Department of Medicine, Gastroenterology, Hepatology, and Nutrition Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Sci Rep. 2019 Jul 3;9(1):9625. doi: 10.1038/s41598-019-44864-2.
Opioid-induced constipation (OIC) has become increasingly prevalent with the rise of prescription opioid use and can significantly impact quality of life, especially in patients with advanced illness. Methylnaltrexone has proven effective in treating cancer patients with OIC who have not responded adequately to conventional laxative therapy, though use is relatively contraindicated in those with peritoneal carcinomatosis due to theoretical risk and reported cases of perforation. The aim of this study was to evaluate the safety of methylnaltrexone in patients with carcinomatosis. We performed a retrospective review of 3058 pediatric and adult patients who received methylnaltrexone at Memorial Sloan Kettering Cancer Center from 2009-2016. Data collected included age, cancer diagnosis, history of abdominal surgery, prior radiation therapy, evidence of peritoneal carcinomatosis, and complications. Charts were reviewed for any complications at 24 hours, 72 hours, and one week following drug administration, as well as at present. We identified 3058 patients (median age 56, range 1-95) who received a total of 3995 doses of methylnaltrexone. Three hundred thirty three (median age 55, range 4-88) had peritoneal carcinomatosis. The most common primary malignancies included pancreatic (17.7%), ovarian (13.5%), colon (7.2%), and lung (6.6%). 228/333 (68.4%) had a history of abdominal surgery and 85/333 (25.5%) underwent prior radiation therapy. Three patients had adverse outcomes or complications, with only one (0.3%) thought to be related to methylnaltrexone use. To our knowledge, this is the largest study to evaluate the outcomes of patients with carcinomatosis receiving methylnaltrexone and the first to include pediatric patients. We found one perforation attributed to methylnaltrexone. Methylnaltrexone should be considered for treatment of refractory OIC in cancer patients with peritoneal carcinomatosis due to low risk of complications.
阿片类药物引起的便秘(OIC)随着处方阿片类药物使用的增加而变得越来越普遍,并且会严重影响生活质量,尤其是在晚期疾病患者中。美沙酮已被证明对接受常规泻药治疗反应不足的 OIC 癌症患者有效,尽管由于理论风险和穿孔报告病例,腹膜转移瘤患者相对禁忌使用。本研究旨在评估美沙酮在转移性肿瘤患者中的安全性。我们对 2009 年至 2016 年期间在 Memorial Sloan Kettering 癌症中心接受美沙酮治疗的 3058 名儿科和成人患者进行了回顾性分析。收集的数据包括年龄、癌症诊断、腹部手术史、既往放疗、腹膜转移瘤证据以及并发症。对给药后 24 小时、72 小时和 1 周以及现在的任何并发症进行了图表审查。我们确定了 3058 名患者(中位年龄 56 岁,范围 1-95 岁),共接受了 3995 剂美沙酮。333 名患者(中位年龄 55 岁,范围 4-88 岁)患有腹膜转移瘤。最常见的原发性恶性肿瘤包括胰腺癌(17.7%)、卵巢癌(13.5%)、结肠癌(7.2%)和肺癌(6.6%)。228/333(68.4%)有腹部手术史,85/333(25.5%)接受过放疗。有 3 名患者出现不良结局或并发症,只有 1 名(0.3%)被认为与美沙酮使用有关。据我们所知,这是评估接受美沙酮治疗的转移性肿瘤患者结局的最大研究,也是第一个纳入儿科患者的研究。我们发现 1 例穿孔归因于美沙酮。由于并发症风险低,美沙酮应考虑用于治疗腹膜转移瘤的癌症患者难治性 OIC。