Department of Pain Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
Department of Pain Medicine, Division of Anesthesia and Critical Care, The University of Texas MD Anderson Cancer Center, Houston, TX.
Pain Physician. 2018 Nov;21(6):571-592.
Chemotherapy-induced peripheral neuropathy (CIPN) is a commonly encountered disease entity following chemotherapy for cancer treatment. Although only duloxetine is recommended by the American Society of Clinical Oncology (ASCO) for the treatment of CIPN in 2014, the evidence of the clinical outcome for new pharmaceutic therapies and non-pharmaceutic treatments has not been clearly determined.
To provide a comprehensive review and evidence-based recommendations on the treatment of CIPN.
A systematic review of each treatment regimen in patients with CIPN.
The literature on the treatment of CIPN published from 1990 to 2017 was searched and reviewed. The 2011 American Academy of Neurology Clinical Practice Guidelines Process Manual was used to grade the evidence and risk of bias. We reviewed and updated the recommendations of the ASCO in 2014, and evaluated new approaches for treating CIPN.
A total of 26 treatment options in 35 studies were identified. Among these, 7 successful RCTs, 6 failed RCTs, 18 prospective studies, and 4 retrospective studies were included. The included studies examined not only pharmacologic therapy but also other modalities, including laser therapy, scrambler therapy, magnetic field therapy and acupuncture, etc. Most of the included studies had small sample sizes, and short follow-up periods. Primary outcome measures were highly variable across the included studies. No studies were prematurely closed owing to its adverse effects.
The limitations of this systematic review included relatively poor homogeneous, with variations in timing of treatment, primary outcomes, and chemotherapeutic agents used.
The evidence is considered of moderate benefit for duloxetine. Photobiomodulation, known as low level laser therapy, is considered of moderate benefit based on the evidence review. Evidence did not support the use of lamotrigine and topical KA (4% ketamine and 2% amitriptyline). The evidence for tricyclic antidepressants was inconclusive as amitriptyline showed no benefit but nortriptyline had insufficient evidence. Further research on CIPN treatment is needed with larger sample sizes, long-term follow-up, standardized outcome measurements, and standardized treatment timing.
Chemotherapy-induced neuropathy, peripheral neuropathy, chemotherapy-tumor, neuropathic pain, chronic pain, toxicology, treatment, reduction of pain, level of evidence.
化疗引起的周围神经病(CIPN)是癌症治疗化疗后常见的疾病实体。尽管美国临床肿瘤学会(ASCO)仅在 2014 年推荐度洛西汀治疗 CIPN,但新药物治疗和非药物治疗的临床疗效证据尚未明确确定。
提供对 CIPN 治疗的全面综述和循证建议。
对 CIPN 患者的每种治疗方案进行系统评价。
检索并回顾了 1990 年至 2017 年发表的关于 CIPN 治疗的文献。使用 2011 年美国神经病学学会临床实践指南制作手册对证据和偏倚风险进行分级。我们回顾并更新了 ASCO 于 2014 年的建议,并评估了治疗 CIPN 的新方法。
确定了 35 项研究中的 26 种治疗方法。其中包括 7 项成功的 RCT 研究,6 项失败的 RCT 研究,18 项前瞻性研究和 4 项回顾性研究。纳入的研究不仅考察了药物治疗,还考察了其他方法,包括激光治疗、 scrambler 治疗、磁场治疗和针灸等。大多数纳入的研究样本量较小,随访时间较短。主要结局指标在纳入的研究中差异很大。没有研究因不良影响而提前关闭。
本系统评价的局限性包括相对较差的同质性,治疗时间、主要结局和使用的化疗药物存在差异。
证据被认为对度洛西汀有中度益处。基于证据综述,光生物调节,称为低水平激光疗法,被认为有中度益处。证据不支持使用拉莫三嗪和局部 KA(4%氯胺酮和 2%阿米替林)。三环类抗抑郁药的证据尚无定论,因为阿米替林没有益处,但去甲替林证据不足。需要进一步研究 CIPN 治疗,方法是采用更大的样本量、长期随访、标准化的结局测量和标准化的治疗时机。
化疗引起的神经病,周围神经病,化疗肿瘤,神经病理性疼痛,慢性疼痛,毒理学,治疗,疼痛减轻,证据水平。