该配方对芳香化酶抑制剂相关肌肉骨骼综合征疗效的影响:一项随机对照试验。
Effects of the efficacy of the formula on aromatase inhibitor associated musculoskeletal syndrome: a randomized controlled trial.
作者信息
Zhang Yan, Chu Meiling, Ye Meina, Cheng Yiqin, Cong Hui, Yin Yulian, Chen Hongfeng
机构信息
Department of Breast Surgery, Longhua Hospital of Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Department of General Surgery, Seventh People's Hospital of Shanghai University of Traditional Chinese Medicine, Shanghai, China.
出版信息
Front Pharmacol. 2025 Jul 25;16:1639714. doi: 10.3389/fphar.2025.1639714. eCollection 2025.
BACKGROUND
Aromatase inhibitor-induced musculoskeletal syndrome (AIMSS) has emerged as a major cause of treatment discontinuation in hormone receptor-positive patients treated with aromatase inhibitors. There are currently no standardized guidelines or universally accepted treatments for AIMSS. Therefore, this exploratory study aimed to preliminarily evaluate the efficacy and safety of Yi Shen Tiao Gan formula in AIMSS patients.
METHODS
A total of 136 patients with AIMSS were included in this single-center, randomized, controlled, single-blind trial and were randomised into the treatment and control groups at a ratio of 1:1. All patients were routinely given Caltrate D. Patients in the treatment group took Breast surgery formula combined with Yi Shen Tiao Gan formula and control group took Breast surgery formula twice a day. The treatment period of Chinese medicine was 3 months as one course of treatment. The clinical efficacy of two courses of treatment was observed in this study. The study observed and compared the following indicators between the two groups: the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scores, Traditional Chinese Medicine symptom and sign scores, bone mineral density, bone metabolism biochemical indicators, bone metabolism-related hormones and safety assessments.
RESULTS
In total, 108 participants were included in the analysis. Before and after treatment, the total WOMAC score of both groups of patients significantly decreased ( < 0.05), with the pain subscale score of the treatment group being significantly lower than that of the control group ( < 0.05). The TCM symptom and sign score significantly decreased in both groups ( < 0.05), with a more pronounced reduction in the treatment group ( < 0.05). The bone mineral density T-score of both groups of patients showed a downward trend. The decrease in the left femoral bone density T-score was smaller in the treatment group, while the decline in the lumbar spine bone density T-score was slower in the control group. There was no significant difference in bone metabolism levels between the two groups ( > 0.05), but the decrease in β-CTX was slightly slower in the treatment group of the AI + OFS population compared to the control group. After applying Bonferroni correction for multiple testing, these associations did not reach statistical significance. No serious adverse events were observed in either group.
CONCLUSION
The YSTG formula significantly reduced WOMAC scores, improving pain, stiffness, physical function in patients with AIMSS, and alleviating the traditional Chinese medicine symptoms and signs of liver and kidney deficiency, thereby enhancing the overall quality of life for patients.
CLINICAL TRIAL REGISTRATION
http://www.chictr.org.cn, identifer ChiCTR2200057785.
背景
芳香化酶抑制剂诱导的肌肉骨骼综合征(AIMSS)已成为接受芳香化酶抑制剂治疗的激素受体阳性患者治疗中断的主要原因。目前尚无针对AIMSS的标准化指南或普遍接受的治疗方法。因此,本探索性研究旨在初步评估益肾调肝方对AIMSS患者的疗效和安全性。
方法
本单中心、随机、对照、单盲试验共纳入136例AIMSS患者,按1:1的比例随机分为治疗组和对照组。所有患者均常规给予钙尔奇D。治疗组患者服用乳癖消方联合益肾调肝方,对照组患者服用乳癖消方,均每日2次。中药治疗期为3个月为1个疗程。本研究观察了两个疗程的临床疗效。研究观察并比较了两组之间的以下指标:西安大略和麦克马斯特大学骨关节炎指数(WOMAC)评分、中医症状体征评分、骨密度、骨代谢生化指标、骨代谢相关激素及安全性评估。
结果
总共108名参与者纳入分析。治疗前后,两组患者的WOMAC总分均显著降低(P<0.05),治疗组的疼痛子量表评分显著低于对照组(P<0.05)。两组的中医症状体征评分均显著降低(P<0.05),治疗组降低更明显(P<0.05)。两组患者的骨密度T值均呈下降趋势。治疗组左股骨骨密度T值下降较小,而对照组腰椎骨密度T值下降较慢。两组骨代谢水平无显著差异(P>0.05),但AI+OFS人群治疗组的β-CTX下降略慢于对照组。在对多重检验应用Bonferroni校正后,这些关联未达到统计学显著性。两组均未观察到严重不良事件。
结论
益肾调肝方显著降低了WOMAC评分,改善了AIMSS患者的疼痛、僵硬、身体功能,并缓解了肝肾亏虚的中医症状体征,从而提高了患者的整体生活质量。
临床试验注册
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