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Poster Display

594P - The treatment pattern and clinical outcome in NSCLC patients with MET alteration: A retrospective real-world analysis in China

Date

02 Dec 2023

Session

Poster Display

Presenters

Yongfeng Yu

Citation

Annals of Oncology (2023) 34 (suppl_4): S1661-S1706. 10.1016/annonc/annonc1391

Authors

Y. Yu1, L. Shen1, W. Li2, B. Jin3, Y. Xia4, S. Zhang3, S. Lu5

Author affiliations

  • 1 Oncology Department, Shanghai Chest Hospital, Shanghai Jiao Tong University, 200030 - Shanghai/CN
  • 2 Respiratory Medicine Department, The Second Affiliated Hospital of Zhejiang University School of Medicine - East Gate 1, 310009 - Hangzhou/CN
  • 3 Oncology Department, The First Affiliated Hospital of China Medical University, 110001 - Shenyang/CN
  • 4 Oncology Department, The Second Affiliated Hospital of Zhejiang University School of Medicine - East Gate 1, 310009 - Hangzhou/CN
  • 5 Medical Oncology Department, Shanghai Chest Hospital, School of Medicine, Shanghai Jiao Tong University, 200030 - Shanghai/CN

Resources

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Abstract 594P

Background

MET alteration, as promising rare target, plays the key role in the development of NSCLC. However, the treatment pattern and efficacy for Chinese NSCLC patients (pts) with MET alteration in real-world setting is limited. Here, we report the treatment pattern and clinical outcome in Chinese NSCLC pts with MET alteration.

Methods

We performed a retrospective, multicenter study in NSCLC pts with MET alteration between Jul. 2021 and Sep. 2022 in China. Patient characteristics, gene profile, and treatment pattern were collected. The objective response rate (ORR) and time to treatment failure (TTF) were analyzed.

Results

202 NSCLC pts with MET alteration were collected. 117 MET exon 14 skipping mutation (MET ex14m) and MET amplification (amp) (MET NGS GCN≥3.5) pts with subsequent efficacy assessment and follow-up data were included for analysis. The ORR of pts with MET ex14m received 1L savolitinib (savo mono), other MET inhibitor (METi) and chemotherapy (chemo)-based regimen were 56.3%, 16.7%, 36.3%, respectively. The ORR of pts with de novo MET amp received savo, other METi, and chemo-based regimen as 1st-line therapy were 66.7%, 0, 20%, respectively. The ORR of post EGFR/ALK-TKI resistance pts with MET amp (resistant MET amp) received savo mono, savo plus osimertinib (osi), other METi and chemo-based regimen were 12.5%, 43.8%, 0, 14.2%, respectively. (Table) Median TTF of 1L savo mono in pts with MET ex14m was 12.6months and median TTF of savo plus osi in pts with resistant MET amp was 11.3 months. Savo discontinuation due to adverse events occurred in MET ex14m, de novo MET amp and resistant MET amp pts were 18.7%, 33.3%, and 7%, respectively. The safety profile of savo were similar to previously reported data. Table: 594P

The ORR result in the analysis

MET ex14m (n=44) De novo MET amp (n=16) Resistant MET amp (n=57)
n ORR n ORR n ORR
1L Savo 16 56.3% 3 66% NA
Other METi 6 16.7% 3 0%
Chemo 22 36.3% 10 20%
2L+ Savo 14 42.8% 2 50% 8 12.5%
Savo+osi 2 50% 2 50% 32 43.8%
Other METi 3 0 0 NA 3 0
Chemo 23 26.1% 14 28.5% 14 14.2%

Conclusions

The real-world analysis results showed the promising clinical benefit of savo in NSCLC pts with MET alterations and the acceptable safety. Follow-up of these pts are still ongoing.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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