Evidence map›Paper›PMID 38776028›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2024

Serum cytokines and creatinine/cystatin C ratio as prognostic biomarkers in advanced cancer patients treated with anti-PD-1/PD-L1 therapy.

Shan-Xiu Jin, Bo-Na Liu, Hong-Juan Ji, Jing-Ran Wu, Bao-Lei Li, Xiao-Li Gao, Na Li, Zhen-Dong Zheng, Cheng Du

Abstract read
In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 3 pooled it
–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

8 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Pooled it
  4. Review
  5. Article
  6. Article
  7. Article
  8. A critical review: serum cytokines and creatinine/cystatin C ratio as prognostic biomarkers in advanced cancer patients treated with anti-PD-1/PD-L1 therapy.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Shan-Xiu Jin *Department of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Bo-Na Liu *Department of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Hong-Juan Ji *Department of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Jing-Ran WuDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Bao-Lei LiDepartment of Oncology, Anshan Tumor Hospital, Anshan, China.
Xiao-Li GaoDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Na LiDepartment of Gynaecology and Obstetrics, The First Hospital of Jilin University, Jilin, China. linawyswcy@163.com.
Zhen-Dong ZhengDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, China. gcp_zzd@sina.com.
Cheng DuDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, China. dc1115010@sina.com.

Funding

Education Department of Jilin Province JJKH20190002KJNatural Science Foundation of Jilin Province 20190201089JCNatural Science Foundation of Liaoning Province 2023020976-JH2/1017
6 · The paper itself

Abstract

objectiveImmune checkpoint inhibitors (ICIs), specifically targeting the programmed cell death protein-1 or its ligand (PD-1/PD-L1), have been extensively used in the treatment of a spectrum of malignancies, although the predictive biomarkers remain to be elucidated. This study aims to investigate the association between baseline circulating levels of cytokines and the creatinine/cystatin C ratio (CCR) with the treatment outcomes of ICIs in patients with advanced cancer.

methodsThe pre-treatment circulating levels of 10 cytokines (PD-L1, CTLA4, CXCL10, LAG3, HGF, CCL2, MIG, GRANB, IL-18, and IL-6) were measured via automated capillary-based immunoassay platform in the serum of 65 advanced cancer patients treated with anti-PD-1/PD-L1-based systemic therapy and 10 healthy volunteers. The levels of cytokines and CCR were quantified and categorized into high and low groups based on the median value. The associations of serum cytokines and CCR with response to treatment, survival, and immune-related adverse events were assessed.

resultsElevated circulating levels of 6 cytokines (PD-L1, CXCL10, HGF, CCL2, MIG, and IL-6) were observed in cancer patients compared with that in healthy volunteers. The correlation coefficients between cytokines, CCR and nutritional risk index were also calculated. In the cancer cohort (N = 65), low circulating HGF (P = 0.023, P = 0.029), low IL-6 (P = 0.002, P < 0.001), and high CCR (P = 0.031, P = 0.008) were associated with significantly improved progression-free survival (PFS) and overall survival (OS). Multi-variable COX analyses adjusted for clinicopathological factors revealed that low HGF, low IL-6, and high CCR were independent favorable prognostic factors for PFS (P = 0.028, P = 0.010, and P = 0.015, respectively) and OS (P = 0.043, P = 0.003, and P = 0.026, respectively). Grade 2 irAEs occurred more frequently in patients with low levels of circulating CCL2 and LAG3.

conclusionsPre-treatment circulating levels of serum IL-6, HGF, and CCR may serve as independent predictive and prognostic biomarkers in advanced cancer patients treated with ICIs-based systemic therapy. These findings might help to identify potential patients who would benefit from these therapies.

Indexed as

Biomarkers, TumorCreatinineCytokinesImmune Checkpoint InhibitorsNeoplasmsAdultAgedAged, 80 and overB7-H1 AntigenCase-Control StudiesFemaleHumansMaleMiddle AgedPrognosisB7-H1 AntigenBiomarkers, TumorCreatinineCytokinesImmune Checkpoint InhibitorsCancerCreatinine/cystatin C ratioImmune checkpoint inhibitorsPrognostic biomarkersSerum cytokines

Identifiers

PMID38776028
PMCPMC11111483

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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.