Evidence map›Paper›PMID 36139571›Full record

ArticleCancers2022

Expression of Nectin-4 in Variant Histologies of Bladder Cancer and Its Prognostic Value-Need for Biomarker Testing in High-Risk Patients?

Severin Rodler, Lennert Eismann, Boris Schlenker, Jozefina Casuscelli, Isabel Brinkmann, Andrea Sendelhofert, Raphaela Waidelich, Alexander Buchner, Christian Stief, Gerald Bastian Schulz and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 31 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

11 authors at 2 institutions in 1 country.

Severin RodlerDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.ORCID 0000-0002-7600-6535
Lennert EismannDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.ORCID 0000-0002-9971-4411
Boris SchlenkerDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.ORCID 0000-0001-6150-776X
Jozefina CasuscelliDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.
Isabel BrinkmannDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.
Andrea SendelhofertDepartment of Pathology, Ludwig Maximilian University Munich, 81377 Munich, Germany.
Raphaela WaidelichDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.
Alexander BuchnerDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.ORCID 0000-0001-7895-7070
Christian StiefDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.
Gerald Bastian SchulzDepartment of Urology, University Hospital of Munich, 81377 Munich, Germany.ORCID 0000-0002-0340-0304
Stephan LedderoseDepartment of Pathology, Ludwig Maximilian University Munich, 81377 Munich, Germany.
München Klinik · DELudwig-Maximilians-Universität München · DE

Funding

Horst-Jürgen Lühl-Stiftung Severin Rodler
6 · The paper itself

Abstract

Variant histologies of bladder cancer (BC) often present with advanced tumor stage and the status of perioperative therapy is unclear. Thereby, squamous cell carcinoma (SCC), adenocarcinoma (ADENO), and sarcomatoid urothelial carcinoma (SARCO) are the most frequent variants. Nectin-4 has emerged as a highly interesting target in BC and might guide therapeutic application of antibody−drug conjugates (ADC). We therefore aimed to investigate expression patterns and prognostic value of Nectin-4 in variant histologies of BC. A single-center retrospective analysis was conducted of patients who underwent radical cystectomy (RC) for BC and revealed variant histologies of BC in the final specimens. Immunohistochemical staining for Nectin-4 was performed on tissue microarrays with 59 SCC, 22 ADENO, and 24 SARCO, and Nectin-4 expression was scored using the histochemical scoring system (H-score). Overall survival (OS) and progression-free survival (PFS) was calculated by Kaplan−Meier method. Median expression of Nectin-4 was 150 (range 0−250) in SCC, 140.5 (range 30−275) in ADENO, and 10 (0−185) in SARCO, with significantly lower levels for SARCO compared to SCC or ADENO (p < 0.001). For SCC, ADENO or SARCO no differences regarding OS or PFS were observed based on Nectin-4 expression levels (p > 0.05). Multivariate analysis revealed nodal stage as an independent prognostic factor for OS and PFS and metastases for PFS but not Nectin-4 expression. In conclusion, Nectin-4 was not prognostic in histological subtypes of BC in our study cohort. However, the high expression of Nectin-4 in SCC and ADENO might guide future treatment with novel Nectin-4-directed ADCs and provide this high-risk patient collective with a new promising therapeutic option. Testing Nectin-4 expression as a biomarker should be considered in trials with SARCO, where low Nectin-4 expression has been observed.

Indexed as

adjuvant therapyantibody–drug conjugateNectin-4neoadjuvant therapysquamous cell carcinoma

Identifiers

PMID36139571
PMCPMC9497069
OpenAlexW4295560411

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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.