Predictive factors for progression of patients with carcinoma in situ of the bladder at long-term follow-up: pure versus non-pure CIS.


Journal

Minerva urologica e nefrologica = The Italian journal of urology and nephrology
ISSN: 1827-1758
Titre abrégé: Minerva Urol Nefrol
Pays: Italy
ID NLM: 8503649

Informations de publication

Date de publication:
Aug 2019
Historique:
pubmed: 31 5 2019
medline: 4 12 2019
entrez: 31 5 2019
Statut: ppublish

Résumé

The aim of this study was to identify the predictive factors for progression defined as any event that shifted the management of the disease from a bladder sparing approach, by comparing patients with pure versus non-pure carcinoma in situ (CIS) of the bladder. A retrospective analysis was carried out in consecutive patients affected by newly-diagnosed pure CIS and non-pure CIS (excluding cases with concomitant muscle invasive cancer). All patients were enrolled a in our institution from 1998 to 2010. Data was prospectively collected. Main end point was progression-free survival. Overall, 149 patients with CIS were identified for the analysis. A total of 98 patients had pure CIS (66%). Median follow-up was 103 months (range: 40-206 months). Progression occurred in 29 patients (19%). A total of 30 patients died during the follow-up (20%). In 13 cases (9%), the death was cancer specific. Progression-free survival estimate was 181 months (95% CI: 169-193 months) and 154 months (95% CI: 133-176 months) respectively for pure and non-pure CIS population (P=0.03). Among examined variables (age, gender, symptoms, smoking habit, ASA score, number of bacillus Calmette-Guérin [BCG] instillations), multivariate analysis disclosed that only CIS type was an independent predictor of progression (P=0.03) with a relative risk of 0.37 in favor of pure CIS. Pure and non-pure CIS are efficiently treated by BCG therapy combined with trans-urethral resection and/or radical cystectomy, with relatively low rate of progression. CIS type was the only significant predictor of progression.

Sections du résumé

BACKGROUND BACKGROUND
The aim of this study was to identify the predictive factors for progression defined as any event that shifted the management of the disease from a bladder sparing approach, by comparing patients with pure versus non-pure carcinoma in situ (CIS) of the bladder.
METHODS METHODS
A retrospective analysis was carried out in consecutive patients affected by newly-diagnosed pure CIS and non-pure CIS (excluding cases with concomitant muscle invasive cancer). All patients were enrolled a in our institution from 1998 to 2010. Data was prospectively collected. Main end point was progression-free survival.
RESULTS RESULTS
Overall, 149 patients with CIS were identified for the analysis. A total of 98 patients had pure CIS (66%). Median follow-up was 103 months (range: 40-206 months). Progression occurred in 29 patients (19%). A total of 30 patients died during the follow-up (20%). In 13 cases (9%), the death was cancer specific. Progression-free survival estimate was 181 months (95% CI: 169-193 months) and 154 months (95% CI: 133-176 months) respectively for pure and non-pure CIS population (P=0.03). Among examined variables (age, gender, symptoms, smoking habit, ASA score, number of bacillus Calmette-Guérin [BCG] instillations), multivariate analysis disclosed that only CIS type was an independent predictor of progression (P=0.03) with a relative risk of 0.37 in favor of pure CIS.
CONCLUSIONS CONCLUSIONS
Pure and non-pure CIS are efficiently treated by BCG therapy combined with trans-urethral resection and/or radical cystectomy, with relatively low rate of progression. CIS type was the only significant predictor of progression.

Identifiants

pubmed: 31144485
pii: S0393-2249.19.03254-5
doi: 10.23736/S0393-2249.19.03254-5
doi:

Substances chimiques

BCG Vaccine 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

406-412

Auteurs

Rodolfo Hurle (R)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Massimo Lazzeri (M)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Alberto Saita (A)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy - alberto.saita@humanitas.it.

Angelo Naselli (A)

Unit of Urology, San Giuseppe Hospital, MultiMedica, Milan, Italy.

Andrea Guarneri (A)

University Unit of Urology, San Giuseppe Hospital, MultiMedica, Milan, Italy.

Nicolò M Buffi (NM)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Giovanni Lughezzani (G)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Vittorio Fasulo (V)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Giulio M Mondellini (GM)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Marco Paciotti (M)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Luigi Domanico (L)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Roberto Peschechera (R)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Alessio Benetti (A)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Silvia Zandegiacomo (S)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Giuliana Lista (G)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Luisa Pasini (L)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

Giorgio Guazzoni (G)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.
Humanitas University, Pieve Emanuele, Milan, Italy.

Paolo Casale (P)

Department of Urology, Humanitas Clinic IRCCS, Rozzano, Milan, Italy.

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Classifications MeSH