D. Lin, A. Klein, D. Cella, A. Beutler, F. Fang, M. Magestro, P. Cremer, M. LeWinter, S. Luis, A. Abbate, A. Ertel, L. Litcher-Kelly, B. Klooster, J. Paolini
{"title":"摘要 241:复发性心包炎患者的健康相关生活质量:利洛那普的2期研究结果","authors":"D. Lin, A. Klein, D. Cella, A. Beutler, F. Fang, M. Magestro, P. Cremer, M. LeWinter, S. Luis, A. Abbate, A. Ertel, L. Litcher-Kelly, B. Klooster, J. Paolini","doi":"10.1161/hcq.13.suppl_1.241","DOIUrl":null,"url":null,"abstract":"\n Background:\n Recurrent pericarditis (RP) episodes and conventional treatments result in morbidity, but the impact on patient health-related quality of life (HRQoL) has not been quantified. The Phase 2 trial NCT03980522 of rilonacept (IL-1α/IL-1β inhibitor) evaluated HRQoL.\n \n \n Methods:\n Patients with active RP who were symptomatic at Baseline (A-RP, n=16) and RP patients who were not currently experiencing a recurrence but were corticosteroid-dependent at Baseline (CSD-RP, n=9) were enrolled. All received rilonacept weekly for 6 weeks to end of base treatment period (TP) plus an optional 18-week extension treatment period (EP). Corticosteroid tapering occurred in the EP. Physical and mental HRQoL (PROMIS Global Health v1.2 Physical and Mental Component Scores [PCS/MCS]) were assessed at baseline and follow-up.\n \n \n Results:\n Figure 1 presents the PROMIS PCS/MCS and pain scale scores (both patient-reported) as well as C-reactive protein levels over time. Mean PCS/MCS scores at baseline were 39.9/44.5 and 43.3/46.5 for A-RP and CSD-RP groups respectively (versus the norm mean of 50). In A-RP, PCS/MCS scores improved by 11.4/5.6 points by end of base TP, and this improvement was sustained throughout the EP (increase of 11.4/6.0 points from baseline at end of EP). In CSD-RP, PCS/MCS scores increased by 1.8/1.4 points by end of TP and improved by 3.5/4.2 points at end of study, after tapering or discontinuation of corticosteroid without disease recurrence.\n \n \n Conclusion:\n Impaired baseline HRQoL suggests negative impact of RP. For A-RP, rilonacept rapidly improved pericarditis signs and symptoms which was associated with HRQoL improvements. For CSD-RP, rilonacept supported tapering/withdrawal of corticosteroids without recurrence, with maintained/improved HRQoL. These results suggest rilonacept can improve RP patient HRQoL while providing an alternative to corticosteroids.\n \n \n \n","PeriodicalId":10239,"journal":{"name":"Circulation: Cardiovascular Quality and Outcomes","volume":"83 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"Abstract 241: Health-related Quality of Life in Patients With Recurrent Pericarditis: Results From a Phase 2 Study of Rilonacept\",\"authors\":\"D. Lin, A. Klein, D. Cella, A. Beutler, F. Fang, M. Magestro, P. Cremer, M. LeWinter, S. Luis, A. Abbate, A. Ertel, L. Litcher-Kelly, B. Klooster, J. Paolini\",\"doi\":\"10.1161/hcq.13.suppl_1.241\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Background:\\n Recurrent pericarditis (RP) episodes and conventional treatments result in morbidity, but the impact on patient health-related quality of life (HRQoL) has not been quantified. The Phase 2 trial NCT03980522 of rilonacept (IL-1α/IL-1β inhibitor) evaluated HRQoL.\\n \\n \\n Methods:\\n Patients with active RP who were symptomatic at Baseline (A-RP, n=16) and RP patients who were not currently experiencing a recurrence but were corticosteroid-dependent at Baseline (CSD-RP, n=9) were enrolled. All received rilonacept weekly for 6 weeks to end of base treatment period (TP) plus an optional 18-week extension treatment period (EP). Corticosteroid tapering occurred in the EP. Physical and mental HRQoL (PROMIS Global Health v1.2 Physical and Mental Component Scores [PCS/MCS]) were assessed at baseline and follow-up.\\n \\n \\n Results:\\n Figure 1 presents the PROMIS PCS/MCS and pain scale scores (both patient-reported) as well as C-reactive protein levels over time. Mean PCS/MCS scores at baseline were 39.9/44.5 and 43.3/46.5 for A-RP and CSD-RP groups respectively (versus the norm mean of 50). In A-RP, PCS/MCS scores improved by 11.4/5.6 points by end of base TP, and this improvement was sustained throughout the EP (increase of 11.4/6.0 points from baseline at end of EP). In CSD-RP, PCS/MCS scores increased by 1.8/1.4 points by end of TP and improved by 3.5/4.2 points at end of study, after tapering or discontinuation of corticosteroid without disease recurrence.\\n \\n \\n Conclusion:\\n Impaired baseline HRQoL suggests negative impact of RP. For A-RP, rilonacept rapidly improved pericarditis signs and symptoms which was associated with HRQoL improvements. For CSD-RP, rilonacept supported tapering/withdrawal of corticosteroids without recurrence, with maintained/improved HRQoL. 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引用次数: 9
摘要
背景:复发性心包炎(RP)发作和常规治疗会导致发病,但对患者健康相关生活质量(HRQoL)的影响尚未量化。利龙赛普(IL-1α/IL-1β抑制剂)的 2 期试验 NCT03980522 对 HRQoL 进行了评估。 研究方法纳入基线时有症状的活动性 RP 患者(A-RP,16 人)和目前未复发但基线时依赖皮质类固醇的 RP 患者(CSD-RP,9 人)。所有患者每周接受利龙赛普治疗 6 周,直至基础治疗期(TP)结束,并可选择接受为期 18 周的延长治疗期(EP)。在延长治疗期,皮质类固醇逐渐减少。在基线和随访期间对患者的身体和心理 HRQoL(PROMIS Global Health v1.2 身体和心理成分评分 [PCS/MCS])进行评估。 结果图 1 显示了随时间变化的 PROMIS PCS/MCS 和疼痛量表评分(均由患者报告)以及 C 反应蛋白水平。A-RP 组和 CSD-RP 组基线时的 PCS/MCS 平均分分别为 39.9/44.5 和 43.3/46.5(标准平均分为 50)。在 A-RP 组中,PCS/MCS 分数在基础 TP 结束时提高了 11.4/5.6 分,而且这种提高在整个 EP 中一直持续(EP 结束时比基线提高了 11.4/6.0 分)。在 CSD-RP 中,PCS/MCS 评分在 TP 结束时提高了 1.8/1.4 分,在研究结束时提高了 3.5/4.2 分,在减量或停用皮质类固醇后疾病没有复发。 结论基线 HRQoL 受损表明 RP 有负面影响。对于A型RP,利隆钠肽能迅速改善心包炎的体征和症状,这与心率质生活改善有关。对于 CSD-RP,利隆塞普支持皮质类固醇的减量/停药,且不会复发,同时还能维持/改善 HRQoL。这些结果表明,利龙赛普可以改善RP患者的HRQoL,同时提供皮质类固醇的替代品。
Abstract 241: Health-related Quality of Life in Patients With Recurrent Pericarditis: Results From a Phase 2 Study of Rilonacept
Background:
Recurrent pericarditis (RP) episodes and conventional treatments result in morbidity, but the impact on patient health-related quality of life (HRQoL) has not been quantified. The Phase 2 trial NCT03980522 of rilonacept (IL-1α/IL-1β inhibitor) evaluated HRQoL.
Methods:
Patients with active RP who were symptomatic at Baseline (A-RP, n=16) and RP patients who were not currently experiencing a recurrence but were corticosteroid-dependent at Baseline (CSD-RP, n=9) were enrolled. All received rilonacept weekly for 6 weeks to end of base treatment period (TP) plus an optional 18-week extension treatment period (EP). Corticosteroid tapering occurred in the EP. Physical and mental HRQoL (PROMIS Global Health v1.2 Physical and Mental Component Scores [PCS/MCS]) were assessed at baseline and follow-up.
Results:
Figure 1 presents the PROMIS PCS/MCS and pain scale scores (both patient-reported) as well as C-reactive protein levels over time. Mean PCS/MCS scores at baseline were 39.9/44.5 and 43.3/46.5 for A-RP and CSD-RP groups respectively (versus the norm mean of 50). In A-RP, PCS/MCS scores improved by 11.4/5.6 points by end of base TP, and this improvement was sustained throughout the EP (increase of 11.4/6.0 points from baseline at end of EP). In CSD-RP, PCS/MCS scores increased by 1.8/1.4 points by end of TP and improved by 3.5/4.2 points at end of study, after tapering or discontinuation of corticosteroid without disease recurrence.
Conclusion:
Impaired baseline HRQoL suggests negative impact of RP. For A-RP, rilonacept rapidly improved pericarditis signs and symptoms which was associated with HRQoL improvements. For CSD-RP, rilonacept supported tapering/withdrawal of corticosteroids without recurrence, with maintained/improved HRQoL. These results suggest rilonacept can improve RP patient HRQoL while providing an alternative to corticosteroids.