Efficacy and safety of fentanyl inhalant for the treatment of breakthrough cancer pain: a multicenter, randomized, double-blind, placebo-controlled trial.

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Rongbo Lin, Binbin Song, Na Li, Biaoxue Rong, Jinghui Bai, Yong Liu, Wei Wang, Anwen Liu, Suxia Luo, Bo Liu, Peng Cheng, Yani Wu, Yujie Li, Xiaohui Yu, Xueying Liu, Xiangrong Dai, Xiaoyi Li, Dongying Liu, Jian Wang, Yan Huang
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引用次数: 0

Abstract

Background: Breakthrough cancer pain (BTcP) has a negative impact on patients' quality of life, general activities, and is related to worse clinical outcomes. Fentanyl inhalant is a hand-held combination drug-device delivery system providing rapid, multi-dose (25μg/dose) administration of fentanyl via inhalation of a thermally generated aerosol. This multicenter, randomized, placebo-controlled, multiple-crossover, double-blind study evaluated the efficacy, safety, and tolerability of fentanyl inhalant in treating BTcP in opioid-tolerant patients.

Methods: The trial was conducted in opioid-tolerant cancer patients with 1 ~ 4 BTcP outbursts per day. Each patient was treated and observed for 6 episodes of BTcP (4 with fentanyl inhalant, 2 with placebo). During each episode of targeted BTcP, patients were allowed up to six inhalations, with an interval of at least 4 min between doses. Primary outcome was the time-weighted sum of PID (pain intensity difference) scores at 30 min (SPID30).

Results: A total of 335 BTcP episodes in 59 patients were treated. The mean SPID30 was -97.4 ± 48.43 for fentanyl inhalant-treated episodes, and -64.6 ± 40.25 for placebo-treated episodes (p < 0.001). Significant differences in PID for episodes treated with fentanyl inhalant versus placebo was seen as early as 4 min and maintained for up to 60 min. The percentage of episodes reported PI (pain intensity) scores ≤ 3, a ≥ 33% or ≥ 50% reduction in PI scores at 30 min, PR30 (pain relief scores at 30 min) and SPID60 favored fentanyl inhalant over placebo. Only 4.4% of BTcP episodes required rescue medication in fentanyl inhalant group. Most AEs were of mild or moderate severity and typical of opioid drugs.

Conclusion: Treatment with fentanyl inhalant was shown to be a promising therapeutic option for BTcP, with significant pain relief starting very soon after dosing. Confirmation of effectiveness requires a larger phase III trial.

Trial registration: ClinicalTrials.gov: NCT05531422 registered on 6 September 2022 after major amendment, NCT04713189 registered on 14 January 2021.

芬太尼吸入剂治疗突破性癌痛的有效性和安全性:一项多中心、随机、双盲、安慰剂对照试验。
背景:突破性癌症疼痛(BTcP)会对患者的生活质量和一般活动产生负面影响,并与更差的临床预后有关。芬太尼吸入剂是一种手持式组合给药装置,可通过吸入热气雾剂快速、多剂量(25 微克/剂量)给药芬太尼。这项多中心、随机、安慰剂对照、多交叉、双盲研究评估了芬太尼吸入剂治疗阿片耐受患者 BTcP 的疗效、安全性和耐受性:该试验在阿片类药物耐受的癌症患者中进行,患者每天爆发 1~4 次 BTcP。每位患者接受 6 次 BTcP 治疗和观察(4 次使用芬太尼吸入剂,2 次使用安慰剂)。在每次有针对性的 BTcP 发作期间,患者最多可吸入 6 次,每次吸入之间至少间隔 4 分钟。主要结果是30分钟时PID(疼痛强度差异)评分的时间加权总和(SPID30):结果:59 名患者共接受了 335 次 BTcP 治疗。芬太尼吸入剂治疗的平均 SPID30 为-97.4±48.43,安慰剂治疗的平均 SPID30 为-64.6±40.25(p 结论:芬太尼吸入剂治疗的平均 SPID30 为-97.4±48.43,安慰剂治疗的平均 SPID30 为-64.6±40.25:使用芬太尼吸入剂治疗 BTcP 是一种很有前景的治疗方案,用药后很快就能明显缓解疼痛。有效性的确认需要更大规模的 III 期试验:试验注册:ClinicalTrials.gov:试验注册:ClinicalTrials.gov:NCT05531422,重大修订后于 2022 年 9 月 6 日注册;NCT04713189,2021 年 1 月 14 日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
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