Effectiveness and optimization of low-sodium oxybate in participants with narcolepsy switching from a high-sodium oxybate: data from the Substitution of Equal Grams of Uninterrupted Xyrem to Xywav study.

IF 3.5 3区 医学 Q1 CLINICAL NEUROLOGY Journal of Clinical Sleep Medicine Pub Date : 2024-09-01 DOI:10.5664/jcsm.11182
Wayne Macfadden, Eileen B Leary, Douglas S Fuller, M Todd Kirby, Asim Roy
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Abstract

Study objectives: Low-sodium oxybate (LXB; calcium, magnesium, potassium, and sodium oxybates; Xywav) contains the same active moiety as high-sodium oxybates (SXBs; SXB [Xyrem] and fixed-dose SXB [Lumryz]), with 92% less sodium, and is approved in the United States for treatment of cataplexy or excessive daytime sleepiness in patients 7 years of age and older with narcolepsy, and idiopathic hypersomnia in adults. Patients with narcolepsy have increased cardiovascular risk relative to people without narcolepsy. LXB's lower sodium content is recognized by the United States Food and Drug Administration in the narcolepsy population as clinically meaningful in reducing cardiovascular morbidity compared with SXBs. The Substitution of Equal Grams of Uninterrupted Xyrem to Xywav study (NCT04794491) examined the transition experience of patients with narcolepsy switching from SXB to LXB.

Methods: Eligible participants were aged 18-80 years with narcolepsy type 1 or 2 on a stable SXB dose/regimen. After 2 weeks, participants transitioned gram-per-gram to LXB for 6 weeks, with opportunity for subsequent titration. Assessments included the Epworth Sleepiness Scale, Patient Global Impression of change, Ease of Switching Medication Scale, and Forced Preference Questionnaire.

Results: The study enrolled 62 participants at baseline; 60 transitioned to LXB and 54 completed the study. At baseline and end of the LXB intervention/early discontinuation, respectively, mean total doses were 8.0 and 8.0 g/night; mean Epworth Sleepiness Scale scores were 9.4 and 8.8. Most participants reported improvement (45%) or no change (48%) in narcolepsy symptoms on the Patient Global Impression of change, reported the transition to LXB was "easy" (easy, extremely easy, not difficult at all; 93%) on the Ease of Switching Medication Scale, and preferred LXB compared with SXB (79%) on the Forced Preference Questionnaire, most commonly due to the lower sodium content.

Conclusions: Most participants switched from SXB to LXB with minimal modifications of dose/regimen and reported the transition process was easy. Effectiveness of oxybate treatment was maintained on LXB, and most participants preferred LXB to SXB. No new safety or tolerability issues were identified.

Clinical trial registration: Registry: ClinicalTrials.gov; Name: An Interventional Safety Switch Study (Segue Study) of XYWAV in Narcolepsy; URL: https://classic.clinicaltrials.gov/ct2/show/NCT04794491; Identifier: NCT04794491.

Citation: Macfadden W, Leary EB, Fuller DS, Kirby MT, Roy A. Effectiveness and optimization of low-sodium oxybate in participants with narcolepsy switching from a high-sodium oxybate: data from the Substitution of Equal Grams of Uninterrupted Xyrem to Xywav study. J Clin Sleep Med. 2024;20(9):1467-1477.

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从高羟丁酸钠转用低羟丁酸钠对嗜睡症患者的疗效和优化:来自 SEGUE 研究的数据。
研究目的:低钠羟贝特盐(LXB;钙、镁、钾和钠羟贝特盐;Xywav)含有与高钠羟贝特盐(羟贝特钠 [SXB;Xyrem]和固定剂量羟贝特钠[Lumryz])相同,但钠含量减少了 92%,在美国被批准用于治疗 7 岁及以上嗜睡症患者的紧张性瘫痪或白天过度嗜睡,以及成人特发性嗜睡症。与没有嗜睡症的人相比,嗜睡症患者的心血管风险更高。与高钠奥昔贝特相比,LXB 在嗜睡症人群中的钠含量较低,这一点已被美国 FDA 认定为在降低心血管发病率方面具有临床意义。等克不间断服用解痉灵至解痉灵(SEGUE)研究(NCT04794491)考察了嗜睡症患者从解痉灵转为解痉灵的过渡经历:符合条件的参与者年龄在18至80岁之间,患有1型或2型嗜睡症,使用稳定的SXB剂量/方案。2 周后,参与者按克过渡到 LXB,持续 6 周,并有机会进行后续滴定。评估包括埃普沃思嗜睡量表(ESS)、患者总体变化印象(PGIc)、换药难易度量表(EOSMS)和强迫偏好问卷(FPQ):该研究共招募了 62 名基线参与者,其中 60 人过渡到 LXB,54 人完成了研究。在基线和 LXB 干预/早期停药结束时,平均总剂量分别为 8.0 克/晚和 8.0 克/晚;ESS 平均得分分别为 9.4 分和 8.8 分。大多数参与者在 PGIc 中表示嗜睡症症状有所改善(45%)或无变化(48%),在 EOSMS 中表示向 LXB 过渡 "容易"(容易、非常容易、一点也不难;93%),在 FPQ 中表示与 SXB 相比更喜欢 LXB(79%),最常见的原因是钠含量较低:大多数参与者从 SXB 转为 LXB 时只需对剂量/治疗方案进行最小程度的调整,并表示转换过程很容易。羟丁酸盐治疗的效果在 LXB 上得以保持,与 SXB 相比,大多数参与者更喜欢 LXB。没有发现新的安全性或耐受性问题:临床试验注册临床试验注册:注册表:ClinicalTrials.gov;名称:介入性安全转换研究(SXB):XYWAV治疗嗜睡症的干预性安全转换研究(Segue 研究);URL:https://classic.clinicaltrials.gov/ct2/show/NCT04794491;识别码:NCT04794491:NCT04794491。
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来源期刊
CiteScore
6.20
自引率
7.00%
发文量
321
审稿时长
1 months
期刊介绍: Journal of Clinical Sleep Medicine focuses on clinical sleep medicine. Its emphasis is publication of papers with direct applicability and/or relevance to the clinical practice of sleep medicine. This includes clinical trials, clinical reviews, clinical commentary and debate, medical economic/practice perspectives, case series and novel/interesting case reports. In addition, the journal will publish proceedings from conferences, workshops and symposia sponsored by the American Academy of Sleep Medicine or other organizations related to improving the practice of sleep medicine.
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