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
[21]   Outcome-Adaptive Randomization: Is It Useful? [J].
Korn, Edward L. ;
Freidlin, Boris .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (06) :771-776
[22]   Anaplastic Lymphoma Kinase Inhibition in Non-Small-Cell Lung Cancer [J].
Kwak, Eunice L. ;
Bang, Yung-Jue ;
Camidge, D. Ross ;
Shaw, Alice T. ;
Solomon, Benjamin ;
Maki, Robert G. ;
Ou, Sai-Hong I. ;
Dezube, Bruce J. ;
Jaenne, Pasi A. ;
Costa, Daniel B. ;
Varella-Garcia, Marileila ;
Kim, Woo-Ho ;
Lynch, Thomas J. ;
Fidias, Panos ;
Stubbs, Hannah ;
Engelman, Jeffrey A. ;
Sequist, Lecia V. ;
Tan, WeiWei ;
Gandhi, Leena ;
Mino-Kenudson, Mari ;
Wei, Greg C. ;
Shreeve, S. Martin ;
Ratain, Mark J. ;
Settleman, Jeffrey ;
Christensen, James G. ;
Haber, Daniel A. ;
Wilner, Keith ;
Salgia, Ravi ;
Shapiro, Geoffrey I. ;
Clark, Jeffrey W. ;
Iafrate, A. John .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) :1693-1703
[23]   Microsatellite Instability and Therapeutic Consequences in Colorectal Cancer [J].
Laghi, Luigi ;
Malesci, Alberto .
DIGESTIVE DISEASES, 2012, 30 (03) :304-309
[24]   Clinical trial designs for testing biomarker-based personalized therapies [J].
Lai, Tze Leung ;
Lavori, Philip W. ;
Shih, Mei-Chiung I. ;
Sikic, Branimir I. .
CLINICAL TRIALS, 2012, 9 (02) :141-154
[25]   Clinical drug tests adapted for speed [J].
Ledford, Heidi .
NATURE, 2010, 464 (7293) :1258-1258
[26]   Bayesian adaptive randomization designs for targeted agent development [J].
Lee, J. Jack ;
Gu, Xuemin ;
Liu, Suyu .
CLINICAL TRIALS, 2010, 7 (05) :584-596
[27]   KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer [J].
Lièvre, A ;
Bachet, JB ;
Le Corre, D ;
Boige, V ;
Landi, B ;
Emile, JF ;
Côté, JF ;
Tomasic, G ;
Penna, C ;
Ducreux, M ;
Rougier, P ;
Penault-Llorca, F ;
Laurent-Puig, P .
CANCER RESEARCH, 2006, 66 (08) :3992-3995
[28]   Locally advanced breast cancers are more likely to present as Interval Cancers: results from the I-SPY 1 TRIAL (CALGB 150007/150012, ACRIN 6657, InterSPORE Trial) [J].
Lin, Cheryl ;
Buxton, Meredith Becker ;
Moore, Dan ;
Krontiras, Helen ;
Carey, Lisa ;
DeMichele, Angela ;
Montgomery, Leslie ;
Tripathy, Debasish ;
Lehman, Constance ;
Liu, Minetta ;
Olapade, Olufunmilayo ;
Yau, Christina ;
Berry, Donald ;
Esserman, Laura J. .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 132 (03) :871-879
[29]   Oxaliplatin/capecitabine vs oxaliplatin/infusional 5-FU in advanced colorectal cancer: the MRC COIN trial [J].
Madi, A. ;
Fisher, D. ;
Wilson, R. H. ;
Adams, R. A. ;
Meade, A. M. ;
Kenny, S. L. ;
Nichols, L. L. ;
Seymour, M. T. ;
Wasan, H. ;
Kaplan, R. ;
Maughan, T. S. .
BRITISH JOURNAL OF CANCER, 2012, 107 (07) :1037-1043
[30]   Predictive biomarker validation in practice: lessons from real trials [J].
Mandrekar, Sumithra J. ;
Sargent, Daniel J. .
CLINICAL TRIALS, 2010, 7 (05) :567-573