Real-world overall survival (OS) of patients (pts) with metastatic urothelial carcinoma (mUC) receiving first-line (1L) systemic therapy (tx): Results from IMPACT UC II.

Authors

Mehmet Asim Bilen

Mehmet Asim Bilen

Winship Cancer Institute of Emory University, Atlanta, GA

Mehmet Asim Bilen, Brandon Diessner, Valerie A. Morris, John White, Melissa Kirker, Amy Sainski-Nguyen, Norbek Gharibian, Louise Murphy, Abhijeet Bhanegaonkar

Organizations

Winship Cancer Institute of Emory University, Atlanta, GA, Optum, Eden Prairie, MN, EMD Serono, Rockland, MA, Pfizer, New York, NY

Research Funding

Pharmaceutical/Biotech Company
This study was sponsored by EMD Serono, Rockland, MA, USA (CrossRef Funder ID: 10.13039/ 100004755), as part of an alliance between the healthcare business of Merck KGaA, Darmstadt, Germany (CrossRef Funder ID: 10.13039/100009945) and Pfizer.

Background: Urothelial cancer (UC) is the most common urinary system cancer. The IMPACT UC II study aimed to assess tx patterns and clinical outcomes in pts with mUC treated with platinum-based chemotherapy or immuno-oncology monotherapy (IO-mono) in 1L. Methods: This was a retrospective claims analysis of pts diagnosed with mUC from July 2015 to June 2020 and continuously enrolled for 6 mo before and ≥6 mo after index date (ie, date of first claim) using Optum Research Database, which represents ≈8% of commercially insured and 18% of Medicare Advantage (MAPD) populations. Pts were followed up until disenrollment, study end in August 2021, or death. Analyses examined OS and time to 2L tx (TT2L) in three tx cohorts: cisplatin (cis)-based, carboplatin (carbo)-based, or IO-mono. Results: Of 3,006 pts diagnosed with mUC, 1,037 received 1L tx: 365 (35.2%) with cis-based tx; 337 (32.5%) with carbo-based tx, and 335 (32.3%) with IO-mono. Among treated pts, mean age was 72.5 years (SD, 9.9 years), 72.3% were male, and 77.4% were MAPD insured. At baseline, pts receiving cis-based tx had a lower percentage of ≥3 comorbidities (defined by National Cancer Institute criteria): cis-based, 22.2%; carbo-based, 39.5%; and IO-mono, 45.1%. Among 290 pts (27.9%) receiving 2L tx, carbo-based tx had the shortest median TT2L (5.7 mo). Pts receiving cis-based tx had the longest median OS (27.4 mo). Relative to cis-based tx, multivariable–adjusted mortality risk was 2 times higher with IO-mono (hazard ratio [HR], 2.0; 95% CI, 1.6-2.5) and 1.5 times higher with carbo-based tx (HR, 1.5; 95% CI, 1.3-1.9) (Table). Conclusions: This study shows that, before avelumab 1L maintenance approval, the majority of pts did not receive any systemic anticancer tx. following mUC diagnosis. In 1L, after multivariable adjustment (including for baseline comorbidities), real-world OS was lower in pts receiving carbo-based tx and IO-mono compared with cis-based tx. Future research should examine outcomes with newer standard of care.

Cis-basedCarbo-basedIO-mono
Pts, n365337335
Median OS (IQR), mo27.4 (10.2-NRa)12.2 (5.4-34.7)8.8 (3.4-26.7)
OS rate, %
6 mo87.372.858.1
12 mo70.450.939.4
24 mo56.028.526.0
OS hazard ratio (95% CI), Multivariable adjusteda1.5 (1.3-1.9)2.0 (1.6-2.5)
Median TT2L (IQR), mo6.5 (4.0-9.2)5.7 (3.1-9.3)5.8 (3.2-8.0)

IQR, interquartile range; NCI, National Cancer Institute; NR, not reached. a>75% of patients were alive at study end. b Adjusted for age, sex, region, NCI comorbidities, and anemia (defined by Agency for Healthcare Research and Quality criteria).

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Abstract Details

Meeting

2023 ASCO Quality Care Symposium

Session Type

Poster Session

Session Title

Poster Session B

Track

Health Care Access, Equity, and Disparities,Technology and Innovation in Quality of Care,Palliative and Supportive Care

Sub Track

Real-World Evidence

Citation

JCO Oncol Pract 19, 2023 (suppl 11; abstr 529)

DOI

10.1200/OP.2023.19.11_suppl.529

Abstract #

529

Poster Bd #

L4

Abstract Disclosures