Systematic review on oncologic outcomes on adjuvant endovesical treatment for non-muscle invasive bladder cancer in patients with solid organ transplant.


Journal

World journal of urology
ISSN: 1433-8726
Titre abrégé: World J Urol
Pays: Germany
ID NLM: 8307716

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 10 04 2022
accepted: 06 10 2022
pubmed: 12 11 2022
medline: 3 12 2022
entrez: 11 11 2022
Statut: ppublish

Résumé

Urothelial carcinoma has a higher incidence in renal transplanted patients according to several registries (relative risk × 3), and the global prognosis is inferior to the general population. The potential impact of immunosuppressive therapy on the feasibility, efficacy, and complications of endovesical treatment, especially Bacillus Calmette-Guerin, has a low level of evidence. We performed a systematic review that aimed to assess the morbidity and oncological outcomes of adjuvant endovesical treatment in solid organ transplanted patients. Medline was searched up to December 2021 for all relevant publications reporting oncologic outcomes of endovesical treatment in solid organ transplanted patients with NMIBC. Data were synthesized in light of methodological and clinical heterogeneity. Twenty-three retrospective studies enrolling 238 patients were included: 206 (96%) kidney transplants, 5 (2%) liver transplants, and 2 (1%) heart transplants. Concerning staging: 25% were pTa, 62% were pT1, and 22% were CIS. 140/238 (59%) patients did not receive adjuvant treatment, 50/238 (21%) received mitomycin C, 4/238 (2%) received epirubicin, and 46/238 (19%) received BCG. Disease-free survival reached 35% with TURBT only vs. 47% with endovesical treatment (Chi-square test p = 0.08 OR 1.2 [0.98-1.53]). The complication rate of endovesical treatment was 12% and was all minor (Clavien-Dindo I). In solid organ transplanted patients under immunosuppressive treatment, both endovesical chemotherapy and BCG are safe, but the level of evidence concerning efficacy in comparison with the general population is low. According to these results, adjuvant treatment should be proposed for NMIC in transplanted patients as in the general population.

Identifiants

pubmed: 36367586
doi: 10.1007/s00345-022-04188-9
pii: 10.1007/s00345-022-04188-9
doi:

Substances chimiques

BCG Vaccine 0
Adjuvants, Immunologic 0

Types de publication

Systematic Review Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2901-2910

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Matthieu Simonet (M)

Department of Urology and Renal Transplantation, Urology, University Hospital La Conception, Aix-Marseille University, Marseille, France.

Ana Dominguez Gutierrez (A)

Urology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Angelo Territo (A)

Oncology and Renal Transplant Units, Puigvert's Foundation, Barcelona, Spain.

Thomas Prudhomme (T)

Department of Urology, Rangueil University Hospital, Toulouse, France.

Ricardo Campi (R)

Department of Urology, Florence University Hospital, Florence, Italy.

Iulia Andras (I)

Department of Urology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Michael Baboudjian (M)

Department of Urology and Renal Transplantation, Urology, University Hospital La Conception, Aix-Marseille University, Marseille, France.

Vital Hevia (V)

Urology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Romain Boissier (R)

Department of Urology and Renal Transplantation, Urology, University Hospital La Conception, Aix-Marseille University, Marseille, France. romain.boissier@ap-hm.fr.
Department of Urology and Kidney Transplantation, Aix-Marseille University, Conception Academic Hospital, APHM147 Boulevard Baille, 13005, Marseille, France. romain.boissier@ap-hm.fr.

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