Xie Yun, Li Qingfeng, Zhao Hongyi, Qi Zuoliang, Sun Jiaming, Tan Qian, Li Dong, Hu Zhiqi, Liu Ziyang, Chawla Smita
Aesthet Surg J. 2025 Jun 16;45(7):699-708. doi: 10.1093/asj/sjaf033.
BACKGROUND: Individuals with chin retrusion may seek chin and lower jawline aesthetic enhancement. OBJECTIVES: To evaluate VYC-25L (Juvéderm Volux XC; Allergan Aesthetics, an AbbVie company), a lidocaine-containing injectable hyaluronic acid dermal filler, for chin retrusion correction. METHODS: In this prospective, Phase 3, multicenter study (NCT04559984), Chinese adults with moderate-to-severe chin retrusion on the China (Allergan) Chin Retrusion Scale (CACRS) and glabella-subnasale-pogonion (G-Sn-Pog) angle <172.5° were randomized 2:1 to VYC-25L (treatment plus optional touch-up 4 weeks later) or no treatment (control). The primary endpoint was change from baseline (CFB) in G-Sn-Pog angle at Week 24. Secondary endpoints included CACRS response (≥1-point improvement), Global Aesthetic Improvement Scale (GAIS) response (improved/much improved), and FACE-Q Satisfaction with Chin score. Procedural pain was rated (0 = none to 10 = worst imaginable); injection-site responses (ISRs) were recorded daily for ≤28 days. RESULTS: The mean age of the patient (VYC-25L, n = 97; control, n = 51) was 31.2 years (range, 20-52 years). Mean CFB in G-Sn-Pog angle at Week 24 was 2.97° (VYC-25L) vs 0.09° (control; between-group difference, 3.08° [P < .0001]); improvement was maintained to Week 52. At Week 24, VYC-25L achieved higher responses vs control for CACRS (78.7% vs 18.8%, respectively; rate difference, 60.0%; P < .0001) and GAIS (92.6% vs 4.2%, respectively; rate difference, 88.4%; P < .0001); mean overall FACE-Q Satisfaction with Chin score was 70.4 vs 34.9, respectively. Mean (standard deviation) procedural pain was 2.6 (1.6); most ISRs were mild (41.8%) or moderate (50.0%) in severity. CONCLUSIONS: In Chinese adults, VYC-25L safely and effectively corrected chin retrusion for at least 1 year.
背景:下巴后缩的个体可能会寻求下巴和下颌轮廓的美学改善。 目的:评估VYC - 25L(乔雅登极致丰颜;艾伯维公司旗下的艾尔建美学),一种含利多卡因的可注射透明质酸真皮填充剂,用于矫正下巴后缩。 方法:在这项前瞻性、3期、多中心研究(NCT04559984)中,根据中国(艾尔建)下巴后缩量表(CACRS)评估为中度至重度下巴后缩且眉间 - 鼻下点 - 颏前点(G - Sn - Pog)角<172.5°的中国成年人,按2:1随机分为VYC - 25L组(治疗并在4周后进行可选的补打)或不治疗组(对照组)。主要终点是第24周时G - Sn - Pog角相对于基线的变化(CFB)。次要终点包括CACRS反应(改善≥1分)、全球美学改善量表(GAIS)反应(改善/显著改善)以及面部Q量表下巴满意度评分。对操作疼痛进行评分(0 = 无疼痛至10 = 难以想象的剧痛);记录注射部位反应(ISR),持续≤28天。 结果:患者的平均年龄(VYC - 25L组,n = 97;对照组,n = 51)为31.2岁(范围20 - 52岁)。第24周时,VYC - 25L组G - Sn - Pog角的平均CFB为2.97°,而对照组为0.09°(组间差异为3.08°[P <.0001]);这种改善维持到了第52周。在第24周时,VYC - 25L组在CACRS反应(分别为78.7%对18.8%;率差为60.0%;P <.0001)和GAIS反应(分别为92.6%对4.2%;率差为88.4%;P <.0001)方面相对于对照组取得了更高的反应;面部Q量表下巴总体满意度评分的平均值分别为70.4和34.9。操作疼痛的平均(标准差)评分为2.6(1.6);大多数ISR的严重程度为轻度(41.8%)或中度(50.0%)。 结论:在中国成年人中,VYC - 25L可安全有效地矫正下巴后缩至少1年。
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