Evidence map›Paper›PMID 35805028›Full record

ArticleCancers2022

Intratumoral Switch of Molecular Phenotype and Overall Survival in Muscle Invasive Bladder Cancer.

Camilla De Carlo, Marina Valeri, Noemi Rudini, Paolo Andrea Zucali, Miriam Cieri, Grazia Maria Elefante, Federica D'antonio, Rodolfo Hurle, Laura Giordano, Alessandra Bressan and 5 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

15 authors at 2 institutions in 1 country.

Camilla De CarloDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Marina ValeriDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.ORCID 0000-0002-9998-8762
Noemi RudiniDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Paolo Andrea ZucaliDepartment of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, Pieve Emanuele, 20090 Milan, Italy.
Miriam CieriDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Grazia Maria ElefanteDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Federica D'antonioDepartment of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, Pieve Emanuele, 20090 Milan, Italy.
Rodolfo HurleDepartment of Urology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Laura GiordanoBiostatistic Unit, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.ORCID 0000-0002-9587-7870
Alessandra BressanDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Massimo LazzeriDepartment of Urology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Matteo PerrinoDepartment of Oncology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Giorgio GuazzoniDepartment of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, Pieve Emanuele, 20090 Milan, Italy.
Luigi Maria TerraccianoDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.
Piergiuseppe ColomboDepartment of Pathology, IRCCS Humanitas Clinical and Research Hospital, Via Manzoni 56, Rozzano, 20089 Milan, Italy.ORCID 0000-0002-6161-6138
Humanitas University · ITIRCCS Humanitas Research Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, immunohistochemical protein expression was studied as a surrogate to the molecular classification of bladder cancer, although no tissue biomarkers are available for clinical use to predict survival or the response to neoadjuvant chemotherapy (CT) in UC, as the literature produced conflicting results. This retrospective study included TURB specimens harboring foci of HG pT2 muscle-invasive bladder carcinoma (MIBC) from 251 patients who subsequently underwent radical cystectomy. We performed immunohistochemical analysis on tumor samples, for relevant gene-expression-based markers for basal type (CD44, CK5/6) and luminal type (CK20 and pPARγ). Piescore, investigated in both non-muscle-invasive (NMI) and muscle-invasive (MI) components of the tumor, divided basal and luminal UC-types when at least three of the four markers were consistent with a specific phenotype, mixed types if one/two luminal and basal markers were present simultaneously, and neu-like types when all four markers investigated were negative. Eighteen selected cases were also investigated with RT-PCR to validate, and to increase the specificity of, the immunohistochemical results. We observe an immunophenotypical difference in the NMI and MI components in 96/251 UC patients (38.25%): half of tumors (44/96 cases) have a transition to basal, 36.46% (35/96 cases) to neu-like, 12.5% (12/96 cases) to mixed, and 5.2% (5/96 cases) to luminal phenotypes. Mixed tumors in the NMI component are more likely to change phenotype than other groups, particularly compared with basal tumors, which demonstrate greater stability (only 8/96 cases, p < 0.00001). The transition of luminal tumors to basal display a better OS compared with the transition toward neu-like tumors (p = 0.027). Overall, the phenotypical switch does not affect lymphovascular invasion, pT, DFS, or OS compared with non-switched cases. In the MI component, the presence of CD44 expression, irrespective of score-related phenotype, shows a protective effect in papillary-type UC (OS p = 0.008, HR 0.453, PFS p = 0.07, HR 0.599), and in UC naïve for CT (p = 0.0479). Piescore immunophenotyping reveals an intratumoral phenotypical transition between the NMI and MI components of the same tumor. The molecular change is a common event in the mixed and luminal categories, but not in basal tumors, which show better phenotypical stability. This phenomenon could partially explain the sensitivity of a subset of luminal UC to chemotherapy: good responders could be “non-real” luminal UC, which acquire nasal markers, such as CD44.

Indexed as

basalbladder cancerCD44CK20CK5/6luminalmolecular phenotypeneu-likeOSPFSphenotypical transitionpPARγ

Identifiers

PMID35805028
PMCPMC9265094
OpenAlexW4283778802

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.