Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin und Humboldt-Universität zu Berlin, Institute for Experimental Pediatric Endocrinology, CVK, Augustenburger Platz 1, 13353, Berlin, Germany.
Division of Pediatric Endocrinology and Diabetes, Center for Rare Endocrine Diseases, Department of Pediatrics and Adolescent Medicine, University of Ulm, Eythstraße 24, 89075, Ulm, Germany.
Orphanet J Rare Dis. 2022 Feb 5;17(1):38. doi: 10.1186/s13023-022-02186-z.
Individuals with proopiomelanocortin (POMC) or leptin receptor (LEPR) deficiency are young and experience severe obesity, hyperphagia, and comorbidities, which can impair quality of life (QOL).
Two pivotal Phase 3 trials explored the effect of setmelanotide on body weight and hunger in individuals with obesity due to POMC (NCT02896192) or LEPR (NCT03287960) deficiency. QOL and depression were investigated in parallel using the disease-specific, age-appropriate Impact of Weight on Quality of Life-Lite (IWQOL-Lite), Pediatric Quality of Life Inventory (PedsQL), and Patient Health Questionnaire-9 (PHQ-9).
In total, the POMC and LEPR trials enrolled 21 patients. Adults (≥ 18 years old; n = 7) had moderate-to-severe impairment in QOL at baseline, with mean (standard deviation [SD]) IWQOL-Lite total score 60.3 (13.2; maximum IWQOL-Lite total score = 100). The effect of setmelanotide on IWQOL-Lite total score was observed as soon as Week 5. Among those with scores at Week 52, 5 of 6 adults experienced a clinically meaningful improvement, with mean (SD) total scores increased from baseline by 24.2 (12.1) points. Children (6-12 years old; n = 2) and adolescents (13-17 years old; n = 4) had impaired QOL at baseline, with mean (SD) self-reported PedsQL total scores 53.3 (6.2) and 63.3 (29.1), respectively (maximum PedsQL total score = 100). Three of 5 patients experienced clinically meaningful improvement in PedsQL, with 2 children whose PedsQL total score increased by 28.3 and 3.3 points and 3 adolescents whose mean (SD) total score increased from baseline by 5.8 (18.3) points. Baseline mean (SD) PHQ-9 score (in those ≥ 12 years old) was 5.3 (3.8) and was generally maintained through Week 52.
Patients with POMC or LEPR deficiency had impaired, and in some cases severely impaired, QOL before setmelanotide treatment. Setmelanotide improved QOL in patients as early as Week 5, with some patients no longer experiencing impaired QOL at Week 52. Improvements in QOL may be related to a reduction in hunger and body weight associated with setmelanotide. Because of the highly complex psychological consequences of rare genetic diseases of obesity, some patients may require a long period of treatment to improve QOL and benefit from interdisciplinary care.
患有前阿黑皮素原(POMC)或瘦素受体(LEPR)缺乏症的个体通常较为年轻,且会经历严重肥胖、食欲过盛和合并症,这些问题会损害生活质量(QOL)。
两项关键性的 3 期临床试验探索了黑素细胞刺激素受体激动剂(setmelanotide)对 POMC(NCT02896192)或 LEPR(NCT03287960)缺乏所致肥胖个体体重和饥饿的影响。使用特定于疾病的、适合年龄的生活质量影响量表-简化版(IWQOL-Lite)、儿科生活质量量表(PedsQL)和患者健康问卷-9(PHQ-9)平行评估 QOL 和抑郁情况。
共有 21 例 POMC 和 LEPR 试验患者入组。成年人(≥18 岁;n=7)基线时 QOL 存在中度至重度受损,平均(标准偏差 [SD])IWQOL-Lite 总分 60.3(13.2;IWQOL-Lite 总分最高值为 100)。从第 5 周开始,setmelanotide 对 IWQOL-Lite 总分的影响即显现。在第 52 周有评分的患者中,6 例成年人中有 5 例经历了有临床意义的改善,平均(SD)总分从基线增加了 24.2(12.1)分。2 例 6-12 岁儿童(n=2)和 4 例 13-17 岁青少年(n=4)基线时 QOL 受损,分别报告平均(SD)PedsQL 总分 53.3(6.2)和 63.3(29.1)(PedsQL 总分最高值为 100)。5 例患者中有 3 例 PedsQL 改善具有临床意义,2 例儿童的 PedsQL 总分分别增加了 28.3 和 3.3 分,3 例青少年的平均(SD)总分从基线增加了 5.8(18.3)分。≥12 岁患者的基线平均(SD)PHQ-9 评分(5.3[3.8])在第 52 周基本保持不变。
在接受 setmelanotide 治疗前,POMC 或 LEPR 缺乏症患者的 QOL 受损,在某些情况下严重受损。setmelanotide 最早在第 5 周即可改善 QOL,一些患者在第 52 周时不再出现 QOL 受损。QOL 的改善可能与 setmelanotide 相关的食欲下降和体重减轻有关。由于罕见肥胖遗传疾病的高度复杂的心理后果,一些患者可能需要长期治疗以改善 QOL,并从多学科护理中获益。