Analysis of phase II studies on targeted agents and subsequent phase III trials: What are the predictors for success?

被引:49
作者
Chan, John K. [1 ]
Ueda, Stefanie M.
Sugiyama, Valerie E.
Stave, Christopher D.
Shin, Jacob Y.
Monk, Bradley J.
Sikic, Branimir I.
Osann, Kathryn
Kapp, Daniel S.
机构
[1] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, Div Gynecol Oncol, Dept Obstet & Gynecol, San Francisco, CA 94143 USA
关键词
D O I
10.1200/JCO.2007.14.8874
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To identify the characteristics of phase II studies that predict for subsequent "positive" phase III trials (those that reached the proposed primary end points of study or those wherein the study drug was superior to the standard regimen investigating targeted agents in advanced tumors. Methods We identified all phase III clinical trials of targeted therapies against advanced cancers published from 1985 to 2005. Characteristics of the preceding phase II studies were reviewed to identify predictive factors for success of the subsequent phase III trial. Data were analyzed using the chi(2) test and logistic regression models. Results Of 351 phase II studies, 167 (47.6%) subsequent phase III trials were positive and 184 (52.4%) negative. Phase II studies from multiple rather than single institutions were more likely to precede a successful trial (60.4% v 39.4%; P < .001). Positive phase II results were more likely to lead to a successful phase III trial (50.8% v 22.5%; P = .003). The percentage of successful trials from pharmaceutical companies was significantly higher compared with academic, cooperative groups, and research institutes (89.5% v 44.2%, 45.2%, and 46.3%, respectively; P = .002). On multivariate analysis, these factors and shorter time interval between publication of phase II results and III study publication were independent predictive factors for a positive phase III trial. Conclusion In phase II studies of targeted agents, multiple-versus single-institution participation, positive phase II trial, pharmaceutical company-based trials, and shorter time period between publication of phase II to phase III trial were independent predictive factors of success in a phase III trial. Investigators should be cognizant of these factors in phase II studies before designing phase III trials.
引用
收藏
页码:1511 / 1518
页数:8
相关论文
共 36 条
[1]   The phase III candidate: Can we improve the science of selection? [J].
Bajorin, D .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (02) :211-213
[2]   Association of industry sponsorship to published outcomes in gastrointestinal clinical research [J].
Brown, Alphonso ;
Kraft, Daniel ;
Schmitz, Sara M. ;
Sharpless, Virginia ;
Martin, Christopher ;
Shah, Ritesh ;
Shaheen, Nicholas J. .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2006, 4 (12) :1445-1451
[3]   Relation between tumour response to first-line chemotherapy and survival in advanced colorectal cancer: a meta-analysis [J].
Buyse, M ;
Thirion, P ;
Carlson, RW ;
Burzykowski, T ;
Molenberghs, G ;
Piedbois, P .
LANCET, 2000, 356 (9227) :373-378
[4]   Risks and benefits of phase 1 clinical trials evaluating new anticancer agents - A case for more innovation [J].
Chen, EX ;
Tannock, IF .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (17) :2150-2151
[5]  
Dickersin K, 1997, AIDS EDUC PREV, V9, P15
[6]   Risks in new drug development: Approval success rates for investigational drugs [J].
DiMasi, JA .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (05) :297-307
[7]   PUBLICATION BIAS IN CLINICAL RESEARCH [J].
EASTERBROOK, PJ ;
BERLIN, JA ;
GOPALAN, R ;
MATTHEWS, DR .
LANCET, 1991, 337 (8746) :867-872
[8]   The phase II/III transition: Toward the proof of efficacy in cancer clinical trials [J].
Fazzari, M ;
Heller, G ;
Scher, HI .
CONTROLLED CLINICAL TRIALS, 2000, 21 (04) :360-368
[9]   Surrogate end points in clinical trials: Are we being misled? [J].
Fleming, TR ;
DeMets, DL .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (07) :605-613
[10]   PHASE-II STUDY OF DOCETAXEL FOR RECURRENT OR METASTATIC NON-SMALL-CELL LUNG-CANCER [J].
FOSSELLA, FV ;
LEE, JS ;
MURPHY, WK ;
LIPPMAN, SM ;
CALAYAG, M ;
PANG, A ;
CHASEN, M ;
SHIN, DM ;
GLISSON, B ;
BENNER, S ;
HUBER, M ;
PEREZSOLER, R ;
HONG, WK ;
RABER, M .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (06) :1238-1244