Impact of Comorbidity on Antiemetic Efficacy in Patients with Esophageal Cancer Treated with Cisplatin-Based Chemotherapy: A Retrospective Study from Japan.

IF 1.8 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2025-07-29 DOI:10.1159/000547684
Masahiro Hatori, Shota Fukuoka, Shunya Kimura, Kazuyoshi Kawakami, Kensei Yamaguchi, Masakazu Yamaguchi
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引用次数: 0

Abstract

Introduction: Cancer patients often have comorbidities due to the aging population or various other factors. However, clinical trials typically exclude specific severe comorbidities, and no prior study has examined their impact on antiemetic efficacy. Our previous research suggested that antiemetic efficacy might be higher in patients with diabetes mellitus (DM) compared to those without DM because of cortisol and substance P. To further investigate this, the current study analyzed which comorbidities affected chemotherapy-induced nausea and vomiting in patients with esophageal cancer treated with cisplatin-based chemotherapy.

Methods: This retrospective study enrolled Japanese patients with esophageal cancer who received fluorouracil and cisplatin (FP) combination chemotherapy as their initial treatment. The primary endpoint was the total control (TC) rate during the first cycle, defined as no emetic episodes, no nausea, and no rescue medication use over the overall period (0-120 h) measured by patients' diary or medical staff interview. Univariate and multivariate logistic regression models were used to analyze the TC rate, including previously reported risk factors (age, sex, performance status, body mass index, cisplatin dose, and number of prophylactic antiemetic agents). Comorbidities showing significance in the univariate analysis were further assessed in the multivariate analysis. The significance level was set at 5%.

Results: Among the 285 eligible patients, the prevalence of comorbidities was as follows: hypertension (36.8%), DM (17.9%), cardiovascular disease (10.6%), and hyperlipidemia (9.5%). Multivariate analysis revealed a significantly higher TC rate during the overall period in patients with cardiovascular disease (50.0%) compared to those without one (32.5%) (adjusted odds ratio 0.455, 95% confidence interval 0.207-0.999, p = 0.0499).

Conclusions: Antiemetic regimen appeared to be more effective in patients with esophageal cancer and cardiovascular disease during the overall period when compared to patients without one. The clinical trial stratified by whether cardiovascular disease should be conducted in the further.

合并症对食管癌顺铂化疗止吐效果的影响:来自日本的一项回顾性研究
导读:由于人口老龄化或其他各种因素,癌症患者往往有合并症。然而,临床试验通常排除特定的严重合并症,并且没有先前的研究检查它们对止吐疗效的影响。我们之前的研究表明,由于皮质醇和p物质的影响,糖尿病患者的止吐效果可能比非糖尿病患者更高。为了进一步研究这一点,本研究分析了哪些合并症影响顺铂化疗的食管癌患者化疗引起的恶心和呕吐。方法:本回顾性研究纳入了日本食管癌患者,他们接受氟尿嘧啶和顺铂联合化疗作为初始治疗。主要终点是第一个周期的总控制率(TC),定义为通过患者日记或医务人员访谈测量的整个期间(0-120 h)无呕吐事件、无恶心、无抢救药物使用。采用单因素和多因素logistic回归模型分析TC率,包括先前报道的危险因素(年龄、性别、运动状态、体重指数、顺铂剂量和预防性止吐药数量)。在单因素分析中显示有意义的合并症在多因素分析中进一步评估。显著性水平设为5%。结果:285例符合条件的患者合并症患病率为:高血压(36.8%)、糖尿病(17.9%)、心血管疾病(10.6%)、高脂血症(9.5%)。多因素分析显示,有心血管疾病患者的总TC率(50.0%)显著高于无心血管疾病患者(32.5%)(校正优势比0.455,95%可信区间0.207-0.999,p = 0.0499)。结论:在食管癌合并心血管疾病的患者中,止吐方案在整个治疗期间比未合并心血管疾病的患者更有效。临床试验按是否应进一步进行心血管疾病分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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