Department of Breast Tumor Surgery, Zhejiang Cancer Hospital, Hangzhou, PR China.
Department of Orthopedics, 413 Hospital of PLA, Zhoushan, PR China.
J Ethnopharmacol. 2019 Jun 28;238:111840. doi: 10.1016/j.jep.2019.111840. Epub 2019 Mar 29.
Cimicifuga racemose is previously proved effective on nature menopausal syndrome (MPS). However, its clinical value in treating with MPS induced by luteinizing-hormone releasing hormone analogue (LHRH-a) therapy of pre-/peri-menopausal breast cancer patients is still unknown.
This perspective randomised-design study is to investigate the effect and safety of cimicifuga racemosa on MPS induced by LHRH-a in breast cancer (clinical trial registered: NCT03339882).
Breast cancer patients planning for LHRH-a treatment were randomly divided into 2 groups. The control group which was being treated with the standard treatment of LHRH-a. The other group was being treated with Remifemin, the commercialized product of cimicifuga racemose extract, combined with LHRH-a, called Remifemin group. Our main endpoint was Kupperman menopause index (KMI). Hormone levels in peripheral blood and gynecological complications were also evaluated.
Totally, 85 patients (42 in Remifemin group and 43 in control group) were enrolled in Zhejiang Cancer Hospital. At the 4th, 8th and 12th week after using LHRH-a, the KMI were all significantly lower in Remifemin group than in control group (P < 0.01), while the hormone levels, including estradiol (E), follicle-stimulating hormone (FSH) and luteinizing hormone (LH) were similar in the two groups. In addition, the incidence of cervical cyst in Remifemin group was higher than that in control group (P = 0.02), and there was no significant difference in the other gynecological complications, including endometrial thickening, ovarian cyst or uterine fibroid (P > 0.05).
Cimicifuga racemose is effective, oncological safe and reliable for treatment of MPS caused by LHRH-a in breast cancer.
升麻属植物先前已被证明对自然绝经综合征(MPS)有效。然而,其在治疗因黄体生成素释放激素类似物(LHRH-a)治疗绝经前/围绝经期乳腺癌患者引起的 MPS 的临床价值尚不清楚。
本前瞻性随机设计研究旨在探讨升麻属植物对 LHRH-a 诱导的乳腺癌(临床试验注册:NCT03339882)中 MPS 的疗效和安全性。
计划接受 LHRH-a 治疗的乳腺癌患者被随机分为 2 组。对照组接受 LHRH-a 的标准治疗,另一组接受 Remifemin(升麻属植物提取物的商业化产品)联合 LHRH-a 治疗,称为 Remifemin 组。我们的主要终点是 Kupperman 绝经指数(KMI)。还评估了外周血激素水平和妇科并发症。
共有 85 名患者(Remifemin 组 42 名,对照组 43 名)入组浙江肿瘤医院。在使用 LHRH-a 后的第 4、8 和 12 周,Remifemin 组的 KMI 均明显低于对照组(P<0.01),而两组的激素水平,包括雌二醇(E)、卵泡刺激素(FSH)和黄体生成素(LH)相似。此外,Remifemin 组宫颈囊肿的发生率高于对照组(P=0.02),而子宫内膜增厚、卵巢囊肿或子宫肌瘤等其他妇科并发症无显著差异(P>0.05)。
升麻属植物对 LHRH-a 治疗乳腺癌引起的 MPS 有效、肿瘤安全可靠。