Evidence map›Paper›PMID 35039462›Full record

ArticleJournal for immunotherapy of cancer2022

Efficacy of pembrolizumab and comprehensive CD274/PD-L1 profiles in patients previously treated with chemoradiation therapy as radical treatment in bladder cancer.

Kazuki Nishimura, Kyosuke Nishio, Kensuke Hirosuna, Kazumasa Komura, Takuo Hayashi, Wataru Fukuokaya, Ayako Ura, Taizo Uchimoto, Ko Nakamura, Tatsuo Fukushima and 16 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 13 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

26 authors at 4 institutions in 1 country.

Kazuki Nishimura *Department of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Kyosuke Nishio *Department of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Kensuke Hirosuna *Translational Research Program, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Kazumasa KomuraDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan kazumasa.komura@ompu.ac.jp.ORCID 0000-0003-4157-1929
Takuo HayashiDepartment of Human Pathology, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Wataru FukuokayaDepartment of Urology, The Jikei University School of Medicine, Tokyo, Japan.ORCID 0000-0003-1044-912X
Ayako UraDepartment of Human Pathology, Juntendo University Graduate School of Medicine, Bunkyo-ku, Tokyo, Japan.
Taizo UchimotoDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Ko NakamuraDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Tatsuo FukushimaDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Yusuke YanoDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Nobushige TakahashiDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Keita NakamoriDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Shoko KinoshitaDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Tomohisa MatsunagaDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Takeshi TsutsumiDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Takuya TsujinoDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Kohei TaniguchiTranslational Research Program, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Tomohito TanakaTranslational Research Program, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Hirofumi UeharaDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Kiyoshi TakaharaDepartment of Urology, Fujita-Health University School of Medicine, Toyoake, Japan.
Teruo InamotoDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Yoshinobu HiroseDepartment of Pathology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Takahiro KimuraDepartment of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Shin EgawaDepartment of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Haruhito AzumaDepartment of Urology, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Osaka University of Pharmaceutical Sciences · JPJikei University School of Medicine · JPJuntendo University · JPFujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemoradiation therapy (CRT) has been increasingly reported as a possible alternative to total cystectomy (TC) for localized bladder cancer (BC). Pembrolizumab is the standard of care for platinum-refractory metastatic urothelial carcinoma, although it is unknown whether the efficacy of pembrolizumab in patients previously treated with curative CRT varies from the results of benchmark trials.

methodsWe retrospectively assessed whether the survival benefit of pembrolizumab differs between patients previously treated with TC or CRT as radical treatment. A total of 212 patient records were collected for a logistic regression propensity score model. An independent dataset with next-generation sequencing (n=289) and PD-L1 Combined Positive Score (CPS: n=266) was analyzed to assess whether CRT-recurrent tumor harbors distinct CD274/PD-L1 profiles.

resultsPropensity score matching was performed using putative clinical factors, from which 30 patients in each arm were identified as pair-matched groups. There was no significant difference in overall survival from the initiation of pembrolizumab (p=0.80) and objective response rate (p=0.59) between CRT and TC treatment groups. In the independent 289 BC cohort, 22 samples (7.6%) were collected as CRT-recurrent tumors. There was no significant difference in CD274 mRNA expression level between CRT-naïve and CRT-recurrent tumors. The compositions of CD274 isoforms were comparable among all isoforms detected from RNAseq between CRT-naïve (n=267) and CRT-recurrent (n=22) tumors. No actionable exonic mutation in CD274 was detected in CRT-recurrent tumors. PD-L1 CPS was positively correlated with CD274 mRNA expression level, and PD-L1 CPS was comparable between CRT-naïve and CRT-recurrent tumors.

conclusionsThe efficacy of pembrolizumab for patients previously treated with CRT was similar to those treated with TC. The enhanced tumor regression by combining programmed cell death protein 1/PD-L1 inhibitor and CRT might be expected only in the concurrent administration.

Indexed as

AgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenChemoradiotherapyFemaleHumansMaleMiddle AgedRetrospective StudiesSurvival AnalysisUrinary Bladder NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenCD274 protein, humanpembrolizumabimmunotherapyradioimmunotherapyurinary bladder neoplasms

Identifiers

PMID35039462
PMCPMC8765067
OpenAlexW4205454312

What OpenQuestion holds

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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.