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

医学 无容量 内科学 中性粒细胞与淋巴细胞比率 肿瘤科 进行性疾病 癌症 胃肠病学 实体瘤疗效评价标准 预测标记 回顾性队列研究 化疗 淋巴细胞 免疫疗法
作者
Hidetake Tachinami,Kei Tomihara,Shin‐ichi Yamada,Atsushi Ikeda,Shuichi Imaue,Hideaki Hirai,Hiromi Nakai,Tomoko Sonoda,Kazuto Kurohara,Yukio Yoshioka,Takumi Hasegawa,Tomofumi Naruse,Takashi Niiyama,Tetsu Shimane,Michihiro Ueda,Souichi Yanamoto,Masaya Akashi,Masahiro Umeda,Hiroshi Kurita,Akihiro Miyazaki,Naoya Arai,Ryuji Hayashi,Makoto Noguchi
出处
期刊:British Journal of Oral & Maxillofacial Surgery [Elsevier]
卷期号:61 (4): 320-326 被引量:5
标识
DOI:10.1016/j.bjoms.2023.03.012
摘要

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.
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