Abstract 368P
Background
Bilateral diffuse metastatic lung adenocarcinoma (BLDM-LUAD) is a special imaging pattern of lung adenocarcinoma (LUAD), characterized by diffuse, innumerable, small metastatic lesions evenly distributed in bilateral lungs. We retrospectively assessed survival outcomes and co-mutation characteristics of BLDM-LUAD patients harboring EGFR mutations who were treated with EGFR-TKIs.
Methods
From May 2016 to May 2021, 1125 patients with NSCLC were admitted to the Second Affiliated Hospital of Nanchang University. Among 458 patients who submitted samples for NGS detection, 44 patients were diagnosed as BLDM-LUAD, and 129 patients were included in control group. In order to analyze the survival outcomes of BLDM-LUAD patients harboring EGFR mutations who were treated with EGFR-TKIs, the factors age, gender, smoking history, hydrothorax, site of EGFR mutations and EGFR-TKIs treatment were adjusted using 1:1 propensity score-matching (PSM). The Kaplan–Meier survival curves and log-rank test were used to analyze progression-free survival (PFS) and overall survival (OS). The co-mutation characteristics of BLDM-LUAD patients harboring EGFR mutations were analyzed by NGS panels.
Results
64 patients with advanced lung adenocarcinoma harboring EGFR mutations and first-line treatment of EGFR-TKIs were successfully matched. BLDM-LUAD (n=32) have significantly longer median PFS than control group (n=32) (mPFS: 14 vs. 6.2 months; HR: 2.58(95%CI: 1.38−4.84); P=0.002) and longer median OS than control group (mOS: 45 vs. 25 months; HR: 2.64(95%CI: 0.96−7.24); P=0.052). The patients with BLDM-LUAD have the higher frequency of EGFR mutation than control group (84.1% vs. 62.0%) before PSM. The co-mutation genes KRAS (9.4%), ATM (7.4%), MET (3.1%), MTOR (3.7%), SMAD4 (3.7%) only appeared in the control group, while he co-mutation genes APC (8.3%), BRCA2 (8.3%), ERBB2 (6.7%), BRAF (3.3%) only appeared in the BLDM-LUAD group after PSM.
Conclusions
The special bilateral diffuse metastases pattern in advanced lung adenocarcinoma harboring EGFR mutations was associated with a favorable prognosis to EGFR-TKIs.
Clinical trial identification
Editorial acknowledgement
We thank Yu Zhong from Berry Oncology, Co., Ltd. for editorial assistance in the writing of the abstract.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
364P - Tepotinib with an EGFR-tyrosine kinase inhibitor (TKI) in patients with EGFR-mutant MET-amplified NSCLC: A case series
Presenter: Azura Ahmad
Session: Poster viewing 05.
365P - Patterns of progression on first-line osimertinib in patients with EGFR mutation-positive advanced non-small cell lung cancer (NSCLC): A Swiss cohort study
Presenter: Alexandra Schuler
Session: Poster viewing 05.
366P - EGFR amplification is a putative resistance mechanism for NSCLC-LM patients with TKI therapy and is associated with poor outcome
Presenter: Hainan Yang
Session: Poster viewing 05.
367P - High-dose aumolertinib in EGFR-mutant NSCLC patients with brain metastases: Primary data from ACHIEVE
Presenter: Yun Fan
Session: 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
Presenter: Fang Cun
Session: Poster viewing 05.
371P - Real-world data of first-line treatment with aumolertinib for elderly EGFR+ NSCLC patients
Presenter: Haitao Zhang
Session: Poster viewing 05.
373P - Safety and efficacy of aumolertinib treatment in patients with advanced NSCLC harboring uncommon EGFR mutations: Cohort 2
Presenter: WenFeng Fang
Session: Poster viewing 05.