AI Article Synopsis

  • Platinum-based chemotherapy combined with anti-PD-1 or PD-L1 monoclonal antibodies is now the standard first-line treatment for advanced non-small cell lung cancer (mNSCLC) without specific mutations.
  • A network meta-analysis was conducted using data from 24 randomized control trials to compare the effectiveness of anti-PD-1 and anti-PD-L1 therapies, focusing on overall survival (OS) and other key outcomes.
  • Results indicated that anti-PD-1 plus chemotherapy offers better overall survival, progression-free survival, and response rates compared to anti-PD-L1 plus chemotherapy, especially in patients with certain PD-L1 expression levels, highlighting the need for future direct comparisons between these treatments.

Article Abstract

Platinum-based chemotherapy combined with anti-PD-1 or PD-L1 monoclonal antibodies (mAbs) is now standard first-line therapy for mNSCLC patients without sensitizing driver mutations. Anti-PD-1 and anti-PD-L1 mAbs are considered to be equivalent in efficacy. In the absence of head-to-head randomized control trials (RCTs), we utilized network meta-analysis (NWM) to provide an indirect comparison of their efficacy. A systematic literature review and NWM were performed using RCTs that investigated anti-PD-1 or PD-L1 mAbs ± chemotherapy in patients with mNSCLC in the first-line setting. The primary outcome was comparative overall survival (OS), while secondary outcomes were comparative progression-free survival (PFS), objective response rate (ORR), and rate of grade 3 and higher toxicities. We identified 24 RCTs. Patients treated with anti-PD-1 mAb + chemotherapy compared with anti-PD-L1 mAb + chemotherapy showed superior mOS, mPFS, and ORR with a similar rate of grade 3 and higher toxicities. This difference in mOS was most pronounced in the PD-L1 TPS 1-49% population. The two mAbs were equivalent as single agents. Anti-PD-1 mAb + chemotherapy improved mOS when compared to anti-PD-1 mAb monotherapy, whereas anti-PD-L1 mAbs + chemotherapy did not when compared to anti-PD-L1 mAb monotherapy. Head-to-head RCTs are warranted in the future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376908PMC
http://dx.doi.org/10.3390/biomedicines11071827DOI Listing

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