Predicting Objective Response of Pembrolizumab in Platinum-Refractory Urothelial Carcinoma Based on Neutrophil-Lymphocyte Ratio Fluctuation and Liver Metastases.

IF 2.5 3区 医学 Q3 ONCOLOGY Oncology Pub Date : 2024-01-01 Epub Date: 2023-10-13 DOI:10.1159/000534554
Kyosuke Nishio, Takuya Higashio, Kazumasa Komura, Wataru Fukuokaya, Takahiro Adachi, Yosuke Hirasawa, Takeshi Hashimoto, Atsuhiko Yoshizawa, Shuya Tsuchida, Takuya Matsuda, Takuya Tsujino, Kazuki Nishimura, Satoshi Tokushige, Keita Nakamori, Taizo Uchimoto, Shutaro Yamamoto, Kosuke Iwatani, Fumihiko Urabe, Keiichiro Mori, Takafumi Yanagisawa, Shunsuke Tsuduki, Kyoshi Takahara, Teruo Inamoto, Jun Miki, Takahiro Kimura, Yoshio Ohno, Ryoichi Shiroki, Haruhito Azuma
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Abstract

Introduction: It is well known that patients with objective response to pembrolizumab have a durable duration of response, leading to favorable survival outcomes. We investigated the possibility of predicting the objective response with concise indicators obtained from daily clinical practice.

Methods: In our multi-institutional cohort, 220 platinum-refractory metastatic urothelial carcinoma (mUC) patients treated with pembrolizumab for at least 6 weeks with complete information of objective response were investigated.

Results: The median follow-up was 7.3 months, and 119 patients deceased during the follow-up. A multivariate logistic regression analysis exhibited two independent variables predicting the objective response, including the neutrophil-lymphocyte ratio (NLR) change at 6 weeks of treatment and liver metastasis. We proposed a risk group using these two indicators. Patients with no predictive indicators/one of those were assigned to favorable (42%)/intermittent (47%) risk groups. Patients with both indicators were assigned to poor risk (11%). Notably, the objective response rate was well delineated in 41%, 25%, and 0% for favorable-, intermediate-, and poor-risk groups, respectively (p < 0.001). Distinct overall survival (OS) between the risk groups was also confirmed with the median OS of 14.1, 11.7, and 4.2 months in favorable-, intermediate-, and poor-risk groups, respectively.

Conclusions: At the 6 weeks of the pembrolizumab treatment, our risk model predicts the objective response rate precisely. Notably, those classified as "poor risk" - marked by liver metastasis and an increased NLR - should be considered for alternative therapy with a different mode of action, highlighting a critical decision point in treatment optimization.

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根据NLR波动和肝转移预测Pembrolizumab对铂难治性尿路上皮癌的客观疗效。
背景和目的:众所周知,对pembrolizumab有客观反应的患者有持久的反应时间,从而获得良好的生存结果。我们研究了用从日常临床实践中获得的简明指标预测客观反应的可能性。方法在我们的多机构队列中,对220例铂类难治性转移性尿路上皮癌(mUC)进行了研究,这些癌用pembrolizumab治疗至少6周,且具有完整的客观反应信息。结果中位随访时间为7.3个月,随访期间死亡119例。多变量逻辑回归分析显示了两个预测客观反应的自变量,包括治疗六周时中性粒细胞-淋巴细胞比率(NLR)的变化和肝转移。我们提出了一个使用这两个指标的风险组。没有预测指标的患者/其中一名患者被分为有利(42%)/间歇性(47%)风险组。具有这两个指标的患者被分配为低风险(11%)。值得注意的是,有利、中等和较差风险组的客观有效率分别为41%、25%和0%,结论:在pembrolizumab治疗的六周时,我们的风险模型准确预测了客观反应率。值得注意的是,那些被归类为“低风险”(以肝转移和NLR升高为标志)的患者应考虑采用不同的作用模式进行替代治疗,这突出了治疗优化的关键决策点。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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