此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

The Role of Simvastatin in The Epithelial-Mesenchymal Transition Process of Breast Cancer

2026年9月16日 更新者:Dr. dr. Erwin Danil Yulian, Sp.B (K) Onk、Universitas Indonesia

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

介入性

注册 (估计的)

26

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • DKI Jakarta
      • Jakarta Pusat、DKI Jakarta、印度尼西亚、10430
        • 招聘中
        • Dr. Cipto Mangunkusumo National Central General Hospital
        • 接触:
          • Erwin D Yulian, MD
          • 电话号码:+6281315249627

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

女性

描述

Inclusion Criteria:

  1. Female patients with advanced breast cancer (locally advanced and distantly advanced) with triple-negative molecular type confirmed by biopsy and immunohistochemical examination.
  2. The patient planned to receive 8 cycles of AC-T chemotherapy.
  3. Patient age > 18 years.
  4. Willing to participate in research by signing informed consent.

Exclusion Criteria:

  1. The patient is pregnant or breastfeeding.
  2. Patients who have received chemotherapy or are on simvastatin therapy.
  3. Allergy to statins.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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
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:
  • 辛伐他汀
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:
  • 安慰剂口服胶囊 40 毫克

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
Vimentin Expression
大体时间:6 months

Vimentin expression is measured based on Histoscore (H-Score) with immunohistochemistry examination:

  • 0-50 : negative (0)
  • 51-100 : weak positive (1+)
  • 101-200 : moderate positive (2+)
  • 201-300 : strong positive (3+)
6 months

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

Pathological Response as Measured by Miller-Payne system

Evaluation before and after chemotherapy, divided into:

  1. Grade 1: There is no significant change or reduction in cancer cells.
  2. Grade 2: Reduction of <30% cancer cells
  3. Grade 3: Reduction of cancer cells between 30-90%
  4. Grade 4: Reduction of > 90% cancer cells
  5. Grade 5 : There are no residual cancer cells. DCIS (Ductal Carcinoma In Situ) might be detected.
6 months
Clinical Response
大体时间:6 months

Clinical response based on WHO (World Health Organization) criteria:

  1. Complete Response (CR): Disappearance
  2. Partial Response (PR): 50% decrease
  3. Stable Disease(SD): Neither PR nor PD criteria met
  4. Progressive Disease (PD):25% increase; no CR, PR, or SD documented before increased disease
6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

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

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2022年8月19日

初级完成 (估计的)

2026年11月1日

研究完成 (估计的)

2026年12月1日

研究注册日期

首次提交

2022年9月19日

首先提交符合 QC 标准的

2022年9月19日

首次发布 (实际的)

2022年9月22日

研究记录更新

最后更新发布 (实际的)

2026年9月21日

上次提交的符合 QC 标准的更新

2026年9月16日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅