Evaluation of Treatment-Effect Heterogeneity Using Biomarkers Measured on a Continuous Scale: Subpopulation Treatment Effect Pattern Plot

被引:78
作者
Lazar, Ann A.
Cole, Bernard F.
Bonetti, Marco
Gelber, Richard D. [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dana Farber Canc Inst, Dept Biostat, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
TREATMENT-COVARIATE INTERACTIONS; EARLY BREAST-CANCER; POSTMENOPAUSAL WOMEN; SUBGROUP ANALYSES; ESTROGEN-RECEPTOR; TAMOXIFEN; LETROZOLE; PROLIFERATION; CHEMOTHERAPY; PREDICTORS;
D O I
10.1200/JCO.2009.27.9182
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The discovery of biomarkers that predict treatment effectiveness has great potential for improving medical care, particularly in oncology. These biomarkers are increasingly reported on a continuous scale, allowing investigators to explore how treatment efficacy varies as the biomarker values continuously increase, as opposed to using arbitrary categories of expression levels resulting in a loss of information. In the age of biomarkers as continuous predictors (eg, expression level percentage rather than positive v negative), alternatives to such dichotomized analyses are needed. The purpose of this article is to provide an overview of an intuitive statistical approach-the subpopulation treatment effect pattern plot (STEPP)-for evaluating treatment-effect heterogeneity when a biomarker is measured on a continuous scale. STEPP graphically explores the patterns of treatment effect across overlapping intervals of the biomarker values. As an example, STEPP methodology is used to explore patterns of treatment effect for varying levels of the biomarker Ki-67 in the BIG (Breast International Group) 1-98 randomized clinical trial comparing letrozole with tamoxifen as adjuvant therapy for postmenopausal women with hormone receptor-positive breast cancer. STEPP analyses showed patients with higher Ki-67 values who were assigned to receive tamoxifen had the poorest prognosis and may benefit most from letrozole. J Clin Oncol 28:4539-4544. (C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:4539 / 4544
页数:6
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