Prognostic factors versus predictive factors: Examples from a clinical trial of erlotinib

被引:111
作者
Clark, Gary M. [1 ]
机构
[1] OSI Pharmaceut Inc, Biostat & Data Management, Boulder, CO 80301 USA
关键词
Prognostic; Predictive; Epidermal growth factor receptor; Non-small lung cancer; Erlotinib; Smoking; Histology;
D O I
10.1016/j.molonc.2007.12.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It would be helpful to have factors that could identify patients who will, or will not, benefit from treatment with specific therapies. Ideally, these should be molecular-based factors. When results with molecular-based factors are disappointing, physicians often use clinical character-is tics to make treatment decisions. Several characteristics have been suggested to predict sensitivity to epidermal growth factor receptor inhibitors in patients with non-small lung cancer, including gender, histology, smoking history. This report demonstrates that gender and histology are actually prognostic, rather than predictive factors. Before biomarkers or clinical characteristics are included in guidelines for selecting patients for specific treatments, it is imperative that the prognostic effects of these factors are distinguished from their ability to predict a differential clinical benefit from the specific treatment. (C) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:406 / 412
页数:7
相关论文
共 12 条
[1]   Gefitinib therapy for non-small cell lung cancer [J].
Birnbaum A. ;
Ready N. .
Current Treatment Options in Oncology, 2005, 6 (1) :75-81
[2]  
Buyse M, 2000, Biostatistics, V1, P49, DOI 10.1093/biostatistics/1.1.49
[3]   Smoking history and epidermal growth factor receptor expression as predictors of survival benefit from erlotinib for patients with non-small-cell lung cancer in the National Cancer Institute of Canada Clinical Trials Group study BR.21 [J].
Clark, Gary M. ;
Zborowski, Denni M. ;
Santabarbara, Pedro ;
Ding, Keyue ;
Whitehead, Marlo ;
Seymour, Lesley ;
Shepherd, Frances A. .
CLINICAL LUNG CANCER, 2006, 7 (06) :389-394
[4]   Clinical utility of epidermal growth factor receptor expression for selecting patients with advanced non-small cell lung cancer for treatment with erlotinib [J].
Clark, Gary M. ;
Zborowski, Denni M. ;
Culbertson, Jennifer L. ;
Whitehead, Marlo ;
Savoie, Michelle ;
Seymour, Lesley ;
Shepherd, Frances A. .
JOURNAL OF THORACIC ONCOLOGY, 2006, 1 (08) :837-846
[5]   Objective response rate as a surrogate end point: A commentary [J].
Fleming, TR .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (22) :4845-4846
[6]   Erlotinib: Optimizing therapy with predictors of response? [J].
Goodin, Susan .
CLINICAL CANCER RESEARCH, 2006, 12 (10) :2961-2963
[7]   Female sex and bronchioloalveolar pathologic subtype predict EGFR mutations in non-small cell lung cancer [J].
Hsieh, RK ;
Lim, KH ;
Kuo, HT ;
Tzen, CY ;
Huang, MJ .
CHEST, 2005, 128 (01) :317-321
[8]   Risk factors differ for non-small-cell lung cancers with and without EGFR mutation:: assessment of smoking and sex by a case-control study in Japanese [J].
Matsuo, Keitaro ;
Ito, Hidemi ;
Yatabe, Yasushi ;
Hiraki, Akio ;
Hirose, Kaoru ;
Wakai, Kenji ;
Kosaka, Takayuki ;
Suzuki, Takeshi ;
Tajima, Kazuo ;
Mitsudomi, Tetsuya .
CANCER SCIENCE, 2007, 98 (01) :96-101
[9]   Practical management of patients with non-small-cell lung cancer treated with gefitinib [J].
Shah, NT ;
Kris, MG ;
Pao, W ;
Tyson, LB ;
Pizzo, BM ;
Heinemann, MH ;
Ben-Porat, L ;
Sachs, DL ;
Heelan, RT ;
Miller, VA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (01) :165-174
[10]   Erlotinib in previously treated non-small-cell lung cancer [J].
Shepherd, FA ;
Pereira, JR ;
Ciuleanu, T ;
Tan, EH ;
Hirsh, V ;
Thongprasert, S ;
Campos, D ;
Maoleekoonpiroj, S ;
Smylie, M ;
Martins, R ;
van Kooten, M ;
Dediu, M ;
Findlay, B ;
Tu, DS ;
Johnston, D ;
Bezjak, A ;
Clark, G ;
Santabárbara, P ;
Seymour, L .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (02) :123-132