The neutrophil-lymphocyte ratio has a role in predicting the effectiveness of nivolumab in Japanese patients with metastatic renal cell carcinoma: a multi-institutional retrospective study.


Journal

BMC urology
ISSN: 1471-2490
Titre abrégé: BMC Urol
Pays: England
ID NLM: 100968571

Informations de publication

Date de publication:
25 Jul 2020
Historique:
received: 10 07 2019
accepted: 20 07 2020
entrez: 27 7 2020
pubmed: 28 7 2020
medline: 23 4 2021
Statut: epublish

Résumé

The neutrophil-lymphocyte ratio (NLR) is a well-known prognostic marker in various cancers. However, its role as a predictive marker for the effectiveness of nivolumab in patients with metastatic RCC (mRCC) remains unclear. We evaluated the relationships between the NLR and progression-free survival (PFS) or overall survival (OS) in mRCC patients treated with nivolumab. The data of 52 mRCC patients who received nivolumab therapy were collected from seven institutes and evaluated. The median follow-up period from treatment with nivolumab was 25.2 months (IQR 15.5-33.2). The median duration of nivolumab therapy was 7.1 months (IQR 2.9-24.4). The objective response rate was 25% and the 1- and 2-year PFS rates were 46.2 and 25.2%, respectively. The median NLR values at baseline and 4 weeks were 3.7 (IQR 2.7-5.1) and 3.3 (IQR 2.4-5.7), respectively. In the multivariate analysis, an NLR of ≥3 at 4 weeks was an independent predictor of PFS (P = 0.013) and OS (P = 0.034). The 1-year PFS of patients with an NLR of < 3 at 4 weeks was better than that of those with an NLR of ≥3 (75% versus 29%, P = 0.011). The 1-year OS of patients with an NLR of < 3 at 4 weeks was also better than that of those with an NLR of ≥3 (95% versus 71%, P = 0.020). Although the baseline NLR was not associated with PFS or OS, an NLR of ≥3 at 4 weeks after the initiation of therapy might be a robust predictor of poor PFS and OS in mRCC patients undergoing sequential treatment with nivolumab.

Sections du résumé

BACKGROUND BACKGROUND
The neutrophil-lymphocyte ratio (NLR) is a well-known prognostic marker in various cancers. However, its role as a predictive marker for the effectiveness of nivolumab in patients with metastatic RCC (mRCC) remains unclear. We evaluated the relationships between the NLR and progression-free survival (PFS) or overall survival (OS) in mRCC patients treated with nivolumab.
METHODS METHODS
The data of 52 mRCC patients who received nivolumab therapy were collected from seven institutes and evaluated. The median follow-up period from treatment with nivolumab was 25.2 months (IQR 15.5-33.2).
RESULTS RESULTS
The median duration of nivolumab therapy was 7.1 months (IQR 2.9-24.4). The objective response rate was 25% and the 1- and 2-year PFS rates were 46.2 and 25.2%, respectively. The median NLR values at baseline and 4 weeks were 3.7 (IQR 2.7-5.1) and 3.3 (IQR 2.4-5.7), respectively. In the multivariate analysis, an NLR of ≥3 at 4 weeks was an independent predictor of PFS (P = 0.013) and OS (P = 0.034). The 1-year PFS of patients with an NLR of < 3 at 4 weeks was better than that of those with an NLR of ≥3 (75% versus 29%, P = 0.011). The 1-year OS of patients with an NLR of < 3 at 4 weeks was also better than that of those with an NLR of ≥3 (95% versus 71%, P = 0.020).
CONCLUSIONS CONCLUSIONS
Although the baseline NLR was not associated with PFS or OS, an NLR of ≥3 at 4 weeks after the initiation of therapy might be a robust predictor of poor PFS and OS in mRCC patients undergoing sequential treatment with nivolumab.

Identifiants

pubmed: 32711491
doi: 10.1186/s12894-020-00679-2
pii: 10.1186/s12894-020-00679-2
pmc: PMC7382809
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Nivolumab 31YO63LBSN

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

110

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Auteurs

Naotaka Nishiyama (N)

Department of Urology, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan. nishiyan@med.u-toyama.ac.jp.

Megumi Hirobe (M)

Department of Urology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Takuya Kikushima (T)

Department of Urology, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

Masahiro Matsuki (M)

Department of Urology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Atsushi Takahashi (A)

Department of Urology, Hakodate Goryoukaku Hospital, Hakodate, Japan.

Masahiro Yanase (M)

Department of Urology, Sunagawa City Medical Center, Sunagawa, Japan.

Keisuke Ichimatsu (K)

Department of Urology, Tonami general hospital, Tonami, Japan.

Masayuki Egawa (M)

Department of Urology, Tonami general hospital, Tonami, Japan.

Norihiro Hayashi (N)

Department of Urology, Takaoka city hospital, Takaoka, Japan.

Takahito Negishi (T)

Department of Urology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Hakata, Japan.

Naoya Masumori (N)

Department of Urology, Sapporo Medical University School of Medicine, Sapporo, Japan.

Hiroshi Kitamura (H)

Department of Urology, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

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Classifications MeSH