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Friday, September 24
Fri, Sep 24, 3:45 PM - 5:00 PM
Virtual
Estimands in Oncology: White Papers from an Industry Working Group

Estimands for Overall Survival in Oncology Clinical Trials with Treatment Switching (303484)

Hannes Buchner, Staburo 
Natalia Kan-Dobrosky, PPD 
*Juliane Manitz, EMD Serono, Inc. 

Keywords: estimands, intercurrent event, treatment switching, overall survival, treatment policy strategy, hypothetical strategy, adjusted survival, reconstructed survival

An addendum of the ICH E9 guideline on Statistical Principles for Clinical Trials was released in November 2019 introducing the estimand framework. This new framework aims to align trial objectives and statistical analyses by requiring a precise definition of the inferential quantity of interest, i.e. the estimand. This definition explicitly accounts for intercurrent events, such as switching to new anticancer therapies for the analysis of overall survival (OS), the gold standard in oncology. Traditionally, OS in confirmatory studies is analyzed using the intention-to-treat (ITT) approach comparing treatment groups as they were initially randomized regardless of whether treatment switching occurred and regardless of any subsequent therapy (treatment-policy strategy). Regulatory authorities and other stakeholders often consider ITT results as most relevant. However, the respective estimand yields a clinically meaningful comparison of two treatment arms only if subsequent therapies are known to be approved and reflect clinical practice. We illustrate different scenarios where subsequent therapies are not yet approved drugs and thus do not reflect clinical practice. In such situations the hypothetical strategy could be more meaningful from patient’s and prescriber’s perspective. The cross-industry Oncology Estimand Working Group (www.oncoestimand.org) was initiated to foster a common understanding and consistent implementation of the estimand framework in oncology clinical trials. This paper summarizes the group’s recommendations for appropriate estimands in the presence of treatment switching, one of the key intercurrent events in oncology clinical trials. We also discuss how different choices of estimands may impact study design, data collection, trial conduct, analysis, and interpretation.