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Articles

The Prognostic Value of Albumin-Globulin Ratio and Eosinophil-Neutrophil Ratio in Patients with Advanced Tumors Undergoing Treatment with PD-1/PD-L1 Inhibitors

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Pages 2815-2828 | Received 01 Jul 2021, Accepted 27 Dec 2021, Published online: 01 Feb 2022
 

Abstract

We investigated the prognostic value of peripheral serum biomarkers, including albumin-globulin ratio (AGR) and eosinophil-neutrophil ratio (ENR), in patients with advanced tumors treated with PD-1/PD-L1 inhibitors. We also retrospectively analyzed the clinical efficacy of PD-1/PD-L1 inhibition in 95 patients with advanced tumors treated at our center. The prognostic value of baseline AGR, baseline ENR, and baseline neutrophil-lymphocyte ratio (NLR) in the serum were evaluated. We also developed a risk scoring tool to stratify patients based on their prognosis. Univariate Cox regression analysis revealed that age, NLR, Eastern Cooperative Oncology Group (ECOG) performance status (PS), platelet-neutrophil ratio (PLR), ENR, AGR, lactate dehydrogenase levels, treatment line, and treatment type were correlated with progression-free survival (PFS). Multivariate Cox regression analysis showed that age, AGR, ENR, and treatment type were independent prognostic factors for PFS. Patients in the low-risk group had significantly longer PFS than those in the high-risk group. The nomogram concordance index (C-index) was 0.716. Patients with a decrease in AGR of over 20% after the first and second treatment cycles had significantly worse PFS than those without decreased AGR. These findings suggest that baseline AGR and ENR may be useful prognostic biomarkers for patients with advanced tumors treated with PD-1/PD-L1 inhibitors.

Acknowledgments

All authors contributed to the study’s conception and design. Material preparation and data collection were performed by Yan Ma, Kun Shang, Jing Wang, and Bangwei Cao. Shanshan Wu provided support with statistical analyses. The first draft of the manuscript was written by Yan Ma. The manuscript was reviewed and approved by all authors.

Beijing key clinical specialty and the pilot project of clinical collaboration with traditional Chinese medicine; Western medicine in major refractory disease—Esophageal cancer.

Disclosure statement

No potential conflict of interest was reported by the authors.

Funding

This study was supported by the capital health research and development of special, the Digestive Medical Coordinated Development Center of Beijing Hospitals Authority (No: XXT01), the Beijing key clinical specialty, and the pilot project of clinical collaboration with traditional Chinese medicine and western medicine in major refractory disease-Esophageal cancer (2019-ZX-005).

Ethics approval

Beijing Friendship Hospital’s Institutional Review Board (2020-P2-176-01) approved our study protocol, which was compliant with the Declaration of Helsinki.

Additional information

Funding

This study was supported by the capital health research and development of special, the Digestive Medical Coordinated Development Center of Beijing Hospitals Authority (No: XXT01), the Beijing key clinical specialty, and the pilot project of clinical collaboration with traditional Chinese medicine and western medicine in major refractory disease-Esophageal cancer (2019-ZX-005).

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