The hepatorenal protective effects of silymarin in cancer patients receiving chemotherapy: a randomized, placebo-controlled trial.

IF 3.3 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE
Safoora Sadat Erfanian, Hourieh Ansari, Shaghayegh Haghjooy Javanmard, Zahra Amini, Ali Hajigholami
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引用次数: 0

Abstract

Background: Breast cancer is one of the most common diseases globally that may have side effects on liver and renal function. Pharmacological treatments to reduce adverse liver and renal effects are still limited. It has been proposed that silymarin may possess hepatoprotective and anti-inflammatory properties. The present trial aims to assess the hepatorenal protective efficacy of silymarin supplementation in cancer patients receiving chemotherapy in an outpatient setting.

Method: This is a randomized, placebo-controlled clinical trial that recruited female breast cancer patients. Participants were randomly assigned to one placebo group and two intervention groups. The control group received 140 mg of placebo daily, while the two intervention groups received 140 mg silymarin daily. Follow-up assessments were conducted at baseline, 3 weeks, and 6 weeks. At the beginning of the study, the patients were subjected to a computed tomography (CT) scan, and the liver and renal parameters such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), bilirubin, Blood urea nitrogen (BUN) and Creatinine (Cr) were examined through laboratory tests.

Results: Despite two deaths and three dropouts, 100 patients completed the study. Silymarin showed significant effects on liver enzymes in the levels of ALP and bilirubin (P < 0.05), with no significant impact on renal function in the levels of Blood urea nitrogen (BUN) and Creatinine (Cr) (P > 0.05). The medication was well-tolerated, with minimal reported side effects (P > 0.05).

Discussion: The study suggests that silymarin may have hepato-renal protective potential in breast cancer patients and improve patient tolerance to chemotherapy. The data presented on the efficacy and safety of silymarin may provide stronger foundation for further trials and for a possible use in clinical practice.

Trial registration information: Registration Number: IRCT20201123049474N2, First Trial Registration: 16/08/2021, Access: https://www.irct.behdasht.gov.ir/trial/57641.

水飞蓟素对接受化疗的癌症患者的肝肾保护作用:随机安慰剂对照试验。
背景:乳腺癌是全球最常见的疾病之一,可能会对肝脏和肾脏功能产生副作用。减少对肝脏和肾脏不良影响的药物治疗仍然有限。有研究认为,水飞蓟素可能具有保肝和抗炎特性。本试验旨在评估在门诊环境中接受化疗的癌症患者补充水飞蓟素的肝肾保护功效:这是一项随机、安慰剂对照临床试验,招募女性乳腺癌患者。参与者被随机分配到一个安慰剂组和两个干预组。对照组每天服用 140 毫克安慰剂,而两个干预组每天服用 140 毫克水飞蓟素。分别在基线、3 周和 6 周进行随访评估。研究开始时,患者接受了计算机断层扫描(CT),并通过实验室检测检查了丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)、碱性磷酸酶(ALP)、胆红素、血尿素氮(BUN)和肌酸酐(Cr)等肝肾指标:尽管有两名患者死亡,三名患者辍学,但仍有 100 名患者完成了研究。水飞蓟素对肝酶中的 ALP 和胆红素水平有明显影响(P 0.05)。药物耐受性良好,副作用极小(P > 0.05):讨论:该研究表明,水飞蓟素可能对乳腺癌患者的肝肾具有保护作用,并能提高患者对化疗的耐受性。有关水飞蓟素疗效和安全性的数据可为进一步试验和临床实践提供更坚实的基础:注册号:IRCT20201123049474N2,首次试验注册:16/08/2021, Access: https://www.irct.behdasht.gov.ir/trial/57641.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Complementary Medicine and Therapies
BMC Complementary Medicine and Therapies INTEGRATIVE & COMPLEMENTARY MEDICINE-
CiteScore
6.10
自引率
2.60%
发文量
300
审稿时长
19 weeks
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