The Role of Simvastatin in The Epithelial-Mesenchymal Transition Process of Breast Cancer
Vimentin Expression-based Therapeutic Response in Triple Negative Breast Cancer Receiving Combination of Simvastatin and NAC: A Randomized, Double-Blind, Placebo-Controlled Trial
Introduction: Most cases of Triple Negative Breast Cancer (TNBC) have a high proliferation rate. TNBC is associated with a poor prognosis, a high recurrence rate, and a high incidence of distant metastases. The Epithelial-Mesenchymal Transition process (EMT) plays an essential role in the metastatic process. EMT markers were also more abundant in TNBC and contributed to a poorer TNBC prognosis. As an important EMT marker, the increased expression of vimentin also contributed to the increase in TNBC aggressiveness and resistance to chemotherapeutic agents. Through the mechanism of action in inhibiting the mevalonate pathway, statins can help inhibit the EMT process in metastases. Notably, simvastatin promotes the down-regulation of vimentin in breast cancer cells. The combination of statins and neoadjuvant chemotherapy (NAC) improves the cancer patient's response. This study is expected to evaluate the role of a combination between NAC and simvastatin on therapeutic response in TNBC patients through vimentin expression.
Methods: This study is a double-blind, randomized, placebo-controlled trial conducted in Dr. Cipto Mangunkusumo National Central General Hospital. An expected total of 26 TNBC patients will be assessed for eligibility and asked for informed consent. Patients with the plan to have ACT (Doxorubicin hydrochloride, Cyclophosphamide, Paclitaxel) chemotherapy regimen will receive either a combination of ACT-Simvastatin (40 mg/day) or ACT-Placebo. The biopsy will be taken pre-NAC to make the histopathological diagnosis and examine the expression of vimentin. Patients will be evaluated for adverse effects reaction every cycle and the clinical response after 8 cycles. The post-intervention biopsy will be conducted after the cycle finish. The pathological response and vimentin expression will be reviewed from the obtained samples.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Erwin D Yulian, MD
- 电话号码:+6281315249627
- 邮箱:erwin.yulian@ui.ac.id
学习地点
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DKI Jakarta
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Jakarta Pusat、DKI Jakarta、印度尼西亚、10430
- 招聘中
- Dr. Cipto Mangunkusumo National Central General Hospital
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接触:
- Erwin D Yulian, MD
- 电话号码:+6281315249627
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Female patients with advanced breast cancer (locally advanced and distantly advanced) with triple-negative molecular type confirmed by biopsy and immunohistochemical examination.
- The patient planned to receive 8 cycles of AC-T chemotherapy.
- Patient age > 18 years.
- Willing to participate in research by signing informed consent.
Exclusion Criteria:
- The patient is pregnant or breastfeeding.
- Patients who have received chemotherapy or are on simvastatin therapy.
- Allergy to statins.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Simvastatin
The group received standard treatment with simvastatin 40mg in capsule by oral route, once a day, for 21 days (every cycle of the chemotherapy regiment) |
The administration of Simvastatin 40 mg in addition to ACT regiment of neoadjuvant chemotherapy
其他名称:
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安慰剂比较:Placebo
The group received standard treatment with placebo 40mg in capsule by oral route, once a day, for 21 days (every cycle of the chemotherapy regiment) |
The administration of Placebo capsule 40 mg in addition to ACT regiment of neoadjuvant chemotherapy
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Vimentin Expression
大体时间:6 months
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Vimentin expression is measured based on Histoscore (H-Score) with immunohistochemistry examination:
|
6 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Pathological Response
大体时间:6 months
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Pathological Response as Measured by Miller-Payne system Evaluation before and after chemotherapy, divided into:
|
6 months
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Clinical Response
大体时间:6 months
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Clinical response based on WHO (World Health Organization) criteria:
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6 months
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合作者和调查者
调查人员
- 首席研究员:Erwin D Yulian, MD、Surgical Oncology Division, Department of Surgery, Universitas Indonesia
- 研究主任:Tantri Hellyanti, MD、Department of Pathological Anatomy, Universitas Indonesia
- 学习椅:Shabrina Adzania, MD、Research Assistant, Department of Surgery, Universitas Indonesia
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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