Evaluating Many Treatments and Biomarkers in Oncology: A New Design

被引:100
作者
Kaplan, Richard [1 ]
Maughan, Timothy [2 ]
Crook, Angela [1 ]
Fisher, David [1 ]
Wilson, Richard [3 ]
Brown, Louise [1 ]
Parmar, Mahesh [1 ]
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.
引用
收藏
页码:4562 / +
页数:9
相关论文
共 43 条
[1]   Toxicity associated with combination oxaliplatin plus fluoropyrimidine with or without cetuximab in the MRC COIN trial experience [J].
Adams, R. A. ;
Meade, A. M. ;
Madi, A. ;
Fisher, D. ;
Kay, E. ;
Kenny, S. ;
Kaplan, R. S. ;
Maughan, T. S. .
BRITISH JOURNAL OF CANCER, 2009, 100 (02) :251-258
[2]   Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer [J].
Amado, Rafael G. ;
Wolf, Michael ;
Peeters, Marc ;
Van Cutsem, Eric ;
Siena, Salvatore ;
Freeman, Daniel J. ;
Juan, Todd ;
Sikorski, Robert ;
Suggs, Sid ;
Radinsky, Robert ;
Patterson, Scott D. ;
Chang, David D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (10) :1626-1634
[3]  
[Anonymous], 2010, NATURE, V464, p1245 1246
[4]   I-SPY 2: An Adaptive Breast Cancer Trial Design in the Setting of Neoadjuvant Chemotherapy [J].
Barker, A. D. ;
Sigman, C. C. ;
Kelloff, G. J. ;
Hylton, N. M. ;
Berry, D. A. ;
Esserman, L. J. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2009, 86 (01) :97-100
[5]   A menu-driven facility for sample-size calculation in novel multiarm, multistage randomized controlled trials with a time-to-event outcome [J].
Barthel, Friederike M-S. ;
Royston, Patrick ;
Parmar, Mahesh K. B. .
STATA JOURNAL, 2009, 9 (04) :505-523
[6]   Molecularly targeted therapies for metastatic triple-negative breast cancer [J].
Bayraktar, Soley ;
Glueck, Stefan .
BREAST CANCER RESEARCH AND TREATMENT, 2013, 138 (01) :21-35
[7]   Triple-negative breast cancer in the older population [J].
Boyle, P. .
ANNALS OF ONCOLOGY, 2012, 23 :7-12
[8]   Survival of patients with Stage III colon cancer is improved in hereditary non-polyposis colorectal cancer compared with sporadic cases. A Danish registry based study [J].
Brixen, L. M. ;
Bernstein, I. T. ;
Bulow, S. ;
Ehrnrooth, E. .
COLORECTAL DISEASE, 2013, 15 (07) :816-823
[9]  
Cortesi L, 2012, TUMORI J, V98, P743, DOI 10.1700/1217.13498
[10]   Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis [J].
De Roock, Wendy ;
Claes, Bart ;
Bernasconi, David ;
De Schutter, Jef ;
Biesmans, Bart ;
Fountzilas, George ;
Kalogeras, Konstantine T. ;
Kotoula, Vassiliki ;
Papamichael, Demetris ;
Laurent-Puig, Pierre ;
Penault-Llorca, Frederique ;
Rougier, Philippe ;
Vincenzi, Bruno ;
Santini, Daniele ;
Tonini, Giuseppe ;
Cappuzzo, Federico ;
Frattini, Milo ;
Molinari, Francesca ;
Saletti, Piercarlo ;
De Dosso, Sara ;
Martini, Miriam ;
Bardelli, Alberto ;
Siena, Salvatore ;
Sartore-Bianchi, Andrea ;
Tabernero, Josep ;
Macarulla, Teresa ;
Di Fiore, Frederic ;
Gangloff, Alice Oden ;
Ciardiello, Fortunato ;
Pfeiffer, Per ;
Qvortrup, Camilla ;
Hansen, Tine Plato ;
Van Cutsem, Eric ;
Piessevaux, Hubert ;
Lambrechts, Diether ;
Delorenzi, Mauro ;
Tejpar, Sabine .
LANCET ONCOLOGY, 2010, 11 (08) :753-762