Chen Ping, Wang Dingyi, Zhan Zhouwei, Chen Ling, Chen Yu
Department of Medical Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, Fujian, China.
Front Immunol. 2024 Dec 5;15:1477310. doi: 10.3389/fimmu.2024.1477310. eCollection 2024.
Cachexia is a leading cause of death among individuals with advanced cancer, yet effective pharmacological treatments are lacking. In this single-center retrospective study, we aimed to investigate the efficacy and safety of tocilizumab for the treatment of cancer cachexia accompanied by systemic hyperinflammation.
Data were collected from 20 patients treated with tocilizumab and a control group of 20 patients matched for age, sex, and comorbidities. Both groups received corticosteroids. In the tocilizumab treatment group, patients received a single dose of tocilizumab (8 mg/kg, maximum 800 mg) in combination with corticosteroids. Weight, body mass index, liver metastasis, Eastern Cooperative Oncology Group score, patient-generated subjective global assessments, the Anorexia/Cachexia Subscale of the Functional Assessment of Anorexia/Cachexia Therapy, handgrip strength, neutrophil-to-lymphocyte ratio, and the C-reactive protein, hemoglobin, prealbumin, and albumin levels were recorded in both groups.
Tocilizumab treatment favorably influenced the levels of patient biomarkers (p<0.05), ameliorated systemic inflammation, and demonstrated enhanced clinical short-term efficacy compared to the control group, including rates of symptomatic relief (60% vs. 20%, p = 0.024), improvement of serum PAB and ALB (70% vs. 25%, p = 0.004), weight gain >2% (45% vs. 15%, p = 0.038), and improvement of grip strength and 6-m walk speed (p<0.05). Treatment with tocilizumab was generally safe, with no observed increase in infection rates (10% vs. 15%, p = 0.633) or intensive care unit admissions (10% vs. 25%, p = 0.405), and was more favorable for restarting antitumor therapy (70% vs. 35%, p = 0.027).
Tocilizumab, in combination with corticosteroids, is favorable for alleviating cancer cachexia with systemic hyperinflammation, despite the small sample size. Thus, this combination holds great potential as a novel strategy for treating cancer cachexia with systemic hyperinflammation.
恶病质是晚期癌症患者死亡的主要原因之一,但目前缺乏有效的药物治疗方法。在这项单中心回顾性研究中,我们旨在探讨托珠单抗治疗伴有全身炎症的癌症恶病质的疗效和安全性。
收集20例接受托珠单抗治疗的患者以及20例年龄、性别和合并症相匹配的对照组患者的数据。两组均接受皮质类固醇治疗。在托珠单抗治疗组中,患者接受单剂量托珠单抗(8mg/kg,最大剂量800mg)联合皮质类固醇治疗。记录两组患者的体重、体重指数、肝转移情况、东部肿瘤协作组评分、患者主观整体评估、厌食/恶病质治疗功能评估中的厌食/恶病质子量表评分、握力、中性粒细胞与淋巴细胞比值以及C反应蛋白、血红蛋白、前白蛋白和白蛋白水平。
与对照组相比,托珠单抗治疗对患者生物标志物水平有积极影响(p<0.05),改善了全身炎症,显示出更高的临床短期疗效,包括症状缓解率(60%对20%,p = 0.024)、血清前白蛋白和白蛋白改善率(70%对25%,p = 0.004)、体重增加>2%(45%对15%,p = 0.038)以及握力和6分钟步行速度改善(p<0.05)。托珠单抗治疗总体安全,未观察到感染率增加(10%对15%,p = 0.633)或重症监护病房入院率增加(10%对25%,p = 0.405),且更有利于重新开始抗肿瘤治疗(70%对35%,p = 0.027)。
尽管样本量较小,但托珠单抗联合皮质类固醇有利于缓解伴有全身炎症的癌症恶病质。因此,这种联合疗法作为治疗伴有全身炎症的癌症恶病质的新策略具有巨大潜力。