Symptom Alleviation/Resolution and Returns to Usual Health/Activities in Immunocompromised Adults with COVID-19 Treated with Nirmatrelvir-Ritonavir: Results from the EPIC-IC Trial.

IF 5.3 3区 医学 Q1 INFECTIOUS DISEASES
Ruth Mokgokong, Paul Cislo, Elena Tudone, Edward Weinstein, Joseph C Cappelleri
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Abstract

Introduction: EPIC-IC was a randomized, double-blind trial comparing the approved 5-day regimen of nirmatrelvir-ritonavir (NMV/r) vs. 10-day and 15-day NMV/r in immunocompromised individuals with mild-to-moderate COVID-19. We describe patient-reported global impressions of illness from EPIC-IC.

Methods: In EPIC-IC, 155 immunocompromised participants received 5-day, 10-day, or 15-day NMV/r (1:1:1). Participants completed the Global Impressions Questionnaire through week 24. Median times to first alleviation and resolution of symptoms and return to usual health and usual activities were estimated using Kaplan-Meier analyses for each treatment arm and post hoc subpopulations with severe vs. non-severe immunocompromise. Five-day arm times were compared vs. 10-day and 15-day arm times.

Results: Symptoms were alleviated after a median 6.0 (95% CI 4.0-9.0) days with 5-day NMV/r, similar to 9.0 (5.0-9.0) days with 10-day NMV/r (p = 0.627) and 10.0 (6.0-11.0) days with 15-day NMV/r (p = 0.528). Symptoms resolved after a median 16.0 (10.0-22.0) days with 5-day NMV/r, similar to 13.0 (9.0-14.0) days with 10-day (p = 0.140) and 13.0 (11.0-21.0) days with 15-day NMV/r (p = 0.471). In the severely immunocompromised subpopulation, symptoms resolved later with 5-day vs. 10-day NMV/r (p = 0.026). Participants returned to usual health after a median 11.0 (6.0-16.0) days with 5-day NMV/r, similar to 9.0 (6.0-13.0) days with 10-day (p = 0.319) and 10.0 (6.0-13.0) days with 15-day NMV/r (p = 0.218), and to usual activities after 10.0 (9.0-15.0) days with 5-day NMV/r, similar to 9.0 (6.0-10.0) days with 10-day (p = 0.102) and 9.0 (5.0-10.0) days with 15-day NMV/r (p = 0.190).

Conclusions: Times to symptom alleviation/resolution and returns to usual health/activities were similar with 5-day vs. extended NMV/r and comparable to those in the EPIC-HR trial. Five-day treatment may be adequate for most immunocompromised individuals, while extended treatment might improve symptom resolution in those with severe immunocompromise; larger studies are needed to confirm these findings.

Trial registration: ClinicalTrials.gov identifier, NCT05438602.

使用尼马特利韦-利托那韦治疗的免疫功能低下成人COVID-19患者症状缓解/解决并恢复正常健康/活动:EPIC-IC试验的结果
EPIC-IC是一项随机双盲试验,比较了在轻中度COVID-19免疫功能受损患者中批准的5天尼马特利韦-利托那韦(NMV/r)方案与10天和15天NMV/r方案。我们描述了从EPIC-IC患者报告的疾病的全球印象。方法:在EPIC-IC中,155名免疫功能低下的参与者接受5天、10天或15天的NMV/r(1:1:1)。参与者在第24周完成了全球印象问卷。使用Kaplan-Meier分析对每个治疗组和严重与非严重免疫功能低下的事后亚群进行估计,首次缓解和解决症状并恢复正常健康和正常活动的中位时间。将5天的手臂时间与10天和15天的手臂时间进行比较。结果:5天NMV/r的中位缓解时间为6.0 (95% CI 4.0-9.0)天,10天NMV/r的中位缓解时间为9.0(5.0-9.0)天(p = 0.627), 15天NMV/r的中位缓解时间为10.0(6.0-11.0)天(p = 0.528)。症状消退的中位时间为16.0(10.0-22.0)天,NMV/r为5天,与13.0(9.0-14.0)天(10天)(p = 0.140)和13.0(11.0-21.0)天(15天NMV/r)相似(p = 0.471)。在严重免疫功能低下亚群中,症状消退较晚,NMV/r为5天vs 10天(p = 0.026)。参与者在中位11.0(6.0-16.0)天,5天NMV/r后恢复正常健康,类似于9.0(6.0-13.0)天,10天(p = 0.319)和10.0(6.0-13.0)天,15天NMV/r (p = 0.218), 10.0(9.0-15.0)天,5天NMV/r,类似于9.0(6.0-10.0)天,10天(p = 0.102)和9.0(5.0-10.0)天,15天NMV/r (p = 0.190)。结论:症状缓解/解决和恢复正常健康/活动的时间与5天与延长NMV/r相似,与EPIC-HR试验相当。对于大多数免疫功能低下的个体,5天治疗可能足够,而延长治疗可能改善严重免疫功能低下患者的症状缓解;需要更大规模的研究来证实这些发现。试验注册:ClinicalTrials.gov识别码,NCT05438602。
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
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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