Abstract 1357P
Background
Cerebral radiotherapy can reduce recurrence and improve overall survival (OS) in patients with brain metastasis (BM) from Epidermal growth factor receptor (EGFR)-mutant lung adenocarcinoma. Bevacizumab (Avastin), an anti-Vascular endothelial growth factor (VEGF) monoclonal antibody, angiogenesis inhibition and alleviates blood-brain barrier (BBB) damage and brain edema through its blocking VEGF. However, whether bevacizumab combined with cerebral radiotherapy can further increase the efficacy and improve the prognosis of patients is unclear. This study aimed to evaluate the effect of bevacizumab on OS in BM patients with EGFR mutation-positive non-small cell lung cancer (NSCLC) undergoing cerebral radiotherapy.
Methods
A total of 178 patients with EGFR-mutant lung adenocarcinoma and BM who received cerebral radiotherapy met the inclusion criteria for this retrospective study, including 70 patients in the bevacizumab treatment group and 108 in the non-bevacizumab group. The Kaplan-Meier method was used for survival analysis. Univariate and multivariate analyses were performed to identify EGFR-mutated BM prognostic factors for these patients. Cerebral radiotherapy included whole-brain radiotherapy (WBRT), local radiotherapy, and WBRT + Boost.
Results
At the end of the last follow-up period, 176 patients (74.3 %) had died, and the median OS was 33.25 months. We observed a significant difference in the median OS between the bevacizumab and non-bevacizumab groups (45.8 months vs 32.0 months, P =0.007). Patients treated with bevacizumab after cerebral radiotherapy had a longer median OS than patients treated with bevacizumab before cerebral radiotherapy (59.4 months vs 33.7months, P=0.0198).
Conclusions
Bevacizumab could improve OS in BM patients with EGFR mutation-positive NSCLC receiving cerebral radiotherapy. This improvement was more obvious after cerebral radiotherapy, possibly as a result of bevacizumab alleviating radiation brain necrosis caused by brain radiotherapy.
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.
Resources from the same session
1352P - Plasma metabolic signatures uncover therapeutic response and prognosis of third-generation EGFR-TKI treatment in patients with NSCLC
Presenter: Ruyun Gao
Session: Poster session 19
1353P - Effect of TP53 co-mutation in non-small cell lung cancer (NSCLC) with driver mutations
Presenter: Jamie Feng
Session: Poster session 19
1354P - Beyond the common mutation: Examining chemotherapy success in uncommon EGFR mutations
Presenter: Chien-Chung Lin
Session: Poster session 19
1355P - Evaluation of the role of variant allele frequency in EGFR mutated non-small cell lung cancer treated with first line osimertinib
Presenter: Marta Brambilla
Session: Poster session 19
1356P - 10-year survivors treated with tyrosine kinase inhibitor for advanced non-small cell lung cancer
Presenter: Yu Tanaka
Session: Poster session 19
1358P - Safety of tepotinib + EGFR TKI (osimertinib or gefitinib) in patients with EGFRm NSCLC
Presenter: Ernest Nadal
Session: Poster session 19
1359P - Relationship between tumor TP53 gene mutation, circulating anti-p53 antibodies and response to first-line osimertinib in EGFR-mutated NSCLC patients
Presenter: Marc Denis
Session: Poster session 19
1361P - Alectinib for treatment-naïve advanced ALK+ NSCLC selected via blood-based NGS: Updated analyses of outcomes, circulating tumour (ct)DNA and biomarker subgroups from BFAST Cohort A
Presenter: Shirish Gadgeel
Session: Poster session 19
1362P - Association of baseline (BL) anaplastic lymphoma kinase (ALK) fusion detected by circulating tumor DNA (ctDNA) with clinical features and outcomes in the phase III ALTA-3 trial
Presenter: Charu Aggarwal
Session: Poster session 19