Song Zhang, Ibrahim Serag, Tangatarova Sofia, Sama Mahmoud Gamal, Mahmoud G. A. Saleh, E. A. Shaban, Mostafa Hossam El Din Moawad
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Randomized controlled trials (RCTs) comparing CLIN/BPO with ADAP/BPO were included. Data on treatment-emergent adverse events (TEAEs), treatment discontinuation due to TEAEs, AS reactions, and total lesion count were extracted and analyzed using RevMan 5.3 with a fixed effects model. Three RCTs from the USA and Argentina, including 556 participants, were analyzed. The risk of bias assessment classified two studies as low-risk and one with some concerns. The meta-analysis demonstrated that CLIN/BPO significantly reduced the risk of TEAEs compared to ADAP/BPO (OR = 0.32; 95% CI: 0.21–0.47; <i>p</i> < 0.0001). Additionally, treatment discontinuation due to TEAEs was lower with CLIN/BPO (OR = 0.10; 95% CI: 0.02–0.55; <i>p</i> = 0.008). CLIN/BPO was associated with fewer application site (AS) side effects (OR = 0.40; 95% CI: 0.28–0.55; <i>p</i> < 0.00001), particularly in terms of reduced pain, dryness, and irritation. However, no significant differences were observed in AS exfoliation, dermatitis, erythema, or pruritus. Both treatments showed comparable efficacy in reducing total lesion count (MD = 2.55; 95% CI: -4.11 to 9.22; <i>p</i> = 0.45). CLIN/BPO exhibits a superior safety and tolerability profile compared to ADAP/BPO, with significantly lower rates of TEAEs and AS reactions, while maintaining equivalent efficacy in lesion reduction. 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Data on treatment-emergent adverse events (TEAEs), treatment discontinuation due to TEAEs, AS reactions, and total lesion count were extracted and analyzed using RevMan 5.3 with a fixed effects model. Three RCTs from the USA and Argentina, including 556 participants, were analyzed. The risk of bias assessment classified two studies as low-risk and one with some concerns. The meta-analysis demonstrated that CLIN/BPO significantly reduced the risk of TEAEs compared to ADAP/BPO (OR = 0.32; 95% CI: 0.21–0.47; <i>p</i> < 0.0001). Additionally, treatment discontinuation due to TEAEs was lower with CLIN/BPO (OR = 0.10; 95% CI: 0.02–0.55; <i>p</i> = 0.008). CLIN/BPO was associated with fewer application site (AS) side effects (OR = 0.40; 95% CI: 0.28–0.55; <i>p</i> < 0.00001), particularly in terms of reduced pain, dryness, and irritation. However, no significant differences were observed in AS exfoliation, dermatitis, erythema, or pruritus. 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引用次数: 0
摘要
寻常痤疮是一种常见的皮肤病,主要影响青少年和年轻人,经常导致身体和心理上的痛苦。克林霉素磷酸/过氧化苯甲酰(CLIN/BPO)和阿达帕林/过氧化苯甲酰(ADAP/BPO)等联合疗法被广泛用于治疗;然而,对其疗效和安全性的直接比较分析仍然有限。本系统综述和荟萃分析旨在比较CLIN/BPO与ADAP/BPO治疗寻常性痤疮的疗效和安全性。在PubMed、Scopus、Web of Science和Cochrane Library数据库中,按照PRISMA指南进行了系统的文献检索。随机对照试验(rct)比较clint /BPO与ADAP/BPO。采用RevMan 5.3固定效应模型提取并分析治疗不良事件(teae)、因teae而停药、AS反应和总病灶数的数据。分析了来自美国和阿根廷的三个随机对照试验,包括556名参与者。偏倚风险评估将两项研究分类为低风险,一项研究分类为有一些问题。荟萃分析显示,与ADAP/BPO相比,CLIN/BPO显著降低了teae的风险(OR = 0.32; 95% CI: 0.21-0.47; p < 0.0001)。此外,由于teae而中断治疗的clini /BPO较低(OR = 0.10; 95% CI: 0.02-0.55; p = 0.008)。CLIN/BPO与较少的应用部位(AS)副作用相关(OR = 0.40; 95% CI: 0.28-0.55; p < 0.00001),特别是在减轻疼痛、干燥和刺激方面。然而,在AS脱落、皮炎、红斑或瘙痒方面没有观察到显著差异。两种治疗方法在减少病变总数方面的疗效相当(MD = 2.55; 95% CI: -4.11 ~ 9.22; p = 0.45)。与ADAP/BPO相比,CLIN/BPO表现出更高的安全性和耐受性,teae和AS反应率显著降低,同时在减少病变方面保持相同的疗效。这些研究结果表明,在不影响治疗效果的前提下,临床/BPO可能是患者优先考虑安全性的首选方案。
Comparative efficacy and safety of clindamycin phosphate/benzoyl peroxide versus adapalene/benzoyl peroxide in acne treatment: a systematic review and meta-analysis
Acne vulgaris is a common dermatological disorder, primarily affecting adolescents and young adults, often leading to both physical and psychological distress. Combination therapies such as Clindamycin phosphate/Benzoyl Peroxide (CLIN/BPO) and Adapalene/Benzoyl Peroxide (ADAP/BPO) are widely used for treatment; however, direct comparative analyses of their efficacy and safety remain limited. This systematic review and meta-analysis aimed to compare the efficacy and safety profiles of CLIN/BPO versus ADAP/BPO in the treatment of acne vulgaris. A systematic literature search was conducted following PRISMA guidelines across PubMed, Scopus, Web of Science, and Cochrane Library databases. Randomized controlled trials (RCTs) comparing CLIN/BPO with ADAP/BPO were included. Data on treatment-emergent adverse events (TEAEs), treatment discontinuation due to TEAEs, AS reactions, and total lesion count were extracted and analyzed using RevMan 5.3 with a fixed effects model. Three RCTs from the USA and Argentina, including 556 participants, were analyzed. The risk of bias assessment classified two studies as low-risk and one with some concerns. The meta-analysis demonstrated that CLIN/BPO significantly reduced the risk of TEAEs compared to ADAP/BPO (OR = 0.32; 95% CI: 0.21–0.47; p < 0.0001). Additionally, treatment discontinuation due to TEAEs was lower with CLIN/BPO (OR = 0.10; 95% CI: 0.02–0.55; p = 0.008). CLIN/BPO was associated with fewer application site (AS) side effects (OR = 0.40; 95% CI: 0.28–0.55; p < 0.00001), particularly in terms of reduced pain, dryness, and irritation. However, no significant differences were observed in AS exfoliation, dermatitis, erythema, or pruritus. Both treatments showed comparable efficacy in reducing total lesion count (MD = 2.55; 95% CI: -4.11 to 9.22; p = 0.45). CLIN/BPO exhibits a superior safety and tolerability profile compared to ADAP/BPO, with significantly lower rates of TEAEs and AS reactions, while maintaining equivalent efficacy in lesion reduction. These findings suggest that CLIN/BPO may be the preferred option for patients prioritizing safety without compromising treatment effectiveness.
期刊介绍:
Archives of Dermatological Research is a highly rated international journal that publishes original contributions in the field of experimental dermatology, including papers on biochemistry, morphology and immunology of the skin. The journal is among the few not related to dermatological associations or belonging to respective societies which guarantees complete independence. This English-language journal also offers a platform for review articles in areas of interest for dermatologists and for publication of innovative clinical trials.