Efficacy of Vinflunine for Patients with Metastatic Urothelial Cancer after Immune Checkpoint Inhibitor Pretreatment-A Retrospective Multicenter Analysis.

bladder cancer chemotherapy immune checkpoint inhibition immunotherapy metastatic urothelial carcinoma vinflunine

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
09 Jun 2022
Historique:
received: 20 03 2022
revised: 24 04 2022
accepted: 20 05 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 25 6 2022
Statut: epublish

Résumé

Immune checkpoint inhibitors (ICI) are standard of care in patients with metastatic urothelial carcinoma (mUC) ineligible for cisplatin, and as second-line therapy after platinum-based chemotherapy. To date, few data exist about the efficacy of the former second-line chemotherapeutic agent vinflunine after the failure of sequential platinum-based chemotherapy and ICI treatment. The aim of this analysis was to examine the efficacy of vinflunine in a post-ICI third- or later-line setting. In this retrospective German multicenter study, data of mUC patients treated with vinflunine were reviewed in six centers between February 2010 and December 2021. All of the 105 included patients had radiologic progression after first-line platinum-based chemotherapy. The objective was to describe the efficacy of vinflunine in terms of overall response rate (ORR), clinical benefit rate (CBR), overall survival (OS), and progression-free survival (PFS) for post-ICI and ICI-naïve patients, respectively. In our cohort, 61 patients (58.1%) had preceding immunotherapy before vinflunine administration, and 44 patients (41.9%) were ICI-naïve. Patients with ICI pretreatment showed an ORR of 22.4% compared to 15.6% within ICI-naïve patients ( This analysis supports the sequential use of vinflunine in post-ICI patients since the vinca-alkaloid retains a measurable clinical activity in these heavily pretreated patients. The therapeutic benefit may be higher than demonstrated in previous studies.

Sections du résumé

BACKGROUND BACKGROUND
Immune checkpoint inhibitors (ICI) are standard of care in patients with metastatic urothelial carcinoma (mUC) ineligible for cisplatin, and as second-line therapy after platinum-based chemotherapy. To date, few data exist about the efficacy of the former second-line chemotherapeutic agent vinflunine after the failure of sequential platinum-based chemotherapy and ICI treatment. The aim of this analysis was to examine the efficacy of vinflunine in a post-ICI third- or later-line setting.
METHODS METHODS
In this retrospective German multicenter study, data of mUC patients treated with vinflunine were reviewed in six centers between February 2010 and December 2021. All of the 105 included patients had radiologic progression after first-line platinum-based chemotherapy. The objective was to describe the efficacy of vinflunine in terms of overall response rate (ORR), clinical benefit rate (CBR), overall survival (OS), and progression-free survival (PFS) for post-ICI and ICI-naïve patients, respectively.
RESULTS RESULTS
In our cohort, 61 patients (58.1%) had preceding immunotherapy before vinflunine administration, and 44 patients (41.9%) were ICI-naïve. Patients with ICI pretreatment showed an ORR of 22.4% compared to 15.6% within ICI-naïve patients (
CONCLUSION CONCLUSIONS
This analysis supports the sequential use of vinflunine in post-ICI patients since the vinca-alkaloid retains a measurable clinical activity in these heavily pretreated patients. The therapeutic benefit may be higher than demonstrated in previous studies.

Identifiants

pubmed: 35740516
pii: cancers14122850
doi: 10.3390/cancers14122850
pmc: PMC9220857
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Felix Riedel (F)

Department of Urology, University Hospital Ulm, 89081 Ulm, Germany.

Mara Münker (M)

Department of Urology, Marien Hospital, Ruhr-University Bochum, 44625 Herne, Germany.

Florian Roghmann (F)

Department of Urology, Marien Hospital, Ruhr-University Bochum, 44625 Herne, Germany.

Johannes Breyer (J)

Department of Urology, Caritas Hospital St. Josef, University of Regensburg, 93053 Regensburg, Germany.

Marco J Schnabel (MJ)

Department of Urology, Caritas Hospital St. Josef, University of Regensburg, 93053 Regensburg, Germany.

Maximilian Burger (M)

Department of Urology, Caritas Hospital St. Josef, University of Regensburg, 93053 Regensburg, Germany.

Danijel Sikic (D)

Department of Urology and Pediatric Urology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, 91054 Erlangen, Germany.

Thomas Büttner (T)

Department of Urology, University Hospital Bonn (UKB), 53127 Bonn, Germany.

Manuel Ritter (M)

Department of Urology, University Hospital Bonn (UKB), 53127 Bonn, Germany.

Kiriaki Hiller (K)

National Center for Tumor Diseases (NCT) Heidelberg, 69120 Heidelberg, Germany.

Felix Wezel (F)

Department of Urology, University Hospital Ulm, 89081 Ulm, Germany.

Christian Bolenz (C)

Department of Urology, University Hospital Ulm, 89081 Ulm, Germany.

Friedemann Zengerling (F)

Department of Urology, University Hospital Ulm, 89081 Ulm, Germany.

Classifications MeSH