Evidence map›Paper›PMID 41647830›Full record

ArticleFrontiers in oncology2025

The modified Glasgow prognostic score serves as a robust predictor of unplanned readmission and 1-year mortality in lung cancer patients receiving immune checkpoint inhibitors.

Fengwang Xue, Ruoqing Lu, Cailian Wang, Qilian Xiong, Ying Liu, Shengmin Guo, Bo Deng

Abstract read
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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Fengwang Xue *School of Nursing, Southwest Medical University, Luzhou, China.
Ruoqing Lu *Department of General Surgery, Luzhou People's Hospital, Luzhou, China.
Cailian WangSchool of Nursing, Southwest Medical University, Luzhou, China.
Qilian XiongEmergency Department & ICU, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
Ying LiuOncology Department, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
Shengmin GuoDepartment of Nursing, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Bo DengOncology Department, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The modified Glasgow Prognostic Score (mGPS), which reflects the degree of systemic inflammation and nutritional status, is associated with prognosis in various common malignancies. However, its association with 30-day unplanned readmission and 1-year mortality in stage III-IV lung cancer (LC) patients remains unvalidated. This study aimed to evaluate the prognostic value of mGPS in stage III-IV LC patients receiving immune checkpoint inhibitors (ICIs). Methods: In this retrospective study, 209 patients diagnosed with stage III-IV LC who underwent ICI therapy between January 2023 and May 2024 were included. Patients were stratified based on mGPS scores into three risk categories: low-risk (0 points), intermediate-risk (1 point), and high-risk (2 points). Kaplan-Meier analyses, multivariate Cox proportional hazard regression, and subgroup analyses were employed to assess primary outcomes. Results: Among the enrolled patients, the rates of 30-day unplanned readmission and 1-year mortality were 35.4% (74/209) and 11.0% (23/209), respectively. Kaplan-Meier analysis indicated significantly elevated cumulative incidences of 30-day unplanned readmission and 1-year mortality in the high-risk group relative to intermediate- and low-risk groups (log-rank Conclusion: Higher mGPS scores significantly correlate with elevated risks of both 30-day unplanned readmission and 1-year mortality among LC patients receiving ICI therapy. Routine mGPS monitoring may warrants further evaluation in prospective multicenter validation studies to inform prophylactic interventions.

Indexed as

immune checkpoint inhibitorslung cancermodified Glasgow prognostic scoreprognosisunplanned readmission

Identifiers

PMID41647830
PMCPMC12867839

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