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

23 mars 2022 mis à jour par: 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)

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

24

Phase

  • Phase 2
  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

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

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 120 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

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)

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Arm I (Phase II)
Patients receive oral sorafenib tosylate on days 1-28 twice daily and bevacizumab IV on days 1 and 15.
Biologique: bévacizumab
Étant donné IV
Médicament: tosylate de sorafénib
Donné oralement
Expérimental: Arm II (Phase II)
Patients receive oral sorafenib tosylate twice daily on days 1-28.
Médicament: tosylate de sorafénib
Donné oralement

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Maximum Tolerated Dose (Phase I)
Délai: 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)
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Overall Survival
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Alliance for Clinical Trials in Oncology

Collaborateurs

National Cancer Institute (NCI)

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 avril 2009

Achèvement primaire (Réel)

1 avril 2012

Achèvement de l'étude (Réel)

1 mai 2013

Dates d'inscription aux études

Première soumission

20 mars 2009

Première soumission répondant aux critères de contrôle qualité

20 mars 2009

Première publication (Estimation)

23 mars 2009

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

19 avril 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

23 mars 2022

Dernière vérification

1 mars 2022

Plus d'information

Termes liés à cette étude

Mots clés

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • NCCTG-N0745
  • NCI-2009-01178 (Identificateur de registre: CTRP (Clinical Trials Reporting System))
  • CDR0000637866 (Identificateur de registre: PDQ (Physician Data Query))

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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