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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00005045
Other study ID # CDR0000067636
Secondary ID ECOG-4896
Status Completed
Phase Phase 2
First received April 6, 2000
Last updated June 20, 2013
Start date March 2000
Est. completion date June 2004

Study information

Verified date December 2005
Source National Cancer Institute (NCI)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

RATIONALE: Carboxyamidotriazole may stop the growth of kidney cancer by stopping blood flow to the tumor.

PURPOSE: Phase II trial to study the effectiveness of carboxyamidotriazole in treating patients who have advanced kidney cancer that has not responded to biological therapy.


Description:

OBJECTIVES: I. Determine the disease free progression at 6 months in patients with locally recurrent or metastatic renal cell cancer (refractory to immunotherapy) treated with carboxyamidotriazole. II. Evaluate the progression free survival rate and response rate in these patients on this regimen. III. Evaluate the toxic effect of this regimen on these patients.

OUTLINE: Patients receive oral carboxyamidotriazole daily. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity. Patients with stable disease may discontinue therapy after 6 courses. Patients are followed every 3 months for 2 years, every 6 months for 3 years, and every 12 months thereafter until death.

PROJECTED ACCRUAL: A total of 55 patients will be accrued for this study within 20 months.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date June 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility DISEASE CHARACTERISTICS: Histologically proven advanced renal cell cancer Locally recurrent or metastatic lesions not amenable to current resection Progressive disease defined as 25% increase from last measurement or new lesions Bidimensionally measurable disease No brain metastases

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: Not specified Hematopoietic: WBC greater than 3,000/mm3 OR Absolute neutrophil count greater than 1,500/mm3 Platelet count greater than 100,000/mm3 Hepatic: Bilirubin less than 1.5 mg/dL SGOT and/or SGPT less than 2 times upper limit of normal Renal: Creatinine less than 2.0 mg/dL Other: Not pregnant or nursing Fertile patients must use effective contraception No other serious medical illness or active infection that would preclude chemotherapy compliance No other prior malignancy unless curatively treated and disease free for the past 5 years

PRIOR CONCURRENT THERAPY: Biologic therapy: At least 4 weeks since prior biologic therapy At least 1 (but no more than 2) prior biologic regimen(s) (i.e., interleukin-2, interferon alfa, or combination) and recovered Regimen defined as at least 8 weeks of treatment Prior sargramostim allowed Chemotherapy: No prior chemotherapy Endocrine therapy: At least 4 weeks since prior hormonal therapy (i.e., megestrol or tamoxifen) and recovered Radiotherapy: No prior radiotherapy to study lesions At least 4 weeks since prior radiotherapy and recovered No concurrent palliative radiotherapy Surgery: Prior nephrectomy allowed Recovered from any recent surgery

Study Design

Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
carboxyamidotriazole


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 Hospital 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 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 Cleveland Clinic Cancer Center Cleveland Ohio
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 Clinical and Medical Center Danville Pennsylvania
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 Veterans Affairs Medical Center - East Orange East Orange New Jersey
United States CCOP - Evanston Evanston Illinois
United States Veterans Affairs Medical Center - Gainsville Gainesville Florida
United States CCOP - Northern New Jersey Hackensack New Jersey
United States Indiana University Cancer Center Indianapolis Indiana
United States Veterans Affairs Medical Center - Indianapolis (Roudebush) Indianapolis Indiana
United States University of Iowa Hospitals and Clinics Iowa City Iowa
United States CCOP - Southern Nevada Cancer Research Foundation Las Vegas Nevada
United States Beckman Research Institute, City of Hope Los Angeles California
United States Sylvester Cancer Center, University of Miami Miami Florida
United States University of Minnesota Cancer Center Minneapolis Minnesota
United States Veterans Affairs Medical Center - Minneapolis Minneapolis Minnesota
United States Cancer Institute of New Jersey New Brunswick New Jersey
United States CCOP - Ochsner New Orleans Louisiana
United States MBCCOP - LSU Medical Center New Orleans Louisiana
United States Kaplan 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 Allegheny University Philadelphia Pennsylvania
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 Mayo Clinic Cancer Center Rochester 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 - Sooner State Tulsa Oklahoma
United States Walter Reed Army Medical Center Washington District of Columbia
United States CCOP - Christiana Care Health Services Wilmington Delaware

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 (2)

Dutcher JP, Leon L, Manola J, Friedland DM, Roth B, Wilding G; Eastern Cooperative Oncology Group. Phase II study of carboxyamidotriazole in patients with advanced renal cell carcinoma refractory to immunotherapy: E4896, an Eastern Cooperative Oncology Gr — View Citation

Friedland D, Leon L, Manola J, et al.: Carboxyamidotriazole (CAI) in patients with advanced renal cell cancer (RCC) refractory to immunotherapy: an ECOG phase II trial. [Abstract] Proceedings of the American Society of Clinical Oncology 21: A-2424, 2002.

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