Prognostic impact of metastasectomy in renal cell carcinoma in the postcytokine therapy era.


Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
01 2021
Historique:
received: 25 05 2020
revised: 21 07 2020
accepted: 05 08 2020
pubmed: 31 8 2020
medline: 23 7 2021
entrez: 1 9 2020
Statut: ppublish

Résumé

To explore the real-world data regarding survival following metastasectomy (MS) for renal cell carcinoma (RCC) in the postcytokine therapy era. Patients diagnosed with metastatic renal cell carcinoma (mRCC) between January 2008 and December 2018 at our institutions were retrospectively evaluated. The patients were classified into three groups according to their MS status: (1) complete MS (cMS), (2) incomplete MS (icMS), and (3) without MS (nonMS). Factors for overall survival (OS) after diagnosis were analyzed. Overall, 314 patients were evaluated. During the follow-up period (median: 25.3 months), a total of 98 patients (31.2%) underwent at least one MS. The cMS group (n = 45, 14.3%) had a significantly longer OS (median: not reached [N.R.]) than the icMS (n = 53, 16.9%) (81.5 months, P= 0.0042) and nonMS groups (28.1 months, P< 0.0001). The icMS group had a significantly longer OS than the nonMS group did (P= 0.0010). Multivariate analysis showed that the MS status was an independent factor for OS (cMS vs. nonMS: P= 0.0004; icMS vs. nonMS: P= 0.0176), together with histopathological type, International Metastatic Renal Cell Carcinoma Database Consortium risk, liver metastasis status, and prior nephrectomy status (all, P< 0.05). In addition, the OS was comparable throughout the eras of systemic therapy (early molecular-targeted therapy, late molecular-targeted therapy, and immune checkpoint inhibitor eras) in the MS group (median: 121.9 vs. N.R. vs. N.R. months, P= 0.948). MS, especially cMS improved survival in selected patients with mRCC in the postcytokine therapy era. In addition, MS still plays a significant role in the current systemic therapy.

Identifiants

pubmed: 32863124
pii: S1078-1439(20)30378-1
doi: 10.1016/j.urolonc.2020.08.011
pii:
doi:

Substances chimiques

Cytokines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

77.e17-77.e25

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Hiroki Ishihara (H)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

Toshio Takagi (T)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan. Electronic address: t.takagi1192@gmail.com.

Tsunenori Kondo (T)

Department of Urology, Tokyo Women's Medical University Medical Center East, Arakawa-ku, Tokyo, Japan.

Hironori Fukuda (H)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

Hidekazu Tachibana (H)

Department of Urology, Tokyo Women's Medical University Medical Center East, Arakawa-ku, Tokyo, Japan.

Kazuhiko Yoshida (K)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

Junpei Iizuka (J)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

Hirohito Kobayashi (H)

Department of Urology, Tokyo Women's Medical University Medical Center East, Arakawa-ku, Tokyo, Japan.

Hideki Ishida (H)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

Kazunari Tanabe (K)

Department of Urology, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

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