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Clorhidrato de pazopanib en el tratamiento de pacientes con tumores carcinoides progresivos

11 de septiembre de 2026 actualizado por: National Cancer Institute (NCI)

Ensayo prospectivo aleatorizado de fase II de pazopanib (NSC n.° 737754) versus placebo en pacientes con tumores carcinoides progresivos

This randomized phase II trial studies how well pazopanib hydrochloride works in treating patients with carcinoid tumors that are growing, spreading, or getting worse. Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Descripción general del estudio

Estado

Activo, no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

PRIMARY OBJECTIVE:

I. For patients with progressive carcinoid tumors, progression-free survival (PFS defined by central review according to Response Evaluation Criteria in Solid Tumors [RECIST] 1.1) will be compared between patients randomized to treatment with pazopanib (pazopanib hydrochloride) versus placebo.

SECONDARY OBJECTIVES:

I. Overall survival (OS) will be compared between treatment arms. II. Objective response rate, duration of response, and time to treatment failure will be compared between treatment arms.

III. Progression free survival (PFS) as assessed by central radiology review and local radiology review will be compared overall and within treatment arms.

IV. Safety and tolerability of treatment with pazopanib/placebo will be evaluated within each treatment arm.

V. PFS and other indicators of efficacy will be estimated in patients who crossover to pazopanib from placebo.

VI. To determine the turn-around time for timely adjudicated central review. VII. To characterize the nature of discordance between local and central radiology review in assessment of progression.

VIII. To characterize the type and rate of progression in carcinoid (at study entry, on-study, and at progression).

IX. To develop new methods for modeling carcinoid growth and detecting treatment effects, and to perform simulations that advance new clinical trial designs to apply to future trials of carcinoid therapeutics.

X. To assess for differences in quality of life (QOL)-related domains between the two treatment groups (pazopanib versus placebo).

XI. To determine if the more brief measures of QOL-related domains provide comparable information to that which is provided by the longer assessments (European Organization for Research and Treatment of Cancer [EORTC], neuroendocrine tumors [NET]21).

XII. To provide validation data for the EORTC NET21 module in terms of responsiveness over time and differences across arms.

XIII. To determine whether components of the plasma angiome panel that have been shown to be predictive previously (interleukin-6 [IL-6] and vascular endothelial growth factor [VEGF]-D) are predictive of a therapeutic advantage for pazopanib treatment in baseline samples from the patients treated on A021202.

XIV. To determine whether other components of the plasma angiome panel tested (not IL-6 and VEGF-D) are predictive of a therapeutic advantage for pazopanib treatment in baseline samples from the patients treated on A021202.

XV. To evaluate the changes in the plasma angiome markers after treatment with or without pazopanib over time.

EXPLORATORY OBJECTIVES:

I. PFS at 6 months will be estimated within each treatment arm. II. Biochemical response (for chromogranin A, defined as a decrease of 50% or more in chromogranin A levels from baseline and for 5-hydroxyindoleacetic acid [5-HIAA], defined as a decrease of 50% or more in urinary 5-HIAA levels from baseline) will be compared between treatment arms among patients with elevated baseline levels of chromogranin A (CGA) and 5-HIAA.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive pazopanib hydrochloride orally (PO) once daily (QD) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo echocardiography (ECHO) or multigated acquisition scan (MUGA) during screening. Patients also undergo computed tomography (CT), magnetic resonance imaging (MRI), and chest x-ray throughout the trial. Patients may optionally undergo blood sample collection during screening and on study.

ARM II: Patients receive placebo PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At the time of progressive disease, patients may cross-over to Arm I. Patients undergo ECHO or MUGA during screening. Patients also undergo CT, MRI, and chest x-ray throughout the trial. Patients may optionally undergo blood sample collection during screening and on study.

After completion of study treatment, patients are followed up every 3-6 months for 5 years.

Tipo de estudio

Intervencionista

Inscripción (Actual)

171

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

  • Canadá
    • Alberta
      • Calgary, Alberta, Canadá, T2N 5G2
        • Arthur J E Child Comprehensive Cancer Centre
    • British Columbia
      • Vancouver, British Columbia, Canadá, V5Z 4E6
        • BCCA-Vancouver Cancer Centre
    • New Brunswick
      • Moncton, New Brunswick, Canadá, E1C 8X3
        • The Vitalite Health Network - Dr Leon Richard Oncology Centre
    • Nova Scotia
      • Halifax, Nova Scotia, Canadá, B3H 2Y9
        • QEII Health Sciences Centre/Nova Scotia Health Authority
    • Ontario
      • Hamilton, Ontario, Canadá, L8V 5C2
        • Juravinski Cancer Centre at Hamilton Health Sciences
      • Kitchener, Ontario, Canadá, N2G 1G3
        • Waterloo Regional Health Network
      • Ottawa, Ontario, Canadá, K1H 8L6
        • Ottawa Hospital and Cancer Center-General Campus
      • Toronto, Ontario, Canadá, M5G 2M9
        • University Health Network-Princess Margaret Hospital
    • Quebec
      • Montreal, Quebec, Canadá, H2X 3E4
        • CHUM - Centre Hospitalier de l'Universite de Montreal
    • Saskatchewan
      • Regina, Saskatchewan, Canadá, S4T 7T1
        • Allan Blair Cancer Centre
      • Saskatoon, Saskatchewan, Canadá, S7N 4H4
        • Saskatoon Cancer Centre
  • Estados Unidos
    • Alaska
      • Anchorage, Alaska, Estados Unidos, 99508
        • Alaska Breast Care and Surgery LLC
      • Anchorage, Alaska, Estados Unidos, 99508
        • Alaska Women's Cancer Care
      • Anchorage, Alaska, Estados Unidos, 99508
        • Anchorage Oncology Centre
      • Anchorage, Alaska, Estados Unidos, 99508
        • Katmai Oncology Group
      • Anchorage, Alaska, Estados Unidos, 99508
        • Providence Alaska Medical Center
    • Arizona
      • Scottsdale, Arizona, Estados Unidos, 85259
        • Mayo Clinic in Arizona
    • California
      • Anaheim, California, Estados Unidos, 92806
        • Kaiser Permanente-Anaheim
      • Baldwin Park, California, Estados Unidos, 91706
        • Kaiser Permanente-Baldwin Park
      • Fontana, California, Estados Unidos, 92335
        • Kaiser Permanente-Fontana
      • Harbor City, California, Estados Unidos, 90710
        • Kaiser Permanente South Bay
      • Irvine, California, Estados Unidos, 92618
        • Kaiser Permanente-Irvine
      • Los Angeles, California, Estados Unidos, 90033
        • USC / Norris Comprehensive Cancer Center
      • Los Angeles, California, Estados Unidos, 90048
        • Cedars-Sinai Medical Center
      • Los Angeles, California, Estados Unidos, 90027
        • Kaiser Permanente Los Angeles Medical Center
      • Los Angeles, California, Estados Unidos, 90034
        • Kaiser Permanente West Los Angeles
      • Los Angeles, California, Estados Unidos, 90033
        • Los Angeles General Medical Center
      • Palo Alto, California, Estados Unidos, 94304
        • Stanford Cancer Institute Palo Alto
      • Palo Alto, California, Estados Unidos, 94301
        • Palo Alto Medical Foundation Health Care
      • Panorama City, California, Estados Unidos, 91402
        • Kaiser Permanente - Panorama City
      • Riverside, California, Estados Unidos, 92505
        • Kaiser Permanente-Riverside
      • San Diego, California, Estados Unidos, 92120
        • Kaiser Permanente-San Diego Zion
      • San Diego, California, Estados Unidos, 92108
        • Kaiser Permanente-Rio San Diego
      • San Francisco, California, Estados Unidos, 94158
        • UCSF Medical Center-Mission Bay
      • San Francisco, California, Estados Unidos, 94115
        • UCSF Medical Center-Mount Zion
      • San Marcos, California, Estados Unidos, 92078
        • Kaiser Permanente-San Marcos
      • Santa Cruz, California, Estados Unidos, 95065
        • Palo Alto Medical Foundation-Santa Cruz
      • Sunnyvale, California, Estados Unidos, 94086
        • Palo Alto Medical Foundation-Sunnyvale
      • Woodland Hills, California, Estados Unidos, 91367
        • Kaiser Permanente-Woodland Hills
    • Colorado
      • Aurora, Colorado, Estados Unidos, 80012
        • The Medical Center of Aurora
      • Boulder, Colorado, Estados Unidos, 80303
        • Boulder Community Foothills Hospital
      • Boulder, Colorado, Estados Unidos, 80304
        • Rocky Mountain Cancer Centers-Boulder
      • Colorado Springs, Colorado, Estados Unidos, 80907
        • Penrose-Saint Francis Healthcare
      • Colorado Springs, Colorado, Estados Unidos, 80907
        • Rocky Mountain Cancer Centers-Penrose
      • Denver, Colorado, Estados Unidos, 80218
        • Presbyterian - Saint Lukes Medical Center - Health One
      • Denver, Colorado, Estados Unidos, 80220
        • Rose Medical Center
      • Denver, Colorado, Estados Unidos, 80218
        • Rocky Mountain Cancer Centers-Midtown
      • Denver, Colorado, Estados Unidos, 80220
        • Rocky Mountain Cancer Centers-Rose
      • Denver, Colorado, Estados Unidos, 80218
        • Colorado Blood Cancer Institute
      • Denver, Colorado, Estados Unidos, 80222
        • Western States Cancer Research NCORP
      • Denver, Colorado, Estados Unidos, 80218
        • Saint Joseph Hospital - Cancer Centers of Colorado
      • Denver, Colorado, Estados Unidos, 80210
        • AdventHealth Porter
      • Durango, Colorado, Estados Unidos, 81301
        • Mercy Medical Center
      • Englewood, Colorado, Estados Unidos, 80113
        • Mountain Blue Cancer Care Center - Swedish
      • Englewood, Colorado, Estados Unidos, 80113
        • Swedish Medical Center
      • Fort Collins, Colorado, Estados Unidos, 80524
        • Poudre Valley Hospital
      • Golden, Colorado, Estados Unidos, 80401
        • Mountain Blue Cancer Care Center
      • Greeley, Colorado, Estados Unidos, 80631
        • Banner North Colorado Medical Center
      • Greenwood Village, Colorado, Estados Unidos, 80111
        • Rocky Mountain Cancer Centers-Greenwood Village
      • Lakewood, Colorado, Estados Unidos, 80228
        • Rocky Mountain Cancer Centers-Lakewood
      • Lakewood, Colorado, Estados Unidos, 80228
        • CommonSpirit Saint Anthony Hospital Cancer Center
      • Littleton, Colorado, Estados Unidos, 80122
        • AdventHealth Littleton
      • Lone Tree, Colorado, Estados Unidos, 80124
        • Sky Ridge Medical Center
      • Lone Tree, Colorado, Estados Unidos, 80124
        • Rocky Mountain Cancer Centers-Sky Ridge
      • Longmont, Colorado, Estados Unidos, 80501
        • Longmont United Hospital
      • Longmont, Colorado, Estados Unidos, 80501
        • Rocky Mountain Cancer Centers-Longmont
      • Loveland, Colorado, Estados Unidos, 80539
        • Banner North Colorado Medical Center - Loveland Campus
      • Parker, Colorado, Estados Unidos, 80138
        • Rocky Mountain Cancer Centers-Parker
      • Parker, Colorado, Estados Unidos, 80138
        • AdventHealth Parker
      • Pueblo, Colorado, Estados Unidos, 81004
        • Saint Mary Corwin Medical Center
      • Pueblo, Colorado, Estados Unidos, 81008
        • Rocky Mountain Cancer Centers - Pueblo
      • Wheat Ridge, Colorado, Estados Unidos, 80401
        • Intermountain Health Lutheran Hospital
    • Connecticut
      • Hartford, Connecticut, Estados Unidos, 06105
        • Smilow Cancer Hospital Care Center at Saint Francis
    • Delaware
      • Lewes, Delaware, Estados Unidos, 19958
        • Beebe Medical Center
      • Newark, Delaware, Estados Unidos, 19713
        • Helen F Graham Cancer Center
      • Newark, Delaware, Estados Unidos, 19713
        • Delaware Clinical and Laboratory Physicians PA
      • Newark, Delaware, Estados Unidos, 19713
        • Medical Oncology Hematology Consultants PA
      • Newark, Delaware, Estados Unidos, 19718
        • Christiana Care Health System-Christiana Hospital
      • Rehoboth Beach, Delaware, Estados Unidos, 19971
        • Beebe Health Campus
      • Seaford, Delaware, Estados Unidos, 19973
        • TidalHealth Nanticoke / Allen Cancer Center
      • Wilmington, Delaware, Estados Unidos, 19801
        • Christiana Care Health System-Wilmington Hospital
    • Florida
      • Tampa, Florida, Estados Unidos, 33612
        • Moffitt Cancer Center
    • Georgia
      • Columbus, Georgia, Estados Unidos, 31904
        • John B Amos Cancer Center
      • Savannah, Georgia, Estados Unidos, 31404
        • Memorial Health University Medical Center
    • Hawaii
      • Honolulu, Hawaii, Estados Unidos, 96813
        • Queen's Medical Center
      • Honolulu, Hawaii, Estados Unidos, 96813
        • Hawaii Cancer Care Inc - Waterfront Plaza
      • Honolulu, Hawaii, Estados Unidos, 96813
        • Straub Clinic and Hospital
      • Honolulu, Hawaii, Estados Unidos, 96813
        • University of Hawaii Cancer Center
      • Honolulu, Hawaii, Estados Unidos, 96817
        • Hawaii Cancer Care Inc-Liliha
      • Honolulu, Hawaii, Estados Unidos, 96817
        • Queen's Cancer Center - Kuakini
      • Honolulu, Hawaii, Estados Unidos, 96826
        • Kapiolani Medical Center for Women and Children
      • Kailua, Hawaii, Estados Unidos, 96734
        • Castle Medical Center
      • Lihue, Hawaii, Estados Unidos, 96766
        • Wilcox Memorial Hospital and Kauai Medical Clinic
      • ‘Aiea, Hawaii, Estados Unidos, 96701
        • Pali Momi Medical Center
      • ‘Aiea, Hawaii, Estados Unidos, 96701
        • Queen's Cancer Center - Pearlridge
    • Idaho
      • Boise, Idaho, Estados Unidos, 83706
        • Saint Alphonsus Cancer Care Center-Boise
      • Post Falls, Idaho, Estados Unidos, 83854
        • Kootenai Clinic Cancer Services - Post Falls
    • Illinois
      • Bloomington, Illinois, Estados Unidos, 61704
        • Illinois CancerCare-Bloomington
      • Canton, Illinois, Estados Unidos, 61520
        • Illinois CancerCare-Canton
      • Carthage, Illinois, Estados Unidos, 62321
        • Illinois CancerCare-Carthage
      • Chicago, Illinois, Estados Unidos, 60611
        • Northwestern University
      • Chicago, Illinois, Estados Unidos, 60637
        • University of Chicago Comprehensive Cancer Center
      • Decatur, Illinois, Estados Unidos, 62526
        • Decatur Memorial Hospital
      • Decatur, Illinois, Estados Unidos, 62526
        • Cancer Care Specialists of Illinois - Decatur
      • Eureka, Illinois, Estados Unidos, 61530
        • Illinois CancerCare-Eureka
      • Galesburg, Illinois, Estados Unidos, 61401
        • Illinois CancerCare-Galesburg
      • Harvey, Illinois, Estados Unidos, 60426
        • Ingalls Memorial Hospital
      • Kewanee, Illinois, Estados Unidos, 61443
        • Illinois CancerCare-Kewanee Clinic
      • Macomb, Illinois, Estados Unidos, 61455
        • Illinois CancerCare-Macomb
      • Maywood, Illinois, Estados Unidos, 60153
        • Loyola University Medical Center
      • Mount Vernon, Illinois, Estados Unidos, 62864
        • SSM Health Good Samaritan
      • Ottawa, Illinois, Estados Unidos, 61350
        • Illinois CancerCare-Ottawa Clinic
      • Pekin, Illinois, Estados Unidos, 61554
        • Illinois CancerCare-Pekin
      • Peoria, Illinois, Estados Unidos, 61615
        • Illinois CancerCare-Peoria
      • Peru, Illinois, Estados Unidos, 61354
        • Illinois CancerCare-Peru
      • Princeton, Illinois, Estados Unidos, 61356
        • Illinois CancerCare-Princeton
    • Indiana
      • Elkhart, Indiana, Estados Unidos, 46515
        • Elkhart General Hospital
      • Elkhart, Indiana, Estados Unidos, 46514
        • Michiana Hematology Oncology PC-Elkhart
      • Elkhart, Indiana, Estados Unidos, 46514-2098
        • Elkhart Clinic
      • Indianapolis, Indiana, Estados Unidos, 46202
        • Indiana University/Melvin and Bren Simon Cancer Center
      • Kokomo, Indiana, Estados Unidos, 46904
        • Community Howard Regional Health
      • La Porte, Indiana, Estados Unidos, 46350
        • IU Health La Porte Hospital
      • Mishawaka, Indiana, Estados Unidos, 46545
        • Michiana Hematology Oncology PC-Mishawaka
      • Mishawaka, Indiana, Estados Unidos, 46545
        • Saint Joseph Regional Medical Center-Mishawaka
      • Plymouth, Indiana, Estados Unidos, 46563
        • Michiana Hematology Oncology PC-Plymouth
      • Richmond, Indiana, Estados Unidos, 47374
        • Reid Health
      • South Bend, Indiana, Estados Unidos, 46601
        • Memorial Hospital of South Bend
      • South Bend, Indiana, Estados Unidos, 46628
        • Northern Indiana Cancer Research Consortium
      • South Bend, Indiana, Estados Unidos, 46617
        • South Bend Clinic
      • Westville, Indiana, Estados Unidos, 46391
        • Michiana Hematology Oncology PC-Westville
    • Iowa
      • Ames, Iowa, Estados Unidos, 50010
        • Mary Greeley Medical Center
      • Ames, Iowa, Estados Unidos, 50010
        • McFarland Clinic - Ames
      • Bettendorf, Iowa, Estados Unidos, 52722
        • University of Iowa Healthcare Cancer Services Quad Cities
      • Boone, Iowa, Estados Unidos, 50036
        • McFarland Clinic - Boone
      • Cedar Rapids, Iowa, Estados Unidos, 52403
        • Mercy Hospital
      • Cedar Rapids, Iowa, Estados Unidos, 52403
        • Oncology Associates at Mercy Medical Center
      • Clive, Iowa, Estados Unidos, 50325
        • Mercy Cancer Center-West Lakes
      • Clive, Iowa, Estados Unidos, 50325
        • UI Health Care Mission Cancer and Blood - West Des Moines Clinic
      • Des Moines, Iowa, Estados Unidos, 50309
        • Iowa Methodist Medical Center
      • Des Moines, Iowa, Estados Unidos, 50314
        • Mercy Medical Center - Des Moines
      • Des Moines, Iowa, Estados Unidos, 50316
        • Iowa Lutheran Hospital
      • Des Moines, Iowa, Estados Unidos, 50309
        • Iowa-Wide Oncology Research Coalition NCORP
      • Des Moines, Iowa, Estados Unidos, 50309
        • UI Health Care Mission Cancer and Blood - Des Moines Clinic
      • Des Moines, Iowa, Estados Unidos, 50314
        • UI Health Care Mission Cancer and Blood - Laurel Clinic
      • Iowa City, Iowa, Estados Unidos, 52242
        • University of Iowa/Holden Comprehensive Cancer Center
      • Jefferson, Iowa, Estados Unidos, 50129
        • McFarland Clinic - Jefferson
      • Marshalltown, Iowa, Estados Unidos, 50158
        • McFarland Clinic - Marshalltown
      • Sioux City, Iowa, Estados Unidos, 51101
        • Siouxland Regional Cancer Center
      • Sioux City, Iowa, Estados Unidos, 51102
        • Mercy Medical Center-Sioux City
      • Sioux City, Iowa, Estados Unidos, 51104
        • Saint Luke's Regional Medical Center
      • West Des Moines, Iowa, Estados Unidos, 50266-7700
        • Methodist West Hospital
      • West Des Moines, Iowa, Estados Unidos, 50266
        • Mercy Medical Center-West Lakes
    • Kansas
      • Emporia, Kansas, Estados Unidos, 66801
        • Newman Regional Health
      • Garden City, Kansas, Estados Unidos, 67846
        • Saint Catherine Hospital
      • Great Bend, Kansas, Estados Unidos, 67530
        • Saint Rose Ambulatory and Surgery Center
      • Hays, Kansas, Estados Unidos, 67601
        • HaysMed
      • Kansas City, Kansas, Estados Unidos, 66160
        • University of Kansas Cancer Center
      • Kansas City, Kansas, Estados Unidos, 66112
        • University of Kansas Cancer Center-West
      • Olathe, Kansas, Estados Unidos, 66061
        • The University of Kansas Cancer Center - Olathe
      • Overland Park, Kansas, Estados Unidos, 66210
        • University of Kansas Cancer Center-Overland Park
      • Overland Park, Kansas, Estados Unidos, 66209
        • Menorah Medical Center
      • Overland Park, Kansas, Estados Unidos, 66213
        • Saint Luke's South Hospital
      • Pittsburg, Kansas, Estados Unidos, 66762
        • Mercy Hospital Pittsburg
      • Prairie Village, Kansas, Estados Unidos, 66208
        • Kansas City NCI Community Oncology Research Program
      • Salina, Kansas, Estados Unidos, 67401
        • Salina Regional Health Center
      • Topeka, Kansas, Estados Unidos, 66606
        • University of Kansas Health System Saint Francis Campus
      • Wichita, Kansas, Estados Unidos, 67214
        • Cancer Center of Kansas - Wichita
    • Kentucky
      • Crestview Hills, Kentucky, Estados Unidos, 41017
        • Oncology Hematology Care Inc-Crestview
      • Elizabethtown, Kentucky, Estados Unidos, 42701
        • Baptist Health Hardin
      • Lexington, Kentucky, Estados Unidos, 40503
        • Baptist Health Lexington
    • Louisiana
      • Baton Rouge, Louisiana, Estados Unidos, 70809
        • Ochsner Health Center-Summa
      • New Orleans, Louisiana, Estados Unidos, 70121
        • Ochsner Medical Center Jefferson
    • Michigan
      • Adrian, Michigan, Estados Unidos, 49221
        • Bixby Medical Center
      • Adrian, Michigan, Estados Unidos, 49221
        • Hickman Cancer Center
      • Ann Arbor, Michigan, Estados Unidos, 48106
        • Michigan Cancer Research Consortium NCORP
      • Ann Arbor, Michigan, Estados Unidos, 48106
        • Trinity Health Saint Joseph Mercy Hospital Ann Arbor
      • Battle Creek, Michigan, Estados Unidos, 49017
        • Bronson Battle Creek
      • Dearborn, Michigan, Estados Unidos, 48124
        • Corewell Health Dearborn Hospital
      • Detroit, Michigan, Estados Unidos, 48236
        • Henry Ford Health Saint John Hospital
      • Escanaba, Michigan, Estados Unidos, 49829
        • OSF Saint Francis Hospital and Medical Group
      • Flint, Michigan, Estados Unidos, 48503
        • Hurley Medical Center
      • Flint, Michigan, Estados Unidos, 48503
        • Genesys Hurley Cancer Institute
      • Grand Rapids, Michigan, Estados Unidos, 49503
        • Cancer Research Consortium of West Michigan NCORP
      • Grand Rapids, Michigan, Estados Unidos, 49503
        • Trinity Health Grand Rapids Hospital
      • Grand Rapids, Michigan, Estados Unidos, 49503
        • Corewell Health Grand Rapids Hospitals - Butterworth Hospital
      • Jackson, Michigan, Estados Unidos, 49201
        • Allegiance Health
      • Lansing, Michigan, Estados Unidos, 48912
        • University of Michigan Health - Sparrow Lansing
      • Livonia, Michigan, Estados Unidos, 48154
        • Trinity Health Saint Mary Mercy Livonia Hospital
      • Monroe, Michigan, Estados Unidos, 48162
        • Mercy Memorial Hospital
      • Monroe, Michigan, Estados Unidos, 48162
        • Toledo Clinic Cancer Centers-Monroe
      • Muskegon, Michigan, Estados Unidos, 49444
        • Trinity Health Muskegon Hospital
      • Niles, Michigan, Estados Unidos, 49120
        • Corewell Health Lakeland Hospitals - Niles Hospital
      • Pontiac, Michigan, Estados Unidos, 48341
        • Trinity Health Saint Joseph Mercy Oakland Hospital
      • Port Huron, Michigan, Estados Unidos, 48060
        • Lake Huron Medical Center
      • Reed City, Michigan, Estados Unidos, 49677
        • Corewell Health Reed City Hospital
      • Saginaw, Michigan, Estados Unidos, 48601
        • MyMichigan Medical Center Saginaw
      • Saint Joseph, Michigan, Estados Unidos, 49085
        • Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center
      • Saint Joseph, Michigan, Estados Unidos, 49085
        • Corewell Health Lakeland Hospitals - Saint Joseph Hospital
      • Traverse City, Michigan, Estados Unidos, 49684
        • Munson Medical Center
      • Warren, Michigan, Estados Unidos, 48093
        • Henry Ford Health Warren Hospital
    • Minnesota
      • Burnsville, Minnesota, Estados Unidos, 55337
        • Fairview Ridges Hospital
      • Coon Rapids, Minnesota, Estados Unidos, 55433
        • Mercy Hospital
      • Duluth, Minnesota, Estados Unidos, 55805
        • Essentia Health Cancer Center
      • Duluth, Minnesota, Estados Unidos, 55805
        • Essentia Health Saint Mary's Medical Center
      • Duluth, Minnesota, Estados Unidos, 55805
        • Miller-Dwan Hospital
      • Edina, Minnesota, Estados Unidos, 55435
        • Fairview Southdale Hospital
      • Fridley, Minnesota, Estados Unidos, 55432
        • Unity Hospital
      • Hutchinson, Minnesota, Estados Unidos, 55350
        • Hutchinson Area Health Care
      • Maplewood, Minnesota, Estados Unidos, 55109
        • Saint John's Hospital - Healtheast
      • Maplewood, Minnesota, Estados Unidos, 55109
        • Minnesota Oncology Hematology PA-Maplewood
      • Minneapolis, Minnesota, Estados Unidos, 55415
        • Hennepin County Medical Center
      • Minneapolis, Minnesota, Estados Unidos, 55407
        • Abbott-Northwestern Hospital
      • Minneapolis, Minnesota, Estados Unidos, 55454
        • Health Partners Inc
      • New Ulm, Minnesota, Estados Unidos, 56073
        • New Ulm Medical Center
      • Robbinsdale, Minnesota, Estados Unidos, 55422
        • North Memorial Medical Health Center
      • Rochester, Minnesota, Estados Unidos, 55905
        • Mayo Clinic in Rochester
      • Saint Louis Park, Minnesota, Estados Unidos, 55416
        • Park Nicollet Clinic - Saint Louis Park
      • Saint Louis Park, Minnesota, Estados Unidos, 55416
        • Metro Minnesota Community Oncology Research Consortium
      • Saint Paul, Minnesota, Estados Unidos, 55101
        • Regions Hospital
      • Saint Paul, Minnesota, Estados Unidos, 55102
        • United Hospital
      • Shakopee, Minnesota, Estados Unidos, 55379
        • Saint Francis Regional Medical Center
      • Stillwater, Minnesota, Estados Unidos, 55082
        • Lakeview Hospital
      • Waconia, Minnesota, Estados Unidos, 55387
        • Ridgeview Medical Center
      • Willmar, Minnesota, Estados Unidos, 56201
        • Rice Memorial Hospital
      • Woodbury, Minnesota, Estados Unidos, 55125
        • Minnesota Oncology Hematology PA-Woodbury
    • Missouri
      • Branson, Missouri, Estados Unidos, 65616
        • Cox Cancer Center Branson
      • Cape Girardeau, Missouri, Estados Unidos, 63703
        • Mercy Cancer Center - Cape Girardeau
      • Columbia, Missouri, Estados Unidos, 65212
        • MU Health - University Hospital/Ellis Fischel Cancer Center
      • Independence, Missouri, Estados Unidos, 64057
        • Centerpoint Medical Center LLC
      • Jefferson City, Missouri, Estados Unidos, 65109
        • MU Health Care Goldschmidt Cancer Center
      • Joplin, Missouri, Estados Unidos, 64804
        • Mercy Hospital Joplin
      • Kansas City, Missouri, Estados Unidos, 64154
        • University of Kansas Cancer Center - North
      • Kansas City, Missouri, Estados Unidos, 64131
        • The University of Kansas Cancer Center-South
      • Kansas City, Missouri, Estados Unidos, 64111
        • Saint Luke's Hospital of Kansas City
      • Kansas City, Missouri, Estados Unidos, 64132
        • Research Medical Center
      • Kansas City, Missouri, Estados Unidos, 64118
        • Heartland Hematology and Oncology Associates Incorporated
      • Kansas City, Missouri, Estados Unidos, 64108
        • University Health Truman Medical Center
      • Lee's Summit, Missouri, Estados Unidos, 64064
        • University of Kansas Cancer Center - Lee's Summit
      • Lee's Summit, Missouri, Estados Unidos, 64086
        • Saint Luke's East - Lee's Summit
      • Liberty, Missouri, Estados Unidos, 64068
        • Liberty Hospital
      • Rolla, Missouri, Estados Unidos, 65401
        • Mercy Clinic-Rolla-Cancer and Hematology
      • Rolla, Missouri, Estados Unidos, 65401
        • Phelps Health Delbert Day Cancer Institute
      • Saint Joseph, Missouri, Estados Unidos, 64506
        • Heartland Regional Medical Center
      • Springfield, Missouri, Estados Unidos, 65804
        • Cancer Research for the Ozarks NCORP
      • Springfield, Missouri, Estados Unidos, 65807
        • CoxHealth South Hospital
      • Springfield, Missouri, Estados Unidos, 65804
        • Mercy Hospital Springfield
      • St Louis, Missouri, Estados Unidos, 63110
        • Washington University School of Medicine
      • St Louis, Missouri, Estados Unidos, 63131
        • Missouri Baptist Medical Center
      • St Louis, Missouri, Estados Unidos, 63109
        • Mercy Infusion Center - Chippewa
      • St Louis, Missouri, Estados Unidos, 63141
        • Mercy Hospital Saint Louis
    • Montana
      • Billings, Montana, Estados Unidos, 59101
        • Billings Clinic Cancer Center
      • Billings, Montana, Estados Unidos, 59101
        • Saint Vincent Healthcare
      • Billings, Montana, Estados Unidos, 59102
        • Montana Cancer Consortium NCORP
      • Bozeman, Montana, Estados Unidos, 59715
        • Bozeman Health Deaconess Hospital
      • Butte, Montana, Estados Unidos, 59701
        • Saint James Community Hospital and Cancer Treatment Center
      • Great Falls, Montana, Estados Unidos, 59405
        • Benefis Sletten Cancer Institute
      • Helena, Montana, Estados Unidos, 59601
        • Saint Peter's Community Hospital
      • Kalispell, Montana, Estados Unidos, 59901
        • Logan Health Medical Center
      • Missoula, Montana, Estados Unidos, 59802
        • Saint Patrick Hospital - Community Hospital
    • Nebraska
      • Lincoln, Nebraska, Estados Unidos, 68510
        • Nebraska Cancer Research Center
      • Omaha, Nebraska, Estados Unidos, 68114
        • Nebraska Methodist Hospital
      • Omaha, Nebraska, Estados Unidos, 68124
        • Alegent Health Bergan Mercy Medical Center
      • Omaha, Nebraska, Estados Unidos, 68122
        • Alegent Health Immanuel Medical Center
      • Omaha, Nebraska, Estados Unidos, 68130
        • Alegent Health Lakeside Hospital
      • Omaha, Nebraska, Estados Unidos, 68106
        • Missouri Valley Cancer Consortium
    • Nevada
      • Henderson, Nevada, Estados Unidos, 89052
        • Comprehensive Cancer Centers of Nevada - Henderson
      • Henderson, Nevada, Estados Unidos, 89052
        • Cancer and Blood Specialists-Henderson
      • Henderson, Nevada, Estados Unidos, 89052
        • Las Vegas Cancer Center-Henderson
      • Henderson, Nevada, Estados Unidos, 89074
        • Comprehensive Cancer Centers of Nevada-Southeast Henderson
      • Henderson, Nevada, Estados Unidos, 89074
        • Oncology Las Vegas - Henderson
      • Las Vegas, Nevada, Estados Unidos, 89106
        • Radiation Oncology Centers of Nevada Central
      • Las Vegas, Nevada, Estados Unidos, 89119
        • Radiation Oncology Centers of Nevada Southeast
      • Las Vegas, Nevada, Estados Unidos, 89128
        • Comprehensive Cancer Centers of Nevada - Northwest
      • Las Vegas, Nevada, Estados Unidos, 89144
        • Comprehensive Cancer Centers of Nevada-Summerlin
      • Las Vegas, Nevada, Estados Unidos, 89148
        • Comprehensive Cancer Centers of Nevada
      • Las Vegas, Nevada, Estados Unidos, 89169
        • Comprehensive Cancer Centers of Nevada - Central Valley
      • Las Vegas, Nevada, Estados Unidos, 89102
        • University Medical Center of Southern Nevada
      • Las Vegas, Nevada, Estados Unidos, 89106
        • Cancer and Blood Specialists-Shadow
      • Las Vegas, Nevada, Estados Unidos, 89109
        • HealthCare Partners Medical Group Oncology/Hematology-Maryland Parkway
      • Las Vegas, Nevada, Estados Unidos, 89113
        • HealthCare Partners Medical Group Oncology/Hematology-San Martin
      • Las Vegas, Nevada, Estados Unidos, 89121
        • Cancer Therapy and Integrative Medicine
      • Las Vegas, Nevada, Estados Unidos, 89128
        • Cancer and Blood Specialists-Tenaya
      • Las Vegas, Nevada, Estados Unidos, 89128
        • HealthCare Partners Medical Group Oncology/Hematology-Tenaya
      • Las Vegas, Nevada, Estados Unidos, 89148-2405
        • Las Vegas Cancer Center-Medical Center
      • Las Vegas, Nevada, Estados Unidos, 89149
        • HealthCare Partners Medical Group Oncology/Hematology-Centennial Hills
      • Las Vegas, Nevada, Estados Unidos, 89120
        • Nevada Cancer Research Foundation NCORP
      • Las Vegas, Nevada, Estados Unidos, 89128
        • Oncology Las Vegas - Tenaya
      • Las Vegas, Nevada, Estados Unidos, 89183
        • OptumCare Cancer Care at Fort Apache
    • New Hampshire
      • Lebanon, New Hampshire, Estados Unidos, 03756
        • Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
    • New Jersey
      • Camden, New Jersey, Estados Unidos, 08103
        • Cooper Hospital University Medical Center
      • New Brunswick, New Jersey, Estados Unidos, 08903
        • Rutgers Cancer Institute of New Jersey
    • New Mexico
      • Albuquerque, New Mexico, Estados Unidos, 87106
        • University of New Mexico Cancer Center
      • Las Cruces, New Mexico, Estados Unidos, 88011
        • Memorial Medical Center-Las Cruces
    • New York
      • Glens Falls, New York, Estados Unidos, 12801
        • Glens Falls Hospital
      • Rochester, New York, Estados Unidos, 14642
        • University of Rochester
      • Syracuse, New York, Estados Unidos, 13210
        • Syracuse Veterans Administration Medical Center
      • The Bronx, New York, Estados Unidos, 10461
        • Montefiore Medical Center-Einstein Campus
      • The Bronx, New York, Estados Unidos, 10467
        • Montefiore Medical Center - Moses Campus
    • North Carolina
      • Chapel Hill, North Carolina, Estados Unidos, 27599
        • UNC Lineberger Comprehensive Cancer Center
      • Goldsboro, North Carolina, Estados Unidos, 27534
        • Wayne Memorial Hospital
      • Hendersonville, North Carolina, Estados Unidos, 28791
        • Margaret R Pardee Memorial Hospital
      • Kinston, North Carolina, Estados Unidos, 28501
        • ECU Health Oncology Kinston
      • Statesville, North Carolina, Estados Unidos, 28677
        • Iredell Memorial Hospital
    • North Dakota
      • Fargo, North Dakota, Estados Unidos, 58103
        • Essentia Health Cancer Center-South University Clinic
    • Ohio
      • Belpre, Ohio, Estados Unidos, 45714
        • Strecker Cancer Center-Belpre
      • Bowling Green, Ohio, Estados Unidos, 43402
        • Toledo Clinic Cancer Centers-Bowling Green
      • Chillicothe, Ohio, Estados Unidos, 45601
        • Adena Regional Medical Center
      • Cincinnati, Ohio, Estados Unidos, 45242
        • Oncology Hematology Care Inc-Blue Ash
      • Cincinnati, Ohio, Estados Unidos, 45202
        • Oncology Hematology Care Inc-Eden Park
      • Cincinnati, Ohio, Estados Unidos, 45211
        • Oncology Hematology Care Inc-Mercy West
      • Cincinnati, Ohio, Estados Unidos, 45230
        • Oncology Hematology Care Inc-Anderson
      • Cincinnati, Ohio, Estados Unidos, 45236
        • Oncology Hematology Care Inc-Kenwood
      • Cleveland, Ohio, Estados Unidos, 44106
        • Case Western Reserve University
      • Columbus, Ohio, Estados Unidos, 43214
        • Riverside Methodist Hospital
      • Columbus, Ohio, Estados Unidos, 43210
        • Ohio State University Comprehensive Cancer Center
      • Columbus, Ohio, Estados Unidos, 43219
        • The Mark H Zangmeister Center
      • Columbus, Ohio, Estados Unidos, 43214
        • Columbus Oncology and Hematology Associates Inc
      • Columbus, Ohio, Estados Unidos, 43228
        • Doctors Hospital
      • Columbus, Ohio, Estados Unidos, 43215
        • Grant Medical Center
      • Columbus, Ohio, Estados Unidos, 43222
        • Mount Carmel Health Center West
      • Columbus, Ohio, Estados Unidos, 43215
        • Columbus NCI Community Oncology Research Program
      • Dayton, Ohio, Estados Unidos, 45406
        • Good Samaritan Hospital - Dayton
      • Dayton, Ohio, Estados Unidos, 45409
        • Miami Valley Hospital
      • Dayton, Ohio, Estados Unidos, 45415
        • Miami Valley Hospital North
      • Dayton, Ohio, Estados Unidos, 45459
        • Dayton NCI Community Oncology Research Program
      • Delaware, Ohio, Estados Unidos, 43015
        • Delaware Health Center-Grady Cancer Center
      • Delaware, Ohio, Estados Unidos, 43015
        • Delaware Radiation Oncology
      • Delaware, Ohio, Estados Unidos, 43015
        • Grady Memorial Hospital
      • Fairfield, Ohio, Estados Unidos, 45014
        • Oncology Hematology Care Inc-Healthplex
      • Findlay, Ohio, Estados Unidos, 45840
        • Blanchard Valley Hospital
      • Franklin, Ohio, Estados Unidos, 45005-1066
        • Atrium Medical Center-Middletown Regional Hospital
      • Greenville, Ohio, Estados Unidos, 45331
        • Wayne Hospital
      • Kettering, Ohio, Estados Unidos, 45429
        • Kettering Medical Center
      • Lancaster, Ohio, Estados Unidos, 43130
        • Fairfield Medical Center
      • Lancaster, Ohio, Estados Unidos, 43130
        • Lancaster Radiation Oncology
      • Lima, Ohio, Estados Unidos, 45804
        • Lima Memorial Hospital
      • Marietta, Ohio, Estados Unidos, 45750
        • Marietta Memorial Hospital
      • Maumee, Ohio, Estados Unidos, 43537
        • Toledo Clinic Cancer Centers-Maumee
      • Maumee, Ohio, Estados Unidos, 43537
        • Toledo Radiation Oncology at Northwest Ohio Onocolgy Center
      • Mount Vernon, Ohio, Estados Unidos, 43050
        • Knox Community Hospital
      • Newark, Ohio, Estados Unidos, 43055
        • Licking Memorial Hospital
      • Newark, Ohio, Estados Unidos, 43055
        • Newark Radiation Oncology
      • Oregon, Ohio, Estados Unidos, 43616
        • Saint Charles Hospital
      • Oregon, Ohio, Estados Unidos, 43616
        • Toledo Clinic Cancer Centers-Oregon
      • Portsmouth, Ohio, Estados Unidos, 45662
        • Southern Ohio Medical Center
      • Springfield, Ohio, Estados Unidos, 45504
        • Springfield Regional Medical Center
      • Sylvania, Ohio, Estados Unidos, 43560
        • ProMedica Flower Hospital
      • Tiffin, Ohio, Estados Unidos, 44883
        • Mercy Hospital of Tiffin
      • Toledo, Ohio, Estados Unidos, 43623
        • Mercy Health - Saint Anne Hospital
      • Toledo, Ohio, Estados Unidos, 43623
        • Toledo Clinic Cancer Centers-Toledo
      • Toledo, Ohio, Estados Unidos, 43614
        • University of Toledo
      • Toledo, Ohio, Estados Unidos, 43617
        • Toledo Community Hospital Oncology Program CCOP
      • Toledo, Ohio, Estados Unidos, 43608
        • Mercy Health - Saint Vincent Hospital
      • Troy, Ohio, Estados Unidos, 45373
        • Upper Valley Medical Center
      • Wauseon, Ohio, Estados Unidos, 43567
        • Fulton County Health Center
      • Westerville, Ohio, Estados Unidos, 43081
        • Saint Ann's Hospital
      • Zanesville, Ohio, Estados Unidos, 43701
        • Genesis Healthcare System Cancer Care Center
    • Oklahoma
      • Lawton, Oklahoma, Estados Unidos, 73505
        • Cancer Centers of Southwest Oklahoma Research
      • Oklahoma City, Oklahoma, Estados Unidos, 73104
        • University of Oklahoma Health Sciences Center
      • Tulsa, Oklahoma, Estados Unidos, 74146
        • Oklahoma Cancer Specialists and Research Institute-Tulsa
    • Oregon
      • Clackamas, Oregon, Estados Unidos, 97015
        • Clackamas Radiation Oncology Center
      • Milwaukie, Oregon, Estados Unidos, 97222
        • Providence Milwaukie Hospital
      • Newberg, Oregon, Estados Unidos, 97132
        • Providence Newberg Medical Center
      • Oregon City, Oregon, Estados Unidos, 97045
        • Providence Willamette Falls Medical Center
      • Portland, Oregon, Estados Unidos, 97213
        • Providence Portland Medical Center
      • Portland, Oregon, Estados Unidos, 97225
        • Providence Saint Vincent Medical Center
    • Pennsylvania
      • Bethlehem, Pennsylvania, Estados Unidos, 18015
        • Saint Luke's University Hospital-Bethlehem Campus
      • Danville, Pennsylvania, Estados Unidos, 17822
        • Geisinger Medical Center
      • Hazleton, Pennsylvania, Estados Unidos, 18201
        • Geisinger Medical Center-Cancer Center Hazleton
      • Sayre, Pennsylvania, Estados Unidos, 18840
        • Guthrie Medical Group PC-Robert Packer Hospital
      • State College, Pennsylvania, Estados Unidos, 16801
        • Geisinger Medical Group
      • Wilkes-Barre, Pennsylvania, Estados Unidos, 18711
        • Geisinger Wyoming Valley/Henry Cancer Center
      • Williamsport, Pennsylvania, Estados Unidos, 17701
        • UPMC Susquehanna
    • South Carolina
      • Boiling Springs, South Carolina, Estados Unidos, 29316
        • Prisma Health Cancer Institute - Spartanburg
      • Florence, South Carolina, Estados Unidos, 29506
        • McLeod Regional Medical Center
      • Greenville, South Carolina, Estados Unidos, 29605
        • Prisma Health Cancer Institute - Faris
      • Greenville, South Carolina, Estados Unidos, 29615
        • Prisma Health Cancer Institute - Eastside
      • Greenville, South Carolina, Estados Unidos, 29605
        • Prisma Health Cancer Institute - Butternut
      • Greenville, South Carolina, Estados Unidos, 29605
        • Prisma Health Greenville Memorial Hospital
      • Greer, South Carolina, Estados Unidos, 29650
        • Prisma Health Cancer Institute - Greer
      • Seneca, South Carolina, Estados Unidos, 29672
        • Prisma Health Cancer Institute - Seneca
    • South Dakota
      • Rapid City, South Dakota, Estados Unidos, 57701
        • Rapid City Regional Hospital
    • Texas
      • Dallas, Texas, Estados Unidos, 75246
        • Baylor University Medical Center
      • Houston, Texas, Estados Unidos, 77030
        • Houston Methodist Hospital
      • San Antonio, Texas, Estados Unidos, 78229
        • University of Texas Health Science Center at San Antonio
    • Utah
      • American Fork, Utah, Estados Unidos, 84003
        • American Fork Hospital / Huntsman Intermountain Cancer Center
      • Cedar City, Utah, Estados Unidos, 84720
        • Sandra L Maxwell Cancer Center
      • Logan, Utah, Estados Unidos, 84321
        • Logan Regional Hospital
      • Murray, Utah, Estados Unidos, 84107
        • Intermountain Medical Center
      • Ogden, Utah, Estados Unidos, 84403
        • McKay-Dee Hospital Center
      • Provo, Utah, Estados Unidos, 84604
        • Utah Valley Regional Medical Center
      • Salt Lake City, Utah, Estados Unidos, 84106
        • Utah Cancer Specialists-Salt Lake City
      • Salt Lake City, Utah, Estados Unidos, 84143
        • LDS Hospital
      • St. George, Utah, Estados Unidos, 84770
        • Saint George Regional Medical Center
    • Vermont
      • Bennington, Vermont, Estados Unidos, 05201
        • Southwestern Vermont Medical Center
    • Virginia
      • Fredericksburg, Virginia, Estados Unidos, 22401
        • Fredericksburg Oncology Inc
    • Washington
      • Vancouver, Washington, Estados Unidos, 98664
        • PeaceHealth Southwest Medical Center
      • Vancouver, Washington, Estados Unidos, 98684
        • Compass Oncology Vancouver
    • West Virginia
      • Huntington, West Virginia, Estados Unidos, 25701
        • Edwards Comprehensive Cancer Center
    • Wisconsin
      • Chippewa Falls, Wisconsin, Estados Unidos, 54729
        • Marshfield Clinic-Chippewa Center
      • Eau Claire, Wisconsin, Estados Unidos, 54701
        • HSHS Sacred Heart Hospital
      • Eau Claire, Wisconsin, Estados Unidos, 54701
        • Marshfield Clinic Cancer Center at Sacred Heart
      • Green Bay, Wisconsin, Estados Unidos, 54301
        • Saint Vincent Hospital Cancer Center Green Bay
      • Green Bay, Wisconsin, Estados Unidos, 54303
        • Saint Vincent Hospital Cancer Center at Saint Mary's
      • Green Bay, Wisconsin, Estados Unidos, 54301-3526
        • Green Bay Oncology at Saint Vincent Hospital
      • Madison, Wisconsin, Estados Unidos, 53792
        • University of Wisconsin Carbone Cancer Center - University Hospital
      • Manitowoc, Wisconsin, Estados Unidos, 54221
        • Holy Family Memorial Hospital
      • Marshfield, Wisconsin, Estados Unidos, 54449
        • Marshfield Medical Center-Marshfield
      • Marshfield, Wisconsin, Estados Unidos, 54449
        • Marshfield Medical Center
      • Milwaukee, Wisconsin, Estados Unidos, 53226
        • Medical College of Wisconsin
      • Minocqua, Wisconsin, Estados Unidos, 54548
        • Marshfield Medical Center - Minocqua
      • New Richmond, Wisconsin, Estados Unidos, 54017
        • Cancer Center of Western Wisconsin
      • Oconto Falls, Wisconsin, Estados Unidos, 54154
        • Saint Vincent Hospital Cancer Center at Oconto Falls
      • Rhinelander, Wisconsin, Estados Unidos, 54501
        • Saint Mary's Hospital
      • Rhinelander, Wisconsin, Estados Unidos, 54501
        • Aspirus Cancer Care-Rhinelander-James Beck Cancer Center
      • Rice Lake, Wisconsin, Estados Unidos, 54868
        • Marshfield Medical Center-Rice Lake
      • Sheboygan, Wisconsin, Estados Unidos, 53081
        • HSHS Saint Nicholas Hospital
      • Stevens Point, Wisconsin, Estados Unidos, 54481
        • Aspirus Cancer Care - Stevens Point
      • Wausau, Wisconsin, Estados Unidos, 54401
        • Marshfield Clinic-Wausau Center
      • Weston, Wisconsin, Estados Unidos, 54476
        • Marshfield Medical Center - Weston
      • Wisconsin Rapids, Wisconsin, Estados Unidos, 54494
        • Marshfield Clinic - Wisconsin Rapids Center
    • Wyoming
      • Casper, Wyoming, Estados Unidos, 82609
        • Rocky Mountain Oncology
      • Sheridan, Wyoming, Estados Unidos, 82801
        • Welch Cancer Center

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Low- or intermediate-grade neuroendocrine carcinoma, including the following subtypes: carcinoid tumor, low- to intermediate-grade or well- to moderately-differentiated neuroendocrine carcinoma or tumor, atypical carcinoid tumor; documentation from a primary tumor or metastatic site is sufficient; patients with poorly differentiated neuroendocrine carcinoma, high-grade neuroendocrine carcinoma, adenocarcinoid tumor, or goblet cell carcinoid tumor are not eligible

  • Locally unresectable or metastatic carcinoid tumors

  • Patients must have histologic documentation or clinical evidence of a carcinoid tumor of primary site (including foregut, midgut, hindgut or other non-pancreatic site); tumors of unknown primary site are eligible provided the treating physician does not suspect medullary thyroid cancer, pancreatic neuroendocrine tumor, paraganglioma, or pheochromocytoma; unknown primary tumors will be classified as small bowel tumors for the purpose of stratification; functional (associated with a clinical syndrome) or nonfunctional tumors are allowed; target lesions must have shown disease progression if therapy included peptide receptor radiotherapy (PRRT) and PRRT must be completed at least 8 weeks prior to registration

  • Radiological evidence for progressive disease (measurable or non-measurable) within 12 months prior to registration; patients who have received anti-tumor therapy during the past 12 months (including octreotide analogs) must have had radiological documentation of progression of disease while on or after receiving therapy

  • No known endobronchial lesions and/or lesions infiltrating major pulmonary vessels that increase the risk of pulmonary hemorrhage; patients with lesions infiltrating major pulmonary vessels (contiguous tumor and vessels) are excluded; however, the presence of a tumor that is touching, but not infiltrating (abutting) the vessels is acceptable (computed tomography [CT] with contrast is strongly recommended to evaluate such lesions); patients with large protruding endobronchial lesions in the main or lobar bronchi are excluded; however, endobronchial lesions in the segmented bronchi are allowed

  • Patients must have measurable disease per RECIST 1.1 by computed tomography (CT) scan or magnetic resonance imaging (MRI); lesions must be accurately measured in at least one dimension (longest diameter to be recorded) as >= 1 cm with CT or MRI (or >= 1.5 cm for lymph nodes); index lesions for the purpose of RECIST 1.1 measurements will not be selected from within the radiation therapy treatment field; however, if there is evidence of disease progression within the radiation treatment field, measurement of the progressing lesions will be documented

  • No prior treatment with an inhibitor of vascular endothelial growth factor (VEGF) or vascular endothelial growth factor receptor (VEGFR)

  • Prior treatment (somatostatin analogs excepted) must be completed at least 2 weeks prior to registration; in addition, prior treatment (somatostatin analogs excepted) must be completed at least 4 weeks prior to initiation of study drug; treatment-related toxicities must have improved to =< grade 1 prior to registration, with the exception of alopecia

  • Concurrent use of somatostatin analogs (SSTa) is allowed, provided that the patient is on a stable dose for at least two months and progressive disease on somatostatin analog has been documented; progression on octreotide is required for patients with tumors arising in the midgut

  • Prior treatment with embolization (including bland embolization, chemoembolization, and selective internal radiation therapy) or ablative therapies is allowed if measurable disease remains outside of the treated area or there is documented disease progression in a treated site; there is no limit on the prior number of procedures; prior liver-directed or other ablative treatment must be completed at least 8 weeks prior to registration; index lesions for the purpose of RECIST 1.1 measurements will not be selected from within the radiation therapy treatment field; however, if there is evidence of disease progression within the radiation treatment field, measurement of the progressing lesions will be documented

  • Patients should have completed any major surgery >= 4 weeks prior to registration and must have completed any minor surgery >= 2 weeks prior to registration; patients must have fully recovered from the procedure

    • The following are examples of procedures considered to be minor: port placement, laparoscopy, thoracoscopy, bronchoscopy, mediastinoscopy, skin biopsies, incisional biopsies, imaging-guided biopsy for diagnostic purposes, and dental extraction procedures
    • Insertion of a vascular access device, thoracentesis, paracentesis, and endoscopic ultrasonographic procedures are not considered to be major or minor surgeries

  • No concurrent condition resulting in immune compromise, including chronic treatment with corticosteroids or other immunosuppressive agents

  • No clinical evidence of central nervous system (CNS) metastases (including carcinomatous meningitis) at baseline, with the exception of those patients who have previously-treated CNS metastases (surgery +/- radiotherapy, radiosurgery, or gamma knife) and who meet both of the following criteria: a) are asymptomatic and b) had no requirement for steroids or enzyme-inducing anticonvulsants within 6 months prior to registration

  • No history of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 28 days prior to registration

  • No clinically significant gastrointestinal abnormalities that may increase the risk for gastrointestinal bleeding within 28 days prior to registration including, but not limited to:

    • Active peptic ulcer
    • Known endoluminal metastatic lesion(s) with history of bleeding
    • Inflammatory bowel disease (e.g. ulcerative colitis, Crohn's disease), or other gastrointestinal conditions with increased risk of perforation

  • No history of serious (i.e., requiring active medical therapy with medication or medical device under the supervision of a physician) non-healing wound, ulcer, trauma, or bone fracture within 28 days prior to study entry

  • Patients with a history of hypertension must have blood pressure that is adequately controlled on antihypertensives; (< 140/90 mm Hg)

  • No symptomatic congestive heart failure (New York Heart Association class II, III, or IV) within 6 months prior to registration

  • No arterial thrombotic events within 6 months of registration, including transient ischemic attack (TIA), cerebrovascular accident (CVA), peripheral arterial thrombus, myocardial infarction (MI), or unstable angina or angina requiring surgical or medical intervention in 6 months prior to registration; patients with clinically significant peripheral artery disease (i.e., claudication on less than one block) are ineligible; patients who have experienced a deep venous thrombosis or pulmonary embolus within 6 months prior to registration must be on stable therapeutic anticoagulation for at least 6 weeks prior to enrollment of this study

  • Patients on therapeutic anticoagulation with low molecular weight heparins, fondaparinux, rivaroxaban or warfarin are eligible, provided that they are on a stable dose of anticoagulants; patients who are currently receiving antiplatelet therapy of prasugrel or clopidogrel or antiaggregation agents (e.g., eptifibatide, epoprostenol, dipyridamole) or low doses of acetylsalicylic acid (up to 100 mg daily) are also eligible

  • No ongoing cardiac dysrhythmias, atrial fibrillation, or prolongation of corrected QT (QTc) interval to > 480 msec

  • No evidence of active bleeding, bleeding diathesis, or hemoptysis (>= 1/2 teaspoon of red blood) within 8 weeks prior to registration

  • No currently unstable angina and/or uncontrolled cardiac arrhythmias

  • Patients with symptomatic peripheral vascular disease are ineligible

  • Ejection fraction on echocardiogram (Echo) or multi gated acquisition scan (MUGA) > 50%

  • Chronic concomitant treatment with strong inhibitors of cytochrome P450, family 3, subfamily A, polypeptide 4 (CYP3A4) is not allowed on this trial; patients on strong CYP3A4 inhibitors must discontinue the drug 14 days prior to the start of study treatment

  • Women must not be pregnant or nursing; women of child bearing potential must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]) within 72 hours prior to registration; women of child-bearing potential include any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy, bilateral tubal ligation or bilateral oophorectomy) or is not postmenopausal (defined as amenorrhea >= 12 consecutive months; or women on hormone replacement therapy [HRT] with documented serum follicle stimulating hormone [FSH] level > 35 mIU/mL)

  • Age >= 18 years of age

  • Eastern Cooperative Oncology Group (ECOG) performance status 0-1

  • Granulocytes >= 1,500/mcL

  • Platelets >= 100,000/mcL

  • International normalized ratio (INR) =< 1.2 X upper limit of normal (ULN); only required for patients receiving anticoagulant therapy; patients are eligible if their INR is stable and within the recommended range for the desired level of anticoagulation

  • QTc =< 480 msecs

  • Thyroid stimulating hormone (TSH) within normal limits (WNL); medications for thyroid dysfunction are allowed as long as TSH is normal at registration; in patients with abnormal TSH, if the free thyroxine (free T4) and free thyroxine index (FTI) are normal and patient is clinically euthyroid, patient is eligible

  • Bilirubin =< 1.5 x ULN

  • Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) & alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 x ULN; concomitant elevations in bilirubin and AST/ALT above 1.0 X ULN are NOT permitted; also, if liver metastases are present, AST & ALT =< 5 x ULN is allowed

  • Serum creatinine =< 1.5 x ULN

  • Urine protein to creatinine ratio < 1, or, 24-hour urine protein < 1 g; if urine protein to creatinine (UPC) >= 1, then a 24-hour urine protein must be assessed; patients must have a 24-hour urine protein value < 1 g to be eligible; use of urine dipstick for renal function assessment is not acceptable

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Arm I (pazopanib hydrochloride)

Patients receive pazopanib hydrochloride PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO or MUGA during screening. Patients also undergo CT, MRI, and chest x-ray throughout the trial. Patients may optionally undergo blood sample collection during screening and on study.
Otro: Laboratory Biomarker Analysis

Correlative studies

Otro: Quality-of-Life Assessment

Ancillary studies

Otros nombres:
  • Evaluación de la calidad de vida
Procedimiento: Biospecimen Collection

Undergo blood sample collection

Otros nombres:
  • Recolección de muestras biológicas
  • Muestra biológica recolectada
  • Coleccion de especimenes
  • Recolección de muestras
Procedimiento: Computed Tomography

Undergo CT

Otros nombres:
  • Connecticut
  • GATO
  • Análisis de gato
  • Tomografía Axial Computarizada
  • Tomografía axial computarizada
  • Tomografía computarizada
  • tomografía
  • Tomografía axial computarizada (procedimiento)
  • Tomografía computarizada (TC)
  • Escaneo de gato de diagnóstico
  • Tipo de servicio de escaneo de gato de diagnóstico
Procedimiento: Magnetic Resonance Imaging

Undergo MRI

Otros nombres:
  • Resonancia magnética
  • Resonancia magnetica
  • Exploración de imágenes por resonancia magnética
  • Imágenes Médicas, Resonancia Magnética / Resonancia Magnética Nuclear
  • SRES
  • Imágenes de RM
  • Imágenes de RMN
  • RMN
  • Imágenes de resonancia magnética nuclear
  • Imágenes por resonancia magnética (IRM)
  • resonancia magnética nuclear
  • Imágenes por resonancia magnética (procedimiento)
  • Resonancias magnéticas
  • Resonancia magnética estructural
Droga: Pazopanib Hydrochloride

Given PO

Otros nombres:
  • GW786034B
  • Votriente
  • Pazopater
  • GW 786034B
  • GW-786034B
Procedimiento: Echocardiography Test

Undergo ECHO

Otros nombres:
  • Ecocardiografía
  • CE
Procedimiento: Multigated Acquisition Scan

Undergo MUGA

Otros nombres:
  • Exploración de la piscina de sangre
  • Angiografía con radionúclidos de equilibrio
  • Imagen de piscina de sangre cerrada
  • MUGA
  • Ventriculografía con radionúclidos
  • RNVG
  • Escaneo SIMA
  • Escaneo de adquisición sincronizado de múltiples puertas
  • Escaneo MUGA
  • Escaneo de adquisición de puertas múltiples
  • Exploración de ventriculograma con radionúclidos
  • Escaneo de grupo de corazón cerrado
  • Escaneo RNV
Procedimiento: X-Ray Imaging

Undergo chest x-ray

Otros nombres:
  • Radiografía convencional
  • Radiología diagnóstica
  • Imágenes médicas, rayos X
  • Imágenes radiográficas
  • Radiografía
  • RG
  • Rayos X estáticos
  • Radiografías simples
  • Procedimiento de imágenes radiográficas (procedimiento)
Comparador de placebos: Arm II (placebo)

Patients receive placebo PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At the time of progressive disease, patients may cross-over to Arm I. Patients undergo ECHO or MUGA during screening. Patients also undergo CT, MRI, and chest x-ray throughout the trial. Patients may optionally undergo blood sample collection during screening and on study.
Otro: Laboratory Biomarker Analysis

Correlative studies

Otro: Quality-of-Life Assessment

Ancillary studies

Otros nombres:
  • Evaluación de la calidad de vida
Procedimiento: Biospecimen Collection

Undergo blood sample collection

Otros nombres:
  • Recolección de muestras biológicas
  • Muestra biológica recolectada
  • Coleccion de especimenes
  • Recolección de muestras
Procedimiento: Computed Tomography

Undergo CT

Otros nombres:
  • Connecticut
  • GATO
  • Análisis de gato
  • Tomografía Axial Computarizada
  • Tomografía axial computarizada
  • Tomografía computarizada
  • tomografía
  • Tomografía axial computarizada (procedimiento)
  • Tomografía computarizada (TC)
  • Escaneo de gato de diagnóstico
  • Tipo de servicio de escaneo de gato de diagnóstico
Procedimiento: Magnetic Resonance Imaging

Undergo MRI

Otros nombres:
  • Resonancia magnética
  • Resonancia magnetica
  • Exploración de imágenes por resonancia magnética
  • Imágenes Médicas, Resonancia Magnética / Resonancia Magnética Nuclear
  • SRES
  • Imágenes de RM
  • Imágenes de RMN
  • RMN
  • Imágenes de resonancia magnética nuclear
  • Imágenes por resonancia magnética (IRM)
  • resonancia magnética nuclear
  • Imágenes por resonancia magnética (procedimiento)
  • Resonancias magnéticas
  • Resonancia magnética estructural
Otro: Placebo Administration

Given PO

Procedimiento: Echocardiography Test

Undergo ECHO

Otros nombres:
  • Ecocardiografía
  • CE
Procedimiento: Multigated Acquisition Scan

Undergo MUGA

Otros nombres:
  • Exploración de la piscina de sangre
  • Angiografía con radionúclidos de equilibrio
  • Imagen de piscina de sangre cerrada
  • MUGA
  • Ventriculografía con radionúclidos
  • RNVG
  • Escaneo SIMA
  • Escaneo de adquisición sincronizado de múltiples puertas
  • Escaneo MUGA
  • Escaneo de adquisición de puertas múltiples
  • Exploración de ventriculograma con radionúclidos
  • Escaneo de grupo de corazón cerrado
  • Escaneo RNV
Procedimiento: X-Ray Imaging

Undergo chest x-ray

Otros nombres:
  • Radiografía convencional
  • Radiología diagnóstica
  • Imágenes médicas, rayos X
  • Imágenes radiográficas
  • Radiografía
  • RG
  • Rayos X estáticos
  • Radiografías simples
  • Procedimiento de imágenes radiográficas (procedimiento)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Progression-free Survival (PFS)
Periodo de tiempo: From date of patient entry until documented progression of disease or death from any cause, assessed up to 5 years

PFS will be measured from date of patient entry until documented progression of disease as determined by central review or death from any cause. If a patient does not have a documented date of progression or death, then PFS will be censored at the date of last adequate assessment. PFS will be estimated within treatment arm using the Kaplan-Meier method. Progression is defined as any new lesion or increase by ≥20% of previously involved sites from nadir based on RECIST criteria.
From date of patient entry until documented progression of disease or death from any cause, assessed up to 5 years

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Best Response
Periodo de tiempo: Up to 5 years

The best response per RECIST 1.1 criteria of participants receiving randomized treatment assignment. Complete response (CR): Disappearance of all evidence of disease, Partial response (PR): Regression of measurable disease and no new sites, Stable disease (SD): Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as references the smallest sum diameters while on study. Progressive disease (PD): Any new lesion or increase by ≥20% of previously involved sites from nadir. Note that those considered evaluable for best response here were those who had disease measurements while on treatment. Those who discontinued therapy early prior to a disease evaluation were not included.
Up to 5 years
Overall Survival
Periodo de tiempo: From randomization until death from any cause, assessed up to 5 years

Overall survival (OS) will be measured from randomization until death from any cause. A patient who is alive at the time of the statistical analysis will be considered censored at the last date of known contact. OS will be estimated by the Kaplan-Meier method within each treatment arm.
From randomization until death from any cause, assessed up to 5 years
Duration of Response for the Subset of Patients With a Confirmed Complete Response or Partial Response
Periodo de tiempo: From first documented evidence of complete response or partial response until first documented disease progression or death from any cause, assessed up to 5 years

Duration of response is defined as the time from documented response to time of progression and/or death. This time-to-event outcome will be summarized descriptively using the methods of Kaplan and Meier to characterize the cohort and distribution of this outcome.
From first documented evidence of complete response or partial response until first documented disease progression or death from any cause, assessed up to 5 years
Time to Treatment Failure
Periodo de tiempo: From randomization until termination of protocol therapy for any reason including progression of disease, adverse events, and death, assessed up to 5 years

Time to treatment failure is defined as the time from randomization to the time that treatment is terminated, including the reasons of disease progression, adverse events, withdrawal from study, or death. This time-to-event outcome will be evaluated using the methods of Kaplan and Meier.
From randomization until termination of protocol therapy for any reason including progression of disease, adverse events, and death, assessed up to 5 years

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Time to Second Progression for Patients Who Crossover From Placebo to Active Therapy
Periodo de tiempo: Up to 5 years

Time to second progression will be defined as the progression free survival from crossover re-registration to documented progression of disease as determined by central review or death from any cause. If a patient does not have a documented date of progression or death, then PFS will be censored at the date of last adequate assessment. PFS will be estimated within treatment arm using the Kaplan-Meier method. Progression is defined as any new lesion or increase by ≥20% of previously involved sites from nadir based on RECIST criteria.
Up to 5 years
PFS Within Each Arm
Periodo de tiempo: At 6 months

Kaplan-Meier methods will be used including calculations of 95% confidence intervals.
At 6 months
Biochemical Response
Periodo de tiempo: Up to 5 years

Biochemical response (for chromogranin A, defined as a decrease of 50% or more in chromogranin A levels from baseline, and for 5-hydroxyindoleacetic acid [5-HIAA], defined as a decrease of 50% or more in urinary 5-HIAA levels from baseline) will be compared between treatment arms among patients with elevated baseline levels of serum chromogranin A (CGA) and 5-HIAA.
Up to 5 years

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

National Cancer Institute (NCI)

Investigadores

  • Investigador principal: Emily K Bergsland, Alliance for Clinical Trials in Oncology

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

20 de septiembre de 2013

Finalización primaria (Actual)

5 de marzo de 2019

Finalización del estudio (Estimado)

10 de septiembre de 2027

Fechas de registro del estudio

Enviado por primera vez

24 de abril de 2013

Primero enviado que cumplió con los criterios de control de calidad

24 de abril de 2013

Publicado por primera vez (Estimado)

26 de abril de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de octubre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

11 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • NCI-2013-00831
  • U10CA180821 (Subvención/contrato del NIH de EE. UU.)
  • U10CA180830 (Subvención/contrato del NIH de EE. UU.)
  • U10CA031946 (Subvención/contrato del NIH de EE. UU.)
  • NCI-2013-00831 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
  • ALLIANCE A021202
  • CALGB-A021202
  • A021202 (Otro identificador: CTEP)
  • A021202 (Otro identificador: Alliance for Clinical Trials in Oncology)

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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