Department of Palliative Care, Rehabilitation and Integrative Medicine, MD Anderson Cancer Center, Houston, Texas, USA.
Department of Palliative Care, Rehabilitation and Integrative Medicine, MD Anderson Cancer Center, Houston, Texas, USA.
J Pain Symptom Manage. 2021 Aug;62(2):223-232.e1. doi: 10.1016/j.jpainsymman.2020.12.023. Epub 2021 Jan 1.
No clinical trials have examined the effect of netupitant/palonosetron (NEPA) on chronic nausea in patients with cancer.
In this pilot randomized trial, we assessed the efficacy of NEPA and placebo on chronic nausea.
This double-blind, parallel, randomized trial enrolled patients with cancer and chronic nausea for at least 1 month, intensity ≥4/10 and not on moderately or highly emetogenic systemic therapies. Patients started with a placebo run-in period from days 1 to 5; those without a placebo response proceeded to the double-blinded phase between days 6 to 15 (NEPA: placebo 2:1 ratio). The primary outcome was within-group change in average nausea over the 24 hours on a 0-10 numeric rating scale between day 5 and 15.
Among the 53 enrolled patients, 46 proceeded to placebo run-in and 33 had blinded treatment (22 NEPA and 11 placebo). We observed a statistically significant within-group improvement in nausea numeric rating scale between day 5 and 15 in the NEPA group (mean change, -2.0; 95% CI, -3.1 to -0.8) and the placebo group (mean change, -2.3; 95% CI, -3.9 to -0.7). A complete response was achieved in 8 (38%) patients in the NEPA group and 2 (20%) in the placebo group by day 15. No grade 3-4 toxicities were attributed to NEPA. There were no statistically significant between-group differences for the primary/secondary outcomes.
NEPA and placebo were associated with similar magnitude of within-group improvement in chronic nausea without significant between-group differences (Clinicaltrials.gov NCT03040726).
尚无临床试验研究奈妥匹坦/帕洛诺司琼(NEPA)对癌症患者慢性恶心的影响。
在这项初步随机试验中,我们评估了 NEPA 和安慰剂对慢性恶心的疗效。
这项双盲、平行、随机试验纳入了至少有 1 个月慢性恶心且强度≥4/10 且未接受中度或高度致吐性全身治疗的癌症患者。患者先进行为期 5 天的安慰剂导入期;如果没有安慰剂反应,则在第 6 至 15 天进行双盲阶段(NEPA:安慰剂 2:1 比例)。主要结局是在第 5 天至第 15 天之间,0-10 数字评分量表上 24 小时内平均恶心的组内变化。
在 53 名入组患者中,46 名患者进入安慰剂导入期,33 名患者接受了盲法治疗(22 名 NEPA 和 11 名安慰剂)。我们观察到 NEPA 组和安慰剂组的恶心数字评分量表在第 5 天至第 15 天之间均有统计学显著的组内改善(NEPA 组平均变化-2.0;95%CI,-3.1 至-0.8;安慰剂组平均变化-2.3;95%CI,-3.9 至-0.7)。在第 15 天,NEPA 组有 8 名(38%)患者达到完全缓解,安慰剂组有 2 名(20%)患者达到完全缓解。没有 3-4 级毒性归因于 NEPA。主要/次要结局无统计学显著的组间差异。
NEPA 和安慰剂在慢性恶心方面都有相似程度的组内改善,且无显著的组间差异(Clinicaltrials.gov NCT03040726)。