RecruitingPhase 2NCT05550415

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


Sponsor

Indonesia University

Enrollment

26 participants

Start Date

Aug 19, 2022

Study Type

INTERVENTIONAL

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.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating whether adding the cholesterol-lowering drug simvastatin to standard chemotherapy can slow the spread of triple-negative breast cancer — one of the most aggressive types of breast cancer, which lacks the three common hormone or protein receptors. **You may be eligible if...** - You are a woman over 18 years old - You have been diagnosed with advanced triple-negative breast cancer, confirmed by biopsy - You are scheduled to receive 8 cycles of AC-T chemotherapy (a standard breast cancer regimen) - You are willing to sign informed consent **You may NOT be eligible if...** - You are pregnant or breastfeeding - You have already received chemotherapy for this cancer - You are currently taking a statin drug like simvastatin - You are allergic to statins Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSimvastatin 40mg

The administration of Simvastatin 40 mg in addition to ACT regiment of neoadjuvant chemotherapy

DRUGPlacebo

The administration of Placebo capsule 40 mg in addition to ACT regiment of neoadjuvant chemotherapy


Locations(1)

Dr. Cipto Mangunkusumo National Central General Hospital

Jakarta Pusat, DKI Jakarta, Indonesia

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NCT05550415