Impact of Complete Surgical Resection of Metastatic Lesions in Patients with Advanced Renal Cell Carcinoma in the Era of Tyrosine Kinase Inhibitors and Immune Checkpoint Inhibitors

Author:

Shimizu Takuto1,Miyake Makito1ORCID,Nishimura Nobutaka1,Yoshida Takanori2,Itami Yoshitaka3,Tachibana Akira4,Omori Chihiro15,Oda Yuki1,Kohashi Mikiko6,Tomizawa Mitsuru1,Onishi Kenta1,Hori Shunta1,Morizawa Yosuke1ORCID,Dotoh Daisuke1,Nakai Yasushi1,Torimoto Kazumasa1,Tanaka Nobumichi7,Fujimoto Kiyohide1ORCID

Affiliation:

1. Department of Urology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan

2. Department of Urology, Nara Prefecture Seiwa Medical Center, Ikoma, Nara 636-0802, Japan

3. Department of Urology, Tane General Hospital, Osaka, Osaka 550-0025, Japan

4. Department of Urology, Hoshigaoka Medical Center, Hirakata, Osaka 573-8511, Japan

5. Department of Urology, Nara Prefecture General Medical Center, Nara, Nara 630-8581, Japan

6. Department of Urology, Nara City Hospital, Nara, Nara 630-8305, Japan

7. Department of Prostate Brachytherapy, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan

Abstract

Complete metastasectomy (CM) in metastatic renal cell carcinoma (mRCC) has demonstrated efficacy in the cytokine era, but its effectiveness in the era of tyrosine kinase inhibitors (TKIs) and immune checkpoint inhibitors (ICIs) remains unclear. A multi-institutional database included clinicopathological data of 367 patients with mRCC. Patients were divided into two groups: the CM group and the non-CM group. These two groups were compared before and after propensity score matching (PSM). Cox proportional hazard models were used to detect factors associated with disease-free survival (DFS) and overall survival (OS) from mRCC diagnosis. The CM group showed a significant association with longer overall survival compared to the non-CM group in the PSM-unadjusted cohorts (p < 0.001, hazard ratio 0.49, 95% confidence interval 0.35–0.69), but no superiority was noted in the adjusted cohorts. The median DFS after CM was 24 months, with no significant differences based on relapse timing. Notably, the international metastatic RCC database consortium risk categories and metastatic burden were associated with DFS. This study supports the potential of CM in mRCC management during the TKI/ICI era, although limitations including sample size and selection bias need to be considered.

Publisher

MDPI AG

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