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Efficacy of oral or intrauterine device-delivered progestin in patients with complex endometrial hyperplasia with atypia or early endometrial adenocarcinoma : a meta-analysis and systematic review of the literature

机译:口服或宫腔内装置孕激素在非典型性或早期子宫内膜腺癌的复杂子宫内膜增生患者中的疗效:一项荟萃分析和系统的文献复习

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摘要

Objectives: udTo investigate the efficacy of progestin treatment to achieve pathological complete response (pCR) in patients with complex atypical endometrial hyperplasia (CAH) or early endometrial adenocarcinoma (EC).ududMethods: udA systematic search identified 3245 potentially relevant citations. Studies containing less than ten eligible CAH or EC patients in either oral or intrauterine treatment arm were excluded. Only information from patients receiving six or more months of treatment and not receiving other treatments was included. Weighted proportions of patients achieving pCR were calculated using R software.ududResults: udTwelve studies met the selection criteria. Eleven studies reported treatment of patients with oral (219 patients, 117 with CAH, 102 with grade 1 Stage I EC) and one reported treatment of patients with intrauterine progestin (11 patients with grade 1 Stage IEC). Overall, 74% (95% confidence interval [CI] 65-81%) of patients with CAH and 72% (95% CI 62-80%) of patients with grade 1 Stage I EC achieved a pCR to oral progestin. Disease progression while on oral treatment was reported for 6/219 (2.7%), and relapse after initial complete response for 32/159 (20.1%) patients. The weighted mean pCR rate of patients with grade 1 Stage I EC treated with intrauterine progestin from one prospective pilot study and an unpublished retrospective case series from the Queensland Centre of Gynaecologic Oncology (QCGC) was 68% (95% CI 45- 86%).ududConclusions: udThere is a lack of high quality evidence for the efficacy of progestin in CAH or EC. The available evidence however suggests that treatment with oral or intrauterine progestin is similarly effective. The risk of progression during treatment is small but longer follow-up is required. Evidence from prospective controlled clinical trials is warranted to establish how the efficacy of progestin for the treatment of CAH and EC can be improved further.
机译:目的: ud研究孕激素治疗在复杂的非典型子宫内膜增生(CAH)或早期子宫内膜腺癌(EC)患者中实现病理完全缓解(pCR)的功效。 。排除口服或宫内治疗组中少于十名合格的CAH或EC患者的研究。仅包括来自接受六个月或更长时间治疗且未接受其他治疗的患者的信息。使用R软件计算达到pCR的患者的加权比例。 ud ud结果: ud十二项研究符合选择标准。十一项研究报告了口服患者的治疗(219例,CAH 117例,I级1期EC 102例),一项宫内孕激素治疗(11例IEC 1级患者)的报道。总体而言,有74%(95%的置信区间[CI] 65-81%)的CAH患者和72%(95%的CI 62-80%)的1级I期EC患者达到了口服孕激素的pCR。据报道口服治疗时疾病进展为6/219(2.7%),初次完全缓解后复发为32/159(20.1%)患者。昆士兰妇科肿瘤中心(QCGC)进行的一项前瞻性先导研究和未发表的回顾性病例系列研究显示,宫内孕激素治疗的1级I期EC患者的加权平均pCR率为68%(95%CI 45-86%)结论:缺乏孕激素在CAH或EC中疗效的高质量证据。但是,现有证据表明,口服或宫内孕激素治疗同样有效。治疗期间进展的风险很小,但需要更长的随访时间。必须进行前瞻性对照临床试验的证据来确定如何进一步改善孕激素治疗CAH和EC的功效。

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