4.6 Article

First-line immune-based combination therapies for advanced non-small cell lung cancer: A Bayesian network meta-analysis

Journal

CANCER MEDICINE
Volume 10, Issue 24, Pages 9139-9155

Publisher

WILEY
DOI: 10.1002/cam4.4405

Keywords

efficacy; immune-based combination therapies; network meta-analysis; non-small cell lung cancer; safety

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The study conducted a Bayesian network meta-analysis of first-line immune-based combination therapies for advanced NSCLC, showing that IO + IO + Chemo may be the best mode in PD-L1 expression non-selective patients, while IO + Anti-angio + Chemo seemed more effective in the PD-L1-high cohort.
Background Immune-based combination therapies have revolutionized the first-line treatment for advanced non-small cell lung cancer (NSCLC). However, for the efficacy and safety, the best treatment option is still uncertain. Methods We conducted a Bayesian network meta-analysis of randomized controlled trials (RCTs) to evaluate first-line immune-based combination therapies for advanced NSCLC. Results Fourteen trials involving 8467 patients were included. For the programmed cell death-ligand 1 (PD-L1) expression non-selective patients, there were no significant differences among all the treatment modes for overall survival (OS), but the ranking profiles indicated that Immunotherapy + Immunotherapy + Chemotherapy (IO + IO + Chemo) was most likely to be the best mode (probability = 68%). Immunotherapy + Immunotherapy + Anti-angiogenic therapy + Chemotherapy (IO + Anti-angio + Chemo) was significantly better than most other treatment modes for progression-free survival (PFS) with better objective response rate (ORR) and more obvious grade >= 3 treatment-related adverse events (TRAEs). In PD-L1-high cohort, IO + Anti-angio + Chemo seemed to be the best mode for OS, PFS, and ORR according to the ranking profiles. In PD-L1-intermediate and PD-L1-negative cohort, IO + IO + Chemo was inclined to be ranked first for prolonging OS (probability = 78%; 37%) and IO + Anti-angio + Chemo was most likely to provide best PFS (probability = 96%; 100%). Conclusion IO + IO + Chemo has great potential to improve the OS regardless of histology type, especially in PD-L1-intermediate and PD-L1-negative cohort. IO + Anti-angio + Chemo shows great superiority in improving the short-term survival accompanied by increasing grade >= 3 TRAEs.

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