Department of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
J Pain Symptom Manage. 2019 Oct;58(4):662-671. doi: 10.1016/j.jpainsymman.2019.06.018. Epub 2019 Jun 26.
The most debilitating symptoms during oxaliplatin-based chemotherapy in patients with colorectal cancer (CRC) are neuropathy and fatigue. Inflammation has been suggested to contribute to these symptoms, and the anti-inflammatory agent minocycline is safe and readily available.
This proof-of-concept study investigated minocycline's capacity to reduce treatment-related neuropathy and fatigue and its impact on inflammatory markers during chemotherapy in a Phase II randomized, double-blind, placebo-controlled clinical trial.
Patients with locally advanced or metastatic CRC who were scheduled for oxaliplatin-based chemotherapy were randomly assigned to receive either minocycline (100 mg twice daily) or placebo over four months from started chemotherapy. Toxicity assessments and blood samples were prospectively collected monthly. The severity of fatigue and numbness/tingling was assessed weekly using the MD Anderson Symptom Inventory. The primary endpoint, area under the curve for numbness/tingling and fatigue over approximately four months, was compared between the two arms.
Of 66 evaluable participants, 32 received minocycline and 34 placebo. There was no observed significant symptom reduction on both fatigue and numbness/tingling in either arm, nor was there a difference in levels of serum proinflammatory and anti-inflammatory markers between arms. No Grade 3 adverse events nor disparity mediating effects on intervention were observed.
Minocycline treatment is feasible and has a low-toxicity profile. However, with 200 mg/day, it did not reduce numbness/tingling or fatigue nor moderate inflammatory biomarkers from this Phase II randomized study. Our results do not support further exploration of minocycline for fatigue or neuropathy symptom intervention in patients treated for CRC.
在接受基于奥沙利铂的化疗的结直肠癌(CRC)患者中,最令人虚弱的症状是周围神经病变和疲劳。炎症被认为与这些症状有关,而米诺环素这种抗炎药物安全且易于获得。
本概念验证研究旨在调查米诺环素在基于奥沙利铂的化疗期间减轻治疗相关神经病变和疲劳的能力,以及其对化疗期间炎症标志物的影响,并在一项 II 期随机、双盲、安慰剂对照临床试验中进行评估。
计划接受基于奥沙利铂的化疗的局部晚期或转移性 CRC 患者被随机分配,在开始化疗后的四个月内每天接受两次米诺环素(100mg)或安慰剂治疗。每月前瞻性采集毒性评估和血液样本。每周使用 MD 安德森症状量表评估疲劳和麻木/刺痛的严重程度。主要终点为大约四个月内麻木/刺痛和疲劳的曲线下面积,在两个治疗组之间进行比较。
在 66 名可评估的参与者中,32 名接受了米诺环素治疗,34 名接受了安慰剂治疗。在两个治疗组中,疲劳和麻木/刺痛均未观察到明显的症状缓解,两个治疗组之间的血清促炎和抗炎标志物水平也没有差异。未观察到 3 级不良事件,也未观察到干预措施的调解作用差异。
米诺环素治疗是可行的,且具有低毒性特征。然而,在这项 II 期随机研究中,每天 200mg 的剂量并未减轻麻木/刺痛或疲劳,也未调节炎症生物标志物。我们的结果不支持进一步探索米诺环素用于结直肠癌患者的疲劳或神经病变症状干预。