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Poster viewing 05.

370P - Outcomes in patients with EGFR-mutant locally advanced or metastatic NSCLC co-mutations receiving aumolertinib as first-line treatment: A retrospective study

Date

03 Dec 2022

Session

Poster viewing 05.

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Fang Cun

Citation

Annals of Oncology (2022) 33 (suppl_9): S1560-S1597. 10.1016/annonc/annonc1134

Authors

F.S. Cun, H. Zhang

Author affiliations

  • Department Of Respiratory Medicine, Nanjing Chest Hospital, The Affiliated Brain Hospital of Nanjing Medical University, 210029 - NAN JING/CN

Resources

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Abstract 370P

Background

1st/2nd generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) is associated with poor outcomes in patients with locally advanced or metastatic non-small-cell lung cancer (NSCLC) harboring EGFR mutations with co-mutations. We aim to explore the efficacy and safety of third-generation TKI aumolertinib in EGFR-mutant NSCLC patients with co-mutations.

Methods

We retrospectively collected data from 52 EGFR-mutant NSCLC patients with co-mutations between April 2020 and June 2022 in the Affiliated Brain Hospital of Nanjing Medical University. The primary endpoint is objective response rate (ORR). The secondary endpoints included progression free survival (PFS), overall survival (OS), disease control rate (DCR) and safety.

Results

Median age was 65 years (ranged 32-84), 61.5 % were female, 84.6 % received aumolertinib monotherapy, 5.8 % received aumolertinib plus bevacizumab and 9.6 % received aumolertinib plus pemetrexed. ORR and DCR for patients receiving aumolertinib monotherapy was 65.9 % and 95.5 %, respectively. In the subgroup analysis of genotypes, ORR and DCR was 71.4 % and 100 % in TP53 mutation, 72.4 % and 100 % in cell cycle signaling pathway related genes, 66.7 % and 100 % in PIK3CA co-mutation, 83.3 % and 97.7 % in PD-L1 TPS 0-1, 55.6 % and 100 % in PD-L1 TPS ≥ 1 (Efficacy; Table). Meanwhile, aumolertinib combination therapy showed superior antitumor activity (ORR: 87.5 % , DCR: 100 %). Both PFS and OS have not been reached. Rash and diarrhea (1-2 grade) were observed in 5.8 % (3/52) and 7.7 % (4/52) patients. Grade ≥ 3 adverse events were observed in 3.8 % (2/52) patients. Table: 370P

Patients (No.) ORR (%) DCR (%)
Aumolertinib monotherapy 44 65.9 % 95.5 %
TP53 co-mutation 21 71.4 % 100 %
cell cycle co-mutation 29 72.4 % 100 %
PIK3CA co-mutation 6 66.7 % 100 %
PD-L1 expression 21 71.4 % 95.2 %
TPS 0-1 12 83.3 % 91.7 %
TPS ≥ 1 9 55.6 % 100 %
Combination therapy 8 87.5 % 100 %
.

Conclusions

Aumolertinib monotherapy or combination therapy might be an appropriate therapeutic choice in EGFR-mutant NSCLC patients with co-mutations.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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