Prognosis of different bone metastases patterns in EGFR-mutant advanced lung adenocarcinoma patients

Author:

Peng Jin1,Hu Fang1,Mao Xiaowei2,Niu Yanjie3,Ma Meili3,Jiang Liyan1

Affiliation:

1. Shanghai Jiao Tong University

2. Sir Run Run Shaw Hospital

3. Shanghai Chest Hospital

Abstract

Abstract Introduction Bone metastases at initial diagnosis of lung cancer was associated with worse prognosis, compared with non-bone metastases. However, whether there was survival difference in different bone metastases patterns between bone metastases without extrathoracic metastases (BM), simultaneous bone metastases and other extrathoracic metastases (BMM) in real-world setting was unclear. Methods Advanced lung adenocarcinoma patients with initial bone metastases who receiving first-line first-generation Epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) and EGFR T790M guided Osimertinib as second-line therapy were retrospectively screened. The first-line real-world progression-free survival (1LrwPFS), second-line real-world progression-free survival (2LrwPFS), post-progression survival (PPS) and real-world overall survival (rwOS) were evaluated. Results A total of 126 patients were enrolled. Patients with BMM had worse rwOS (35.2 months vs. 42.9 months, HR = 0.512, P = 0.005) and shorter 2LrwPFS (12.8months vs. 17.0 months, HR = 0.575, P = 0.011), compared with BM group. There was no statistically significant difference in 1LrwPFS (12.7months vs. 14.0months, HR = 0.838, P = 0.333) and PPS (10.6 months vs. 6.2months, HR = 0.731, P = 0.152) between BM and BMM group. Linear regression and Spearman rank correlation analysis demonstrated 2LrwPFS was strongly correlated with rwOS (r = 0.621, P = 0.000, R2 = 0.568). In multivariate analysis, patients with BMM (P = 0.002), performance status(PS) score ≥ 2 (P <0.001) and TP53 alteration positive (P = 0.003) were independent prognostic factors of worse rwOS. Conclusion Different bone metastases patterns had different survival outcome. In addition, 2LrwPFS had a high impact on rwOS for EGFR-mutant advanced lung adenocarcinoma patients receiving first-line first-generation EGFR-TKI and Osimertinib as second-line therapy.

Publisher

Research Square Platform LLC

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