Evidence map›Paper›PMID 40240996›Full record

ArticleBMC gastroenterology2025

Dynamic variations in peripheral blood indices and their association with efficacy and adverse reactions of pd- 1 inhibitor combined chemotherapy in patients with advanced gastric cancer.

Rui Wang, Huihui Zeng, Mengting Shi, Yue Wu, Yang Liu, Tiantian Zhang

Abstract read
In one paragraph

Article in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Observational
  4. Article
  5. Circulating PD-1Frontiers in immunology · 2025
    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

6 authors.

Rui Wang *Departments of Medical Oncology, The First Affiliated Hospital of Bengbu Medical University, 233004, Anhui, People's Republic of China.
Huihui Zeng *Departments of Medical Oncology, The First Affiliated Hospital of Bengbu Medical University, 233004, Anhui, People's Republic of China.
Mengting ShiDepartments of Medical Oncology, The First Affiliated Hospital of Bengbu Medical University, 233004, Anhui, People's Republic of China.
Yue WuDepartments of Medical Oncology, The First Affiliated Hospital of Bengbu Medical University, 233004, Anhui, People's Republic of China.
Yang LiuDepartments of Medical Oncology, The First Affiliated Hospital of Bengbu Medical University, 233004, Anhui, People's Republic of China.
Tiantian ZhangDepartments of Medical Oncology, The First Affiliated Hospital of Bengbu Medical University, 233004, Anhui, People's Republic of China. 18355336906@163.com.

Funding

Anhui Provincial Natural Science Foundation 2208085MH248Bengbu Medical College Natural Science Foundation 2022byzd035The First Affiliated Hospital of Bengbu Medical University Science Found for Distinguished Young Scholars 2019byyfyjq03
6 · The paper itself

Abstract

backgroundGastric cancer (GC) continues to pose a significant global health challenge, particularly in advanced stages where treatment options are severely constrained. Immunotherapy represents a groundbreaking advancement in cancer treatment, exhibiting promising therapeutic effects in patients diagnosed with gastric cancer. However, the efficacy of immunotherapy is not universally applicable to all individuals. Revealing precise biomarkers for tumor immunotherapy as targets or indicators for detection and evaluation can facilitate the resolution of this predicament. This study aims to identify serum tumor markers and blood cell ratios as predictive biomarkers to aid in the selection of gastric cancer patients who may benefit from PD-1 inhibitors therapy.

methodsA retrospective analysis was conducted on the medical records and hematological data of 98 patients with HER2-negative and microsatellite-stable (MSS) metastatic gastric cancer who received first-line treatment with PD-1 inhibitors in combination with chemotherapy at our institution. We investigated peripheral blood parameters, including Neutrophil-to-Lymphocyte Ratio (NLR), Platelet-to-Lymphocyte Ratio (PLR), C-Reactive Protein-to-Albumin Ratio (CAR), AFP, Carcinoembryonic Antigen (CEA), and Sugar antigens 199 (CA199). Logistic regression and Cox regression analyses were employed to assess the correlation of these parameters with treatment response and survival duration. The relationship between these indicators and overall survival was assessed by employing Kaplan-Meier survival curves, in conjunction with an analysis of Overall Response Rate (ORR), Disease Control Rate (DCR), Progression-Free Survival (PFS), Overall Survival (OS), and safety profiles..

resultsHigher pre-treatment levels of NLR, CAR, AFP, and CA199, along with subsequent reductions in NLR, CAR, and CA199 at 12 weeks post-treatment, were significantly associated with extended PFS and OS. Multivariate Cox analysis suggested that pre-treatment levels of AFP, as well as the reduction in NLR and CA199 at 12 weeks post-treatment, were strongly correlated with PFS and OS in patients with gastric cancer undergoing immunotherapy. Additionally, the reduction in NLR, CAR, and CA199 observed at 12 weeks after treatment showed a significant positive correlation with improved DCR and ORR. Multivariate logistic regression analysis indicated that the decline in NLR and CA199 levels at 12 weeks post-treatment might be associated with DCR, while pre-treatment CAR levels and the decrease in CAR after 12 weeks could potentially predict ORR in immunotherapy for gastric cancer. Notably, patients with normal AFP levels exhibited significantly prolonged median progression-free survival (mPFS) of 6.8 months and median overall survival (mOS) of 13.2 months compared to those with elevated AFP levels (mPFS: 5.2 months; mOS: 9.4 months), and this difference was statistically significant (P < 0.05).

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorImmune Checkpoint InhibitorsStomach NeoplasmsAdultAgedAntigens, Tumor-Associated, CarbohydrateCarcinoembryonic AntigenC-Reactive ProteinFemaleHumansLymphocytesMaleMiddle AgedNeutrophilsProgrammed Cell Death 1 ReceptorAntigens, Tumor-Associated, CarbohydrateBiomarkers, Tumorcarbohydrate antigen 199, humanCarcinoembryonic AntigenC-Reactive ProteinImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorSerum Albumincarbohydrate antigen 199C-reactive protein-to-albumin ratioGastric cancerneutrophil-to-lymphocyte ratioPD-1 inhibitor

Identifiers

PMID40240996
PMCPMC12004548

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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 OpenQuestion graph.