The Efficacy and Safety of Immune Checkpoint Inhibitor and Tyrosine Kinase Inhibitor Combination Therapy for Advanced or Metastatic Renal Cell Carcinoma: A Multicenter Retrospective Real-World Cohort Study

Author:

Iinuma Koji1ORCID,Yamada Toyohiro1,Kameyama Koji2,Taniguchi Tomoki3ORCID,Kawada Kei4,Ishida Takashi5,Nagai Shingo6,Enomoto Torai7,Ueda Shota8,Takagi Kimiaki9ORCID,Kawase Makoto1,Takeuchi Shinichi1,Kawase Kota1,Kato Daiki1ORCID,Takai Manabu1,Nakane Keita1ORCID,Koie Takuya1ORCID

Affiliation:

1. Department of Urology, Graduate School of Medicine, Gifu University, Gifu 5011194, Japan

2. Department of Urology, Central Japan International Medical Center, 1-1 Kenkonomachi, Minokamo 5058510, Japan

3. Department of Urology, Ogaki Municipal Hospital, Ogaki 5038502, Japan

4. Department of Urology, Gifu Prefectural General Medical Center, Gifu 5008717, Japan

5. Department of Urology, Gifu Municipal Hospital, Gifu 5008513, Japan

6. Department of Urology, Toyota Memorial Hospital, Toyota 4718513, Japan

7. Department of Urology, Matsunami General Hospital, Hashima-gun 5016062, Japan

8. Department of Urology, Japanese Red Cross Takayama Hospital, 3-113-11 Tenman-machi, Takayama 5068550, Japan

9. Department of Urology, Daiyukai Daiichi Hospital, Ichinomiya 4918551, Japan

Abstract

We evaluated the efficacy and safety of combination therapy with immune checkpoint inhibitors (ICIs) and tyrosine kinase inhibitors (TKI) as first-line therapy for patients diagnosed as having advanced or metastatic renal cell carcinoma (mRCC). We enrolled 51 patients to receive ICI+TKI therapy for mRCC at 9 Japanese institutions. The overall survival (OS) of the patients treated with ICI+TKI was the primary endpoint., and the secondary endpoints were progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR). Furthermore, we analyzed the clinical prognostic and predictive factors in patients with mRCC treated with ICI+TKI therapy. Seven months was the median follow-up period. The OS rates at 6, 12, and 18 months were 93.1, 82.5, and 68.8%, respectively. The median PFS for patients who received ICI+TKI was 19.0 months, ORR was 68.6%, and DCR was 88.2%. ICI+TKI-related adverse events occurred in 43 patients (84.3%) with any grade and in 22 patients (43.1%) with grade ≥3. Treatment selection with poor prognostic factors may be prudent, even though ICI+TKI is an efficacious and safe first-line treatment in patients with mRCC.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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