Treatment Patterns and Outcomes by Age in Metastatic Urinary Tract Cancer: A Retrospective Tertiary Cancer Center Analysis

Author:

Tripathi Nishita12,Gebrael Georges1ORCID,Chigarira Beverly1,Sahu Kamal Kant1ORCID,Balasubramanian Ishwarya1,Caparas Constance1,Mathew Thomas Vinay1ORCID,Cohan Jessica N.1,Pelletier Kaitlyn1,Maughan Benjamin L.1,Agarwal Neeraj1ORCID,Swami Umang1ORCID,Gupta Sumati13ORCID

Affiliation:

1. Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA

2. Detroit Medical Center, Wayne State University, Detroit, MI 48201, USA

3. George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, UT 84148, USA

Abstract

Metastatic urinary tract cancer (mUTC) is challenging to treat in older adults due to comorbidities. We compared the clinical courses of younger and older (≥70 years) adults with mUTC receiving first-line (1L) systemic therapy in a tertiary cancer center. Baseline clinical characteristics, treatments received, tolerability, and survival outcomes were analyzed. Among 212 patients (103 older vs. 109 younger), the older patients had lower hemoglobin at baseline (84% vs. 71%, p = 0.03), the majority were cisplatin-ineligible (74% vs. 45%, p < 0.001), received more immunotherapy-based treatments in the 1L (52% vs. 36%, p = 0.01), received fewer subsequent lines of treatment (median 0 vs. 1, p = 0.003), and had lower clinical trial participation (30% vs. 18%, p = 0.05) compared to the younger patients. When treated with 1L chemotherapy, older patients required more dose adjustments (53.4% vs. 23%, p = 0.001) and received fewer cycles of chemotherapy (median 4 vs. 5, p= 0.01). Older patients had similar OS (11.2 months vs. 14 months, p = 0.06) and similar rates of treatment-related severe toxicity and healthcare visits, independent of the type of systemic treatment received, compared to younger patients. We conclude that select older adults with mUTC can be safely treated with immunotherapy and risk-adjusted regimens of chemotherapy with tangible survival benefits.

Publisher

MDPI AG

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