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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00003864
Other study ID # CDR0000067028
Secondary ID E-2298
Status Completed
Phase Phase 2
First received
Last updated
Start date September 3, 1999

Study information

Verified date June 2023
Source Eastern Cooperative Oncology Group
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of docetaxel plus carboplatin in treating patients who have advanced cancer of the esophagus.


Description:

OBJECTIVES: I. Evaluate the objective response rate in patients with advanced squamous cell carcinoma of the esophagus treated with carboplatin and docetaxel. II. Assess the toxicity of this regimen in these patients. III. Assess the time to progression and overall survival of this patient population. OUTLINE: Patients receive docetaxel IV over 1 hour on day 1, followed by carboplatin IV over 15-30 minutes on day 1. Treatment is repeated every 3 weeks for 6 courses in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months until year 2, every 6 months during years 2-5, and then annually thereafter until death. PROJECTED ACCRUAL: A total of 18-35 patients will be accrued for this study at a rate of 30 patients per year.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date January 2004
Accepts healthy volunteers No
Gender All
Age group 18 Years to 120 Years
Eligibility DISEASE CHARACTERISTICS: Histologically confirmed metastatic or incurable, locally advanced squamous cell carcinoma of the esophagus Measurable disease outside of a previously radiated field required PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: Not specified Hematopoietic: Absolute granulocyte count at least 1500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin normal SGOT no greater than 2 times upper limit of normal Renal: Creatinine normal Cardiovascular: No congestive heart failure or angina pectoris, even if medically controlled No prior myocardial infarction within the past year No clinically significant conduction system abnormalities, such as 2nd or 3rd degree heart block or bundle branch block Pulmonary: Not specified Other: Not pregnant or nursing Fertile patients must use effective contraception No active infections or medical illnesses that are uncontrolled No second malignancy other than previously treated nonmelanoma skin cancer or carcinoma in situ of the cervix or a prior malignancy from which patient has been disease free for past 3 years Caloric intake greater than 1500 calories/day Fluid intake greater than 1500 mL/day PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior chemotherapy Endocrine therapy: Not specified Radiotherapy: At least 4 weeks since prior radiotherapy Surgery: Not specified

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
carboplatin

docetaxel


Locations

Country Name City State
Puerto Rico MBCCOP - San Juan San Juan
Puerto Rico Veterans Affairs Medical Center - San Juan San Juan
South Africa Pretoria Academic Hospitals Pretoria
United States Veterans Affairs Medical Center - Albany Albany New York
United States CCOP - Ann Arbor Regional Ann Arbor Michigan
United States Emory University Hospital - Atlanta Atlanta Georgia
United States Johns Hopkins Oncology Center Baltimore Maryland
United States Beth Israel Deaconess Medical Center Boston Massachusetts
United States New England Medical Center Hospital Boston Massachusetts
United States Albert Einstein Comprehensive Cancer Center Bronx New York
United States Veterans Affairs Medical Center - Brooklyn Brooklyn New York
United States CCOP - Cedar Rapids Oncology Project Cedar Rapids Iowa
United States Robert H. Lurie Comprehensive Cancer Center, Northwestern University Chicago Illinois
United States Veterans Affairs Medical Center - Lakeside Chicago Chicago Illinois
United States Ireland Cancer Center Cleveland Ohio
United States Veterans Affairs Medical Center - Cleveland Cleveland Ohio
United States CCOP - Columbus Columbus Ohio
United States CCOP - Geisinger Clinic and Medical Center Danville Pennsylvania
United States CCOP - Central Illinois Decatur Illinois
United States Veterans Affairs Medical Center - Atlanta (Decatur) Decatur Georgia
United States CCOP - Colorado Cancer Research Program, Inc. Denver Colorado
United States CCOP - Iowa Oncology Research Association Des Moines Iowa
United States CCOP - Duluth Duluth Minnesota
United States Veterans Affairs Medical Center - East Orange East Orange New Jersey
United States CCOP - Evanston Evanston Illinois
United States CCOP - Merit Care Hospital Fargo North Dakota
United States Veterans Affairs Medical Center - Gainsville Gainesville Florida
United States CCOP - Northern New Jersey Hackensack New Jersey
United States Hackensack University Medical Center Hackensack New Jersey
United States Indiana University Cancer Center Indianapolis Indiana
United States Veterans Affairs Medical Center - Indianapolis (Roudebush) Indianapolis Indiana
United States CCOP - Kalamazoo Kalamazoo Michigan
United States CCOP - Southern Nevada Cancer Research Foundation Las Vegas Nevada
United States Cancer Center and Beckman Research Institute, City of Hope Los Angeles California
United States University of Wisconsin Comprehensive Cancer Center Madison Wisconsin
United States Veterans Affairs Medical Center - Madison Madison Wisconsin
United States CCOP - Marshfield Medical Research and Education Foundation Marshfield Wisconsin
United States Medical College of Wisconsin Milwaukee Wisconsin
United States Veterans Affairs Medical Center - Milwaukee (Zablocki) Milwaukee Wisconsin
United States University of Minnesota Cancer Center Minneapolis Minnesota
United States Veterans Affairs Medical Center - Minneapolis Minneapolis Minnesota
United States Fox Chase Cancer Center at Virtua Memorial Hospital Burlington County Mount Holly New Jersey
United States Vanderbilt-Ingram Cancer Center Nashville Tennessee
United States Veterans Affairs Medical Center - Nashville Nashville Tennessee
United States Cancer Institute of New Jersey New Brunswick New Jersey
United States CCOP - Ochsner New Orleans Louisiana
United States MBCCOP - LSU Health Sciences Center New Orleans Louisiana
United States NYU School of Medicine's Kaplan Comprehensive Cancer Center New York New York
United States Veterans Affairs Medical Center - New York New York New York
United States CCOP - Missouri Valley Cancer Consortium Omaha Nebraska
United States Veterans Affairs Medical Center - Palo Alto Palo Alto California
United States CCOP - Illinois Oncology Research Association Peoria Illinois
United States Raritan Bay Medical Center Perth Amboy New Jersey
United States Fox Chase Cancer Center Philadelphia Pennsylvania
United States Hahnemann University Hospital Philadelphia Pennsylvania
United States Kimmel Cancer Center of Thomas Jefferson University - Philadelphia Philadelphia Pennsylvania
United States University of Pennsylvania Cancer Center Philadelphia Pennsylvania
United States University of Pittsburgh Cancer Institute Pittsburgh Pennsylvania
United States Veterans Affairs Medical Center - Pittsburgh Pittsburgh Pennsylvania
United States Riverview Medical Center Red Bank New Jersey
United States Mayo Clinic Cancer Center Rochester Minnesota
United States University of Rochester Cancer Center Rochester New York
United States CCOP - Metro-Minnesota Saint Louis Park Minnesota
United States CCOP - Scottsdale Oncology Program Scottsdale Arizona
United States CCOP - Sioux Community Cancer Consortium Sioux Falls South Dakota
United States Stanford University Medical Center Stanford California
United States H. Lee Moffitt Cancer Center and Research Institute Tampa Florida
United States Veterans Affairs Medical Center - Tampa (Haley) Tampa Florida
United States CCOP - Toledo Community Hospital Oncology Program Toledo Ohio
United States CCOP - Sooner State Tulsa Oklahoma
United States CCOP - Carle Cancer Center Urbana Illinois
United States Walter Reed Army Medical Center Washington District of Columbia
United States CCOP - Christiana Care Health Services Wilmington Delaware
United States CCOP - MainLine Health Wynnewood Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Eastern Cooperative Oncology Group National Cancer Institute (NCI)

Countries where clinical trial is conducted

United States,  Puerto Rico,  South Africa, 

References & Publications (1)

Rossman JF, Falkson CI, Xu R, Slabber CF, Mason BA, Mulcahy MF, Benson AB 3rd. Phase II Trial of Docetaxel and Carboplatin in Patients With Advanced Squamous Carcinoma of the Esophagus (E2298): A Trial of the Eastern Cooperative Oncology Group. Gastrointe — View Citation

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