Neutrophil-to-lymphocyte ratio as an early marker of outcomes in patients with recurrent oral squamous cell carcinoma treated with nivolumab.


Journal

The British journal of oral & maxillofacial surgery
ISSN: 1532-1940
Titre abrégé: Br J Oral Maxillofac Surg
Pays: Scotland
ID NLM: 8405235

Informations de publication

Date de publication:
05 2023
Historique:
received: 13 09 2021
revised: 14 02 2023
accepted: 20 03 2023
medline: 15 5 2023
pubmed: 16 4 2023
entrez: 15 4 2023
Statut: ppublish

Résumé

The immune checkpoint inhibitor (ICI), nivolumab, has revolutionised the treatment of recurrent and metastatic oral cancer. However, the response rate to ICIs remains low, and identifying predictors of nivolumab response is critical. Although the neutrophil-to-lymphocyte ratio (NLR) has been suggested as a predictive marker of nivolumab response in patients with various types of cancer, its utility in oral squamous cell carcinoma (OSCC) has not been elucidated. In this retrospective multicentre cohort study, we evaluated the association between NLR and outcome of nivolumab treatment in 64 patients with OSCC treated between 2017 and 2020. The objective response and disease control rates were 25.1% and 32.9%, respectively. The rates for complete and partial responses were 15.7% (10/64) and 9.4% (6/64), respectively; stable and progressive disease rates were 7.8% (5/64) and 67.1% (43/64), respectively. Complete and partial responses were classified as responders, and stable and progressive diseases were classified as non-responders. The median (range) pre-treatment NLR among responders was 4.3 (2.8-8.0), which decreased to 4.0 (2.6-6.3) after nivolumab treatment, and the median (range) pre-treatment NLR among non-responders was 5.1 (2.7-7.9), which increased to 6.4 (4.0-14.0) with tumour growth. Moreover, overall survival was significantly worse in the group with a higher post-treatment NLR (≥5) than in the group with a lower NLR (<5). Patients with a post-treatment NLR of ≥6 had worse outcomes for salvage chemotherapy following nivolumab treatment. Thus, post-treatment NLR could be a useful marker for predicting the response to nivolumab treatment or salvage chemotherapy in patients with OSCC.

Identifiants

pubmed: 37061418
pii: S0266-4356(23)00086-4
doi: 10.1016/j.bjoms.2023.03.012
pii:
doi:

Substances chimiques

Nivolumab 31YO63LBSN
Antineoplastic Agents, Immunological 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

320-326

Informations de copyright

Copyright © 2023 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.

Auteurs

Hidetake Tachinami (H)

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan. Electronic address: hidetake@med.u-toyama.ac.jp.

Kei Tomihara (K)

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan; Division of Oral and Maxillofacial Surgery, Niigata University Graduate School of Medical and Dental Science, Niigata, Japan.

Shin-Ichi Yamada (SI)

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.

Atsushi Ikeda (A)

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.

Shuichi Imaue (S)

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.

Hideaki Hirai (H)

Division of Oral and Maxillofacial Surgery, Niigata University Graduate School of Medical and Dental Science, Niigata, Japan.

Hiromi Nakai (H)

Department of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.

Tomoko Sonoda (T)

Department of Public Health, Sapporo Medical University School of Medicine, Sapporo, Japan.

Kazuto Kurohara (K)

Department of Oral and Maxillofacial Surgery, Department of Clinical Sciences, Medical Life Science, Mie University, Graduate School of Medicine, Mie, Japan.

Yukio Yoshioka (Y)

Department of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Takumi Hasegawa (T)

Department of Oral and Maxillofacial Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

Tomofumi Naruse (T)

Department of Clinical Oral Oncology, Unit of Translational Medicine, Course of Medical and Dental Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Takashi Niiyama (T)

Department of Clinical Oral Oncology, National hospital organization, Hokkaido Cancer Center, Sapporo, Japan.

Tetsu Shimane (T)

Department of Dentistry and Oral Surgery, Shinshu University School of Medicine, Matsumoto, Japan.

Michihiro Ueda (M)

Department of Clinical Oral Oncology, National hospital organization, Hokkaido Cancer Center, Sapporo, Japan.

Souichi Yanamoto (S)

Department of Oral Oncology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Masaya Akashi (M)

Department of Oral and Maxillofacial Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

Masahiro Umeda (M)

Department of Clinical Oral Oncology, Unit of Translational Medicine, Course of Medical and Dental Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Hiroshi Kurita (H)

Department of Dentistry and Oral Surgery, Shinshu University School of Medicine, Matsumoto, Japan.

Akihiro Miyazaki (A)

Department of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.

Naoya Arai (N)

Department of Oral and Maxillofacial Surgery, Department of Clinical Sciences, Medical Life Science, Mie University, Graduate School of Medicine, Mie, Japan.

Ryuji Hayashi (R)

Department of Medical Oncology, Toyama University Hospital, Toyama, Japan.

Makoto Noguchi (M)

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.

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