The BATTLE Trial: Personalizing Therapy for Lung Cancer

被引:661
作者
Kim, Edward S. [1 ]
Herbst, Roy S. [1 ]
Wistuba, Ignacio I. [1 ,2 ]
Lee, J. Jack [3 ]
Blumenschein, George R., Jr. [1 ]
Tsao, Anne [1 ]
Stewart, David J. [1 ]
Hicks, Marshall E. [4 ]
Erasmus, Jeremy, Jr. [4 ]
Gupta, Sanjay [4 ]
Alden, Christine M. [1 ]
Liu, Suyu [1 ]
Tang, Ximing [1 ]
Khuri, Fadlo R. [5 ]
Tran, Hai T. [1 ]
Johnson, Bruce E. [6 ]
Heymach, John V. [1 ]
Mao, Li [7 ]
Fossella, Frank [1 ]
Kies, Merrill S. [1 ]
Papadimitrakopoulou, Vassiliki [1 ]
Davis, Suzanne E. [1 ]
Lippman, Scott M. [1 ]
Hong, Waun K. [1 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[4] Univ Texas Houston, MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
[5] Emory Univ, Winship Canc Ctr, Atlanta, GA 30322 USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
[7] Univ Maryland, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
PHASE-III; GEFITINIB; MUTATIONS; DOCETAXEL; CARBOPLATIN; PACLITAXEL; PREDICTORS; ERLOTINIB;
D O I
10.1158/2159-8274.CD-10-0010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Biomarker-integrated Approaches of Targeted Therapy for Lung Cancer Elimination (BATTLE) trial represents the first completed prospective, biopsy-mandated, biomarker-based, adaptively randomized study in 255 pretreated lung cancer patients. Following an initial equal randomization period, chemorefractory non-small cell lung cancer (NSCLC) patients were adaptively randomized to erlotinib, vandetanib, erlotinib plus bexarotene, or sorafenib, based on relevant molecular biomarkers analyzed in fresh core needle biopsy specimens. Overall results include a 46% 8-week disease control rate (primary end point), confirm prespecified hypotheses, and show an impressive benefit from sorafenib among mutant-KRAS patients. BATTLE establishes the feasibility of a new paradigm for a personalized approach to lung cancer clinical trials. (ClinicalTrials.gov numbers: NCT00409968, NCT00411671, NCT00411632, NCT00410059, and NCT00410189.) SIGNIFICANCE: The BATTLE study is the first completed prospective, adaptively randomized study in heavily pretreated NSCLC patients that mandated tumor profiling with "real-time" biopsies, taking a substantial step toward realizing personalized lung cancer therapy by integrating real-time molecular laboratory findings in delineating specific patient populations for individualized treatment. Cancer Discovery; 1(1); 44-53. (C) 2011 AACR.
引用
收藏
页码:44 / 53
页数:10
相关论文
共 29 条
[1]  
[Anonymous], CANC PREV R IN PRESS
[2]   Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer [J].
Cappuzzo, F ;
Hirsch, FR ;
Rossi, E ;
Bartolini, S ;
Ceresoli, GL ;
Bemis, L ;
Haney, J ;
Witta, S ;
Danenberg, K ;
Domenichini, I ;
Ludovini, V ;
Magrini, E ;
Gregorc, V ;
Doglioni, C ;
Sidoni, A ;
Tonato, M ;
Franklin, WA ;
Crino, L ;
Bunn, PA ;
Varella-Garcia, M .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (09) :643-655
[3]   Molecular Predictors of Outcome With Gefitinib and Docetaxel in Previously Treated Non-Small-Cell Lung Cancer: Data From the Randomized Phase III INTEREST Trial [J].
Douillard, Jean-Yves ;
Shepherd, Frances A. ;
Hirsh, Vera ;
Mok, Tony ;
Socinski, Mark A. ;
Gervais, Radj ;
Liao, Mei-Lin ;
Bischoff, Helge ;
Reck, Martin ;
Sellers, Mark V. ;
Watkins, Claire L. ;
Speake, Georgina ;
Armour, Alison A. ;
Kim, Edward S. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (05) :744-752
[4]   Phase II trial of the novel retinoid, bexarotene, and gemcitabine plus carboplatin in advanced non-small-cell lung cancer [J].
Edelman, MJ ;
Smith, R ;
Hausner, P ;
Doyle, LA ;
Kalra, K ;
Kendall, J ;
Bedor, M ;
Bisaccia, S .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5774-5778
[5]   Randomized phase III trial of docetaxel versus vinorelbine or ifosfamide in patients with advanced non-small-cell lung cancer previously treated with platinum-containing chemotherapy regimens [J].
Fossella, FV ;
DeVore, R ;
Kerr, RN ;
Crawford, J ;
Natale, RR ;
Dunphy, F ;
Kalman, L ;
Miller, V ;
Lee, JS ;
Moore, M ;
Gandara, D ;
Karp, D ;
Vokes, E ;
Kris, M ;
Kim, Y ;
Gamza, F ;
Hammershaimb, L .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (12) :2354-2362
[6]   Molecular origins of cancer: Lung cancer [J].
Herbst, Roy S. ;
Heymach, John V. ;
Lippman, Scott M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (13) :1367-1380
[7]   Epidermal growth factor receptor immunohistochemistry - Comparison of antibodies and cutoff points to predict benefit from gefitinib in a phase 3 placebo-controlled study in advanced nonsmall-cell lung cancer [J].
Hirsch, Fred R. ;
Dziadziuszko, Rafal ;
Thatcher, Nick ;
Mann, Helen ;
Watkins, Claire ;
Parums, Dinah V. ;
Speake, Georgina ;
Holloway, Brian ;
Bunn, Paul A., Jr. ;
Franklin, Wilbur A. .
CANCER, 2008, 112 (05) :1114-1121
[8]   Gefitinib versus docetaxel in previously treated non-small-cell lung cancer (INTEREST): a randomised phase III trial [J].
Kim, Edward S. ;
Hirsh, Vera ;
Mok, Tony ;
Socinski, Mark A. ;
Gervais, Radj ;
Wu, Yi-Long ;
Li, Long-Yun ;
Watkins, Claire L. ;
Sellers, Mark V. ;
Lowe, Elizabeth S. ;
Sun, Yan ;
Liao, Mei-Lin ;
Osterlind, Kell ;
Reck, Martin ;
Armour, Alison A. ;
Shepherd, Frances A. ;
Lippman, Scott M. ;
Douillard, Jean-Yves .
LANCET, 2008, 372 (9652) :1809-1818
[9]   Disease control rate at 8 weeks predicts clinical benefit in advanced non-small-cell lung cancer: Results from southwest oncology group Randomized trials [J].
Lara, Primo N., Jr. ;
Redman, Mary W. ;
Kelly, Karen ;
Edelman, Martin J. ;
Williamson, Stephen K. ;
Crowley, John J. ;
Gandara, David R. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (03) :463-467
[10]   Bayesian adaptive randomization designs for targeted agent development [J].
Lee, J. Jack ;
Gu, Xuemin ;
Liu, Suyu .
CLINICAL TRIALS, 2010, 7 (05) :584-596