Your browser doesn't support javascript.
loading
Adjuvant vs. progression-triggered treatment with gemcitabine in platinum-ineligible high-risk bladder cancer patients: Long-term follow-up of a randomized phase 3 trial.
Heinzelbecker, Julia; Spieler, Natalie; Kuehn, Michael; Fischer, Claus; Volkmer, Björn; von Rundstedt, Friedrich; Albers, Peter; Becht, Eduard; Bannowsky, Andreas; Weber, H Matthias; Hofmann, Rainer; Müller, Markus; Langbein, Sigrun; Steiner, Gabriel; Retz, Margitta; Kamradt, Jörn; Wagenpfeil, Gudrun; Wellek, Stefan; Lehmann, Jan; Stoeckle, Michael.
Affiliation
  • Heinzelbecker J; Department of Urology and Pediatric Urology, University Medical Centre Saarland, Saarland University, Homburg/Saar, Germany. Electronic address: julia.heinzelbecker@uks.eu.
  • Spieler N; Department of Urology and Pediatric Urology, University Medical Centre Saarland, Saarland University, Homburg/Saar, Germany.
  • Kuehn M; Department of Urology, Johanniter Krankenhaus Genthin-Stendal, Stendal, Germany.
  • Fischer C; Department of Urology and Pediatric Urology, Klinikum Bayreuth GmbH, Bayreuth, Germany.
  • Volkmer B; Department of Urology, Klinikum Kassel GmbH, Kassel, Germany.
  • von Rundstedt F; Department of Urology, Helios University Hospital Wuppertal, Witten/Herdecke University, Wuppertal, Germany.
  • Albers P; Department of Urology, University Hospital, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.
  • Becht E; Department of Urology and Pediatric Urology, Krankenhaus Nordwest, Frankfurt, Germany.
  • Bannowsky A; Department of Urology, Imland Klinik, Rendsburg, Germany.
  • Weber HM; Department of Urology, Helios Krankenhaus Blankenhain, Blankenhain, Germany.
  • Hofmann R; Department of Urology and Pediatric Urology, University Hospital Marburg, Marburg, Germany.
  • Müller M; Department of Urology, Klinikum Ludwigshafen gGmbH, Ludwigshafen, Germany.
  • Langbein S; MVZ-Urology, Medical Faculty of Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
  • Steiner G; Department of Urology, Helios Klinikum Meiningen, Meiningen, Germany.
  • Retz M; Department of Urology, Rechts der Isar Medical Center, Technische Universität München, Munich, Germany.
  • Kamradt J; Department of Urology, Zentrum für Urologie und Nephrologie, Bern, Switzerland.
  • Wagenpfeil G; Institute of Medical Biometry, Epidemiology and Medical Informatics, Saarland University Campus Homburg, Saar, Germany.
  • Wellek S; Division of Biostatistics, Center of Mental Health Mannheim, Mannheim, Germany; Department of Medical Biostatistics, Epidemiology and Informatics, University Medical Center, University of Mainz, Mainz, Germany.
  • Lehmann J; Department of Urology and Pediatric Urology, University Medical Centre Saarland, Saarland University, Homburg/Saar, Germany; Städtisches Krankenhaus Kiel, Kiel, Germany; Urologische Gemeinschaftspraxis Pruener Gang, Kiel, Germany.
  • Stoeckle M; Department of Urology and Pediatric Urology, University Medical Centre Saarland, Saarland University, Homburg/Saar, Germany.
Urol Oncol ; 41(8): 356.e19-356.e30, 2023 08.
Article in En | MEDLINE | ID: mdl-37198025
ABSTRACT

BACKGROUND:

Cisplatin-based chemotherapy (ChT) is the preferred perioperative treatment in muscle-invasive urothelial carcinoma of the urinary bladder (UCUB). Nevertheless, a certain number of patients are ineligible for platinum-based ChT. This trial compared immediate adjuvant vs. delayed gemcitabine ChT at progression in platinum-ineligible patients with high-risk UCUB.

METHODS:

High-risk platinum-ineligible UCUB patients (n = 115) were randomized 11 to adjuvant gemcitabine (n = 59) or gemcitabine at progression (n = 56). Overall survival was analyzed. Additionally, we analyzed progression-free survival (PFS), toxicity and quality of life (QoL).

RESULTS:

After a median follow-up of 3.0 years (inter quartile range [IQR] 1.3-11.6), adjuvant ChT did not significantly prolong overall survival (OS) (HR 0.84; 95% CI 0.57-1.24; P = 0.375), with 5-year OS of 44.1% (95% CI 31.2-56.2) and 30.4% (95% CI 19.0-42.5), respectively. We noted no significant difference in PFS (HR 0.76; 95% CI 0.49-1.18; P = 0.218), with 5-year PFS of 36.2% (95% CI 22.8-49.7) in the adjuvant group and 22.2% (95% CI 11.5%-35.1%) when treated at progression. Patients with adjuvant treatment showed a significantly worse QoL. The trial was prematurely closed after recruitment of 115 of the planned 178 patients.

CONCLUSIONS:

There was no statistically significant difference in terms of OS and PFS for patients with platinum-ineligible high-risk UCUB receiving adjuvant gemcitabine compared to patients treated at progression. These findings underline the importance of implementing and developing new perioperative treatments for platinum-ineligible UCUB patients.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Urinary Bladder Neoplasms / Carcinoma, Transitional Cell Type of study: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Urol Oncol Journal subject: NEOPLASIAS / UROLOGIA Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Urinary Bladder Neoplasms / Carcinoma, Transitional Cell Type of study: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Urol Oncol Journal subject: NEOPLASIAS / UROLOGIA Year: 2023 Document type: Article