Comprehensive Weight Control Center, Division of Endocrinology, Diabetes, and Metabolism, Weill Cornell Medicine, New York, New York.
BHF Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom.
JAMA. 2024 Jan 2;331(1):38-48. doi: 10.1001/jama.2023.24945.
The effect of continued treatment with tirzepatide on maintaining initial weight reduction is unknown.
To assess the effect of tirzepatide, with diet and physical activity, on the maintenance of weight reduction.
DESIGN, SETTING, AND PARTICIPANTS: This phase 3, randomized withdrawal clinical trial conducted at 70 sites in 4 countries with a 36-week, open-label tirzepatide lead-in period followed by a 52-week, double-blind, placebo-controlled period included adults with a body mass index greater than or equal to 30 or greater than or equal to 27 and a weight-related complication, excluding diabetes.
Participants (n = 783) enrolled in an open-label lead-in period received once-weekly subcutaneous maximum tolerated dose (10 or 15 mg) of tirzepatide for 36 weeks. At week 36, a total of 670 participants were randomized (1:1) to continue receiving tirzepatide (n = 335) or switch to placebo (n = 335) for 52 weeks.
The primary end point was the mean percent change in weight from week 36 (randomization) to week 88. Key secondary end points included the proportion of participants at week 88 who maintained at least 80% of the weight loss during the lead-in period.
Participants (n = 670; mean age, 48 years; 473 [71%] women; mean weight, 107.3 kg) who completed the 36-week lead-in period experienced a mean weight reduction of 20.9%. The mean percent weight change from week 36 to week 88 was -5.5% with tirzepatide vs 14.0% with placebo (difference, -19.4% [95% CI, -21.2% to -17.7%]; P < .001). Overall, 300 participants (89.5%) receiving tirzepatide at 88 weeks maintained at least 80% of the weight loss during the lead-in period compared with 16.6% receiving placebo (P < .001). The overall mean weight reduction from week 0 to 88 was 25.3% for tirzepatide and 9.9% for placebo. The most common adverse events were mostly mild to moderate gastrointestinal events, which occurred more commonly with tirzepatide vs placebo.
In participants with obesity or overweight, withdrawing tirzepatide led to substantial regain of lost weight, whereas continued treatment maintained and augmented initial weight reduction.
ClinicalTrials.gov Identifier: NCT04660643.
重要性:尚不清楚替西帕肽持续治疗对维持初始减重的效果。
目的:评估替西帕肽联合饮食和体力活动对维持体重减轻的效果。
设计、地点和参与者:这是一项 3 期、随机停药临床试验,在 4 个国家的 70 个地点进行,包括一个 36 周的开放性替西帕肽导入期,随后是 52 周的双盲、安慰剂对照期。参与者为患有 BMI 大于或等于 30 或大于或等于 27 且存在与体重相关的并发症(不包括糖尿病)的成年人。
干预措施:参与者(n = 783)参加了 36 周的开放性导入期,接受每周一次皮下最大耐受剂量(10 或 15 mg)的替西帕肽治疗。在第 36 周时,共有 670 名参与者(1:1)被随机分为继续接受替西帕肽(n = 335)或转为安慰剂(n = 335)治疗 52 周。
主要终点和次要终点:主要终点是从第 36 周(随机化)到第 88 周体重的平均百分比变化。关键次要终点包括在导入期至少减轻 80%体重的参与者在第 88 周时的比例。
结果:完成 36 周导入期的参与者(n = 670;平均年龄 48 岁;473 [71%]名女性;平均体重 107.3 kg)体重平均减轻 20.9%。从第 36 周到第 88 周的体重百分比变化平均为替西帕肽组为-5.5%,安慰剂组为 14.0%(差异,-19.4% [95%CI,-21.2%至-17.7%];P < .001)。总体而言,在第 88 周时,接受替西帕肽治疗的 300 名参与者(89.5%)维持了导入期至少 80%的体重减轻,而接受安慰剂治疗的参与者比例为 16.6%(P < .001)。从第 0 周到第 88 周,替西帕肽组的总体平均体重减轻为 25.3%,安慰剂组为 9.9%。最常见的不良反应大多为轻度至中度胃肠道事件,替西帕肽组比安慰剂组更常见。
结论和相关性:在肥胖或超重的参与者中,停用替西帕肽会导致体重明显反弹,而继续治疗则维持并增加了初始体重减轻。
试验注册:ClinicalTrials.gov 标识符:NCT04660643。