First-line immune checkpoint inhibitor use in cisplatin-eligible patients with advanced urothelial carcinoma: a secular trend analysis

Author:

Parikh Ravi B1ORCID,Feld Emily K1,Galsky Matthew D2,Adamson Blythe JS34ORCID,Cohen Aaron B35,Baxi Shrujal S3,Boursi Shimon Ben1,Christodouleas John P6,Vaughn David J1,Meropol Neal J37,Mamtani Ronac1

Affiliation:

1. Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA

2. Tisch Cancer Institute, Icahn School of Medicine, New York, NY 10029, USA

3. Flatiron Health, New York, NY 10013, USA

4. Comparative Health Outcomes, Policy & Economics (CHOICE) Institute, University of Washington, Seattle, WA 98195, USA

5. NYU Grossman School of Medicine, New York University, New York, NY 10016, USA

6. Department of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, USA

7. Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH 44106, USA

Abstract

Aim: Standard first-line treatment of advanced urothelial cell carcinoma involves cisplatin-based chemotherapy, with carboplatin or immune checkpoint inhibitor therapy (ICI) reserved for cisplatin-ineligible individuals. Methods: Using a large de-identified electronic health record-derived database of patients with advanced urothelial cell carcinoma in the USA, we examined trends in utilization of first-line systemic therapies in cisplatin-eligible patients from 1 January 2015 to 31 March 2018. Results: Among 1181 cisplatin-eligible patients, the quarterly proportion who received first-line ICI increased from 1 to 42% (ptrend <0.001), while the proportion who received cisplatin-based chemotherapy decreased from 53 to 33% (ptrend = 0.018). Patients receiving ICI were older than those receiving cisplatin (median age: 75 vs 68). Conclusion: Our analysis suggests rising off-label ICI use in cisplatin-eligible individuals, potentially because of ICI’s favorable toxicity profile.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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