Prognostic impact of renin-angiotensin system blockade in esophageal squamous cell carcinoma

Yen-Hao Chen1, Cheng-Hua Huang1, Hung-I Lu2

  • 1Department of Hematology-Oncology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.

Abstract

Insights

Renin-angiotensin system (RAS) inhibitors, including angiotensin-I converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs), are linked to better survival in esophageal squamous cell carcinoma patients. These drugs also inhibit cancer cell growth and vascular endothelial growth factor (VEGF) secretion in vitro.

Area of Science:

  • Oncology
  • Pharmacology
  • Gastroenterology

Background:

  • Esophageal squamous cell carcinoma (ESCC) is a significant global health concern.
  • The role of renin-angiotensin system (RAS) inhibitors in cancer treatment outcomes is an area of ongoing research.

Purpose of the Study:

  • To investigate the association between RAS inhibitor use (ACEIs/ARBs) and treatment outcomes in ESCC patients undergoing esophagectomy.
  • To evaluate the in vitro effects of ACEIs/ARBs on ESCC cell proliferation and VEGF secretion.

Main Methods:

  • Retrospective analysis of 141 ESCC patients, comparing outcomes between ACEI/ARB users (n=20) and non-users (n=121).
  • In vitro studies using ESCC cell lines (CE81T/VGH, TE2) to assess proliferation (MTT assay) and VEGF secretion (ELISA) under ACEI/ARB treatment.

Main Results:

  • ACEI/ARB use was significantly associated with superior overall survival (p=0.032) and was an independent prognosticator in multivariate analysis (p=0.006).
  • ACEIs/ARBs demonstrated a dose-dependent inhibition of ESCC cell proliferation and VEGF secretion in vitro.

Conclusions:

  • Administration of ACEIs/ARBs is independently associated with improved overall survival in ESCC patients post-esophagectomy.
  • RAS inhibitors show potential as an adjunct therapy for ESCC, warranting further investigation.

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