Impact of renin angiotensin system inhibitors on survival of patients with metastatic non-small cell lung cancer.

Annals of Saudi medicine Pub Date : 2025-01-01 Epub Date: 2025-02-06 DOI:10.5144/0256-4947.2025.18
Nadiye Sever, Emil Yunusov, Abdussamet Çelebi, Alper Yaşar, Nargiz Majidova, Erkam Kocaaslan, Pınar Erel, Yeşim Ağyol, Ali Kaan Güren, Selver Işık, Rukiye Arıkan, Özlem Ercelep, Osman Köstek, İbrahim Vedat Bayoğlu, Murat Sarıc
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Abstract

Background: We aimed to explore the correlation between anti-hypertensive treatment and survival rates in patients with metastatic non-small cell lung cancer (mNSCLC).

Objective: In this study, we analyzed the correlation between antihypertensive treatment and survival in 300 patients with mNSCLC.

Design: Retrospective.

Settings: Medical faculty hospital.

Patients and methods: We investigated the relationship between antihypertensive treatment and survival in 300 patients who were diagnosed with mNSCLC. We also examined the relationship between histological type, performance status, gender, age and type of antihypertensive medication used and survival.

Main outcomes and measures: Survival difference between mNSCLC patients with and without antihypertensive treatment.

Sample size: 300 patients with mNSCLC.

Results: Among patients receiving concomitant antihypertensive treatment, 107 (35.7%) were prescribed angiotensin-converting enzyme inhibitors (ACEi) or angiotensin II receptor blockers (ARB), 64 (21.3%) beta-blockers and 36 (11%) calcium channel blockers. The study found that the overall survival rates for all patients at 36 and 60 months were 11.5% and 7%, respectively. However, the ACEi/ARB group had higher survival rates at 18.1% and 12% for 36 and 60 months, respectively, compared to the non-ACEi/ARB group with rates of 8.7% and 5% (P<.05).

Conclusion: These results strongly suggest that renin-angiotension system (RAS) inhibitors hold great promise as potential adjunctive therapies for mNSCLC due to their significant inhibitory effects on cell proliferation, angiogenesis and tumor progression.

Limitations: Retrospective and non-randomized nature. Additionally, the retrospective analysis did not allow for verification of the duration or regularity of drug use, which made it infeasible to examine dose-response relationships with reliability.

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