Genomic characterization of non-schistosomiasis-related squamous cell carcinoma of the urinary bladder: A retrospective exploratory study.
Aged
Aged, 80 and over
Biomarkers, Tumor
/ genetics
CREB-Binding Protein
/ genetics
Carcinoma, Squamous Cell
/ genetics
Class I Phosphatidylinositol 3-Kinases
/ genetics
Cyclin D1
/ genetics
ErbB Receptors
/ genetics
F-Box-WD Repeat-Containing Protein 7
/ genetics
Female
Humans
Male
Middle Aged
Mutation
PTEN Phosphohydrolase
/ genetics
Receptor, Fibroblast Growth Factor, Type 3
/ genetics
Telomerase
/ genetics
Tumor Suppressor Protein p53
/ genetics
Urinary Bladder Neoplasms
/ genetics
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2021
2021
Historique:
received:
11
04
2021
accepted:
16
10
2021
entrez:
1
12
2021
pubmed:
2
12
2021
medline:
4
1
2022
Statut:
epublish
Résumé
Non-schistosomiasis related-squamous cell carcinoma of urinary bladder (NSR-SCCUB) is a rare tumor subtype distinct from urothelial carcinoma (UC). Studies assessing molecular biomarkers in bladder cancer have generally focused on UC, and genomic data of NSR-SCCUB is limited. We aim to provide additional insight into the molecular underpinnings of this rare entity. NSR-SCCUB patients were identified retrospectively at Princess Margaret Cancer Centre between 2002 and 2017. Demographics, disease characteristics, therapeutic approaches, and outcomes were collected. Tissue samples were interrogated using the Oncomine Comprehensive Assay v3 (ThermoFisher). Kaplan-Meier method was used to estimate the disease-free survival and overall survival (OS). Overall, 11 patients with NSR-SCCUB were identified between 2002 and 2017 with adequate tissue samples. Median age was 71 years (45-86), predominantly male (63.6%). At time of diagnosis, 9 patients (81.8%) had muscle-invasive disease, 1 (9.1%) had non-muscle invasive, and 1 (9.1%) had advanced disease. Nine (81.8%) patients had radical cystectomy and pelvic lymph nodes dissection. Eight (72.7%) patients had pT3 or pT4 with N0, and 5 (45.5%) were grade 3. Median OS was 12.5 months (95% CI 7.7-17.2 months). Single nucleotide variants or insertion/deletions were identified in TP53, TERT, PIK3CA, PTEN, CREBBP, FBXW7, and FGFR3. Amplifications were found in CCND1, and EGFR. NSR-SCCUB has potentially actionable genomic alterations with anticancer agents and many of these aberrations are also seen in UC. The recruitment of NSR-SCCUB patients harboring such mutations should be considered in biomarker driven urinary bladder cancer studies.
Sections du résumé
BACKGROUND
Non-schistosomiasis related-squamous cell carcinoma of urinary bladder (NSR-SCCUB) is a rare tumor subtype distinct from urothelial carcinoma (UC). Studies assessing molecular biomarkers in bladder cancer have generally focused on UC, and genomic data of NSR-SCCUB is limited. We aim to provide additional insight into the molecular underpinnings of this rare entity.
METHODS
NSR-SCCUB patients were identified retrospectively at Princess Margaret Cancer Centre between 2002 and 2017. Demographics, disease characteristics, therapeutic approaches, and outcomes were collected. Tissue samples were interrogated using the Oncomine Comprehensive Assay v3 (ThermoFisher). Kaplan-Meier method was used to estimate the disease-free survival and overall survival (OS).
RESULTS
Overall, 11 patients with NSR-SCCUB were identified between 2002 and 2017 with adequate tissue samples. Median age was 71 years (45-86), predominantly male (63.6%). At time of diagnosis, 9 patients (81.8%) had muscle-invasive disease, 1 (9.1%) had non-muscle invasive, and 1 (9.1%) had advanced disease. Nine (81.8%) patients had radical cystectomy and pelvic lymph nodes dissection. Eight (72.7%) patients had pT3 or pT4 with N0, and 5 (45.5%) were grade 3. Median OS was 12.5 months (95% CI 7.7-17.2 months). Single nucleotide variants or insertion/deletions were identified in TP53, TERT, PIK3CA, PTEN, CREBBP, FBXW7, and FGFR3. Amplifications were found in CCND1, and EGFR.
CONCLUSIONS
NSR-SCCUB has potentially actionable genomic alterations with anticancer agents and many of these aberrations are also seen in UC. The recruitment of NSR-SCCUB patients harboring such mutations should be considered in biomarker driven urinary bladder cancer studies.
Identifiants
pubmed: 34851968
doi: 10.1371/journal.pone.0259272
pii: PONE-D-21-11959
pmc: PMC8635362
doi:
Substances chimiques
Biomarkers, Tumor
0
CCND1 protein, human
0
F-Box-WD Repeat-Containing Protein 7
0
FBXW7 protein, human
0
TP53 protein, human
0
Tumor Suppressor Protein p53
0
Cyclin D1
136601-57-5
CREB-Binding Protein
EC 2.3.1.48
CREBBP protein, human
EC 2.3.1.48
Class I Phosphatidylinositol 3-Kinases
EC 2.7.1.137
PIK3CA protein, human
EC 2.7.1.137
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
FGFR3 protein, human
EC 2.7.10.1
Receptor, Fibroblast Growth Factor, Type 3
EC 2.7.10.1
TERT protein, human
EC 2.7.7.49
Telomerase
EC 2.7.7.49
PTEN Phosphohydrolase
EC 3.1.3.67
PTEN protein, human
EC 3.1.3.67
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0259272Déclaration de conflit d'intérêts
Adrian G. Sacher received funding from AstraZeneca, Bayer (Consulting, Advisory Boards) and AstraZeneca, Merck, Genentech-Roche, Bayer (Honoraria & Sponsored CME/Symposia) outside this project. Girish. Kulkarni received funding from Janssen, Astellas, Roche, Merck, Sanofi (Ad boards) and Ferring (Ad board, conference travel) outside this project. Alexandre R. Zlotta, received funding from Sanofi, Ferring, Janssen (Ad Board) outside this project. Aaron R. Hansen received funding from Genentech/Roche, Merck, GSK, Bristol-Myers Squibb, Novartis, Boston Biomedical, Boehringer-Ingelheim, AstraZeneca, Medimmune (Advisory/ Consulting/ Research) outside this project. Esmail M. Al-ezzi, Zachary. Veitch, Samer. Salah, Theodorus. Van der Kwast, Tracy. Stockley, Shamini. Selvarajah, Tong. Zhang, Srikala S. Sridhar, Nazanin. Fallah-rad, and Antonio. Finelli have no conflict of interest.]. The aforementioned conflict of interests does not alter our adherence to PLOS ONE policies on sharing data and materials.
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