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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Gastrointest Oncol. Aug 15, 2026; 18(8): 120245
Published online Aug 15, 2026. doi: 10.4251/wjgo.v18.i8.120245
C-reactive protein/albumin ratio in immunochemotherapy for advanced gastric cancer: Prognostic value, clinical challenges, and future directions
Yan-Song Hou, Ze-Yuan Yu, Xiao-Jun Yang
Yan-Song Hou, Ze-Yuan Yu, Department of Gastrointestinal Surgery, The Second Hospital of Lanzhou University, Lanzhou 730000, Gansu Province, China
Xiao-Jun Yang, Department of Hepatobiliary Surgery, Gansu Provincial Hospital, Lanzhou 730000, Gansu Province, China
Co-corresponding authors: Ze-Yuan Yu and Xiao-Jun Yang.
Author contributions: Hou YS contributed to this paper, the writing, and editing the manuscript; Yu ZY and Yang XJ contributed to manuscript review; and all of the authors have read and approved the final manuscript.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Corresponding author: Xiao-Jun Yang, MD, Associate Professor, Chief Physician, Department of Hepatobiliary Surgery, Gansu Provincial Hospital, No. 199 Donggang West Road, Chengguan District, Lanzhou 730000, Gansu Province, China. yangxjmd@aliyun.com
Received: February 24, 2026
Revised: March 9, 2026
Accepted: May 6, 2026
Published online: August 15, 2026
Processing time: 163 Days and 19.1 Hours
Core Tip

Core Tip: C-reactive protein/albumin ratio (CAR) has attracted attention because it is easy to obtain, highly reproducible in clinical practice, and biologically linked to systemic inflammation, malnutrition, cachexia, treatment tolerance, and immune competence. We argue that, in Immunochemotherapy for advanced gastric cancer, the greatest value of CAR is not as an independent determinant of treatment selection, but as a complementary host-state biomarker that should be interpreted alongside programmed death ligand 1, mismatch repair status, metastatic burden, and performance status. The field now needs prospective validation, dynamic monitoring of CAR, and clinical trials testing whether CAR-guided nutritional or anti-inflammatory interventions can improve clinically meaningful outcomes.

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