Evidence map›Paper›PMID 31080803›Full record

ArticleFrontiers in medicine2019

Association of Baseline Serum Levels of CXCL5 With the Efficacy of Nivolumab in Advanced Melanoma.

Taku Fujimura, Yota Sato, Kayo Tanita, Chunbing Lyu, Yumi Kambayashi, Ryo Amagai, Atsushi Otsuka, Yasuhiro Fujisawa, Koji Yoshino, Shigeto Matsushita and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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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

20 authors at 9 institutions in 1 country.

Taku FujimuraDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yota SatoDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kayo TanitaDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Chunbing LyuDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yumi KambayashiDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Ryo AmagaiDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Atsushi OtsukaDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yasuhiro FujisawaDepartment of Dermatology, University of Tsukuba, Tsukuba, Japan.
Koji YoshinoDepartment of Dermatology, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Tokyo, Japan.
Shigeto MatsushitaDepartment of Dermato-Oncology/Dermatology, National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan.
Hiroshi UchiDepartment of Dermatology, Kyushu University Graduate School of Medicine, Fukuoka, Japan.
Yuki YamamotoDepartment of Dermatology, Wakayama Medical University, Wakayama, Japan.
Hiroo HataDepartment of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Takeru FunakoshiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
Yumi NonomuraDepartment of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Ryota TanakaDepartment of Dermatology, University of Tsukuba, Tsukuba, Japan.
Hisako OkuhiraDepartment of Dermatology, Wakayama Medical University, Wakayama, Japan.
Naoko WadaDepartment of Dermatology, Kyushu University Graduate School of Medicine, Fukuoka, Japan.
Akira HashimotoDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Setsuya AibaDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tohoku University · JPKyoto University · JPKyushu University · JPUniversity of Tsukuba · JPWakayama Medical University · JPHokkaido University · JPKeio University · JPNational Hospital Organization · JPTokyo Metropolitan Komagome Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-programmed cell death protein 1 (PD1) antibodies are in wide use for the treatment of various cancers. PD1 antibody-based immunotherapy, co-administration of nivolumab and ipilimumab, is one of the optimal immunotherapies, especially in advanced melanoma with high tumor mutation burden. Since this combined therapy leads to a high frequency of serious immune-related adverse events (irAEs) in patients with advanced melanoma, biomarkers are needed to evaluate nivolumab efficacy to avoid serious irAEs caused by ipilimumab. This study analyzed baseline serum levels of CXCL5, CXCL10, and CCL22 in 46 cases of advanced cutaneous melanoma treated with nivolumab. Baseline serum levels of CXCL5 were significantly higher in responders than in non-responders. In contrast, there were no significant differences in baseline serum levels of CXCL10 and CCL22 between responders and non-responders. These results suggest that baseline serum levels of CXCL5 may be useful as a biomarker for identifying patients with advanced cutaneous melanoma most likely to benefit from anti-melanoma immunotherapy.

Indexed as

baseline levels of CXCL5melanomanivolumabnivolumab and ipilimumab combined therapyprediction of efficacy

Identifiers

PMID31080803
PMCPMC6497728
OpenAlexW2942473792

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.