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  • COVID-19 outbreak has rapidly evolved into a global pandemic. The impact of COVID-19 on patient journeys in oncology represents a new risk to interpretation of trial results and its broad applicability for future clinical practice. We identify key intercurrent events that may occur due to COVID-19 in oncology clinical trials with a focus on time-to-event endpoints and discuss considerations pertaining to the other estimand attributes introduced in the ICH E9 addendum. We propose strategies to handle COVID-19 related intercurrent events, depending on their relationship with malignancy and treatment and the interpretability of data after them. We argue that the clinical trial objective from a world without COVID-19 pandemic remains valid. The estimand framework provides a common language to discuss the impact of COVID-19 in a structured and transparent manner. This demonstrates that the applicability of the framework may even go beyond what it was initially intended for.
Subject
  • Biotechnology
  • Oncology
  • Pharmacy
  • Life sciences industry
  • Biopharmaceuticals
  • Pharmaceutical industry
  • Biotechnology products
  • Specialty drugs
  • Physics institutes
  • ETH Domain
  • 1988 establishments in Switzerland
  • Forensics organizations
  • Neutron facilities
  • Research institutes in Switzerland
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