Caveolin-1 Expression in Upper Tract Urothelial Carcinoma.


Journal

European urology focus
ISSN: 2405-4569
Titre abrégé: Eur Urol Focus
Pays: Netherlands
ID NLM: 101665661

Informations de publication

Date de publication:
01 2019
Historique:
received: 14 03 2017
revised: 23 05 2017
accepted: 13 06 2017
pubmed: 30 7 2017
medline: 1 6 2019
entrez: 30 7 2017
Statut: ppublish

Résumé

Improvement in postoperative risk stratification of upper tract urothelial carcinoma (UTUC) is required to better predict outcomes and counsel patients on adjuvant treatment. To validate the association between caveolin-1 and oncological outcomes in patients treated with radical nephroureterectomy (RNU) for UTUC. Caveolin-1 expression was evaluated via immunochemistry on a tissue microarray from 621 patients. Caveolin-1 was considered overexpressed when at least 50% of the tumor cells stained positive. The median follow-up in this retrospective study was 35 mo (interquartile range 16-65). Radical nephroureterectomy. Univariate and multivariable Cox proportional hazards regression models were used to assess the association between caveolin-1 expression and recurrence and cancer-specific mortality (CSM). Caveolin-1 was overexpressed in 150 patients (24%). Overexpression was associated with higher pathological stage (p<0.001) and grade (p<0.001). In univariate analyses, overexpression of caveolin-1 was significantly associated with lower recurrence (hazard ratio [HR] 1.7, 95% confidence interval [CI] 1.2-2.6; p=0.004) and CSM (HR 1.8, 95% CI 1.2-2.7; p=0.005); however, multivariable analyses did not prove its independent association with outcomes. The study is limited by its retrospective nature. Despite overexpression in a quarter of UTUC patients, caveolin-1 was not independently associated with oncological outcomes. Its use could be evaluated to improve clinical staging of biopsy specimens and to help in clinical decision-making regarding a kidney-sparing approach or neoadjuvant systemic treatment. Development of a panel of prognostic and predictive markers is mandatory for patient consultations in the era of personalized medicine. We evaluated the role of caveolin-1 in a large series of patients treated with radical nephroureterectomy for upper tract urothelial carcinoma (UTUC) and found that it was not independently associated with oncological outcomes. Nevertheless, it was associated with adverse pathological features. Considering caveolin-1 in UTUC biopsy specimens could help in improving clinical staging and decision-making regarding a kidney-sparing approach or neoadjuvant systemic treatment.

Sections du résumé

BACKGROUND
Improvement in postoperative risk stratification of upper tract urothelial carcinoma (UTUC) is required to better predict outcomes and counsel patients on adjuvant treatment.
OBJECTIVE
To validate the association between caveolin-1 and oncological outcomes in patients treated with radical nephroureterectomy (RNU) for UTUC.
DESIGN, SETTING, AND PARTICIPANTS
Caveolin-1 expression was evaluated via immunochemistry on a tissue microarray from 621 patients. Caveolin-1 was considered overexpressed when at least 50% of the tumor cells stained positive. The median follow-up in this retrospective study was 35 mo (interquartile range 16-65).
INTERVENTION
Radical nephroureterectomy.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS
Univariate and multivariable Cox proportional hazards regression models were used to assess the association between caveolin-1 expression and recurrence and cancer-specific mortality (CSM).
RESULTS AND LIMITATIONS
Caveolin-1 was overexpressed in 150 patients (24%). Overexpression was associated with higher pathological stage (p<0.001) and grade (p<0.001). In univariate analyses, overexpression of caveolin-1 was significantly associated with lower recurrence (hazard ratio [HR] 1.7, 95% confidence interval [CI] 1.2-2.6; p=0.004) and CSM (HR 1.8, 95% CI 1.2-2.7; p=0.005); however, multivariable analyses did not prove its independent association with outcomes. The study is limited by its retrospective nature.
CONCLUSIONS
Despite overexpression in a quarter of UTUC patients, caveolin-1 was not independently associated with oncological outcomes. Its use could be evaluated to improve clinical staging of biopsy specimens and to help in clinical decision-making regarding a kidney-sparing approach or neoadjuvant systemic treatment.
PATIENT SUMMARY
Development of a panel of prognostic and predictive markers is mandatory for patient consultations in the era of personalized medicine. We evaluated the role of caveolin-1 in a large series of patients treated with radical nephroureterectomy for upper tract urothelial carcinoma (UTUC) and found that it was not independently associated with oncological outcomes. Nevertheless, it was associated with adverse pathological features. Considering caveolin-1 in UTUC biopsy specimens could help in improving clinical staging and decision-making regarding a kidney-sparing approach or neoadjuvant systemic treatment.

Identifiants

pubmed: 28753840
pii: S2405-4569(17)30162-1
doi: 10.1016/j.euf.2017.06.011
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
CAV1 protein, human 0
Caveolin 1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

97-103

Informations de copyright

Copyright © 2017 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

David D'Andrea (D)

Department of Urology, Medical University of Vienna, Vienna, Austria.

Marco Moschini (M)

Department of Urology, Medical University of Vienna, Vienna, Austria; Urological Research Institute, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

Beat Foerster (B)

Department of Urology, Medical University of Vienna, Vienna, Austria; Department of Urology, Kantonsspital Winterthur, Winterthur, Switzerland.

Mohammad Abufaraj (M)

Department of Urology, Medical University of Vienna, Vienna, Austria.

Vitaly Margulis (V)

Department of Urology, University of Texas Southwestern, Dallas, TX, USA.

Jose Karam (J)

Department of Urology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Yair Lotan (Y)

Department of Urology, University of Texas Southwestern, Dallas, TX, USA.

Jay Raman (J)

Division of Urology, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, USA.

Romain Mathieu (R)

Department of Urology, Rennes University Hospital, Rennes, France.

Morgan Rouprêt (M)

Department of Urology, Pitié-Salpétrière Hospital, APHP, University Paris VI, Paris, France.

Pierre I Karakiewicz (PI)

Cancer Prognostics and Health Outcomes Unit, University of Montreal Health Center, Montreal, Canada.

Alberto Briganti (A)

Urological Research Institute, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

Andrea Haitel (A)

Department of Clinical Pathology, Medical University of Vienna, Vienna, Austria.

Sharhrokh F Shariat (SF)

Department of Urology, Medical University of Vienna, Vienna, Austria; Department of Urology, University of Texas Southwestern, Dallas, TX, USA; Department of Urology, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY, USA. Electronic address: shahrokh.shariat@meduniwien.ac.at.

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Classifications MeSH