Real-World Outcomes in Patients With Metastatic Renal Cell Carcinoma Treated With First-Line Nivolumab Plus Ipilimumab in the United States

被引:3
作者
Doshi, Gurjyot K. [1 ]
Osterland, Andrew J. [2 ]
Shi, Ping [2 ]
Yim, Annette [2 ]
Del Tejo, Viviana [3 ]
Guttenplan, Sarah B. [3 ]
Eiffert, Samantha [3 ]
Yin, Xin [3 ]
Rosenblatt, Lisa [3 ]
Conkling, Paul R. [2 ]
机构
[1] Texas Oncol, Houston, TX USA
[2] Ontada, Boston, MA 02109 USA
[3] Bristol Myers Squibb, Princeton, NJ USA
关键词
D O I
10.1200/CCI.24.00132
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSENivolumab plus ipilimumab (NIVO + IPI) is a first-in-class combination immunotherapy for the treatment of intermediate- or poor (I/P)-risk advanced or metastatic renal cell carcinoma (mRCC). Currently, there are limited real-world data regarding clinical effectiveness beyond 12-24 months from treatment initiation. In this real-world study, treatment patterns and clinical outcomes were evaluated for NIVO + IPI in a community oncology setting.METHODSA retrospective analysis using electronic medical record data from The US Oncology Network examined patients with I/P-risk clear cell mRCC who initiated first-line (1L) NIVO + IPI between January 4, 2018, and December 31, 2019, with follow-up until June 30, 2022. Baseline demographics, clinical characteristics, treatment patterns, clinical effectiveness, and safety outcomes were assessed descriptively. Overall survival (OS) and real-world progression-free survival (rwPFS) were analyzed using Kaplan-Meier methods.RESULTSAmong 187 patients identified (median follow-up, 22.4 months), with median age 63 (range, 30-89) years, 74 (39.6%) patients had poor risk and 37 (19.8%) patients had Eastern Cooperative Oncology Group performance status score >= 2. Of 86 patients who received second-line therapy, 54.7% received cabozantinib and 10.5% received pazopanib. The median (95% CI) OS and rwPFS were 38.4 (24.7-46.1) months and 11.1 (7.5-15.0) months, respectively. Treatment-related adverse events (TRAEs) were reported in 89 (47.6%) patients, including fatigue (n = 25, 13.4%) and rash (n = 19, 10.2%).CONCLUSIONThis study provides data to support the understanding of the real-world utilization and long-term effectiveness of 1L NIVO + IPI in patients with I/P-risk mRCC. TRAE rates were low relative to clinical trials.
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页数:10
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