Literature DB >> 34592192

Basket clinical trial design for targeted therapies for cancer: a French National Authority for Health statement for health technology assessment.

Etienne Lengliné1, Julien Peron2, Antoine Vanier3, François Gueyffier4, Serge Kouzan5, Patrick Dufour6, Bernard Guillot7, Hugues Blondon8, Michel Clanet9, Pierre Cochat9, Françoise Degos9, Sylvie Chevret10, Mathilde Grande9, Jade Putzolu11.   

Abstract

During the past decade, health technology assessment bodies have faced new challenges in establishing the benefits of new drugs for individuals and health-care systems. A topic of increasing importance to the field of oncology is the so-called agnostic regulatory approval of targeted therapies for cancer (independent of tumour location and histology) granted on the basis of basket trials. Basket trials in oncology offer the advantage of simultaneously evaluating treatments for multiple tumours, even rare cancers, in a single clinical trial. To address the novel challenges introduced by these trials, an interdisciplinary panel was convened on behalf of the Transparency Committee of the French National Authority for Health to clarify an approach designed to guarantee a transparent, reproducible, and fair assessment of histology-agnostic treatments for reimbursement by the French National Health Insurance Fund. The requirements of this approach include the need for randomisation, clinically relevant endpoints, appropriate correction for multiple significance testing, characterisation of subgroup heterogeneity, and validation of underlying biomarker assays. A prospectively designated external control is encouraged when the implementation of a direct comparison is deemed infeasible. We also underline the importance of recording outcomes from basket trials in a registry for use as future external controls.
Copyright © 2021 Elsevier Ltd. All rights reserved.

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Year:  2021        PMID: 34592192     DOI: 10.1016/S1470-2045(21)00337-5

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  4 in total

Review 1.  Innovations in Clinical Development in Rare Diseases of Children and Adults: Small Populations and/or Small Patients.

Authors:  Robert A Beckman; Zoran Antonijevic; Mercedeh Ghadessi; Heng Xu; Cong Chen; Yi Liu; Rui Tang
Journal:  Paediatr Drugs       Date:  2022-10-15       Impact factor: 3.930

2.  How can a joint European health technology assessment provide an 'additional benefit' over the current standard of national assessments? : Insights generated from a multi-stakeholder survey in hematology/oncology.

Authors:  Elaine Julian; Fabrizio Gianfrate; Oriol Sola-Morales; Peter Mol; Jean-François Bergmann; Tomas Salmonson; Ansgar Hebborn; Mathilde Grande; Jörg Ruof
Journal:  Health Econ Rev       Date:  2022-06-02

Review 3.  Extrapolating evidence for molecularly targeted therapies from common to rare cancers: a scoping review of methodological guidance.

Authors:  Doah Cho; Saskia Cheyne; Sarah J Lord; John Simes; Chee Khoon Lee
Journal:  BMJ Open       Date:  2022-07-12       Impact factor: 3.006

Review 4.  Implications of Oncology Trial Design and Uncertainties in Efficacy-Safety Data on Health Technology Assessments.

Authors:  Dario Trapani; Kiu Tay-Teo; Megan E Tesch; Felipe Roitberg; Manju Sengar; Sara C Altuna; Michael J Hassett; Armando A Genazzani; Aaron S Kesselheim; Giuseppe Curigliano
Journal:  Curr Oncol       Date:  2022-08-16       Impact factor: 3.109

  4 in total

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