First-line therapy for metastatic renal cell carcinoma: A propensity score-matched comparison of efficacy and safety

被引:0
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作者
Yanagisawa, Takafumi [1 ]
Mori, Keiichiro [1 ]
Kawada, Tatsushi [2 ]
Katayama, Satoshi [2 ]
Uchimoto, Taizo [3 ]
Tsujino, Takuya [3 ]
Nishimura, Kazuki [3 ]
Adachi, Takahiro [4 ]
Toyoda, Shingo [5 ]
Nukaya, Takuhisa [6 ]
Fukuokaya, Wataru [1 ]
Urabe, Fumihiko [1 ]
Murakami, Masaya [1 ]
Yamanoi, Tomoaki
Bekku, Kensuke [2 ]
Komura, Kazumasa
Takahara, Kiyoshi
Hashimoto, Takeshi [4 ]
Fujita, Kazutoshi
Azuma, Haruhito
Ohno, Yoshio
Shiroki, Ryoichi [6 ]
Uemura, Hirotsugu [5 ]
Araki, Motoo [2 ]
Kimura, Takahiro [1 ]
机构
[1] Jikei Univ, Sch Med, Dept Urol, Tokyo, Japan
[2] Okayama Univ, Dept Urol, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[3] Osaka Med & Pharmaceut Univ, Dept Urol, Osaka, Japan
[4] Tokyo Med Univ, Dept Urol, Tokyo, Japan
[5] Kindai Univ, Fac Med, Dept Urol, Osaka, Japan
[6] Fujita Hlth Univ, Sch Med, Dept Urol, Aichi, Japan
关键词
Metastatic renal cell carcinoma; Clear cell carcinoma; Immune checkpoint inhibitor; Tyrosine kinase inhibitor; Propensity-score matching;
D O I
10.1016/j.urolonc.2024.06.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Immune checkpoint inhibitor (ICI)-based combination therapy is a standard systemic treatment for metastatic renal cell carcinoma (mRCC). Although differential pharmacologic action between ICI+ICI and ICI+tyrosine kinase inhibitor (TKI) combinations may affect outcomes, comparative studies using real-world data are few. Methods: We retrospectively analyzed the records of 447 mRCC patients treated with 1st-line ICI-based combinations at multiple institutions between January 2018 and August 2023, and selected 320 patients diagnosed with clear cell RCC (ccRCC) for further study. Cohorts were matched using one-to-one propensity scores based on IMDC risk classification. Overall survival (OS), progression-free survival (PFS), objective response rates (ORRs), and treatment-related adverse events (TrAE) were compared. Results: The matching process yielded 228 metastatic ccRCC patients treated with ICI+ICI (n =114) or ICI+TKI (n =114). Median OS was 53 months (95%CI: 33-NA) in patients treated with ICI+ICI and was not reached (95%CI: 43-NA) with ICI+TKI (P = 0.24). Median PFS was significantly shorter for ICI+ICI (13 months, 95%CI: 7-25) than for ICI+TKI (25 months, 95%CI: 13-NA) (P = 0.047). There were no differences in second-line PFS for sequential therapy after 1st-line combinations of ICI+ICI or ICI+TKI (6 vs. 8 months, P = 0.6). There were no differences in ORR between the 2 groups (ICI+ICI: 51% vs. ICI+TKI: 55%, P = 0.8); the progressive disease (PD) rate was significantly higher in patients treated with the ICI+ICI combination (24% vs. 11%, P = 0.029). The rate of any grade TrAE was significantly higher in patients treated with ICI+TKI (71% vs. 85%, P = 0.016), but we found no differences in severe TrAE between the 2 groups Conclusions: In a matched cohort of real-world data, we confirmed comparable OS benefits between ICI+ICI and ICI+TKI combinations. However, differential clinical behaviors in terms of PFS, PD rates, and TrAE between ICI-based combinations may enrich clinical decisionmaking. (c) 2024 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页数:9
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