Evidence map›Paper›PMID 40959711›Full record

ArticleOncology letters2025

Prognostic value of inflammation- and nutrition-based biomarkers in patients with recurrent or metastatic oral squamous cell carcinoma treated with immune checkpoint inhibitors: A retrospective study.

Sachiko Yamasaki, Nanako Ito, Atsuko Hamada, Fumitaka Obayashi, Mirai Higaki, Takayuki Nakagawa, Shigehiro Ono, Koichi Koizumi, Tomonao Aikawa, Souichi Yanamoto

Abstract read
In one paragraph

Article in Oncology letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sachiko YamasakiDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Nanako ItoDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Atsuko HamadaDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Fumitaka ObayashiDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Mirai HigakiDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Takayuki NakagawaDepartment of Oral and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Shigehiro OnoDepartment of Oral and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Koichi KoizumiDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Tomonao AikawaDepartment of Oral and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.
Souichi YanamotoDepartment of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima 734-8553, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognostic value of inflammation- and nutrition-based biomarkers in oral squamous cell carcinoma (OSCC) remains unclear. The present study evaluated the prognostic significance of these biomarkers in patients with recurrent or metastatic OSCC (R/M-OSCC) undergoing immune checkpoint inhibitor (ICI) therapy. The retrospective study analyzed 45 patients with R/M-OSCC who were treated with ICIs at Hiroshima University Hospital (Hiroshima, Japan) between October 2017 and December 2024. Clinical and treatment data were collected alongside inflammation-based prognostic scores (IBPSs). These biomarkers were calculated prior to and 4-6 weeks after ICI initiation. The 1- and 2-year overall survival (OS) rates for patients were 40 and 22%, respectively, with a median OS of 8.1 months [95% confidence interval (CI): 5.2-14.2). The 1- and 2-year progression-free survival (PFS) rates for patients were 34 and 6.7%, respectively (median PFS, 5.3 months; 95% CI: 2.7-7.9). Post-treatment biomarkers demonstrated superior prognostic value compared with pre-treatment values. Male sex [hazard ratio (HR)=4.11, P=0.0059] and lower body mass index (HR=3.33, P=0.0188) were significantly associated with poorer OS. Post-treatment neutrophil-to-lymphocyte ratio (NLR) (HR=4.17, P=0.0337) and prognostic nutritional index (PNI) (HR=3.92, P=0.0073) were significantly associated with OS. Post-treatment NLR (HR=3.80, P=0.0339), lymphocyte-to-monocyte ratio (LMR) (HR=4.02, P=0.0304) and PNI (HR=2.96, P=0.0342) were significantly associated with PFS. Furthermore, post-treatment IBPS markers, including NLR (P=0.0006), LMR (P=0.0065), platelet-to-lymphocyte ratio (P=0.0396), C-reactive protein-to-albumin ratio (P=0.0062), PNI (P=0.0358) and lymphocyte counts (P=0.0321), were significantly associated with the disease control rate. In conclusion, post-treatment inflammation- and nutrition-based biomarkers could help clinicians identify early those patients most likely to benefit from ICIs and support the development of individualized treatment strategies.

Indexed as

CARDCRIBPSICIsMLROSOSCCPFS

Identifiers

PMID40959711
PMCPMC12434332

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.