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Alvocidib in Treating Patients With Metastatic or Unresectable Refractory Solid Tumors or Hematologic Malignancies

2013년 12월 13일 업데이트: National Cancer Institute (NCI)

A Phase I Clinical, Pharmacokinetic and Pharmacodynamic Study of Flavopiridol in Patients With Refractory Solid Tumors and Hematologic Malignancies

This phase I trial is studying the side effects and best dose of alvocidib in treating patients with metastatic or unresectable refractory solid tumors or hematologic malignancies. Drugs used in chemotherapy, such as alvocidib, work in different ways to stop cancer cells from dividing so they stop growing or die.

연구 개요

상세 설명

PRIMARY OBJECTIVE:

I. Determine the maximum tolerated dose of flavopiridol in patients with metastatic or unresectable refractory solid tumors or hematologic malignancies. (Accrual for patients with hematologic malignancies temporarily closed as of 11/30/04)

SECONDARY OBJECTIVES:

I. Determine the safety profile and toxic effects of this drug in these patients.

II. Determine the pharmacokinetics of this drug in these patients. III. Determine, by pharmacodynamic assays, the ability of this drug to inhibit cyclin-dependent kinase activity in tumor tissue, normal proliferating tissues, circulating tumor cells, and in plasma in these patients.

IV. Determine, preliminarily, the antitumor activity of this drug in these patients.

OUTLINE: This is a 2-part, dose-escalation, multicenter study.

PART 1 (closed to accrual as of 8/2005): Patients receive alvocidib IV over 1 hour on days 1, 8, and 15.

Cohorts of 3-6 patients receive escalating doses of alvocidib until the maximum tolerated dose (MTD)* is determined.

PART 2: Patients receive alvocidib IV over 1 hour at or below the MTD determined in part 1 and then receive a maintenance dose of alvocidib IV over 1-6 hours on days 1, 8, and 15. Cohorts of 3-6 patients receive escalating durations of the maintenance dose of alvocidib until the MTD* is determined. An additional cohort of 10-20 patients receives alvocidib over 1 hour on days 1 and 15 at the MTD.

NOTE: *The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

In both parts, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Patients are followed at 1 month and then every 2 months thereafter.

연구 유형

중재적

등록 (실제)

100

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Massachusetts
      • Boston, Massachusetts, 미국, 02115
        • Dana-Farber Cancer Institute

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Histologically confirmed malignancy, including the following types:

    • Hematologic malignancy, including any of the following: (Accrual for patients with hematologic malignancies temporarily closed as of 11/30/04)
    • Mantle cell lymphoma
    • Morphologically confirmed disease
    • CD20 and CD5 positive
    • Any other refractory lymphoma
    • Chronic lymphocytic leukemia
  • Rai stage III or IV and meeting at least 1 of the following criteria for active disease:

    • Weight loss > 10% in the last 6 months
    • Fatigue
    • Fever or night sweats with no evidence of infection
    • Progressive anemia or thrombocytopenia
    • Progressive lymphocytosis with a lymphocyte doubling time of < 6 months
    • Marked hypogammaglobulinemia or paraproteinemia
    • Progressive splenomegaly and/or lymphadenopathy
    • Multiple myeloma
    • Disease confirmed by bone marrow aspirate and/or biopsy
    • Relapsed or refractory disease after the most recent treatment regimen
    • Quantifiable monoclonal immunoglobulin in serum and/or urine
  • Solid tumor, including but not limited to any of the following:

    • Breast cancer
    • Histologically or cytologically confirmed stage IV invasive disease
    • HER-2 positivity not required for study enrollment
    • Tumor overexpressing HER-2 should be confirmed by immunohistochemistry OR fluorescence in situ hybridization
    • Small cell lung cancer
    • Extensive stage or limited stage disease in relapse
    • Extrapulmonary small cell carcinoma allowed
    • Squamous cell carcinoma of the head and neck
    • Metastatic, recurrent, or refractory disease
    • Renal cell carcinoma
    • Mesothelioma
    • Pleural or peritoneal disease of epithelial, sarcomatoid, or mixed subtype
    • Melanoma
    • Kaposi's sarcoma
    • Metastatic or unresectable disease for which standard therapy does not exist or is no longer effective
    • Measurable or nonmeasurable disease (solid tumor patients)
    • Measurable disease defined as at least 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques or 10 mm by spiral CT scan
  • Nonmeasurable disease includes any of the following:

    • All other lesions, including lesions < 20 mm by conventional techniques or 10 mm by spiral CT scan
    • Bone lesions
    • Cytologically positive pleural or peritoneal disease
    • Elevated tumor marker (e.g., CEA, CA 125, CA 19-9, or other tumor marker)
    • Multinodular or confluent nonmeasurable pulmonary, hepatic, adrenal, intra-abdominal, or skin metastases
    • Previously treated with at least 1 chemotherapy regimen*
    • Prior therapy may have included combined modality treatment (e.g., full-dose chemotherapy and radiotherapy with radiosensitizing chemotherapy)
    • Prior therapy with flavopiridol allowed provided the patient was enrolled in a flavopiridol clinical trial employing a different schedule NOTE: *Except in cases where chemotherapy is not known to be effective (e.g., renal cell carcinoma, chondrosarcoma, or gastrointestinal stromal tumor)
    • No active CNS metastases
  • History of CNS metastases allowed provided all of the following criteria are met:

    • Previously treated and stable and asymptomatic for at least 4 weeks since the completion of treatment
    • Image documentation required
    • Off steroids or on a stable dose of steroids for at least 1 week
  • Hormone receptor status:

    • Not specified
  • Age

    • 18 and over
  • Sex

    • Male or female
  • Menopausal status

    • Not specified
  • Performance status

    • ECOG 0-1 OR
    • Karnofsky 70-100%
  • Life expectancy

    • More than 12 weeks
  • Hematopoietic

    • Absolute neutrophil count > 1,000/mm^3*
    • Platelet count > 75,000/mm^3 (50,000 for hematologic malignancies)* (Accrual for patients with hematologic malignancies temporarily closed as of 11/30/04) NOTE: *Unless abnormality is caused by tumor burden and not cumulative prior chemotherapy
  • Hepatic

    • Bilirubin normal
    • AST/ALT ≤ 2.5 times upper limit of normal (ULN) (5 times ULN if liver metastases are present)
  • Renal

    • Creatinine ≤ 2.0 mg/dL OR
    • Creatinine clearance ≥ 60 mL/min
  • Cardiovascular

    • No myocardial infarction within the past 6 months
    • No unstable angina within the past 6 months
    • No transient ischemic attack or cerebrovascular accident within the past 6 months
    • No history of arterial vascular events
    • No new cardiac arrhythmias likely to be related to cardiac ischemia within the past 6 months
    • No symptomatic congestive heart failure
  • Pulmonary

    • No history of pulmonary embolism within the past 6 months
  • Gastrointestinal

    • No chronic diarrheal disease within the past 6 months
    • No severe malnutrition
    • No intractable emesis
  • Other

    • Not pregnant or nursing
    • Negative pregnancy test
    • Fertile patients must use effective hormonal or barrier contraception
    • No ongoing or active infection
    • No other concurrent uncontrolled illness
    • No psychiatric illness or social situation that would preclude study compliance
  • At least 3 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin)
  • At least 3 weeks since prior radiotherapy No prior radiotherapy to 50% or more of bone marrow
  • Recovered from all prior therapy No other concurrent investigational agents No concurrent combination antiretroviral therapy for HIV-positive patients

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

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
실험적: Treatment

PART 1 (closed to accrual as of 8/2005): Patients receive alvocidib IV over 1 hour on days 1, 8, and 15.

Cohorts of 3-6 patients receive escalating doses of alvocidib until the MTD* is determined.

PART 2: Patients receive alvocidib IV over 1 hour at or below the MTD determined in part 1 and then receive a maintenance dose of alvocidib IV over 1-6 hours on days 1, 8, and 15. Cohorts of 3-6 patients receive escalating durations of the maintenance dose of alvocidib until the MTD* is determined. An additional cohort of 10-20 patients receives alvocidib over 1 hour on days 1 and 15 at the MTD.

NOTE: *The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

In both parts, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

주어진 IV
다른 이름들:
  • 플라보
  • 플라보피리돌
  • HMR 1275
  • L-868275
상관 연구
다른 이름들:
  • 약리학 연구
상관 연구
다른 이름들:
  • 18FDG
  • FDG
Correlative studies
다른 이름들:
  • 18F-FLT
  • 3'-데옥시-3'-[18F]플루오로티미딘
  • 플루오로티미딘 F-18
상관 연구
다른 이름들:
  • 애완 동물
  • FDG-펫
  • PET 스캔
  • 단층 촬영, 방출 계산

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
용량 제한 독성(DLT)
기간: 28일
28일
MTD (or recommended phase II dose), defined as one dose level below that which produces two instances of DLT during the first 28-day course and the level at which no more than one of six patients experiences DLT during course 1
기간: 28 days
28 days

2차 결과 측정

결과 측정
측정값 설명
기간
Pharmacokinetic parameters, including maximum concentration (Cmax), half-life, area under the curve (AUC), clearance, and volume of distribution
기간: 24 hours, 48 hours, 72 hours, and 8 weeks
Determined by nonlinear regression analysis of geometric mean plasma profile. Cmax in patients w/stable disease or response at 8 weeks compared to those who progressed using Mann-Whitney test. Wilcoxon signed-rank test to compare concentration and metabolic ratios directly following infusion and 24, 48, 72 hrs later. Concentration and metabolic ratios compared in patients w/ and w/o toxicities of diarrhea, neutropenia, and asthenia using Mann- Whitney test. Fisher's exact test to assess association of flavopiridol systemic metabolism (low vs. high metabolic ratio) w/development of toxicity.
24 hours, 48 hours, 72 hours, and 8 weeks
Potency of alvocidib in plasma based on change in proliferation of stimulated peripheral blood mononuclear cells (PBMCs)
기간: Baseline to up to 72 hours of day 1 course 1
Baseline to up to 72 hours of day 1 course 1
Change in tumor metabolism and proliferation assessed by fludeoxyglucose F 18 (FDG) and fluorine F 18 fluorothymidine (FLT) positron emission tomography (PET)
기간: Baseline to up to day 19 of course 2
Each type of pre- and post-treatment scans may be analyzed as paired data. The FDG and FLT data will be correlated to explore the relationship between tumor metabolism and tumor proliferation, for example, using Pearson or Spearman correlation coefficient.
Baseline to up to day 19 of course 2

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Geoffrey Shapiro, Dana-Farber Cancer Institute

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2003년 8월 1일

기본 완료 (실제)

2006년 6월 1일

연구 완료

2022년 12월 7일

연구 등록 날짜

최초 제출

2003년 10월 3일

QC 기준을 충족하는 최초 제출

2003년 10월 6일

처음 게시됨 (추정)

2003년 10월 7일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2013년 12월 16일

QC 기준을 충족하는 마지막 업데이트 제출

2013년 12월 13일

마지막으로 확인됨

2013년 12월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • NCI-2009-00039 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
  • 03-082 (Dana-Farber Cancer Institute)
  • P 6052
  • CDR0000331689
  • 6052 (CTEP)
  • U01CA062490 (미국 NIH 보조금/계약)

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

미국에서 제조되어 미국에서 수출되는 제품

아니

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. .

알보시딥에 대한 임상 시험

3
구독하다