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Peer-reviewedCC BY 4.0Cancers

Association of HBsAg Positivity and HBV Reactivation in EGFR-Mutant Lung Adenocarcinoma Treated with EGFR-TKIs: A Retrospective Cohort Study

  1. 1Department of Pulmonary and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu 610041, China
  2. 2State Key Laboratory of Respiratory Health and Multimorbidity, Institute of Respiratory Health and Multimorbidity, Institute of Respiratory Health, Frontiers Science Center for Disease-Related Molecular Network, Precision Medicine Center/Precision Medicine Key Laboratory of Sichuan Province, Sichuan University, Chengdu 610041, China
  3. 3Lung Cancer Center/Lung Cancer Institute, West China Hospital, Sichuan University, Chengdu 610041, China

Abstract

Background: EGFR-TKIs serve as standard first-line targeted therapy for EGFR-mutant lung adenocarcinoma (LUAD). Real-world data on the prognostic role of baseline HBsAg positivity and the risk of HBV reactivation during EGFR-TKI treatment remain limited, particularly in HBV-endemic Chinese populations. Methods: This retrospective single-center cohort study enrolled 580 consecutive patients with stage III–IV EGFR-mutant LUAD who received EGFR-TKIs between 2013 and 2026. Patients were grouped by baseline HBsAg status; Kaplan–Meier curves and multivariable Cox models adjusted for key clinical covariates were used to evaluate progression-free survival (PFS) and overall survival (OS). HBV reactivation was defined by EASL criteria, with virological evaluation available for 51 of 82 HBsAg-positive patients. Results: Among all enrolled patients, 14.1% were HBsAg-positive. The HBV reactivation rate was 9.8% among evaluable HBsAg-positive patients, and reactivation was not independently linked to survival. After adjustment, baseline HBsAg positivity showed a borderline trend toward poorer OS (HR = 1.42, 95% CI, 0.99–2.04, p = 0.054) without significant PFS association (HR = 1.14, 95% CI, 0.80–1.62, p = 0.481). Liver metastasis independently predicted worse OS in HBsAg-positive patients (HR = 3.84, 95% CI, 1.65–8.94, p = 0.002). Conclusions: HBV reactivation was uncommon but warrants close monitoring during EGFR-TKI therapy. Baseline HBsAg positivity demonstrated only a non-significant trend toward inferior OS without affecting PFS. Routine HBsAg screening at diagnosis may facilitate risk stratification, and HBsAg-positive patients with liver metastasis require intensified surveillance.

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BibTeX
@article{sun2026association,
  title = {{Association of HBsAg Positivity and HBV Reactivation in EGFR-Mutant Lung Adenocarcinoma Treated with EGFR-TKIs: A Retrospective Cohort Study}},
  author = {Jiayi Sun and Jingwen Lin and Honglin Li and Weimin Li and Panwen Tian and Yalun Li},
  journal = {Cancers},
  year = {2026},
  month = oct,
  doi = {10.3390/cancers18203373},
  url = {https://www.mdpi.com/2072-6694/18/20/3373},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Association of HBsAg Positivity and HBV Reactivation in EGFR-Mutant Lung Adenocarcinoma Treated with EGFR-TKIs: A Retrospective Cohort Study
AU  - Jiayi Sun
AU  - Jingwen Lin
AU  - Honglin Li
AU  - Weimin Li
AU  - Panwen Tian
AU  - Yalun Li
PY  - 2026
DA  - 2026/10/01
JO  - Cancers
DO  - 10.3390/cancers18203373
UR  - https://www.mdpi.com/2072-6694/18/20/3373
AB  - Background: EGFR-TKIs serve as standard first-line targeted therapy for EGFR-mutant lung adenocarcinoma (LUAD). Real-world data on the prognostic role of baseline HBsAg positivity and the risk of HBV reactivation during EGFR-TKI treatment remain limited, particularly in HBV-endemic Chinese populations. Methods: This retrospective single-center cohort study enrolled 580 consecutive patients with stage III–IV EGFR-mutant LUAD who received EGFR-TKIs between 2013 and 2026. Patients were grouped by baseline HBsAg status; Kaplan–Meier curves and multivariable Cox models adjusted for key clinical covariates were used to evaluate progression-free survival (PFS) and overall survival (OS). HBV reactivation was defined by EASL criteria, with virological evaluation available for 51 of 82 HBsAg-positive patients. Results: Among all enrolled patients, 14.1% were HBsAg-positive. The HBV reactivation rate was 9.8% among evaluable HBsAg-positive patients, and reactivation was not independently linked to survival. After adjustment, baseline HBsAg positivity showed a borderline trend toward poorer OS (HR = 1.42, 95% CI, 0.99–2.04, p = 0.054) without significant PFS association (HR = 1.14, 95% CI, 0.80–1.62, p = 0.481). Liver metastasis independently predicted worse OS in HBsAg-positive patients (HR = 3.84, 95% CI, 1.65–8.94, p = 0.002). Conclusions: HBV reactivation was uncommon but warrants close monitoring during EGFR-TKI therapy. Baseline HBsAg positivity demonstrated only a non-significant trend toward inferior OS without affecting PFS. Routine HBsAg screening at diagnosis may facilitate risk stratification, and HBsAg-positive patients with liver metastasis require intensified surveillance.
SN  - 2072-6694
ER  -