Sophie Leducq, Wei Chern Gavin Fong, Hywel C Williams, Lucy Bradshaw, Kim S Thomas
{"title":"报告特应性皮炎的伴随和救援局部治疗评估全身治疗的随机对照试验:范围综述。","authors":"Sophie Leducq, Wei Chern Gavin Fong, Hywel C Williams, Lucy Bradshaw, Kim S Thomas","doi":"10.1093/bjd/ljaf031","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Randomized controlled trials (RCTs) evaluating new systemic treatments for atopic dermatitis (AD) have increased dramatically over the last decade. These trials often incorporate topical therapies either as permitted concomitant or rescue treatments. Differential use of these topicals postrandomization introduces potential bias as they may nullify or exaggerate treatment responses.</p><p><strong>Objectives: </strong>To determine the proportion of RCTs that clearly report the allowance or prohibition of concomitant and rescue topical treatments; and to examine the reporting of specific key parameters for these topicals.</p><p><strong>Methods: </strong>We included RCTs of systemic AD medication included in a recent living systematic review. Inclusion criteria were published RCTs evaluating systemic immunomodulatory treatments in AD. Only anti-inflammatory topical therapies were included treatments in this review; emollients were not considered.</p><p><strong>Results: </strong>We screened 83 AD trials and included 67 RCTs published between 1991 and 2023. The majority adequately reported the allowance or prohibition of concomitant topical treatments (n = 64/67; 96%), but this clarity was less prevalent with regard to rescue topicals (n = 49/67; 73%). All trials that permitted concomitant treatments consistently reported the type, although details on potency (n = 31/35; 89%), duration (n = 19/35; 54%), application frequency (n = 12/35; 34%) and quantity (n = 2/35; 6%) were less frequently reported. Similarly, trials that allowed rescue treatments often specified the type (n = 31/34; 91%) but provided limited information on potency (n = 18/34; 53%), duration (n = 3/34; 9%), application frequency (n = 2/34; 6%) and quantity (n = 0/34; 0%). Notably, only 24% (n = 8/34) clearly reported the criteria for using rescue topical treatments, with the phrase 'at investigator's discretion' used in most cases (n = 21/34; 62%). In the multivariable logistic regression analysis including impact factor, the journal's policy on adhering to CONSORT guidelines, publication year, funding, number of patients randomized and blinding status, only publication year (≥ 2020) was associated with having better reporting for rescue topical treatments (adjusted odds ratio 9.55, 95% confidence interval 1.76-39.80).</p><p><strong>Conclusions: </strong>While most clinical trials of systemic treatments in AD report concomitant topical treatments, reporting practices for rescue topicals are less consistent and inadequate. A standardized approach to reporting topical treatment in AD trials is needed to enhance transparency and interpretability.</p>","PeriodicalId":9238,"journal":{"name":"British Journal of Dermatology","volume":" ","pages":"818-825"},"PeriodicalIF":9.6000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reporting of concomitant and rescue topical therapies in randomized controlled trials evaluating a systemic treatment in atopic dermatitis: a scoping review.\",\"authors\":\"Sophie Leducq, Wei Chern Gavin Fong, Hywel C Williams, Lucy Bradshaw, Kim S Thomas\",\"doi\":\"10.1093/bjd/ljaf031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Randomized controlled trials (RCTs) evaluating new systemic treatments for atopic dermatitis (AD) have increased dramatically over the last decade. These trials often incorporate topical therapies either as permitted concomitant or rescue treatments. Differential use of these topicals postrandomization introduces potential bias as they may nullify or exaggerate treatment responses.</p><p><strong>Objectives: </strong>To determine the proportion of RCTs that clearly report the allowance or prohibition of concomitant and rescue topical treatments; and to examine the reporting of specific key parameters for these topicals.</p><p><strong>Methods: </strong>We included RCTs of systemic AD medication included in a recent living systematic review. Inclusion criteria were published RCTs evaluating systemic immunomodulatory treatments in AD. Only anti-inflammatory topical therapies were included treatments in this review; emollients were not considered.</p><p><strong>Results: </strong>We screened 83 AD trials and included 67 RCTs published between 1991 and 2023. The majority adequately reported the allowance or prohibition of concomitant topical treatments (n = 64/67; 96%), but this clarity was less prevalent with regard to rescue topicals (n = 49/67; 73%). All trials that permitted concomitant treatments consistently reported the type, although details on potency (n = 31/35; 89%), duration (n = 19/35; 54%), application frequency (n = 12/35; 34%) and quantity (n = 2/35; 6%) were less frequently reported. Similarly, trials that allowed rescue treatments often specified the type (n = 31/34; 91%) but provided limited information on potency (n = 18/34; 53%), duration (n = 3/34; 9%), application frequency (n = 2/34; 6%) and quantity (n = 0/34; 0%). Notably, only 24% (n = 8/34) clearly reported the criteria for using rescue topical treatments, with the phrase 'at investigator's discretion' used in most cases (n = 21/34; 62%). 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引用次数: 0
摘要
背景:在过去十年中,评估特应性皮炎(AD)新的全身治疗方法的随机对照试验(rct)急剧增加。这些试验通常将局部治疗作为允许的伴随治疗或挽救治疗。随机化后这些局部药物的不同使用会引入潜在的偏倚,因为它们可能会使治疗反应无效或夸大。目的:确定明确报道允许或禁止伴随治疗和挽救性局部治疗的随机对照试验的比例。次要结果包括检查这些主题的特定关键参数的报告。方法:我们纳入了Drucker等人的活系统综述(更新于2023年3月,在本综述发表时可用)中的AD全身药物随机对照试验。纳入标准是发表的评估AD全身免疫调节治疗的随机对照试验。本综述仅包括抗炎局部治疗;没有考虑润肤剂。结果:我们筛选了1991年至2023年间发表的83项AD试验,包括67项随机对照试验。大多数人充分报告了允许或禁止伴随的局部治疗(95.5%,N=64/67),但这种明确性在救援局部治疗方面不太普遍(73.1%,N=49/67)。所有允许联合治疗的试验均一致报告了其类型,但对效价(88.6%,N=31/35)、持续时间(54.3%,N=19/35)、应用频率(34.3%,N=12/35)和数量(5.7%,N=2/35)的详细报道较少。类似地,允许挽救治疗的试验通常指定了类型(91.2%,N=31/34),但提供的效力(52.9%,N=18/34)、持续时间(8.8%,N=3/34)、应用频率(5.9%,N=2/34)和数量(0%,N=0/34)的信息有限。值得注意的是,只有23.5% (N=8/34)明确报告了使用救援局部治疗的标准,大多数情况下使用的是“根据研究者的判断”(61.8%,N=21/34)。在多变量logistic回归分析中,包括影响因子、期刊坚持CONSORT指南的政策、出版年份、资金、随机分组的患者数量和盲法状态,只有出版年份(≥2020年)与更好的救援局部治疗报道相关(aOR 9.55, 95% CI 1.76-39.8)。结论:虽然大多数系统性治疗的阿尔茨海默病临床试验报告了伴随的局部治疗,但救援局部治疗的报告实践不太一致和不充分。需要一种标准化的方法来报告局部治疗在AD试验中,以提高透明度和可解释性。
Reporting of concomitant and rescue topical therapies in randomized controlled trials evaluating a systemic treatment in atopic dermatitis: a scoping review.
Background: Randomized controlled trials (RCTs) evaluating new systemic treatments for atopic dermatitis (AD) have increased dramatically over the last decade. These trials often incorporate topical therapies either as permitted concomitant or rescue treatments. Differential use of these topicals postrandomization introduces potential bias as they may nullify or exaggerate treatment responses.
Objectives: To determine the proportion of RCTs that clearly report the allowance or prohibition of concomitant and rescue topical treatments; and to examine the reporting of specific key parameters for these topicals.
Methods: We included RCTs of systemic AD medication included in a recent living systematic review. Inclusion criteria were published RCTs evaluating systemic immunomodulatory treatments in AD. Only anti-inflammatory topical therapies were included treatments in this review; emollients were not considered.
Results: We screened 83 AD trials and included 67 RCTs published between 1991 and 2023. The majority adequately reported the allowance or prohibition of concomitant topical treatments (n = 64/67; 96%), but this clarity was less prevalent with regard to rescue topicals (n = 49/67; 73%). All trials that permitted concomitant treatments consistently reported the type, although details on potency (n = 31/35; 89%), duration (n = 19/35; 54%), application frequency (n = 12/35; 34%) and quantity (n = 2/35; 6%) were less frequently reported. Similarly, trials that allowed rescue treatments often specified the type (n = 31/34; 91%) but provided limited information on potency (n = 18/34; 53%), duration (n = 3/34; 9%), application frequency (n = 2/34; 6%) and quantity (n = 0/34; 0%). Notably, only 24% (n = 8/34) clearly reported the criteria for using rescue topical treatments, with the phrase 'at investigator's discretion' used in most cases (n = 21/34; 62%). In the multivariable logistic regression analysis including impact factor, the journal's policy on adhering to CONSORT guidelines, publication year, funding, number of patients randomized and blinding status, only publication year (≥ 2020) was associated with having better reporting for rescue topical treatments (adjusted odds ratio 9.55, 95% confidence interval 1.76-39.80).
Conclusions: While most clinical trials of systemic treatments in AD report concomitant topical treatments, reporting practices for rescue topicals are less consistent and inadequate. A standardized approach to reporting topical treatment in AD trials is needed to enhance transparency and interpretability.
期刊介绍:
The British Journal of Dermatology (BJD) is committed to publishing the highest quality dermatological research. Through its publications, the journal seeks to advance the understanding, management, and treatment of skin diseases, ultimately aiming to improve patient outcomes.