Waissengrin Barliz, Mirelman Dan, Pelles Sharon, Bukstein Felix, Blumenthal Deborah T, Wolf Ido, Geva Ravit
Division of Oncology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Oncology Division, Tel-Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv, 6423906, Israel.
Ther Adv Med Oncol. 2021 Feb 9;13:1758835921990203. doi: 10.1177/1758835921990203. eCollection 2021.
Chemotherapy-induced peripheral neuropathy (CIPN) is a common and dosage-limited oxaliplatin-related toxicity. To date, there are no successful interventions for CIPN prevention or treatment. A therapeutic role for cannabis in diabetic and HIV-related peripheral neuropathy and a protective role in CIPN have been suggested. We examined the effect of cannabis on oncologic patients with CIPN.
Medical records of 768 consecutive patients treated with oxaliplatin and 5-fluorouracil-based combinations at a tertiary medical center from October 2015 to January 2018 were reviewed. Excluded patients were those with pre-existing neuropathy or patients who received fewer than two cycles of oxaliplatin treatment. CIPN grade, oxaliplatin cumulative dose, and neuropathy-free survival were evaluated. The patients were divided based upon the exposure to cannabis: prior to oxaliplatin (cannabis-first), cannabis following the initiation of oxaliplatin treatment (oxaliplatin-first), and no exposure (control).
In total, 513 patients met the inclusion criteria, of whom 248 were treated with cannabis and 265 served as controls. The cannabis-first group included 116 (46.7%) patients and the oxaliplatin-first group included 132 (53.3%) patients. Demographic parameters were comparable between groups. There was a significant difference in CIPN grade 2-3 between cannabis-exposed patients and controls (15.3% and 27.9%, respectively, < 0.001). The protective effect of cannabis was more pronounced among cannabis-first patients compared to oxaliplatin-first patients (75% and 46.2%, respectively, < 0.001). The median oxaliplatin cumulative doses were higher in the cannabis-first the oxaliplatin-first the control groups (545 mg/m, 340 mg/m, and 425 mg/m respectively, < 0.001).
The rate of neuropathy was reduced among patients treated with cannabis and oxaliplatin. This reduction was more significant in patients who received cannabis prior to treatment with oxaliplatin, suggesting a protective effect. A large prospective trial is planned.
化疗引起的周围神经病变(CIPN)是一种常见且剂量受限的与奥沙利铂相关的毒性反应。迄今为止,尚无成功的干预措施来预防或治疗CIPN。大麻在糖尿病和HIV相关周围神经病变中的治疗作用以及在CIPN中的保护作用已被提出。我们研究了大麻对患有CIPN的肿瘤患者的影响。
回顾了2015年10月至2018年1月在一家三级医疗中心接受奥沙利铂和基于5-氟尿嘧啶联合治疗的768例连续患者的病历。排除的患者为既往患有神经病变的患者或接受奥沙利铂治疗少于两个周期的患者。评估了CIPN分级、奥沙利铂累积剂量和无神经病变生存期。根据大麻暴露情况将患者分为:在奥沙利铂治疗之前(大麻优先)、奥沙利铂治疗开始后使用大麻(奥沙利铂优先)和未暴露(对照组)。
共有513例患者符合纳入标准,其中248例接受了大麻治疗,265例作为对照。大麻优先组包括116例(46.7%)患者,奥沙利铂优先组包括132例(53.3%)患者。各组间人口统计学参数具有可比性。暴露于大麻的患者与对照组之间在2-3级CIPN方面存在显著差异(分别为15.3%和