Division of Pharmacy, Gunma Prefectural Cancer Center, Ota 373-8550, Gunma, Japan.
Division of Respiratory Medicine, Gunma Prefectural Cancer Center, Ota 373-8550, Gunma, Japan.
Medicina (Kaunas). 2021 Nov 11;57(11):1233. doi: 10.3390/medicina57111233.
: Naldemedine is a peripherally acting μ-opioid receptor antagonist that improves opioid-induced constipation. Although clinical trials have excluded patients with poor performance status (PS) and those started on naldemedine early after opioid initiation, clinical practice has used naldemedine for the same patients. Therefore, we investigated the treatment patterns of naldemedine in a real-world setting. : This was a multicenter, retrospective chart review study of opioid-treated patients with cancer receiving naldemedine. Adverse events that occurred within 7 days of naldemedine initiation were evaluated in those who received one or more doses of the same. Effectiveness was assessed in patients who used naldemedine for more than 7 days. : A total of 296 patients satisfied the eligibility criteria, among whom 129 (43.6%) had a PS of ≥3 and 176 (59.5%) started naldemedine within 2 weeks of opioid initiation. Moreover, 203 (79.6%) patients had ≥3 bowel movements per week. Incidences of all grades of diarrhea and abdominal pain were 87 (29.4%) and 12 (4.1%), respectively. No patient had grade 4 or higher adverse events. : Although nearly half of the patients receiving naldemedine in clinical practice belonged to populations that were not included in the clinical trials, our results suggested that naldemedine in clinical practice had the same efficacy and safety as that in clinical trials.
纳洛美丁是一种外周作用μ-阿片受体拮抗剂,可改善阿片类药物引起的便秘。尽管临床试验排除了表现状态差(PS)的患者和在开始使用阿片类药物后早期开始使用纳洛美丁的患者,但临床实践中已经将纳洛美丁用于相同的患者。因此,我们在真实环境中调查了纳洛美丁的治疗模式。
这是一项多中心、回顾性图表审查研究,涉及接受纳洛美丁治疗的癌症阿片类药物治疗患者。评估了在接受一剂或多剂纳洛美丁的患者中,在纳洛美丁开始后 7 天内发生的不良事件。在使用纳洛美丁超过 7 天的患者中评估了疗效。
共有 296 名患者符合入选标准,其中 129 名(43.6%)PS 为≥3,176 名(59.5%)在开始使用阿片类药物后 2 周内开始使用纳洛美丁。此外,203 名(79.6%)患者每周有≥3 次排便。所有级别腹泻和腹痛的发生率分别为 87 例(29.4%)和 12 例(4.1%)。没有患者发生 4 级或更高级别的不良事件。
尽管在临床实践中接受纳洛美丁治疗的患者中近一半属于未纳入临床试验的人群,但我们的结果表明,纳洛美丁在临床实践中的疗效和安全性与临床试验相同。