Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas Y Nutrición Salvador Zubirán, Vasco de Quiroga 15, Belisario Domínguez Sección XVI, Tlalpan, Mexico City, Mexico.
Bioinformatics, Biostatistics and Computational Biology Unit, Red de apoyo a la investigación Coordinación de Investigación Científica, Universidad Nacional Autónoma de México, Mexico City, Mexico.
J Gen Intern Med. 2022 Jan;37(1):4-14. doi: 10.1007/s11606-021-07203-8. Epub 2021 Nov 9.
Colchicine is an available, safe, and effective anti-inflammatory drug and has been suggested as a COVID-19 treatment, but its usefulness in hospitalized severe COVID-19 patients has not been thoroughly demonstrated.
To address the safety and efficacy of colchicine in hospitalized patients with severe COVID-19.
We conducted a triple-blind parallel non-stratified placebo-controlled clinical trial.
We recruited 116 hospitalized patients with severe COVID-19 in Mexico.
Patients were randomized to receive 1.5 mg of colchicine or placebo at the time of the recruitment in the study (baseline) and 0.5 mg BID PO to complete 10 days of treatment.
The primary composite outcome was the progression to critical disease or death. Besides, we evaluated immunological features at baseline and after recovery or disease progression in 20 patients.
Fifty-six patients were allocated to colchicine and 60 patients received placebo. The study was suspended after the second interim analysis demonstrated colchicine had no effect on the primary outcome (OR 0.83, 95%CI 0.35-1.93, P = 0.67), nor in the days of ICU and hospital stays. Adverse events were similar between groups (OR 1.63, 95% CI 0.66-3.88, P = 0.37). After colchicine treatment, patients had higher BUN and lower serum levels of IL-8, IL-12p70, and IL-17A.
Colchicine is safe but not effective in the treatment of severe COVID-19.
ClinicalTrials.gov Identifier: NCT04367168.
秋水仙碱是一种可用的、安全的、有效的抗炎药物,已被提议用于治疗 COVID-19,但它在住院的重症 COVID-19 患者中的有效性尚未得到充分证实。
探讨秋水仙碱在住院的重症 COVID-19 患者中的安全性和疗效。
我们进行了一项三盲、平行、非分层、安慰剂对照的临床试验。
我们招募了墨西哥的 116 名住院的重症 COVID-19 患者。
患者在研究(基线)入组时随机接受 1.5mg 秋水仙碱或安慰剂,并每天两次口服 0.5mg 完成 10 天的治疗。
主要复合结局是进展为危重症或死亡。此外,我们在 20 名患者康复或疾病进展时评估了基线时的免疫特征。
56 名患者分配到秋水仙碱组,60 名患者接受安慰剂。第二次中期分析显示秋水仙碱对主要结局没有影响(OR 0.83,95%CI 0.35-1.93,P=0.67),也没有影响 ICU 和住院天数后,研究被暂停。两组的不良事件相似(OR 1.63,95%CI 0.66-3.88,P=0.37)。秋水仙碱治疗后,患者的 BUN 升高,血清中 IL-8、IL-12p70 和 IL-17A 水平降低。
秋水仙碱治疗重症 COVID-19 安全,但无效。
ClinicalTrials.gov 标识符:NCT04367168。