Assessment of treatment patterns and real-world outcomes following changes in the treatment paradigm for locally advanced/metastatic urothelial carcinoma (la/mUC) in the US.

Authors

null

Melissa Kirker

Pfizer, New York, NY

Melissa Kirker , Anup Abraham , Anna Vlahiotis , Abhijeet Bhanegaonkar , Darrin Benjumea , Chai Kim , Haiyan Sun , Mairead Kearney , Sanjana Chandrasekar , Benjamin Li , Sheena Thakkar , Helen H Moon

Organizations

Pfizer, New York, NY, Genesis Research, LLC, Hoboken, NJ, EMD Serono, Rockland, MA, Pfizer Inc, New York, NY, The Healthcare Business of Merck KGaA, Darmstadt, Germany, Hematology-Oncology, Kaiser Permanente Southern California Region, Riverside, CA

Research Funding

Pharmaceutical/Biotech Company
This study was sponsored by Pfizer as part of an alliance between Pfizer and the healthcare business of Merck KGaA, Darmstadt, Germany (CrossRef Funder ID: 10.13039/100009945)

Background: The standard-of-care first-line (1L) treatment for la/mUC is platinum-based chemotherapy (PBC) followed by avelumab 1L maintenance (1LM) in those who have not progressed following 1L PBC. This study aims to understand treatment patterns and real-world outcomes in patients with la/mUC in the US, including the early adoption of avelumab 1LM since its FDA approval in June 2020. Methods: Patients aged ≥18 years diagnosed with la/mUC between Jan 2015 and Jul 2021 were identified using electronic health records from the Flatiron Health database. Patient characteristics at baseline (la/mUC diagnosis) and clinical outcomes were described by 1L treatment received using the Kaplan-Meier method. Results: Of 4,387 patients included in this study, 3,706 (84.5%) received systemic treatments. Cisplatin-based therapy was the most common 1L therapy (33.3%), followed by carboplatin-based (30.9%) and immuno-oncology (IO) therapies (28.0%). Patients treated with cisplatin-based therapies had longer median progression-free survival compared with patients treated with carboplatin-based and IO therapies (8.0, 6.4, and 6.1 months, respectively). Median overall survival (mOS) in the treated cohort was 14.6 months from the initiation of 1L therapy. Patients treated with 1L cisplatin-based therapies had the longest mOS (18.3 months), followed by 1L IO therapies (14.6 months), and 1L carboplatin (13.2 months). Since July 2020, 89 patients received avelumab 1LM; the median follow-up time from the start of 1LM avelumab was 6.0 months and clinical outcomes data were immature. Of 1L-treated patients, 50.6% (n=1,874) moved onto second-line (2L) therapy during the study period. Notably, the cohort with the lowest 2L treatment rates were patients treated with 1L IO. The table demonstrates treatment sequences for this population. Conclusions: In this real-world cohort, most patients received standard-of-care platinum-based chemotherapy in 1L, with those on cisplatin-based therapy demonstrating the best outcomes. Early uptake of avelumab as 1LM was observed, and future analysis should examine the clinical outcomes of patients who received avelumab 1LM following 1L PBC.

Sequence of treatment groups* (%) from 1L to 2L.

2L cisplatin
(n=107)
2L carboplatin
(n=201)
2L IO
(n=1,148)
2L antibody-drug conjugate (ADC)
(n=66)
2L other
(n=352)
Not treated with 2L
(n=1,832)
1L cisplatin (n=1,235)4.02.842.30.67.742.6
1L carboplatin
(n=1,147)
1.55.844.30.68.139.7
1L IO
(n=1,038)
2.16.66.14.711.968.6
1L other
(n=286)
6.310.819.20.714.049.0

* Treatment groups are mutually exclusive. Patients were placed into each group regardless of cross-treatment group combination with this hierarchy: IO, targeted, ADC, cisplatin, carboplatin, any other. Percentages represent row percentages

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Abstract Details

Meeting

2023 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session B: Prostate Cancer and Urothelial Carcinoma

Track

Urothelial Carcinoma,Prostate Cancer - Advanced

Sub Track

Quality of Care/Quality Improvement and Real-World Evidence

Citation

J Clin Oncol 41, 2023 (suppl 6; abstr 468)

DOI

10.1200/JCO.2023.41.6_suppl.468

Abstract #

468

Poster Bd #

H9

Abstract Disclosures