Real-World Study of Treatment with Pembrolizumab Among Patients with Advanced Urothelial Tract Cancer in Denmark.

ICI Urothelial tract cancer bladder cancer immunotherapy pembrolizumab real-world treatment

Journal

Bladder cancer (Amsterdam, Netherlands)
ISSN: 2352-3735
Titre abrégé: Bladder Cancer
Pays: Netherlands
ID NLM: 101668567

Informations de publication

Date de publication:
2021
Historique:
received: 28 03 2021
accepted: 25 06 2021
medline: 13 12 2021
pubmed: 13 12 2021
entrez: 12 7 2024
Statut: epublish

Résumé

Investigating the effect of newly approved oncological drugs in the real-world is warranted. With emerging novel treatments rapidly being approved for urothelial tract cancers, we aimed to assess real-world data, regarding effect and safety, during the first year after approval of pembrolizumab in Denmark for patients with locally advanced and unresectable or metastatic urothelial tract cancer (mUTC) in the first- and second-line setting. At the six oncological departments treating mUTC in Denmark, we identified all mUTC patients receiving pembrolizumab during the first year after approval, between March 1, 2018 and February 28, 2019. A retrospective data collection was conducted from January to June 2020. Patient characteristics matching that of the relevant clinical trials for pembrolizumab in first- and second-line treatment-setting, overall survival (OS), progression-free survival (PFS), toxicity and tumor response were assessed. 139 patients were identified, 53 in first-line treatment, 77 in second-line, and 9 receiving third or later lines of treatment. The population was characterized by a majority of males (70%), most patients had ECOG PS 0-1 (60.4%) and primary tumor in the bladder was predominant (90.6%). The overall response rate (ORR) in first-line was 30.2%, PFS was 3,5 months (95%CI 2,3-7,9 months) and OS 9,2 months (95%CI 7,0-20.9 months). For second-line treatment the ORR was 27,3%, PFS 2,9 months (95%CI 2,5-5,3) and OS 9.1 months (95%CI 5,4-12,8 months). Toxicity was comparable to clinical trials without any new toxicities registered. Real-world data on response rates, OS, PFS and toxicity for patients with mUTC receiving pembrolizumab in first- and second-line, shows comparable results to clinical trials. This study further establishes immunotherapy as an effective and tolerable treatment for mUTC.

Sections du résumé

BACKGROUND BACKGROUND
Investigating the effect of newly approved oncological drugs in the real-world is warranted. With emerging novel treatments rapidly being approved for urothelial tract cancers, we aimed to assess real-world data, regarding effect and safety, during the first year after approval of pembrolizumab in Denmark for patients with locally advanced and unresectable or metastatic urothelial tract cancer (mUTC) in the first- and second-line setting.
MATERIALS AND METHOD METHODS
At the six oncological departments treating mUTC in Denmark, we identified all mUTC patients receiving pembrolizumab during the first year after approval, between March 1, 2018 and February 28, 2019. A retrospective data collection was conducted from January to June 2020. Patient characteristics matching that of the relevant clinical trials for pembrolizumab in first- and second-line treatment-setting, overall survival (OS), progression-free survival (PFS), toxicity and tumor response were assessed.
RESULTS RESULTS
139 patients were identified, 53 in first-line treatment, 77 in second-line, and 9 receiving third or later lines of treatment. The population was characterized by a majority of males (70%), most patients had ECOG PS 0-1 (60.4%) and primary tumor in the bladder was predominant (90.6%). The overall response rate (ORR) in first-line was 30.2%, PFS was 3,5 months (95%CI 2,3-7,9 months) and OS 9,2 months (95%CI 7,0-20.9 months). For second-line treatment the ORR was 27,3%, PFS 2,9 months (95%CI 2,5-5,3) and OS 9.1 months (95%CI 5,4-12,8 months). Toxicity was comparable to clinical trials without any new toxicities registered.
CONCLUSION CONCLUSIONS
Real-world data on response rates, OS, PFS and toxicity for patients with mUTC receiving pembrolizumab in first- and second-line, shows comparable results to clinical trials. This study further establishes immunotherapy as an effective and tolerable treatment for mUTC.

Identifiants

pubmed: 38993987
doi: 10.3233/BLC-211523
pii: BLC211523
pmc: PMC11181703
doi:

Types de publication

Journal Article

Langues

eng

Pagination

413-425

Informations de copyright

© 2021 – The authors. Published by IOS Press.

Déclaration de conflit d'intérêts

H.P. has received research grants from Roche, MSD, Pfizer, and Pierre-Fabre. D.R.S has no conflict of interest to report. L.H.O has no conflict of interest to report. A.C. has no conflict of interest to report. G.A.T. has no conflict of interest to report. A.T. has no conflict of interest to report. L.H.D. has no conflict of interest to report. N.V.J. has no conflict of interest to report. A.B.A has no conflict of interest to report.

Auteurs

Lise Høj Omland (LH)

Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Dag Rune Stormoen (DR)

Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Line Hammer Dohn (LH)

Department of Oncology, Herlev and Gentofte University Hospital, Copenhagen, Denmark.

Andreas Carus (A)

Department of Oncology, Aalborg University Hospital, Aalborg, Denmark.

Anne Birgitte Als (AB)

Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

Niels Viggo Jensen (NV)

Department of Oncology, Odense University Hospital, Odense, Denmark.

Gry Assam Taarnhøj (GA)

Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Anders Tolver (A)

Department of Mathematical Sciences, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.

Helle Pappot (H)

Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Classifications MeSH