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Poster session 20

1387P - Efficacy of first-line treatment options in advanced HER2-altered non-small cell lung cancer: A multi-center retrospective study

Date

21 Oct 2023

Session

Poster session 20

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

haifeng sun

Citation

Annals of Oncology (2023) 34 (suppl_2): S755-S851. 10.1016/S0923-7534(23)01943-9

Authors

H. sun1, Y. ge1, J. Wu1, Y. Sun1, J. zhang1, Q. Cheng1, D. wang1, X. wang1, J. li1, X. Fu2, H. Sun2, A. gao2

Author affiliations

  • 1 Phase I Clinical Research Center, Cancer Hospital Affiliated to Shandong First Medical University, 25011 - jinan/CN
  • 2 Department Of Thoracic Radiation Oncology, Cancer Hospital Affiliated to Shandong First Medical University, 25011 - jinan/CN

Resources

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Abstract 1387P

Background

HER2 alterations are identified in 2-4% of non-small cell lung cancer (NSCLC), indicating poor clinical outcomes. Due to the deficiency of effective targeted therapies in the first-line setting, chemotherapy alone or combined with Bevacizumab, immune checkpoint inhibitors (ICIs) or both are recommended as standard options. However, the optimal therapy is still undetermined.

Methods

Stage IV NSCLC patients with HER2 alteration were retrospectively analyzed from 6 cancer centers in China between May 2017 and February 2023. All the patients received chemotherapy alone (C), chemotherapy combined with Bevacizumab (BC), chemotherapy combined with ICIs (IC), or chemotherapy combined with Bevacizumab and ICIs (IBC) as first-line strategies. The clinical outcomes were evaluated.

Results

Eighty patients with HER2 mutation (75/80) or amplification (5/80) were included, in which 10 patients received chemotherapy alone, 37 received BC, 24 received IC, and 9 received IBC treatment. Compared with chemotherapy, combination therapy significantly improved mPFS (8.47 months VS 4.97 months, p<0.0001). Further analysis based on different combination mode showed that, each of the combination therapeutics, including BC (mPFS 7.27 m, HR=0.31, 95% CI: 0.14-0.68, p<0.001), IC (mPFS 8.47m, HR=0.20, 95% CI:0.08-0.48, p=0.004) and IBC (mPFS 16.3m, HR=0.08, 95% CI: 0.02-0.25, p<0.001), gave beneficial PFS compared with chemotherapy. In our effort to determine the optimal combination strategy, we found IBC treatment gave longer mPFS compared with BC (HR=0.15, 95% CI: 0.04-0.50, p<0.001) and IC (HR=0.43, 95% CI: 0.16-1.18, p=0.092). However, the efficacy of IC and BC schemes are comparable. Table: 1387P

Groups Patient number ORR, % (95% CI) DCR, % (95% CI) mPFS, months (95% CI)
Chemotherapy n=10 30.0(1.60,58.4) 100(100,100) 4.97 (4.09, 5.84)
Combination n=70 25.7(15.5,36.0) 91.4(84.9,98.0) 8.47 (7.28, 9.35)
IC n=24 29.2(11.0,47.4) 87.5(74.3,101) 8.47 (7.15, 9.78)
BC n=37 18.9(6.30,31.5) 91.9(83.1,101) 7.27 (6.27, 8.26)
IBC n=9 44.4(12.0,76.9) 100(100,100) 16.3 (8.83, 23.8)
ALL n=80 26.3(16.6,35.9) 92.5(86.7,98.3) 7.63 (6.35, 8.92)
.

Conclusions

Chemotherapy-based combination strategies improve patient survival compared with chemotherapy in the first-line therapy of HER2-altered NSCLC, while the IBC mode lead to the optimal PFS.

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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