| Literature DB >> 32409306 |
Cyrus Chargari1,2,3,4, Antonin Levy5,2,3, Xavier Paoletti6,7, Jean-Charles Soria2, Christophe Massard2,8, Ralph R Weichselbaum9, Eric Deutsch5,2,3.
Abstract
Newer technical improvements in radiation oncology have been rapidly implemented in recent decades, allowing an improved therapeutic ratio. The development of strategies using local and systemic treatments concurrently, mainly targeted therapies, has however plateaued. Targeted molecular compounds and immunotherapy are increasingly being incorporated as the new standard of care for a wide array of cancers. A better understanding of possible prior methodology issues is therefore required and should be integrated into upcoming early clinical trials including individualized radiotherapy-drug combinations. The outcome of clinical trials is influenced by the validity of the preclinical proofs of concept, the impact on normal tissue, the robustness of biomarkers and the quality of the delivery of radiation. Herein, key methodological aspects are discussed with the aim of optimizing the design and implementation of future precision drug-radiotherapy trials. ©2020 American Association for Cancer Research.Entities:
Mesh:
Year: 2020 PMID: 32409306 PMCID: PMC7717106 DOI: 10.1158/1078-0432.CCR-19-4155
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531