Study of Metformin With Carboplatin/Paclitaxel Chemotherapy in Patients With Advanced Ovarian Cancer (OVMET)

University Medical Center Groningen (UMCG)

Status and phase

Completed

Phase 1

Conditions

Epithelial Ovarian Cancer

Treatments

Drug: Carboplatin

Drug: Paclitaxel

Drug: Metformin

Study type

Interventional

Funder types

Other

Identifiers

NCT02312661

30102012

Details and patient eligibility

About

Molecularly targeted agents which inhibit the mammalian target of rapamycin (mTOR) pathway and/or circumvent p53 in the induction of apoptosis are exciting potential targets in ovarian cancer. Metformin is a biguanide, widely used in the treatment of type 2 diabetes mellitus, that has shown anti-cancer activity in preclinical studies. The main mechanism of metformin's effect is mTOR pathway inhibition and, in addition, it has been shown to circumvent p53-induced apoptosis making it an exciting, potentially effective drug in ovarian cancer.

Full description

A phase Ib, single-centre, dose-escalation trial with a traditional escalation rule with fixed dose levels ("3 + 3" rule). The recommended phase II dose will be defined as the maximum predefined dose level at which 0 of 3 or ≤ 1 of 6 subjects experience a drug-related dose limiting toxicity (DLT) during cycle 1 and 2 of treatment. An estimated 10-20 patients will be required for this study.

Enrollment

15 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with advanced stage (FIGO III-IV), histologically confirmed and documented epithelial ovarian carcinoma
Patients eligible for neo-adjuvant carboplatin/paclitaxel chemotherapy prior to surgical debulking OR patients with relapsed or progressive ovarian cancer after initial treatment eligible for palliative carboplatin/paclitaxel chemotherapy
Eastern Cooperative Oncology Group-performance status (ECOG-PS) of 0-2
Age ≥ 18 years
Laboratory Requirements - within 7 days prior to enrolment:
absolute neutrophil count (ANC) ≥1.5 x 109/L
platelets > 100 x 109/L
hemoglobin >9g/dl. Patients may be transfused or use erythropoietin to maintain hemoglobin values ≥ 9 g/dl.
hepatic function: bilirubin ≤1.5×upper limit of normal (ULN), aspartate aminotransferase (AST)/ALT≤2.5×ULN
estimated creatinine clearance ≥ 60ml/min
Before patient registration/randomization, written informed consent for the trial must be given according to International Conference on Harmonisation (ICH)/ good clinical practice (GCP), and national/local regulations.

Exclusion criteria

Current or recent (within 30 days of first study dosing) treatment with another investigational drug or participation in another investigational study.
Metformin within 4 weeks prior to enrolment.
Symptomatic central nervous system (CNS) metastasis
Pre-existing peripheral neuropathy ≥ Common toxicity criteria (CTC) grade 2.
Pregnant or lactating females. Serum pregnancy test to be assessed within 7 days prior to study treatment start, or within 14 days with a confirmatory urine pregnancy test within 7 days prior to study treatment start.
Women of childbearing potential (defined as <2 years after last menstruation and not surgically sterile) not using effective, non-hormonal means of contraception (intrauterine contraceptive device, barrier method of contraception in conjunction with spermicidal jelly) during the study and for 6 months after the last study medication.
Known hypersensitivity to any of the study drugs or excipients.
Serious active infection requiring i.v. antibiotics at enrolment.
Unstable medical conditions.
Evidence of any other medical conditions, physical examination or laboratory findings that may interfere with the planned treatment, affect patient compliance or place the patient at high risk from treatment related complications.