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Bevacizumab and Sorafenib as First-Line Therapy in Treating Patients With Locally Advanced or Metastatic Liver Cancer

23. mars 2022 oppdatert av: Alliance for Clinical Trials in Oncology

Phase I/II Randomized Trial of Sorafenib and Bevacizumab as First-Line Therapy in Patients With Locally Advanced or Metastatic Hepatocellular Carcinoma

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab and sorafenib may also stop the growth of liver cancer by blocking blood flow to the tumor.

PURPOSE: This randomized phase I/II trial is studying the best dose of bevacizumab when given together with sorafenib as first-line therapy in treating patients with locally advanced or metastatic liver cancer.(Phase I closed to accrual as of 11/03/2010)

Studieoversikt

Status

Fullført

Forhold

Leverkreft

Intervensjon / Behandling

Detaljert beskrivelse

OBJECTIVES:

Primary

Determine the maximum tolerated dose of bevacizumab in combination with sorafenib tosylate in patients with locally advanced or metastatic hepatocellular carcinoma. (Phase I closed to accrual as of 11/03/2010)
Determine time to progression in these patients. (Phase II)

Secondary

Determine the safety of this regimen in these patients. (Phase I closed to accrual as of 11/03/2010)
Assess tolerability of this regimen in these patients. (Phase I closed to accrual as of 11/03/2010)
Determine overall survival of these patients. (Phase II)
Determine tumor response (at 6 months) in patients treated with this regimen. (Phase II)
Determine progression-free survival of these patients. (Phase II)
Determine response rate in patients treated with this regimen. (Phase II)
Assess the occurrence of adverse events in these patients. (Phase II)

Tertiary

Determine the relationship between tumor biomarkers and circulating biomarkers of vascular response and clinical outcome in patients treated with this regimen.

OUTLINE: This is a phase I, dose escalation study followed by a randomized phase II study.

Phase I (closed to accrual as of 11/03/2010): Patients receive oral sorafenib tosylate twice daily on days 1-28 and bevacizumab IV on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Phase II: Patients are stratified according to gender (female vs male), ECOG performance status (0 vs 1), and Child-Pugh class (A vs B7). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive oral sorafenib tosylate on days 1-28 twice daily and bevacizumab IV on days 1 and 15.
- Arm II: Patients receive oral sorafenib tosylate twice daily on days 1-28. In both arms, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Blood samples are collected periodically for analysis of circulating endothelial cells and circulating endothelial progenitor cells and angiogenic proteins in plasma by ELISA.

After completion of study treatment, patients are followed for 3 years.

Studietype

Intervensjonell

Registrering (Faktiske)

Fase

Fase 2
Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

Forente stater
- Arizona
  - Scottsdale, Arizona, Forente stater, 85259-5499
    - Mayo Clinic Scottsdale
- Colorado
  - Aurora, Colorado, Forente stater, 80012
    - Aurora Presbyterian Hospital
  - Boulder, Colorado, Forente stater, 80301-9019
    - Boulder Community Hospital
  - Colorado Springs, Colorado, Forente stater, 80933
    - Penrose Cancer Center at Penrose Hospital
  - Denver, Colorado, Forente stater, 80210
    - Porter Adventist Hospital
  - Denver, Colorado, Forente stater, 80220
    - Rose Medical Center
  - Denver, Colorado, Forente stater, 80218
    - Presbyterian - St. Luke's Medical Center
  - Denver, Colorado, Forente stater, 80204
    - St. Anthony Central Hospital
  - Denver, Colorado, Forente stater, 80218
    - St. Joseph Hospital
  - Denver, Colorado, Forente stater, 80224-2522
    - CCOP - Colorado Cancer Research Program
  - Englewood, Colorado, Forente stater, 80110
    - Swedish Medical Center
  - Grand Junction, Colorado, Forente stater, 81502
    - St. Mary's Regional Cancer Center at St. Mary's Hospital and Medical Center
  - Greeley, Colorado, Forente stater, 80631
    - North Colorado Medical Center
  - Lone Tree, Colorado, Forente stater, 80124
    - Sky Ridge Medical Center
  - Longmont, Colorado, Forente stater, 80501
    - Hope Cancer Care Center at Longmont United Hospital
  - Loveland, Colorado, Forente stater, 80539
    - McKee Medical Center
  - Pueblo, Colorado, Forente stater, 81004
    - St. Mary - Corwin Regional Medical Center
  - Thornton, Colorado, Forente stater, 80229
    - North Suburban Medical Center
  - Wheat Ridge, Colorado, Forente stater, 80033
    - Exempla Lutheran Medical Center
- Connecticut
  - Hartford, Connecticut, Forente stater, 06105
    - Saint Francis/Mount Sinai Regional Cancer Center at Saint Francis Hospital and Medical Center
- Illinois
  - Bloomington, Illinois, Forente stater, 61701
    - Illinois CancerCare - Bloomington
  - Bloomington, Illinois, Forente stater, 61701
    - St. Joseph Medical Center
  - Canton, Illinois, Forente stater, 61520
    - Illinois CancerCare - Canton
  - Canton, Illinois, Forente stater, 61520
    - Graham Hospital
  - Carthage, Illinois, Forente stater, 62321
    - Memorial Hospital
  - Carthage, Illinois, Forente stater, 62321
    - Illinois CancerCare - Carthage
  - Eureka, Illinois, Forente stater, 61530
    - Illinois CancerCare - Eureka
  - Eureka, Illinois, Forente stater, 61530
    - Eureka Community Hospital
  - Galesburg, Illinois, Forente stater, 61401
    - Illinois CancerCare - Galesburg
  - Galesburg, Illinois, Forente stater, 61401
    - Galesburg Clinic, PC
  - Havana, Illinois, Forente stater, 62644
    - Mason District Hospital
  - Havana, Illinois, Forente stater, 62644
    - Illinois CancerCare - Havana
  - Kewanee, Illinois, Forente stater, 61443
    - Illinois CancerCare - Kewanee Clinic
  - Macomb, Illinois, Forente stater, 61455
    - Illinois CancerCare - Macomb
  - Macomb, Illinois, Forente stater, 61455
    - Mcdonough District Hospital
  - Moline, Illinois, Forente stater, 61265
  - Moline, Illinois, Forente stater, 61265
    - Trinity Cancer Center at Trinity Medical Center - 7th Street Campus
  - Monmouth, Illinois, Forente stater, 61462
    - Illinois CancerCare - Monmouth
  - Monmouth, Illinois, Forente stater, 61462
    - OSF Holy Family Medical Center
  - Normal, Illinois, Forente stater, 61761
    - Bromenn Regional Medical Center
  - Normal, Illinois, Forente stater, 61761
    - Community Cancer Center
  - Normal, Illinois, Forente stater, 61761
    - Illinois CancerCare - Community Cancer Center
  - Ottawa, Illinois, Forente stater, 61350
    - Community Hospital of Ottawa
  - Ottawa, Illinois, Forente stater, 61350
    - Oncology Hematology Associates of Central Illinois, PC - Ottawa
  - Pekin, Illinois, Forente stater, 61554
    - Cancer Treatment Center at Pekin Hospital
  - Pekin, Illinois, Forente stater, 61603
    - Illinois CancerCare - Pekin
  - Peoria, Illinois, Forente stater, 61636
    - Methodist Medical Center of Illinois
  - Peoria, Illinois, Forente stater, 61614
    - Proctor Hospital
  - Peoria, Illinois, Forente stater, 61637
    - OSF St. Francis Medical Center
  - Peoria, Illinois, Forente stater, 61615
    - CCOP - Illinois Oncology Research Association
  - Peoria, Illinois, Forente stater, 61615
    - Oncology Hematology Associates of Central Illinois, PC - Peoria
  - Peru, Illinois, Forente stater, 61354
    - Illinois CancerCare - Peru
  - Peru, Illinois, Forente stater, 61354
    - Illinois Valley Community Hospital
  - Princeton, Illinois, Forente stater, 61356
    - Perry Memorial Hospital
  - Princeton, Illinois, Forente stater, 61356
    - Illinois CancerCare - Princeton
  - Spring Valley, Illinois, Forente stater, 61362
    - Illinois CancerCare - Spring Valley
- Iowa
  - Bettendorf, Iowa, Forente stater, 52722
  - Clive, Iowa, Forente stater, 50325
    - Medical Oncology and Hematology Associates - West Des Moines
  - Des Moines, Iowa, Forente stater, 50309
    - CCOP - Iowa Oncology Research Association
  - Des Moines, Iowa, Forente stater, 50309
    - John Stoddard Cancer Center at Iowa Methodist Medical Center
  - Des Moines, Iowa, Forente stater, 50309
    - Medical Oncology and Hematology Associates at John Stoddard Cancer Center
  - Des Moines, Iowa, Forente stater, 50314
    - Medical Oncology and Hematology Associates at Mercy Cancer Center
  - Des Moines, Iowa, Forente stater, 50314
    - Mercy Cancer Center at Mercy Medical Center - Des Moines
  - Des Moines, Iowa, Forente stater, 50316
    - John Stoddard Cancer Center at Iowa Lutheran Hospital
  - Sioux City, Iowa, Forente stater, 51101
    - Siouxland Hematology-Oncology Associates, LLP
  - Sioux City, Iowa, Forente stater, 51104
    - St. Luke's Regional Medical Center
  - Sioux City, Iowa, Forente stater, 51104
    - Mercy Medical Center - Sioux City
- Kansas
  - Chanute, Kansas, Forente stater, 66720
    - Cancer Center of Kansas, PA - Chanute
  - Dodge City, Kansas, Forente stater, 67801
    - Cancer Center of Kansas, PA - Dodge City
  - El Dorado, Kansas, Forente stater, 67042
    - Cancer Center of Kansas, PA - El Dorado
  - Fort Scott, Kansas, Forente stater, 66701
    - Cancer Center of Kansas - Fort Scott
  - Independence, Kansas, Forente stater, 67301
    - Cancer Center of Kansas-Independence
  - Kingman, Kansas, Forente stater, 67068
    - Cancer Center of Kansas, PA - Kingman
  - Lawrence, Kansas, Forente stater, 66044
    - Lawrence Memorial Hospital
  - Liberal, Kansas, Forente stater, 67905
    - Cancer Center of Kansas, PA - Liberal
  - Newton, Kansas, Forente stater, 67114
    - Cancer Center of Kansas, PA - Newton
  - Parsons, Kansas, Forente stater, 67357
    - Cancer Center of Kansas, PA - Parsons
  - Pratt, Kansas, Forente stater, 67124
    - Cancer Center of Kansas, PA - Pratt
  - Salina, Kansas, Forente stater, 67401
    - Cancer Center of Kansas, PA - Salina
  - Wellington, Kansas, Forente stater, 67152
    - Cancer Center of Kansas, PA - Wellington
  - Wichita, Kansas, Forente stater, 67208
    - Cancer Center of Kansas, PA - Medical Arts Tower
  - Wichita, Kansas, Forente stater, 67214
    - Cancer Center of Kansas, PA - Wichita
  - Wichita, Kansas, Forente stater, 67214
    - CCOP - Wichita
  - Wichita, Kansas, Forente stater, 67214
    - Via Christi Cancer Center at Via Christi Regional Medical Center
  - Wichita, Kansas, Forente stater, 67208
    - Associates in Womens Health, PA - North Review
  - Winfield, Kansas, Forente stater, 67156
    - Cancer Center of Kansas, PA - Winfield
- Michigan
  - Ann Arbor, Michigan, Forente stater, 48106-0995
    - Saint Joseph Mercy Cancer Center
  - Ann Arbor, Michigan, Forente stater, 48106
    - CCOP - Michigan Cancer Research Consortium
  - Battle Creek, Michigan, Forente stater, 49017
    - Battle Creek Health System Cancer Care Center
  - Big Rapids, Michigan, Forente stater, 49307
    - Mecosta County Medical Center
  - Dearborn, Michigan, Forente stater, 48123-2500
    - Oakwood Cancer Center at Oakwood Hospital and Medical Center
  - Escanaba, Michigan, Forente stater, 49431
    - Green Bay Oncology, Limited - Escanaba
  - Flint, Michigan, Forente stater, 48503
    - Hurley Medical Center
  - Flint, Michigan, Forente stater, 48503
    - Genesys Hurley Cancer Institute
  - Grand Rapids, Michigan, Forente stater, 49503
    - Butterworth Hospital at Spectrum Health
  - Grand Rapids, Michigan, Forente stater, 49503
    - CCOP - Grand Rapids
  - Grand Rapids, Michigan, Forente stater, 49503
    - Lacks Cancer Center at Saint Mary's Health Care
  - Grosse Pointe Woods, Michigan, Forente stater, 48236
    - Van Elslander Cancer Center at St. John Hospital and Medical Center
  - Iron Mountain, Michigan, Forente stater, 49801
    - Dickinson County Healthcare System
  - Jackson, Michigan, Forente stater, 49201
    - Foote Memorial Hospital
  - Lansing, Michigan, Forente stater, 48912-1811
    - Sparrow Regional Cancer Center
  - Livonia, Michigan, Forente stater, 48154
    - St. Mary Mercy Hospital
  - Muskegon, Michigan, Forente stater, 49443
    - Mercy General Health Partners
  - Pontiac, Michigan, Forente stater, 48341-2985
    - St. Joseph Mercy Oakland
  - Port Huron, Michigan, Forente stater, 48060
    - Mercy Regional Cancer Center at Mercy Hospital
  - Saginaw, Michigan, Forente stater, 48601
    - Seton Cancer Institute at Saint Mary's - Saginaw
  - Traverse City, Michigan, Forente stater, 49684
    - Munson Medical Center
  - Warren, Michigan, Forente stater, 48093
    - St. John Macomb Hospital
  - Wyoming, Michigan, Forente stater, 49519
    - Metro Health Hospital
- Minnesota
  - Bemidji, Minnesota, Forente stater, 56601
    - MeritCare Bemidji
  - Burnsville, Minnesota, Forente stater, 55337
    - Fairview Ridges Hospital
  - Coon Rapids, Minnesota, Forente stater, 55433
    - Mercy and Unity Cancer Center at Mercy Hospital
  - Duluth, Minnesota, Forente stater, 55805
    - CCOP - Duluth
  - Duluth, Minnesota, Forente stater, 55805-1983
    - Duluth Clinic Cancer Center - Duluth
  - Duluth, Minnesota, Forente stater, 55805
    - Miller - Dwan Medical Center
  - Edina, Minnesota, Forente stater, 55435
    - Fairview Southdale Hospital
  - Fergus Falls, Minnesota, Forente stater, 56537
    - Fergus Falls Medical Group, PA
  - Fridley, Minnesota, Forente stater, 55432
    - Mercy and Unity Cancer Center at Unity Hospital
  - Hutchinson, Minnesota, Forente stater, 55350
    - Hutchinson Area Health Care
  - Maplewood, Minnesota, Forente stater, 55109
    - Minnesota Oncology Hematology, PA - Maplewood
  - Maplewood, Minnesota, Forente stater, 55109
    - HealthEast Cancer Care at St. John's Hospital
  - Minneapolis, Minnesota, Forente stater, 55407
    - Virginia Piper Cancer Institute at Abbott - Northwestern Hospital
  - Minneapolis, Minnesota, Forente stater, 55415
    - Hennepin County Medical Center - Minneapolis
  - Robbinsdale, Minnesota, Forente stater, 55422-2900
    - Hubert H. Humphrey Cancer Center at North Memorial Outpatient Center
  - Rochester, Minnesota, Forente stater, 55905
    - Mayo Clinic Cancer Center
  - Saint Louis Park, Minnesota, Forente stater, 55416
    - CCOP - Metro-Minnesota
  - Saint Louis Park, Minnesota, Forente stater, 55416
    - Park Nicollet Cancer Center
  - Saint Paul, Minnesota, Forente stater, 55102
    - United Hospital
  - Saint Paul, Minnesota, Forente stater, 55101
    - Regions Hospital Cancer Care Center
  - Shakopee, Minnesota, Forente stater, 55379
    - St. Francis Cancer Center at St. Francis Medical Center
  - Stillwater, Minnesota, Forente stater, 55082
    - Lakeview Hospital
  - Waconia, Minnesota, Forente stater, 55387
    - Ridgeview Medical Center
  - Willmar, Minnesota, Forente stater, 56201
    - Willmar Cancer Center at Rice Memorial Hospital
  - Woodbury, Minnesota, Forente stater, 55125
    - Minnesota Oncology Hematology, PA - Woodbury
- Missouri
  - Jefferson City, Missouri, Forente stater, 65109
    - Goldschmidt Cancer Center
  - Saint Louis, Missouri, Forente stater, 63131
    - Missouri Baptist Cancer Center
  - Saint Louis, Missouri, Forente stater, 63141
    - Comprehensive Cancer Care, PC
- Montana
  - Billings, Montana, Forente stater, 59101
    - CCOP - Montana Cancer Consortium
  - Billings, Montana, Forente stater, 59101
    - St. Vincent Healthcare Cancer Care Services
  - Billings, Montana, Forente stater, 59107-7000
    - Billings Clinic - Downtown
  - Billings, Montana, Forente stater, 59102
    - Hematology-Oncology Centers of the Northern Rockies - Billings
  - Bozeman, Montana, Forente stater, 59715
    - Bozeman Deaconess Cancer Center
  - Butte, Montana, Forente stater, 59701
    - St. James Healthcare Cancer Care
  - Great Falls, Montana, Forente stater, 59405
    - Great Falls Clinic - Main Facility
  - Great Falls, Montana, Forente stater, 59405
    - Sletten Cancer Institute at Benefis Healthcare
  - Havre, Montana, Forente stater, 59501
    - Northern Montana Hospital
  - Helena, Montana, Forente stater, 59601
    - St. Peter's Hospital
  - Kalispell, Montana, Forente stater, 59901
    - Kalispell Regional Medical Center
  - Kalispell, Montana, Forente stater, 59901
    - Glacier Oncology, PLLC
  - Kalispell, Montana, Forente stater, 59901
    - Kalispell Medical Oncology at KRMC
  - Missoula, Montana, Forente stater, 59807-7877
    - Montana Cancer Specialists at Montana Cancer Center
  - Missoula, Montana, Forente stater, 59807
    - Montana Cancer Center at St. Patrick Hospital and Health Sciences Center
- North Dakota
  - Bismarck, North Dakota, Forente stater, 58501
    - Bismarck Cancer Center
  - Bismarck, North Dakota, Forente stater, 58501
    - Medcenter One Hospital Cancer Care Center
  - Bismarck, North Dakota, Forente stater, 58501
    - Mid Dakota Clinic, PC
  - Bismarck, North Dakota, Forente stater, 58502
    - St. Alexius Medical Center Cancer Center
  - Fargo, North Dakota, Forente stater, 58122
    - CCOP - MeritCare Hospital
  - Fargo, North Dakota, Forente stater, 58122
    - MeritCare Broadway
- Oklahoma
  - Tulsa, Oklahoma, Forente stater, 74136
    - Natalie Warren Bryant Cancer Center at St. Francis Hospital
- Pennsylvania
  - Danville, Pennsylvania, Forente stater, 17822-0001
    - Geisinger Cancer Institute at Geisinger Health
  - Hazleton, Pennsylvania, Forente stater, 18201
    - Geisinger Hazleton Cancer Center
  - State College, Pennsylvania, Forente stater, 16801
    - Geisinger Medical Group - Scenery Park
  - Wilkes-Barre, Pennsylvania, Forente stater, 18711
    - Frank M. and Dorothea Henry Cancer Center at Geisinger Wyoming Valley Medical Center
- South Dakota
  - Rapid City, South Dakota, Forente stater, 57701
    - Rapid City Regional Hospital
  - Sioux Falls, South Dakota, Forente stater, 57105
    - Medical X-Ray Center, PC
  - Sioux Falls, South Dakota, Forente stater, 57117-5039
    - Sanford Cancer Center at Sanford USD Medical Center
- Wisconsin
  - Green Bay, Wisconsin, Forente stater, 54307-3508
    - St. Vincent Hospital Regional Cancer Center
  - Green Bay, Wisconsin, Forente stater, 54301-3526
    - Green Bay Oncology, Limited at St. Vincent Hospital Regional Cancer Center
  - Green Bay, Wisconsin, Forente stater, 54303
    - Green Bay Oncology, Limited at St. Mary's Hospital
  - Green Bay, Wisconsin, Forente stater, 54303
    - St. Mary's Hospital Medical Center - Green Bay
  - Manitowoc, Wisconsin, Forente stater, 54221-1450
    - Holy Family Memorial Medical Center Cancer Care Center
  - Marinette, Wisconsin, Forente stater, 54143
    - Bay Area Cancer Care Center at Bay Area Medical Center
  - Oconto Falls, Wisconsin, Forente stater, 54154
    - Green Bay Oncology, Limited - Oconto Falls
  - Sheboygan, Wisconsin, Forente stater, 53081
    - St. Nicholas Hospital
  - Sturgeon Bay, Wisconsin, Forente stater, 54235
    - Green Bay Oncology, Limited - Sturgeon Bay
- Wyoming
  - Casper, Wyoming, Forente stater, 82609
    - Rocky Mountain Oncology
  - Sheridan, Wyoming, Forente stater, 82801
    - Welch Cancer Center at Sheridan Memorial Hospital

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 120 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

DISEASE CHARACTERISTICS:

Histologically or cytologically confirmed hepatocellular carcinoma
- Locally advanced or metastatic disease that is not amenable to treatment with surgery or to orthotopic liver transplant
- Child Pugh class A or B7 disease
Measurable disease
No mixed cholangiocarcinoma/hepatocellular carcinoma
No current or previously resected brain metastases

PATIENT CHARACTERISTICS:

ECOG performance status 0-1
Life expectancy ≥ 3 months
ANC ≥ 1,200/mm³
Platelet count ≥ 75,000/mm³
Hemoglobin ≥ 9.0 g/dL
Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
AST ≤ 5 times ULN
Alkaline phosphatase ≤ 5 times ULN
Urine protein ≤ 1+ by urine protein:creatinine ratio OR 24-hour urine protein < 1 g
QTc interval ≤ 500 msec on baseline EKG
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception during and for ≥ 2 weeks after sorafenib tosylate and 6 months after bevacizumab
None of the following risk factors for decreased LVEF:
- Prior treatment with anthracyclines
- History of myocardial infarction within the past 12 months
No uncontrolled hypertension (defined as systolic blood pressure [BP] > 150 mm Hg or diastolic BP > 100 mm Hg) despite optimal medical management
No New York Heart Association class III-IV congestive heart failure
No cardiac ventricular arrhythmias requiring antiarrhythmic therapy
No history of hypertensive crisis or hypertensive encephalopathy
No cardiac ventricular arrhythmia requiring anti-arrhythmic therapy within the past 6 months
None of the following within the past 6 months:
- Transient ischemic attack
- Cerebrovascular accident
- Unstable angina or angina
- Clinically significant peripheral artery disease (i.e., claudication in less than one block) or any other arterial thrombotic event
- Abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess
- Significant vascular disease (e.g., aortic aneurysm, aortic dissection) or recent peripheral arterial thrombosis
No active or recent history of hemoptysis (≥ ½ teaspoon of bright red blood per episode) within the past 30 days
No evidence of bleeding diathesis (greater than normal risk of bleeding) or coagulopathy (in the absence of therapeutic anticoagulation)
No significant traumatic injury within the past 4 weeks
No serious or non-healing wound, ulcer, or bone fracture
No uncontrolled intercurrent illness, including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements
No other active malignancy within the past 3 years, except nonmelanotic skin cancer or carcinoma in situ of the cervix
No comorbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens
No history of allergic reactions attributed to compounds of similar chemical or biologic composition to bevacizumab or sorafenib tosylate

PRIOR CONCURRENT THERAPY:

No prior systemic chemotherapy regimens for hepatocellular carcinoma
No prior external beam radiation to the primary site
No prior central thoracic radiation therapy (RT), including RT to the heart
No prior radiation (if given for another malignancy) to ≥ 25% of the bone marrow
At least 6 weeks since prior chemoembolization, radioembolization, radiofrequency ablation, or other local ablative therapies
More than 4 weeks since prior biologic, hormonal, or immune therapy
More than 4 weeks since prior and no concurrent major surgical procedure or open biopsy
More than 7 days since prior core biopsy or other minor surgical procedure (placement of a vascular access device allowed)
No concurrent investigational agent which would be considered as a treatment for the primary neoplasm
No concurrent anticoagulants, except low-dose warfarin or heparin for deep venous thrombosis prophylaxis
No other concurrent treatment for prior malignancy (other than hormonal therapy)

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Primært formål: Behandling
Tildeling: Randomisert
Intervensjonsmodell: Parallell tildeling
Masking: Ingen (Open Label)

Antall våpen

Våpen og intervensjoner

Deltakergruppe / Arm	Intervensjon / Behandling
Eksperimentell: Arm I (Phase II) Patients receive oral sorafenib tosylate on days 1-28 twice daily and bevacizumab IV on days 1 and 15.	Biologisk: bevacizumab Gitt IV Legemiddel: sorafenibtosylat Gis muntlig
Eksperimentell: Arm II (Phase II) Patients receive oral sorafenib tosylate twice daily on days 1-28.	Legemiddel: sorafenibtosylat Gis muntlig

Hva måler studien?

Primære resultatmål

Resultatmål	Tiltaksbeskrivelse	Tidsramme
Maximum Tolerated Dose (Phase I) Tidsramme: From baseline up to 3 years post treatment	MTD is defined as the dose level below the lowest dose that induces dose limiting toxicity in at least one-third of patients (at least 2 of a maximum of 6 new patients). If dose level (-1) is not tolerable, but dose (-3) or (-2) is below or at MTD, testing of alternate dose levels (-2a, -3a, -3b) will occur as outlined in the table. The number of dose limiting toxicities will be reported here.	From baseline up to 3 years post treatment
Time to Progression (TTP) (Phase II) Tidsramme: From baseline up to 3 years post treatment	Time to progression is defined to be the length of time from study registration to a) date of disease progression as defined by section 11.0, or b) last follow-up. If a patient dies without documentation of disease progression, the patient will be considered to have had a tumor progression at the time of death unless there is sufficient documented evidence to conclude no progression occurred prior to death. Kaplan-Meier survival curves will be used to estimate the distribution of TTP.	From baseline up to 3 years post treatment

Sekundære resultatmål

Resultatmål	Tiltaksbeskrivelse	Tidsramme
Overall Survival Tidsramme: Up to 3 years post treatment	Overall survival (OS) is defined as the length of time from date of registration to a) date of death due to any cause or b) last follow-up. Kaplan-Meier survival curves will be used to estimate the distribution of OS.	Up to 3 years post treatment
Tumor Response at 6 Months Tidsramme: 6 months	Tumor response (at 6 months) is defined as the number of responses (complete or partial response per Section 11) over the number of eligible patients observed for at least 6 months. Tumor response will be evaluated using simple estimates of proportions.	6 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Alliance for Clinical Trials in Oncology

Samarbeidspartnere

National Cancer Institute (NCI)

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Hubbard JM, Mahoney MR, Loui WS, Roberts LR, Smyrk TC, Gatalica Z, Borad M, Kumar S, Alberts SR. Phase I/II Randomized Trial of Sorafenib and Bevacizumab as First-Line Therapy in Patients with Locally Advanced or Metastatic Hepatocellular Carcinoma: North Central Cancer Treatment Group Trial N0745 (Alliance). Target Oncol. 2017 Apr;12(2):201-209. doi: 10.1007/s11523-016-0467-0.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. april 2009

Primær fullføring (Faktiske)

1. april 2012

Studiet fullført (Faktiske)

1. mai 2013

Datoer for studieregistrering

Først innsendt

20. mars 2009

Først innsendt som oppfylte QC-kriteriene

20. mars 2009

Først lagt ut (Anslag)

23. mars 2009

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

19. april 2022

Siste oppdatering sendt inn som oppfylte QC-kriteriene

23. mars 2022

Sist bekreftet

1. mars 2022

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

NCCTG-N0745
NCI-2009-01178 (Registeridentifikator: CTRP (Clinical Trials Reporting System))
CDR0000637866 (Registeridentifikator: PDQ (Physician Data Query))

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Leverkreft

National Health Research Institutes, Taiwan

Rekruttering

Effekter av mindfulness eller hjernestimuleringsintervensjon for voksne i sent liv i Taiwan urbane og landlige områder (PredictNPI)

Tankefullhet | Senlivsdepresjon | Voksne for sent liv | Prodromal depresjon av sen liv | Hjernestimuleringsintervensjon

Taiwan
Universidad Complutense de Madrid

Rekruttering

Meningsfokusert intervensjon i hæren

Meningsfullt liv

Spania
Université de Reims Champagne-Ardenne

Fullført

Støtte til foreldreskap: Utdanning for det følelsesmessige og seksuelle livet til ungdom i alderen 11 til 15 år (educ-parent)

Adolescenters følelsesmessige og seksuelle liv

Frankrike
Tatsuhiro Hisatsune

Rekruttering

En randomisert kontrollert studie av en flerdomene smartphone-intervensjon som inkorporerer generativ kunstig intelligens for friske eldre voksne

Sunn langvarig liv

Japan
Sisli Hamidiye Etfal Training and Research Hospital

Har ikke rekruttert ennå

Våre anestesiopplevelser innen hepatopankreatobiliær kirurgi: en retrospektiv studie

Erfaring, liv

Tyrkia
Bournemouth University
Dorset County Hospital NHS Foundation Trust

Fullført

Implementering av babyvennlig initiativ: Erfaringer fra barselpersonalet

Erfaring, liv

Storbritannia
Swiss Federal Institute of Technology

Fullført

Gjennomførbarhet og effektivitet av et hjemmebasert motorisk-kognitivt treningsprogram hos eldre voksne (COCARE)

Eldret | Uavhengig liv

Sveits
Centre Hospitalier Universitaire Dijon

Fullført

Ekstubering av pasienter på ECLS er assosiert med en reduksjon i komplikasjoner relatert til mekanisk ventilasjon: Retrospektiv enkeltsenterstudie (EXTUB ECLS)

Støtte for liv utenom kropp

Frankrike
Calydial
OZ'IRIS Santé

Fullført

Hva representerer pasienterfaringen for pasienter og pleiere i dialyse? (EnquêteXP)

Pasientengasjement | Pasientmedvirkning | Pasienttilfredshet | Dialyse | Pasientforhold, sykepleier | Erfaring, liv

Frankrike
University of California, Los Angeles
VA Greater Los Angeles Healthcare System

Tilbaketrukket

UCLA FOCUS Forskningsstudie om familieresiliency Training (FOCUS)

Veteranfamilier | Familiekommunikasjon | Reintegrering av sivilt liv

Forente stater

Kliniske studier på bevacizumab

National Cancer Institute (NCI)

Aktiv, ikke rekrutterende

TORC1/2-hemmer MLN0128 og Bevacizumab i behandling av pasienter med tilbakevendende glioblastom eller avanserte solide svulster

Tilbakevendende egglederkarsinom | Tilbakevendende ovariekarsinom | Tilbakevendende primært peritonealt karsinom | Klarcellet ovariecystadenokarsinom | Endometrioid adenokarsinom på eggstokkene | Serøst cystadenokarsinom på eggstokkene | Endometrie klarcellet adenokarsinom | Endometrial serøst adenokarsinom og andre forhold

Forente stater
Blokhin's Russian Cancer Research Center

Aktiv, ikke rekrutterende

Omfattende analyse av resultater ved kjemoterapi og målrettet terapi ved tilbakevendende maligne gliomer (GLIOTARG)

Glioblastom | Anaplastisk astrocytom | Pleomorfisk xanthoastrocytom | Tilbakevendende ondartet gliom

Russland
National Cancer Institute (NCI)

Fullført

Atezolizumab og Bevacizumab i behandling av pasienter med tilbakevendende, vedvarende eller metastatisk livmorhalskreft

Cervical Adenocarcinoma | Cervical Adenosquamous Carcinoma | Livmorhalsplateepitelkarsinom, ikke spesifisert på annen måte | Stage IVA Livmorhalskreft AJCC v6 og v7 | Tilbakevendende livmorhalskreft | Stadium IV Livmorhalskreft AJCC v6 og v7 | Stadium IVB Livmorhalskreft AJCC v6 og v7

Forente stater
Roswell Park Cancer Institute
Merck Sharp & Dohme LLC; United States Department of Defense; Celldex Therapeutics

Rekruttering

Pembrolizumab kombinert med bevacizumab med eller uten agonist Anti-CD40 CDX-1140 for behandling av pasienter med tilbakevendende eggstokkreft

Tilbakevendende egglederkarsinom | Tilbakevendende ovariekarsinom | Tilbakevendende primært peritonealt karsinom | Tilbakevendende endometrie serøst adenokarsinom | Klarcellet adenokarsinom i eggstokkene | Tilbakevendende platina-resistent ovariekarsinom | Platinasensitivt ovariekarsinom | Tilbakevendende... og andre forhold

Forente stater
National Cancer Institute (NCI)
NRG Oncology

Fullført

Bevacizumab med eller uten trebananib ved behandling av pasienter med tilbakevendende hjernesvulster

Glioblastom | Gliosarkom | Tilbakevendende glioblastom | Oligodendrogliom | Kjempecelleglioblastom | Tilbakevendende hjerneneoplasma

Forente stater, Canada
M.D. Anderson Cancer Center

Aktiv, ikke rekrutterende

Atezolizumab og Bevacizumab før kirurgi for behandling av resektabel leverkreft

Stage IB hepatocellulært karsinom AJCC v8 | Stage II hepatocellulært karsinom AJCC v8 | Resektabelt hepatocellulært karsinom | Stage I hepatocellulært karsinom AJCC v8 | Stage IA hepatocellulært karsinom AJCC v8

Forente stater
National Cancer Institute (NCI)

Aktiv, ikke rekrutterende

Bevacizumab og Anetumab Ravtansin eller Paclitaxel ved behandling av pasienter med refraktær ovarie-, eggleder- eller primær bukkreft

Endometrioid adenokarsinom på eggstokkene | Primært peritonealt høygradig serøst adenokarsinom | Endometrioid adenokarsinom i egglederen | Platina-resistent egglederkarsinom | Platina-resistent primært peritonealt karsinom | Ovarial høygradig serøst adenokarsinom | Platina-resistent ovariekarsinom | Eggleder...

Forente stater, Canada
Northwestern University
National Cancer Institute (NCI); Ipsen Biopharmaceuticals

Fullført

Irinotecan Liposome og Bevacizumab for behandling av platinaresistent, tilbakevendende eller refraktær ovarie-, eggleder- eller primær peritonealkreft

Tilbakevendende egglederkarsinom | Tilbakevendende ovariekarsinom | Tilbakevendende primært peritonealt karsinom | Platina-resistent egglederkarsinom | Platina-resistent primært peritonealt karsinom | Platina-resistent ovariekarsinom | Ildfast ovariekarsinom | Ildfast egglederkarsinom | Refraktært primært...

Forente stater
National Cancer Institute (NCI)

Aktiv, ikke rekrutterende

Cediranib Maleate og Olaparib sammenlignet med Bevacizumab ved behandling av pasienter med tilbakevendende glioblastom

Tilbakevendende glioblastom

Forente stater
National Cancer Institute (NCI)

Aktiv, ikke rekrutterende

Testing av Atezolizumab alene eller Atezolizumab Plus Bevacizumab hos personer med avansert alveolar myk delsarkom

Metastatisk alveolar myk delsarkom | Ikke-opererbart alveolært mykt sarkom

Forente stater

Bevacizumab and Sorafenib as First-Line Therapy in Treating Patients With Locally Advanced or Metastatic Liver Cancer

Phase I/II Randomized Trial of Sorafenib and Bevacizumab as First-Line Therapy in Patients With Locally Advanced or Metastatic Hepatocellular Carcinoma

Studieoversikt

Status

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

Studietype

Registrering (Faktiske)

Fase

Kontakter og plasseringer

Studiesteder

Deltakelseskriterier

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

Tar imot friske frivillige

Kjønn som er kvalifisert for studier

Beskrivelse

Studieplan

Hvordan er studiet utformet?

Designdetaljer

Antall våpen

Våpen og intervensjoner

Deltakergruppe / Arm

Intervensjon / Behandling

Hva måler studien?

Primære resultatmål

Resultatmål

Tiltaksbeskrivelse

Tidsramme

Sekundære resultatmål

Resultatmål

Tiltaksbeskrivelse

Tidsramme

Samarbeidspartnere og etterforskere

Sponsor

Samarbeidspartnere

Publikasjoner og nyttige lenker

Generelle publikasjoner

Studierekorddatoer

Studer hoveddatoer

Studiestart

Primær fullføring (Faktiske)

Studiet fullført (Faktiske)

Datoer for studieregistrering

Først innsendt

Først innsendt som oppfylte QC-kriteriene

Først lagt ut (Anslag)

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

Siste oppdatering sendt inn som oppfylte QC-kriteriene

Sist bekreftet

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

Kliniske studier på Leverkreft

Kliniske studier på bevacizumab

Søk i lignende forsøk

Sponsorer og samarbeidspartnere

Medisinsk tilstand

Legemiddelintervensjoner

CROs by country

CROs in Turkmenistan

Forhold

Sjeldne sykdommer

Legemiddelintervensjoner

Kosttilskudd

Sponsor / samarbeidspartnere

Steder