- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT05550415
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.
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
- Navn: Erwin D Yulian, MD
- Telefonnummer: +6281315249627
- E-post: erwin.yulian@ui.ac.id
Studiesteder
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-
DKI Jakarta
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Jakarta Pusat, DKI Jakarta, Indonesia, 10430
- Rekruttering
- Dr. Cipto Mangunkusumo National Central General Hospital
-
Ta kontakt med:
- Erwin D Yulian, MD
- Telefonnummer: +6281315249627
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: 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
Andre navn:
|
|
Placebo komparator: 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
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Vimentin Expression
Tidsramme: 6 months
|
Vimentin expression is measured based on Histoscore (H-Score) with immunohistochemistry examination:
|
6 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Pathological Response
Tidsramme: 6 months
|
Pathological Response as Measured by Miller-Payne system Evaluation before and after chemotherapy, divided into:
|
6 months
|
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Clinical Response
Tidsramme: 6 months
|
Clinical response based on WHO (World Health Organization) criteria:
|
6 months
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Erwin D Yulian, MD, Surgical Oncology Division, Department of Surgery, Universitas Indonesia
- Studieleder: Tantri Hellyanti, MD, Department of Pathological Anatomy, Universitas Indonesia
- Studiestol: Shabrina Adzania, MD, Research Assistant, Department of Surgery, Universitas Indonesia
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Neoplasmer etter nettsted
- Neoplasmer
- Hudsykdommer
- Bryst sykdommer
- Brystneoplasmer
- Hud- og bindevevssykdommer
- Trippel negative brystneoplasmer
- Organiske kjemikalier
- Hydrokarboner
- Hydrokarboner, syklisk
- Naftalener
- Polysykliske aromatiske hydrokarboner
- Hydrokarboner, aromatisk
- Polysykliske forbindelser
- Lovastatin
- Simvastatin
Andre studie-ID-numre
- IndonesiaU2022
Legemiddel- og utstyrsinformasjon, studiedokumenter
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