Evidence map›Paper›PMID 38423597›Full record

ArticleCancer genomics & proteomics

Association of Androgen Receptor and PD-L1 Expression in Upper Urinary Tract Urothelial Carcinoma.

Yohei Okuda, Taigo Kato, Kazutoshi Fujita, Hiroaki Fushimi, Hiroshi Miyamoto, George J Netto, Norio Nonomura

Open access · diamondAbstract read
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Article in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.9field-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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

7 authors at 5 institutions in 2 countries.

Yohei OkudaDepartment of Urology, Osaka University Graduate School of Medicine, Suita, Japan.
Taigo KatoDepartment of Urology, Osaka University Graduate School of Medicine, Suita, Japan; kato@uro.med.oaska-u.ac.jp.
Kazutoshi FujitaDepartment of Urology, Kindai University Faculty of Medicine, Sayama, Japan.
Hiroaki FushimiDepartment of Pathology, Osaka General Medical Center, Osaka, Japan.
Hiroshi MiyamotoDepartments of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, U.S.A.
George J NettoDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL, U.S.A.
Norio NonomuraDepartment of Urology, Osaka University Graduate School of Medicine, Suita, Japan.
The University of Osaka · JPKindai University · JPOsaka Prefectural Medical Center · JPUniversity of Alabama at Birmingham · USUniversity of Rochester Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimThe response to immune checkpoint inhibitors (ICIs) or enfortumab vedotin is limited in patients with upper urinary tract urothelial carcinoma (UTUC), and the development of new targeted therapy for UTUC is eagerly needed. Several biomarkers, including programmed cell death-ligand 1 (PD-L1), have already been reported as predictors of response to ICIs therapy for UTUC. Recently, several studies have shown that steroid hormone receptors, including the androgen receptor (AR), are associated with progression of urothelial carcinoma. MATERIALS AND

methodsWe prepared tissue microarrays (TMA) from paraffin blocks of UTUC specimens in 99 non-metastatic UTUC patients who underwent radical nephroureterectomy. With these TMA sections, we performed immunohistochemical staining for PD-L1 and AR and examined PD-L1 and AR expression levels in tumor cells. In addition, we analyzed the correlation between these markers and clinical prognosis in UTUC cases.

resultsPD-L1 was positive in 24 (24%) of the 99 samples, whereas AR was positive in 20 (20%) patients. AR-negative samples had significantly higher PD-L1 expression level than that the AR-positive samples (mean value 4.70% versus 2.55%, p=0.0324). Among AR-positive cases, patients with absence of PD-L1 expression had significantly lower cancer-specific survival (CSS) than that in PD-L1 expression-positive cases (p=0.049), although PD-L1 expression had no significant impact on CSS in AR-negative cases (p=0.920).

conclusionOur findings suggest that AR is the promising target for UTUC treatment, especially in PD-L1-negative cases.

Indexed as

Carcinoma, Transitional CellKidney NeoplasmsUreteral NeoplasmsUrinary Bladder NeoplasmsUrinary TractB7-H1 AntigenHumansPrognosisReceptors, AndrogenRetrospective StudiesB7-H1 AntigenReceptors, AndrogenAndrogen receptorARPD-L1programmed cell death ligand 1upper urinary tract urothelial carcinomaUTUC

Identifiers

PMID38423597
PMCPMC10905274
OpenAlexW4392296214

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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.