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环丙氯地孕酮治疗乳腺纤维瘤的疗效与安全性:一项系统评价和荟萃分析

Efficacy and Safety of Centchroman in the Treatment of Breast Fibroadenoma: A Systematic Review and Meta-Analysis.

作者信息

Kumar Keshav, Pallavi Kumari, Martand Kumar, Mohan Lalit, Roy Sukalyan Saha, Prakash Prem, Maharshi Vikas

机构信息

Department of Pharmacology and Therapeutics, Indira Gandhi Institute of Medical Sciences, Patna, IND.

Department of Anatomy, Employees State Insurance-Post Graduate Institute of Medical Sciences and Research (ESI-PGIMSR) Employees State Insurance Corporation (ESIC) Medical College, Joka, Kolkata, IND.

出版信息

Cureus. 2025 Jun 30;17(6):e87046. doi: 10.7759/cureus.87046. eCollection 2025 Jun.

Abstract

Breast fibroadenoma is a benign disease in women of reproductive age group which usually presents as painless, solitary, or multiple lumps located in the same or both breasts. Management of breast fibroadenoma ranges from watchful observation for self-regression to surgical interventions. Many studies have evaluated centchroman for its efficacy and safety in the treatment of breast fibroadenoma, but their findings were conflicting. We, therefore, aimed to conduct this systematic review and meta-analysis to resolve the conflict. The primary objective was to assess the efficacy whereas the secondary objective was to assess the safety of centchroman compared with no intervention-only watchful waiting, placebo or any active control in patients with breast fibroadenoma.  The protocol for this systematic review and meta-analysis was designed and registered in PROSPERO (CRD42024552160). Randomized controlled trials (RCTs), non-randomized interventional studies and prospective observational studies that evaluated efficacy and safety of centchroman in patients of breast fibroadenoma were included in the systematic review whereas only RCTs were included in the meta-analysis. Review articles, case reports and communications were excluded. A comprehensive search of databases such as Medline, Science Direct, Cochrane Library and Google Scholar and trial registries such as ClinicalTrial.gov and Clinical Trials Registry-India (CTRI) till 31/12/2024 was carried out by two independent authors. The efficacy outcome was regression of fibroadenoma measured in terms of the number of responders in each arm whereas the safety outcome was the number of patients who developed any adverse reaction. Risk ratio (RR) was used as effect measure and random effect model was used for data analysis. During the preliminary search, we found 8113 search results, of which 60 remained after removing irrelevant and duplicate results and the results available in non-English languages. We obtained full texts of 26 studies that were screened further for eligibility. Eventually, seven studies were eligible for systematic review, of which two studies were included in the meta-analysis. In the meta-analysis of two RCTs with pooled sample size of 234, the pooled estimate (RR) of efficacy outcome was 1.44 [95% CI 0.59 to 3.50; =0.42] and heterogeneity was found to be moderate with value equal to 46%. The pooled estimate (RR) of safety outcome was 13.08 [95% CI 3.72 to 46.02; =0.0001]. With these findings of meta-analysis, we conclude that centchroman is as efficacious as the control in causing regression of fibroadenoma and centchroman has significantly higher number of adverse effects than the control, although none of the adverse effects were serious. More RCTs with larger sample size and from diverse geographical settings are needed to generate more robust evidence and to expand generalizability over a broader population.

摘要

乳腺纤维瘤是育龄期女性的一种良性疾病,通常表现为无痛、单发或多发肿块,位于一侧或双侧乳房。乳腺纤维瘤的治疗方法多样,从密切观察等待其自行消退到手术干预。许多研究评估了棉酚治疗乳腺纤维瘤的有效性和安全性,但结果相互矛盾。因此,我们旨在进行这项系统评价和荟萃分析以解决这一冲突。主要目的是评估有效性,次要目的是评估棉酚与不进行干预(仅密切观察)、安慰剂或任何积极对照相比,在乳腺纤维瘤患者中的安全性。本系统评价和荟萃分析的方案已设计完成并在国际前瞻性注册系统(PROSPERO,注册号:CRD42024552160)中注册。系统评价纳入了评估棉酚在乳腺纤维瘤患者中有效性和安全性的随机对照试验(RCT)、非随机干预研究和前瞻性观察性研究,而荟萃分析仅纳入RCT。综述文章、病例报告和通讯类文章被排除。两名独立作者对Medline、Science Direct、Cochrane图书馆和谷歌学术等数据库以及ClinicalTrial.gov和印度临床试验注册中心(CTRI)等试验注册库进行了全面检索,检索截至2024年12月31日。有效性结局以每组中出现纤维瘤消退的应答者数量来衡量,安全性结局是以出现任何不良反应的患者数量来衡量。风险比(RR)用作效应量度,采用随机效应模型进行数据分析。在初步检索中,我们共找到8113条检索结果,去除不相关、重复结果以及非英文语言的结果后,还剩下60条。我们获取了26项研究的全文,并进一步筛选其是否符合纳入标准。最终,有7项研究符合系统评价的标准,其中2项研究纳入了荟萃分析。在两项RCT的荟萃分析中,合并样本量为234,有效性结局的合并估计值(RR)为1.44 [95%置信区间0.59至3.50;P = 0.42],发现异质性为中度,I²值等于46%。安全性结局的合并估计值(RR)为13.08 [95%置信区间3.72至46.02;P = 0.0001]。基于这些荟萃分析结果,我们得出结论,棉酚在促使纤维瘤消退方面与对照组效果相当,但棉酚引起的不良反应数量明显多于对照组,不过所有不良反应均不严重。需要更多样本量更大且来自不同地理区域的RCT,以产生更有力的证据,并扩大在更广泛人群中的可推广性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3be8/12310075/1bb7cfe307b0/cureus-0017-00000087046-i01.jpg

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