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Two-stage stratified designs with survival outcomes and adjustment for misclassification in predictive biomarkers.
Chen, Yanping; Lin, Yong; Lu, Shou-En; Shih, Weichung J; Quan, Hui.
Affiliation
  • Chen Y; Global Biometrics and Data Sciences, Bristol Myers Squibb, Berkeley Heights, New Jersey, USA.
  • Lin Y; Biostatistics and Epidemiology Department, School of Public Health, Rutgers University, Piscataway, New Jersey, USA.
  • Lu SE; Biometrics Division, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
  • Shih WJ; Biostatistics and Epidemiology Department, School of Public Health, Rutgers University, Piscataway, New Jersey, USA.
  • Quan H; Biometrics Division, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
Stat Med ; 43(10): 1883-1904, 2024 May 10.
Article in En | MEDLINE | ID: mdl-38634277
ABSTRACT
Biomarker stratified clinical trial designs are versatile tools to assess biomarker clinical utility and address its relationship with clinical endpoints. Due to imperfect assays and/or classification rules, biomarker status is prone to errors. To account for biomarker misclassification, we consider a two-stage stratified design for survival outcomes with an adjustment for misclassification in predictive biomarkers. Compared to continuous and/or binary outcomes, the test statistics for survival outcomes with an adjustment for biomarker misclassification is much more complicated and needs to take special care. We propose to use the information from the observed biomarker status strata to construct adjusted log-rank statistics for true biomarker status strata. These adjusted log-rank statistics are then used to develop sequential tests for the global (composite) hypothesis and component-wise hypothesis. We discuss the power analysis with the control of the type-I error rate by using the correlations between the adjusted log-rank statistics within and between the design stages. Our method is illustrated with examples of the recent successful development of immunotherapy in nonsmall-cell lung cancer.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Limits: Humans Language: En Journal: Stat Med Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Limits: Humans Language: En Journal: Stat Med Year: 2024 Document type: Article Affiliation country: Estados Unidos