Ecteinascidin 743 in Treating Children With Refractory Solid Tumors
Phase I Study of ET-743 in Pediatric Refractory Solid Tumors
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Ecteinascidin 743 may be an effective treatment for solid tumors.
PURPOSE: Phase I trial to study the effectiveness of ecteinascidin 743 in treating children who have refractory solid tumors.
연구 개요
상세 설명
OBJECTIVES: I. Determine the maximum tolerated dose and dose-limiting toxicity of ecteinascidin 743 in pediatric patients with refractory solid tumors. II. Determine the pharmacokinetics of this drug in these patients. III. Determine the antitumor activity of this drug in this patient population.
OUTLINE: This is a dose escalation, multicenter study. Patients are stratified according to pretreatment (pretreated vs less heavily pretreated). Patients receive ecteinascidin 743 IV over 3 hours on day 1. Treatment continues every 3 weeks in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of ecteinascidin 743 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicities.
PROJECTED ACCRUAL: A total of 3-20 patients will be accrued for this study within 2 years.
연구 유형
등록 (실제)
단계
- 1단계
연락처 및 위치
연구 장소
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Arkansas
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Little Rock, Arkansas, 미국, 72205
- University of Arkansas for Medical Sciences
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California
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La Jolla, California, 미국, 92093-0658
- University of California San Diego Cancer Center
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Los Angeles, California, 미국, 90095-1781
- Jonsson Comprehensive Cancer Center, UCLA
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Los Angeles, California, 미국, 91010
- Beckman Research Institute, City of Hope
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Los Angeles, California, 미국, 90027-0700
- Children's Hospital Los Angeles
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Orange, California, 미국, 92868
- Children's Hospital of Orange County
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Palo Alto, California, 미국, 94304
- Lucile Packard Children's Hospital at Stanford
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San Francisco, California, 미국, 94115-0128
- UCSF Cancer Center and Cancer Research Institute
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District of Columbia
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Washington, District of Columbia, 미국, 20010-2970
- Children's National Medical Center
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Florida
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Gainesville, Florida, 미국, 32610-100277
- Shands Hospital and Clinics, University of Florida
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Georgia
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Atlanta, Georgia, 미국, 30322
- Emory University Hospital - Atlanta
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Illinois
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Chicago, Illinois, 미국, 60614
- Children's Memorial Hospital, Chicago
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Indiana
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Indianapolis, Indiana, 미국, 46202-5265
- Indiana University Cancer Center
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Maryland
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Baltimore, Maryland, 미국, 21231
- Johns Hopkins Oncology Center
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Massachusetts
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Boston, Massachusetts, 미국, 02115
- Dana-Farber Cancer Institute
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Boston, Massachusetts, 미국, 02111
- Boston Floating Hospital Infants and Children
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Michigan
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Ann Arbor, Michigan, 미국, 48109
- Mott Children's Hospital
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Detroit, Michigan, 미국, 48201
- Children's Hospital of Michigan
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Minnesota
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Rochester, Minnesota, 미국, 55905
- Mayo Clinic Cancer Center
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Mississippi
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Jackson, Mississippi, 미국, 39216-4505
- University of Mississippi Medical Center
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Missouri
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Kansas City, Missouri, 미국, 64108
- Children's Mercy Hospital
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Saint Louis, Missouri, 미국, 63104
- Cardinal Glennon Children's Hospital
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New Jersey
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Hackensack, New Jersey, 미국, 07601
- Hackensack University Medical Center
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New York
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Buffalo, New York, 미국, 14263-0001
- Roswell Park Cancer Institute
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New York, New York, 미국, 10021
- Memorial Sloan-Kettering Cancer Center
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New York, New York, 미국, 10032
- Columbia Presbyterian Hospital
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Syracuse, New York, 미국, 13210
- State University of New York - Upstate Medical University
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North Carolina
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Durham, North Carolina, 미국, 27710
- Duke Comprehensive Cancer Center
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Ohio
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Cincinnati, Ohio, 미국, 45229-3039
- Children's Hospital Medical Center - Cincinnati
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Pennsylvania
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Philadelphia, Pennsylvania, 미국, 19104
- Children's Hospital of Philadelphia
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Pittsburgh, Pennsylvania, 미국, 15213
- Children's Hospital of Pittsburgh
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South Carolina
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Charleston, South Carolina, 미국, 29425-0721
- Medical University of South Carolina
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Tennessee
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Memphis, Tennessee, 미국, 38105-2794
- Saint Jude Children's Research Hospital
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Nashville, Tennessee, 미국, 37232-6838
- Vanderbilt Cancer Center
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Texas
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Fort Worth, Texas, 미국, 76104
- Cook Children's Medical Center - Fort Worth
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Houston, Texas, 미국, 77030
- Baylor College of Medicine
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Houston, Texas, 미국, 77030-4009
- University of Texas - MD Anderson Cancer Center
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San Antonio, Texas, 미국, 78284-7811
- University of Texas Health Science Center at San Antonio
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Utah
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Salt Lake City, Utah, 미국, 84132
- Huntsman Cancer Institute
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Washington
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Seattle, Washington, 미국, 98105
- Children's Hospital and Regional Medical Center - Seattle
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Wisconsin
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Madison, Wisconsin, 미국, 53792-0001
- University of Wisconsin Hospital and Clinics
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Milwaukee, Wisconsin, 미국, 53226
- Midwest Children's Cancer Center
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Ontario
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Toronto, Ontario, 캐나다, M5G 1X8
- Hospital for Sick Children
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Quebec
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Montreal, Quebec, 캐나다, H3H 1P3
- Montreal Children's Hospital
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Montreal, Quebec, 캐나다, H3T 1C5
- Hôpital Sainte Justine
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Victoria
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Parkville, Victoria, 호주, 3052
- Royal Children's Hospital
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Western Australia
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Perth, Western Australia, 호주, 6001
- Princess Margaret Hospital for Children
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
DISEASE CHARACTERISTICS: Histologically confirmed malignant solid tumor at original diagnosis Refractory to standard treatment or no curative therapy available No CNS tumor No bone marrow metastases (for less heavily pretreated stratum only)
PATIENT CHARACTERISTICS: Age: At least 365 days to 17 years Performance status: Karnofsky 50-100% (for patients older than 10 years) Lansky 50-100% (for patients 10 years and younger) Life expectancy: At least 8 weeks Hematopoietic: Absolute neutrophil count at least 1,500/mm3 Platelet count at least 100,000/mm3 (transfusion independent) Hemoglobin at least 8.0 g/dL (RBC transfusion allowed) Hepatic: Bilirubin no greater than normal SGPT no greater than 2.5 times normal Albumin at least 2 g/dL Alkaline phosphatase normal Gamma glutamyl transferase less than 2.5 times normal Renal: Creatinine no greater than 1.5 times normal OR Creatinine clearance or GFR at least lower limit of normal Other: Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception Creatine phosphokinase less than 2 times normal No uncontrolled infection Seizure disorder allowed if well controlled on anticonvulsants No CNS toxicity greater than grade II
PRIOR CONCURRENT THERAPY: Biologic therapy: At least 1 week since prior biologic therapy and recovered At least 1 week since prior growth factor therapy At least 6 months since prior peripheral blood stem cell transplantation and no evidence of graft-vs-host disease For less heavily pretreated stratum: No prior peripheral blood stem cell transplantation Chemotherapy: At least 4 weeks since prior myelosuppressive chemotherapy (6 weeks for nitrosoureas) and recovered No prior ecteinascidin 743 For less heavily pretreated stratum: No more than 2 prior chemotherapy regimens Endocrine therapy: Not specified Radiotherapy: At least 2 weeks since prior local palliative radiotherapy (small port) At least 6 weeks since prior substantial bone marrow radiotherapy At least 6 months since prior craniospinal radiotherapy or radiotherapy to 50% or greater of pelvis For less heavily pretreated stratum: No prior craniospinal irradiation of 18Gy or greater No prior irradiation to greater than 50% of pelvis Recovered from toxic effects of prior radiotherapy Surgery: Not specified Other: No concurrent foods or medication that interferes with P-450 metabolism Anticonvulsants allowed
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Therapy ECTEINASCIDIN 743 (1100 ug/m2 )
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다른 이름들:
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실험적: ECTEINASCIDIN 743 (1300 ug/m2)
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다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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무진행 생존
기간: 공부 기간
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공부 기간
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Dose Limiting Toxicity
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To determine the maximum tolerated dose (MTD) of vincristine, when used in combination with irinotecan, and the dose-limiting toxicity (DLT) of this combination; irinotecan will be administered IV over 1 hour x 5 days, q 21 days, with vincristine IVP days 1, 8, 15, 22, 29, every 42 days, to children with refractory solid tumors.
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Determine a safe and tolerable dose of vincristine, when administered with irinotecan
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To determine a safe and tolerable dose of vincristine, when administered with irinotecan, for future evaluation in phase II clinical trials.
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Determine the pharmacokinetics of vincristine and irinotecan
기간: Length of study
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To determine the pharmacokinetics of vincristine and irinotecan (and its active metabolite SN-38) when administered in combination to children with refractory cancer.
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Length of study
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Determine the incidence and severity of other toxicities
기간: Length of study
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To determine the incidence and severity of other toxicities of this combination.
|
Length of study
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Seek preliminary evidence of anti-tumor activity of irinotecan plus vincristine
기간: Length of study
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To seek preliminary evidence of anti-tumor activity of irinotecan plus vincristine against recurrent solid tumors.
|
Length of study
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공동 작업자 및 조사자
수사관
- 연구 의자: Sylvain Baruchel, MD, The Hospital for Sick Children
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- P9972
- COG-P9972 (기타 식별자: Children's Oncology Group)
- POG-P9972 (기타 식별자: Pediatric Oncology Group)
- CDR0000068273 (기타 식별자: Clinical Trials.gov)
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .