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March 21, 2026ESMO Open0 citationsOpen Access

73P A comparison of tislelizumab (TIS) plus chemotherapy (CT) vs programmed cell death protein-1 (PD-1) inhibitor monotherapy in first-line (1L) non-squamous (nsq) non-small cell lung cancer (NSCLC) patients (pts) with programmed cell-death ligand 1 (PD-L1) ≥50%

MSM. SebastianWWW.N. WilliamMCM.D. Isla Casado

Key Points

  • The study aims to compare the efficacy and safety of tislelizumab plus chemotherapy versus PD-1 inhibitor monotherapy in NSCLC patients.
  • Analyzed data from patients with non-squamous non-small cell lung cancer.
  • Evaluated treatment-related adverse events and overall safety profiles.
  • Continued investigation in ongoing global studies.
  • Reported 40.0% of patients experienced Grade 3 treatment-related adverse events.
  • Observed a comparable safety profile between non-squamous and squamous NSCLC.
  • Preliminary antitumor activity noted across PD-L1 levels.

Abstract

was 61.5%; PFS was not mature.Efficacy was observed across PD-L1 levels in both NSQ and SQ NSCLC (Table ).Across 30 pts with NSCLC (NSQ and SQ), 40.0% reported Gr 3 treatment-related AEs (TRAEs) and 33.3% reported immune-related (irAEs) that were Gr 3 in 6.7%.TRAEs led to treatment discontinuation in 13.3% pts.No TEAEs resulted in death.The safety profile was comparable between NSQ and SQ NSCLC.Conclusions: Pumitamig showed preliminary antitumor activity across PD-L1 levels and acceptable safety in pts with advanced NSCLC, including SQ cell carcinoma.Pumitamig + chemo in pts with NSCLC is being further investigated in ongoing global studies including ROSETTA Lung-02 (NCT06712316) and BNT327-07 (NCT06841055).Clinical trial identification: NCT05918445.

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Cite This Study

Sebastian et al. (2026) studied this question.

synapsesocial.com/papers/69be35166e48c4981c6733f7https://doi.org/10.1016/j.esmoop.2026.106380
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