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Poster Display

81P - Is PD-1 inhibitor based treatment better than chemotherapy for metastatic NSCLC patients with PD-L1≥50% who develop EGFR-TKI resistance? A real-world investigation

Date

08 Dec 2022

Session

Poster Display

Presenters

Yujing Li

Citation

Annals of Oncology (2022) 16 (suppl_1): 100102-100102. 10.1016/iotech/iotech100102

Authors

Y. Li1, H. Jiang1, F. Qian2, Y. Cheng2, Y. Zhang2, J. Lu3, Y. Lou2, B. Han2, W. Zhang4

Author affiliations

  • 1 Shanghai Chest Hospital, Shanghai/CN
  • 2 Shanghai Chest Hospital Affiliated to Shanghai Jiao Tong University, Shanghai/CN
  • 3 Shanghai Chest Hospital Affiliated to Shanghai Jiao Tong University, 200030 - Shanghai/CN
  • 4 Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai/CN

Resources

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Abstract 81P

Background

Platinum-based chemotherapy is still the standard of care for Epidermal growth factor receptor (EGFR) mutated non-small cell lung cancer (NSCLC) patients after developing EGFR-TKI resistance. However, no study focusing on the role of PD-1 inhibitor based treatments for EGFR mutated NSCLC patients who carried PD-L1 TPS ≥ 50% progressed after EGFR-TKI therapy. Thus, we aimed to investigate the outcomes of PD-1 inhibitor based treatments for these patients and to explore the population that may benefited from PD-1 inhibitor based therapies.

Methods

We retrospectively collected data of EGFR mutated advanced NSCLC patients with PD-L1 TPS≥50% who have failed prior EGFR-TKI therapies without T790M mutation at Shanghai Chest Hospital between January 2018 and June 2021. Progression-free survival (PFS) and overall survival (OS) were utilized to evaluate the outcomes.

Results

A total of 146 patients were included. The median follow-up was 36.7 months (IQR, 12.5-44.2 months). Among the population, 66 patients (45.2%) received chemotherapy, the remaning (54.8%) received PD-1 inhibitor based therapies, including 56 patients(70.0%) received PD-1 inhibitor combined with chemotherapy (PC) and 24 patients (30.0%) received PD-1 inhibitor monotherapy (PM). Survival analysis shown that patients who received PD-1 inhibitor based therapies had better PFS and OS compared with those treated with other therapy (median PFS, 4.0 vs. 10.0 months, P<0.001; median OS, 39.5 vs. 24.2 months, P<0.001). What’s more, patients who treated with PC treatment had a superior survival time than those received PM treatment (median PFS, 10.3 vs. 7.0 months, P<0.001; median OS, 32.4 vs. 41.6 months, P<0.001). Subgroup analysis found that the PFS and OS benefit of PC was evident in all subgroups.

Conclusions

For advanced NSCLC patients with EGFR mutations and PD-L1 TPS≥50% who have failed prior EGFR-TKI therapies without T790M mutation, PD-1 inhibitor based treatment could provide a more favorable survival than classical chemotherapy. What's more, compared with PD-1 inhibitor monotherapy, PD-1 inhibitor combined with chemotherapy seems to be the preferred treatment.

Legal entity responsible for the study

The authors.

Funding

Shanghai Shenkang Organization.

Disclosure

All authors have declared no conflicts of interest.

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