Continued Treatment With Tirzepatide for Maintenance of Weight Reduction in Adults With Obesity

被引:335
作者
Aronne, Louis J. [1 ,2 ]
Sattar, Naveed [3 ]
Horn, Deborah B. [4 ]
Bays, Harold E. [5 ]
Wharton, Sean [6 ,7 ]
Lin, Wen-Yuan [8 ]
Ahmad, Nadia N. [9 ]
Zhang, Shuyu [9 ]
Liao, Ran [9 ]
Bunck, Mathijs C. [9 ]
Jouravskaya, Irina [10 ]
Murphy, Madhumita A. [9 ]
机构
[1] Weill Cornell Med, Comprehens Weight Control Ctr, Div Endocrinol Diabet & Metab, 1305 York Ave,Fourth Floor, New York, NY 10065 USA
[2] Comprehens Weight Control Ctr, Div Endocrinol Diabet & Metab, New York, NY USA
[3] Univ Glasgow, BHF Glasgow Cardiovasc Res Ctr, Sch Cardiovasc & Metab Hlth, Glasgow, Scotland
[4] Univ Texas Houston, Univ Texas Ctr Obes Med & Metab Performance, McGovern Med Sch, Dept Surg, Houston, TX USA
[5] Louisville Metab & Atherosclerosis Res Ctr, Louisville, KY USA
[6] McMaster Univ, Toronto, ON, Canada
[7] York Univ, Wharton Weight Management Clin, Toronto, ON, Canada
[8] China Med Univ Hosp, Dept Family Med, Taichung, Taiwan
[9] Eli Lilly & Co, Indianapolis, IN USA
[10] Eli Lilly & Co, Moscow, Russia
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2024年 / 331卷 / 01期
关键词
PLACEBO-CONTROLLED TRIAL; GLP-1 RECEPTOR AGONIST; DOUBLE-BLIND; DUAL GIP; LIRAGLUTIDE; MULTICENTER; ORLISTAT; EFFICACY; PEOPLE;
D O I
10.1001/jama.2023.24945
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Importance The effect of continued treatment with tirzepatide on maintaining initial weight reduction is unknown.Objective 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.Interventions 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.Main Outcomes and MeasuresThe 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.Results 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.Conclusions and Relevance In participants with obesity or overweight, withdrawing tirzepatide led to substantial regain of lost weight, whereas continued treatment maintained and augmented initial weight reduction.Trial RegistrationClinicalTrials.gov Identifier: NCT04660643
引用
收藏
页码:38 / 48
页数:11
相关论文
共 32 条
[1]  
[Anonymous], 2016, Endocr Pract, V22, P1
[2]   Pharmacological Management of Obesity: An Endocrine Society Clinical Practice Guideline [J].
Apovian, Caroline M ;
Aronne, Louis J. ;
Bessesen, Daniel H. ;
McDonnell, Marie E. ;
Murad, M. Hassan ;
Pagotto, Uberto ;
Ryan, Donna H. ;
Still, Christopher D. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2015, 100 (02) :342-362
[3]   Describing the Weight-Reduced State: Physiology, Behavior, and Interventions [J].
Aronne, Louis J. ;
Hall, Kevin D. ;
Jakicic, John M. ;
Leibel, Rudolph L. ;
Lowe, Michael R. ;
Rosenbaum, Michael ;
Klein, Samuel .
OBESITY, 2021, 29 :S9-S24
[4]   LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: From discovery to clinical proof of concept [J].
Coskun, Tamer ;
Sloop, Kyle W. ;
Loghin, Corina ;
Alsina-Fernandez, Jorge ;
Urva, Shweta ;
Bokvist, Krister B. ;
Cui, Xuewei ;
Briere, Daniel A. ;
Cabrera, Over ;
Roell, William C. ;
Kuchibhotla, Uma ;
Moyers, Julie S. ;
Benson, Charles T. ;
Gimeno, Ruth E. ;
D'Alessio, David A. ;
Haupt, Axel .
MOLECULAR METABOLISM, 2018, 18 :3-14
[5]   Effect of Subcutaneous Tirzepatide vs Placebo Added to Titrated Insulin Glargine on Glycemic Control in Patients With Type 2 Diabetes The SURPASS-5 Randomized Clinical Trial [J].
Dahl, Dominik ;
Onishi, Yukiko ;
Norwood, Paul ;
Huh, Ruth ;
Bray, Ross ;
Patel, Hiren ;
Rodriguez, Angel .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2022, 327 (06) :534-545
[6]   Tirzepatide versus insulin glargine in type 2 diabetes and increased cardiovascular risk (SURPASS-4): a randomised, open-label, parallel-group, multicentre, phase 3 trial [J].
Del Prato, Stefano ;
Kahn, Steven E. ;
Pavo, Imre ;
Weerakkody, Govinda J. ;
Yang, Zhengyu ;
Doupis, John ;
Aizenberg, Diego ;
Wynne, Alan G. ;
Riesmeyer, Jeffrey S. ;
Heine, Robert J. ;
Wiese, Russell J. .
LANCET, 2021, 398 (10313) :1811-1824
[7]   Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes [J].
Frias, Juan P. ;
Davies, Melanie J. ;
Rosenstock, Julio ;
Manghi, Federico C. Perez ;
Lando, Laura Fernandez ;
Bergman, Brandon K. ;
Liu, Bing ;
Cui, Xuewei ;
Brown, Katelyn .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (06) :503-515
[8]   Efficacy and tolerability of tirzepatide, a dual glucose-dependent insulinotropic peptide and glucagon-like peptide-1 receptor agonist in patients with type 2 diabetes: A 12-week, randomized, double-blind, placebo-controlled study to evaluate different dose-escalation regimens [J].
Frias, Juan Pablo ;
Nauck, Michael A. ;
Van, Joanna ;
Benson, Charles ;
Bray, Ross ;
Cui, Xuewei ;
Milicevic, Zvonko ;
Urva, Shweta ;
Haupt, Axel ;
Robins, Deborah A. .
DIABETES OBESITY & METABOLISM, 2020, 22 (06) :938-946
[9]   Efficacy and safety of LY3298176, a novel dual GIP and GLP-1 receptor agonist, in patients with type 2 diabetes: a randomised, placebo-controlled and active comparator-controlled phase 2 trial [J].
Frias, Juan Pablo ;
Nauck, Michael A. ;
Van, Joanna ;
Kutner, Mark E. ;
Cui, Xuewei ;
Benson, Charles ;
Urva, Shweta ;
Gimeno, Ruth E. ;
Milicevic, Zvonko ;
Robins, Deborah ;
Haupt, Axel .
LANCET, 2018, 392 (10160) :2180-2193
[10]   Tirzepatide once weekly for the treatment of obesity in people with type 2 diabetes (SURMOUNT-2): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial [J].
Garvey, W. Timothy ;
Frias, Juan P. ;
Jastreboff, Ania M. ;
Roux, Carel W. le ;
Sattar, Naveed ;
Aizenberg, Diego ;
Mao, Huzhang ;
Zhang, Shuyu ;
Ahmad, Nadia N. ;
Bunck, Mathijs C. ;
Benabbad, Imane ;
Zhang, Xiaotian M. .
LANCET, 2023, 402 (10402) :613-626