- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00139360
Efficacy of Bevacizumab Monotherapy in Treatment of Metastatic Melanoma
Efficacy of Bevacizumab Monotherapy in Treatment of Metastatic Melanoma and Predictive Value of Angiogenic Markers
연구 개요
상세 설명
In Norway, cutaneous malignant melanoma is the second most frequent and the most frequent cancer type in middle-aged (30-54 years) females and males, respectively, and the incidence has six-doubled during the last 30 years. Median survival for patients with metastatic melanoma is 6 months.
Many agents have been investigated for anti-tumor effect in melanoma, but there is no accepted standard therapy. Biochemotherapy, combining cytotoxic drugs with Interleukin-2 or Interferon alpha, has not been shown to be superior to single agent Dacarbazine (DTIC), which is regarded to be the most active agent. Other biological approaches like vaccination are currently under investigation, but still no efficient treatment for metastatic melanoma is available. DTIC induces objective remission in 20% of the patients, but without significant impact on survival.
The need of a new and effective treatment for the group of melanoma patients is urgently needed. This will be the first study to assess response rates of bevacizumab monotherapy in first line treatment of metastatic melanoma. In addition there will be a major focus on the identification of predictive biomarkers of bevacizumab efficacy.
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
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Bergen, 노르웨이, 5020
- Department of Oncology, Haukeland University Hospital
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
LEVEL A (second line): after confirmed progression on standard first line treatment with dacarbazine.
LEVEL B (first line): when objective clinical response is observed in LEVEL A, patients will be included for first line treatment with bevacizumab
Inclusion Criteria:
- Histologically confirmed metastatic (unresectable) melanoma and with progressive disease
- WHO performance status 0-2
- Age >18 years
- Able to undergo outpatient treatment
- Patients must have clinically and/or radiographically documented measurable disease according to RECIST criteria
- At least 4 weeks since adjuvant interferon alpha
- Recovered from prior chemotherapy
- Major surgical procedure or significant traumatic injury within 28 days prior to study treatment start. Biopsy or fine needle aspiration within 5 days prior to study treatment start. Central venous line placement must be inserted at least 5 days prior to treatment start.
- Minimum required laboratory data:
Hematology: absolute granulocytes > 1.0 x 109/L platelets > 100 x 109/L Biochemistry: bilirubin < 1.5 x upper normal limit serum creatinine within normal limits INR < 1.5
- Before patient registration/randomization, written informed consent must be given according to national and local regulations.
Exclusion Criteria:
- No pregnant or lactating patients can be included
- No prior interferon alpha or IL-2 for metastatic disease
- No more than 1 prior chemotherapy regimen for metastatic disease
- No clinical evidence of coagulopathy
- No brain metastases
- No symptomatic congestive heart failure
- No unstable angina pectoris
- No cardiac arrhythmia
- No history of thrombosis
- No full-dose oral coumarin-derived anticoagulants (INR>1.5) or heparin, thrombolytic agents, or chronic, daily treatment with aspirin (>325 mg/day)
- No non-steroidal anti-inflammatory medications (those known to inhibit platelet function at doses used to treat chronic inflammatory diseases)
- No uncontrolled hypertension
- Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: 1
Active drug
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Anti angiogenesis treatment
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Clinical Response rates
기간: Evaluated by CT scans every 12 weeks, later every 6 monts. Up to 10 years.
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Evaluated by CT scans every 12 weeks, later every 6 monts. Up to 10 years.
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Time to progression
기간: Evaluated by CT scans every 12 weeks, later every 6 monts. Up to 10 years.
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Evaluated by CT scans every 12 weeks, later every 6 monts. Up to 10 years.
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Overall survival
기간: Evaluated by CT scans every 12 weeks, later every 6 monts. Up to 10 years.
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Evaluated by CT scans every 12 weeks, later every 6 monts. Up to 10 years.
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Safety data
기간: Evaluated by consultations every 12 weeks, later every 6 monts. Up to 10 years.
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CTCAEv2 side effects
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Evaluated by consultations every 12 weeks, later every 6 monts. Up to 10 years.
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공동 작업자 및 조사자
수사관
- 수석 연구원: Oddbjorn Straume, MD, PhD, Department of Oncology, Haukeland University Hospital
간행물 및 유용한 링크
일반 간행물
- Schuster C, Akslen LA, Straume O. Expression of Heat Shock Protein 27 in Melanoma Metastases Is Associated with Overall Response to Bevacizumab Monotherapy: Analyses of Predictive Markers in a Clinical Phase II Study. PLoS One. 2016 May 11;11(5):e0155242. doi: 10.1371/journal.pone.0155242. eCollection 2016.
- Schuster C, Eikesdal HP, Puntervoll H, Geisler J, Geisler S, Heinrich D, Molven A, Lonning PE, Akslen LA, Straume O. Clinical efficacy and safety of bevacizumab monotherapy in patients with metastatic melanoma: predictive importance of induced early hypertension. PLoS One. 2012;7(6):e38364. doi: 10.1371/journal.pone.0038364. Epub 2012 Jun 15.
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
- NSD-11933
- 94070/013
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