Evidence map›Paper›PMID 37101524›Full record

ArticleClinical Medicine Insights. Oncology2023

Early Changes of Serum Interleukin 14α Levels Predicts the Response to Anti-PD-1 Therapy in Cancer.

Buhai Wang, Caiyue Chen, Shiyu Jiang, Yuxiang Huang, Yichun Zeng, Lei Li, Maoqi Wang, Jingliang Guo, Qiuxian Li, Jin Cao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Clinical Medicine Insights. Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 66% of its field
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

13 authors at 3 institutions in 1 country.

Buhai WangDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.
Caiyue ChenDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.ORCID https://orcid.org/0000-0001-8214-7142
Shiyu JiangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yuxiang HuangDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.
Yichun ZengDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.
Lei LiMedical College, Dalian Medical University, Dalian, China.
Maoqi WangMedical College, Dalian Medical University, Dalian, China.
Jingliang GuoMedical College, Dalian Medical University, Dalian, China.
Qiuxian LiMedical College, Dalian Medical University, Dalian, China.
Jin CaoDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.ORCID https://orcid.org/0000-0002-5433-2911
Long ShenDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.
Juan J GuDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.
Yichen LiangDepartment of Oncology and Cancer Institute Affiliated to Northern Jiangsu People's Hospital, Northern Jiangsu People's Hospital, Medical College, Yangzhou University, Yangzhou, China.
Northern Jiangsu People's Hospital · CNDalian Medical University · CNFudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Programmed cell death-1 (PD-1) blockade has been shown to confer clinical benefit in cancer patients. Here, we assessed the level of serum interleukin 14α (IL14α) in patients receiving anti-PD-1 treatment. Methods: This prospective study recruited 30 patients with advanced solid cancer who received pembrolizumab treatment in Northern Jiangsu People's Hospital between April 2016 and June 2018. The western blot analysis was used to assess the expression level of serum IL14α in patients at baseline and after 2 cycles of treatment. Interleukin 14α was performed using the unpaired 2-tailed Student test. The progression-free survival (PFS) and overall survival (OS) were calculated using the Kaplan-Meier method and compared by the log-rank test. Results: The early change of IL14α after 2 cycles of anti-PD-1 therapy was calculated as delta IL14α % change = (IL14α level after 2 cycles - IL14α level before treatment)/IL14α level before treatment × 100%. Receiver operating characteristic (ROC) was analyzed to get a cutoff point of delta IL14α % change as 2.46% (sensitivity = 85.71%, specificity = 62.5%; area under the ROC curve [AUC] = 0.7277, Conclusions: Early changes of serum IL14α levels may be a promising biomarker to predict outcomes in patients with solid cancer following anti-PD-1 treatment.

Indexed as

cancerInterleukin 14αprognosisprogrammed cell death-1 inhibitor

Identifiers

PMID37101524
PMCPMC10123909
OpenAlexW4366419899

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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.