- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00098527
FR901228 in Treating Patients With Refractory Stomach Cancer or Gastroesophageal Junction Cancer
A Phase 2 Study of Single Agent Depsipeptide (FK228) in Gastric and Esophageal Cancers
연구 개요
상세 설명
PRIMARY OBJECTIVES:
I. Determine the radiographic response rate (complete response and partial response) in patients with refractory adenocarcinoma of the stomach or gastroesophageal junction treated with FR901228 (depsipeptide).
SECONDARY OBJECTIVES:
I. Determine the median time to progression and progression-free survival of patients treated with this drug.
II. Determine the grade 3 and 4 toxic effects of this drug in these patients.
OUTLINE: This is an open-label, multicenter study.
Patients receive FR901228 (depsipeptide) IV over 4 hours on days 1, 8, and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
PROJECTED ACCRUAL: A total of 13-20 patients will be accrued for this study within 6.5-10 months.
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
-
-
North Carolina
-
Durham, North Carolina, 미국, 27710
- Duke University Medical Center
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Histologically or cytologically confirmed adenocarcinoma of the stomach or gastroesophageal junction
Measurable disease
- At least 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral CT scan
Refractory* to at least 1, but no more than 3, of the following first-line agents:
- Fluoropyrimidine (e.g., capecitabine or fluorouracil)
- Taxane (e.g., paclitaxel or docetaxel)
- Platinum (e.g., carboplatin, cisplatin, or oxaliplatin)
No known active brain metastases
- Treated brain metastases allowed provided metastases are stable off steroids for ≥ 30 days
- Performance status - ECOG 0-2
- Performance status - Karnofsky 60-100%
- At least 3 months
- WBC ≥ 3,000/mm^3
- Absolute neutrophil count ≥ 1,500/mm^3
- Platelet count ≥ 100,000/mm^3
- Bilirubin ≤ 1.5 times upper limit of normal (ULN)
- AST and ALT ≤ 2.5 times ULN (5 times ULN if liver metastases are present)
- Creatinine clearance ≥ 50 mL/min
- No congestive heart failure
- No New York Heart Association class III or IV heart disease
- No myocardial infarction within the past 6 months
- No ventricular arrhythmias requiring medication
- No angioplasty or vascular stenting within the past 3 months
- No unstable angina
- No left ventricular hypertrophy by EKG
- No known history of serious ventricular arrhythmia (e.g., ventricular tachycardia or ventricular fibrillation ≥ 3 beats in a row)
- QTc < 500 msec
- LVEF > 40% by MUGA or echocardiogram
- No other significant cardiac disease
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- Potassium ≥ 4.0 mmol/L (stable level with no change in supplementation within the past 2 weeks)
- Magnesium ≥ 2.0 mg/dL (stable level with no change in supplementation within the past 2 weeks)
- No history of allergic reaction attributed to compounds of similar chemical or biologic composition to study drug
- No ongoing or active infection
- No psychiatric illness or social situation that would preclude study compliance
- No other uncontrolled illness
- Prior biological agents allowed
- No concurrent prophylactic filgrastim (G-CSF)
- No concurrent biologic therapy
- More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered
- No other concurrent chemotherapy
- More than 4 weeks since prior radiotherapy and recovered
- No concurrent radiotherapy
- Prior targeted agents allowed
- No other prior or concurrent cytotoxic agents
- No other concurrent investigational agents
- No other concurrent anticancer therapy
- No concurrent medications causing QTc prolongation
- No concurrent potassium supplementation > 40 mg/day or magnesium supplementation > 1 g/week
- No concurrent hydrochlorothiazide
- No concurrent combination antiretroviral therapy for HIV-positive patients
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 |
|---|---|
|
실험적: 치료(로미뎁신)
환자는 1일, 8일 및 15일에 4시간에 걸쳐 FR901228(depsipeptide) IV를 투여받습니다.
과정은 질병 진행 또는 허용할 수 없는 독성이 없는 경우 28일마다 반복됩니다.
|
상관 연구
주어진 IV
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Radiographic response rate (complete response & partial response)
기간: Not Provided
|
Not Provided
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Progression-free survival (PFS) according to RECIST
기간: Up to more than 6 months
|
The median time to progression and median PFS for all eligible patients, along with their CIs, will be reported.
The Kaplan-Meier analysis approach may be used to summarize these time-to-event endpoints.
|
Up to more than 6 months
|
|
Frequency of treatment related grade 1-4 toxicities and cardiac toxicities as assessed by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 3.0
기간: Up to 12 months
|
Up to 12 months
|
|
|
Correlation of changes in gene expression profile in dermal granulation tissue pre- and post-treatment with gene expression profile
기간: Not Provided
|
Not Provided
|
|
|
Correlation of wound vascular scores pre- and post-treatment with gene/protein changes
기간: Not Provided
|
Not Provided
|
|
|
Toxicity
기간: Not Provided
|
Not Provided
|
|
|
Changes in gene expression profile
기간: At pre- and post-treatment
|
At pre- and post-treatment
|
|
|
Changes in levels of p21 and thymidine kinase expression, and tubulin acetylation using Western blotting
기간: From baseline to 3 weeks
|
From baseline to 3 weeks
|
|
|
Changes in gene expression profile in dermal granulation tissue
기간: From baseline to up to 3 weeks
|
From baseline to up to 3 weeks
|
|
|
Change in plasma and urine TGFB levels
기간: At pre-and post-treatment
|
At pre-and post-treatment
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Herbert Hurwitz, Duke University
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 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 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. .