Dokumentenart: | Artikel | ||||
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Titel eines Journals oder einer Zeitschrift: | European Urology | ||||
Verlag: | Elsevier | ||||
Ort der Veröffentlichung: | AMSTERDAM | ||||
Band: | 81 | ||||
Nummer des Zeitschriftenheftes oder des Kapitels: | 6 | ||||
Seitenbereich: | S. 606-614 | ||||
Datum: | 2022 | ||||
Institutionen: | Medizin > Lehrstuhl für Urologie | ||||
Identifikationsnummer: |
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Stichwörter / Keywords: | FGFR3 MUTATIONS; UROTHELIAL CARCINOMA; GUIDELINES; BCG; PEMBROLIZUMAB; ASSOCIATION; PROGRESSION; RECURRENCE; BIOMARKER; NMIBC; Bacillus Calmette-Gu?rin; Bladder cancer; Fibroblast growth factor receptor; FGFR alterations; Non-muscle-invasive bladder; cancer | ||||
Dewey-Dezimal-Klassifikation: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||
Status: | Veröffentlicht | ||||
Begutachtet: | Ja, diese Version wurde begutachtet | ||||
An der Universität Regensburg entstanden: | Ja | ||||
Dokumenten-ID: | 57166 |
Zusammenfassung
Background: Limited data are available on the prognostic and predictive value of fibroblast growth factor receptor alterations (FGFRa) relative to clinical outcomes in patients with non-muscle-invasive bladder cancer (NMIBC).Objective: To determine whether FGFRa may be clinically useful in stratifying for treatment response in a real-world cohort of patients with pT1 NMIBC treated and untreated ...
Zusammenfassung
Background: Limited data are available on the prognostic and predictive value of fibroblast growth factor receptor alterations (FGFRa) relative to clinical outcomes in patients with non-muscle-invasive bladder cancer (NMIBC).Objective: To determine whether FGFRa may be clinically useful in stratifying for treatment response in a real-world cohort of patients with pT1 NMIBC treated and untreated with bacillus Calmette-Guerin (BCG) instillation therapy.Design, setting, and participants: A pooled dataset of matched clinical and genomic data (1992-2015) for pT1 NMIBC patients was assessed by the Bladder Cancer Research Initiative for Drug Targets in Germany consortium.Outcome measurements and statistical analysis: Key efficacy outcomes were recurrence-free survival (RFS), progression-free survival (PFS), and disease-specific survival (DSS), which were estimated by Kaplan-Meier analysis, with hazard ratios calculated using a multivariate Cox proportional-hazard model.Results and limitations: In this retrospective study of 263 patients with high-grade NMIBC, at a median follow-up of 63 mo, 32% showed recurrence and 15% progressed to muscle-invasive bladder cancer. FGFRa were found in 43% of patients, including 39% mutations and 5.7% fusions. FGFRa were associated with lower rates of concomitant carcinoma in situ. Among patients with or without FGFRa, there was no significant dif-ference in PFS, RFS, and DSS in those who were BCG treated or BCG naive, or in the over-all population. Limitations include the retrospective design from a single-center setting. Conclusions: In patients with high-risk NMIBC, FGFRa were frequently observed. Patients with FGFRa who often exhibit recurrence/relapse after BCG treatment have a high unmet need. Patient summary: Our retrospective study suggests that fibroblast growth factor recep-tor alterations (FGFRa) occur frequently in non-muscle-invasive bladder cancer (NMIBC).Outcomes were similar with or without FGFRa in patients with NMIBC, both overall and for standard bacillus Calmette-Guerin (BCG) treatment. (c) 2022 The Authors.Published by Elsevier B.V. on behalf of European Association of Urology. This is an open access article under the CC BY-NC-ND license (http://creative-commons.org/licenses/by-nc-nd/4.0/).
Metadaten zuletzt geändert: 29 Feb 2024 12:52