共 43 条
Evaluating Many Treatments and Biomarkers in Oncology: A New Design
被引:100
作者:

Kaplan, Richard
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Clin Trials Unit, London WC2B 6NH, England MRC, Clin Trials Unit, London WC2B 6NH, England

Maughan, Timothy
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, Oxford, England MRC, Clin Trials Unit, London WC2B 6NH, England

Crook, Angela
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Clin Trials Unit, London WC2B 6NH, England MRC, Clin Trials Unit, London WC2B 6NH, England

Fisher, David
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Clin Trials Unit, London WC2B 6NH, England MRC, Clin Trials Unit, London WC2B 6NH, England

Wilson, Richard
论文数: 0 引用数: 0
h-index: 0
机构:
Queens Univ Belfast, Belfast, Antrim, North Ireland MRC, Clin Trials Unit, London WC2B 6NH, England

Brown, Louise
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Clin Trials Unit, London WC2B 6NH, England MRC, Clin Trials Unit, London WC2B 6NH, England

Parmar, Mahesh
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Clin Trials Unit, London WC2B 6NH, England MRC, Clin Trials Unit, London WC2B 6NH, England
机构:
[1] MRC, Clin Trials Unit, London WC2B 6NH, England
[2] Univ Oxford, Oxford, England
[3] Queens Univ Belfast, Belfast, Antrim, North Ireland
基金:
英国医学研究理事会;
关键词:
METASTATIC COLORECTAL-CANCER;
CLINICAL-TRIAL DESIGNS;
NEGATIVE BREAST-CANCER;
MRC COIN TRIAL;
ADAPTIVE RANDOMIZATION;
MUTATION STATUS;
LUNG-CANCER;
CETUXIMAB;
CHEMOTHERAPY;
VALIDATION;
D O I:
10.1200/JCO.2013.50.7905
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
There is a pressing need for more-efficient trial designs for biomarker-stratified clinical trials. We suggest a new approach to trial design that links novel treatment evaluation with the concurrent evaluation of a biomarker within a confirmatory phase II/III trial setting. We describe a new protocol using this approach in advanced colorectal cancer called FOCUS4. The protocol will ultimately answer three research questions for a number of treatments and biomarkers: (1) After a period of first-line chemotherapy, do targeted novel therapies provide signals of activity in different biomarker-defined populations? (2) If so, do these definitively improve outcomes? (3) Is evidence of activity restricted to the biomarker-defined groups? The protocol randomizes novel agents against placebo concurrently across a number of different biomarker-defined population-enriched cohorts: BRAF mutation; activated AKT pathway: PI3K mutation/absolute PTEN loss tumors; KRAS and NRAS mutations; and wild type at all the mentioned genes. Within each biomarker-defined population, the trial uses a multistaged approach with flexibility to adapt in response to planned interim analyses for lack of activity. FOCUS4 is the first test of a protocol that assigns all patients with metastatic colorectal cancer to one of a number of parallel population-enriched, biomarker-stratified randomized trials. Using this approach allows questions regarding efficacy and safety of multiple novel therapies to be answered in a relatively quick and efficient manner, while also allowing for the assessment of biomarkers to help target treatment.
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页码:4562 / +
页数:9
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Univ Oxford, Churchill Hosp, Dept Oncol, Gray Inst Radiat Oncol & Biol, Oxford OX3 7DQ, England Univ Oxford, Churchill Hosp, Dept Oncol, Gray Inst Radiat Oncol & Biol, Oxford OX3 7DQ, England
[30]
Predictive biomarker validation in practice: lessons from real trials
[J].
Mandrekar, Sumithra J.
;
Sargent, Daniel J.
.
CLINICAL TRIALS,
2010, 7 (05)
:567-573

Mandrekar, Sumithra J.
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Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA

Sargent, Daniel J.
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Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA