Tibau A, Kesselheim AS, Hwang TJ - Lancet Regional Health - Europe
The authors comment on a meta-analysis by Rahimzadeh et al. evaluating the clinical benefit and toxicity of cancer drugs approved in Switzerland. Beyond the Swiss context, they explore the global implications of regulatory approvals based on surrogate endpoints and immature survival data, highlighting challenges for evidence standards, patient access, reimbursement decisions, and value-based cancer care.
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Daval CJR, Kesselheim AS - STAT
Mulsant SS, Kesselheim AS, Naci H - Journal of Cancer Policy
Jaiswal N, Gorijavolu R, Thomas S, Hwang TJ, Celi LA, Kesselheim AS - Food and Drug Administration (FDA)