The Role of Simvastatin in The Epithelial-Mesenchymal Transition Process of Breast Cancer
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: 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) |
Drug: Simvastatin 40mg
The administration of Simvastatin 40 mg in addition to ACT regiment of neoadjuvant chemotherapy
Other Names:
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| Placebo Comparator: 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) |
Drug: Placebo
The administration of Placebo capsule 40 mg in addition to ACT regiment of neoadjuvant chemotherapy
Other Names:
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Outcome Measures
Primary Outcome Measures
- Vimentin Expression [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+)
Secondary Outcome Measures
- Pathological Response [6 months]
Pathological Response as Measured by Miller-Payne system Evaluation before and after chemotherapy, divided into: Grade 1: There is no significant change or reduction in cancer cells. Grade 2: Reduction of <30% cancer cells Grade 3: Reduction of cancer cells between 30-90% Grade 4: Reduction of > 90% cancer cells Grade 5 : There are no residual cancer cells. DCIS (Ductal Carcinoma In Situ) might be detected.
- Clinical Response [6 months]
Clinical response based on WHO (World Health Organization) criteria: Complete Response (CR): Disappearance Partial Response (PR): 50% decrease Stable Disease(SD): Neither PR nor PD criteria met Progressive Disease (PD):25% increase; no CR, PR, or SD documented before increased disease
Eligibility Criteria
Criteria
Inclusion Criteria:
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Female patients with advanced breast cancer (locally advanced and distantly advanced) with triple-negative molecular type confirmed by biopsy and immunohistochemical examination.
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The patient planned to receive 8 cycles of AC-T chemotherapy.
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Patient age > 18 years.
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Willing to participate in research by signing informed consent.
Exclusion Criteria:
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The patient is pregnant or breastfeeding.
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Patients who have received chemotherapy or are on simvastatin therapy.
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Allergy to statins.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Dr. Cipto Mangunkusumo National Central General Hospital | Jakarta Pusat | DKI Jakarta | Indonesia | 10430 |
Sponsors and Collaborators
- Indonesia University
Investigators
- Principal Investigator: Erwin D Yulian, MD, Surgical Oncology Division, Department of Surgery, Universitas Indonesia
- Study Director: Tantri Hellyanti, MD, Department of Pathological Anatomy, Universitas Indonesia
- Study Chair: Shabrina Adzania, MD, Research Assistant, Department of Surgery, Universitas Indonesia
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- IndonesiaU2022