M10MKO: Study With Wee-1 Inhibitor MK-1775 and Carboplatin to Treat p53 Mutated Refractory and Resistant Ovarian Cancer

Sponsor

The Netherlands Cancer Institute (Other)

Overall Status

Active, not recruiting

CT.gov ID

NCT01164995

Collaborator

Merck Sharp & Dohme LLC (Industry)

Enrollment

Location

Arm

143

Duration (Months)

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to determine if patients with p53 mutated epithelial ovarian cancer that have been treated with first line treatment (paclitaxel - carboplatin combination therapy) and that have shown early relapse (within 3 months) or progression during treatment will benefit from treatment with Wee-1 inhibitor MK-1775 and carboplatin.

Condition or Disease	Intervention/Treatment	Phase
Epithelial Ovarian Cancer	Drug: MK-1775 and carboplatin	Phase 2

Detailed Description

Platinum-based drugs are used in first line treatment of epithelial ovarian cancer. Despite high overall initial response rates, resistance or early relapse can occur. MK-1775 is a potent and selective inhibitor of Wee-1 kinase, a kinase that regulates the G2/M checkpoint. Since most human cancers retain p53-related G1 checkpoint abnormalities, they are dependent on the G2 checkpoint. Annulment of the G2 checkpoint may therefore make p53 deficient tumor cells more susceptible to anti-cancer agents. The Phase I study with MK-1775 combined with gemcitabine, carboplatin or cisplatin in patients with advanced solid tumors already confirmed target engagement of MK-1775.

In this study Carboplatin will be administered in combination with MK-1775 in a 21 day cycle. Ovarian cancer patients with a p53 mutation based on PCR/sequencing will be eligible for the study. p53 immunohistochemistry (IHC) wil also be performed.

This study is a proof of concept (POC) study. To proof the hypothesis that MK-1775 is more effective in tumors harboring p53 mutations a single stage study with 21 patients will be performed. The final conclusion will then be made as follows: Applying a A'Hern's Single Stage Phase II Design, a minimum of 6 responses (RECIST 1.0 or CA125) out of 21 patients will provide a 61% power to declare an efficacy of at least a 30% (α=0.05). A response of 13% or less would definitively indicate no efficacy of interest.

Patients will remain on treatment until they no longer have clinical benefit from treatment or when toxicity leads to patient withdrawal. Patients will be followed for at least 30 days following their last dose of study therapy, or until death, whichever comes first.

For patients with stable disease follow-up will take place at least until disease progression has been documented = until time of progression. Patients discontinued from the study for unacceptable adverse experiences will be followed until time of progression and until the resolution or stabilization of the adverse experience. These patients with stable disease at the end of treatment or who discontinued for unacceptable adverse experiences will be evaluated every 2 months at the outpatient department, and CA-125 will be determined. In case of CA-125 increase a CT scan will be performed. In patients for whom CA-125 is not a good marker, a CT-scan will need to be performed every 2 cycles (42 days), until disease progression.

Study Design

Study Type:

Interventional

Actual Enrollment :

24 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase II Pharmacological Study With Wee-1 Inhibitor MK-1775 Combined With Carboplatin in Patients With p53 Mutated Epithelial Ovarian Cancer and Early Relapse (< 3 Months) or Progression During Standard First Line Treatment

Study Start Date :

Jul 1, 2010

Actual Primary Completion Date :

Mar 1, 2014

Anticipated Study Completion Date :

Jun 1, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: MK-1775 and carboplatin MK-1775: oral capsules. Carboplatin: intravenous infusion in 30 minutes	Drug: MK-1775 and carboplatin Carboplatin will be administered in a dose resulting in AUC5 (i.v. 30 min) at day 1 of each cycle. Concomittantly with the start of the carboplatin infusion 225 mg of MK-1775 will be administered as an oral capsule, followed by 4 additional doses at 12 hour increments ( = 5 BID doses of MK-1775 in 2.5 days in total). One cycle will last 21 days. Other Names: CBDCA

Arm

Intervention/Treatment

Experimental: MK-1775 and carboplatin

MK-1775: oral capsules. Carboplatin: intravenous infusion in 30 minutes

Drug: MK-1775 and carboplatin

Carboplatin will be administered in a dose resulting in AUC5 (i.v. 30 min) at day 1 of each cycle. Concomittantly with the start of the carboplatin infusion 225 mg of MK-1775 will be administered as an oral capsule, followed by 4 additional doses at 12 hour increments ( = 5 BID doses of MK-1775 in 2.5 days in total). One cycle will last 21 days.

Other Names:

CBDCA

Outcome Measures

Primary Outcome Measures

Number and percentage of Participants with Adverse Events [During treatment with carboplatin and MK-1775 AEs will be recorded up to 30 days after treatment (or until death whatever comes first). Treatment will occur until progressive disease]
Descriptive tables that summarize the number and percentage of patients that experience adverse events as categorized in the NCI CTCAE version 4.0 will be generated for the overall population. Laboratory assessments: screening/day 1, 8, 15 of each cycle, and regular physical examination at the start of each cycle or on indication will be performed and followed until 30 days after the end of study (defined as disease progression or unacceptable toxicity (AEs) or patient withdrawal or patient death) or in case of AEs or Stable disease until time of progression.
Radiological antitumor activity [As long as the patient is treated with carboplatin and MK-1775 radiological assessments will be performed every 2 cycles (42 days) until progressive disease occurs, and evaluated in comparison to the baseline scan]
Radiological assessment (CT scan or MRI)
Laboratory anti-tumor activity [As long as the patient is treated with carboplatin and MK-1775 CA-125 laboratory assessments will be performed every 2 cycles (42 days) until progressive disease occurs, and evaluated in comparison to baseline CA-125.]
CA-125 will be assessed according to the Gynecologic Cancer Intergroup (GCIG) CA-125 response criteria.

Secondary Outcome Measures

Pharmacokinetics assessments [Cycle 1: day 1, 2, 3]
Pharmacokinetic analysis will be performed by using nonlinear mixed effect modeling (NONMEM). The pharmacokinetic profile of MK-1775, when given in combination with carboplatin, will be determined in plasma and dry blood on day 1,2,3 of cycle 1. Pharmacokinetics of carboplatin, when given in combination with MK-1775, will be determined in plasma and ultrafiltrates on day 1 of cycle 1. Correlations between pharmacokinetic data and toxicity are subsequently analyzed for their significance.
Pharmacodynamic assessments [Cycle 1: Day 1 (pre-dose) and day 3 and Cycle 2: day 1]
Pharmacodynamic changes induced by MK-1775 in combination with carboplatin, measured as changes in pCDC2, will be determined in surrogate tissue (skin). Skin biopsies will be performed on day 1 of cycle 1 (pre-dose) and on day 3 of cycle 1 within 2 hours of the last intake of MK-1775. The relationship of various pharmacokinetic parameters to the pharmacodynamic endpoints will also be explored. Disease response, accompanied by available p53-pathway status, will be descriptively summarized.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Inclusion Criteria:

Histological or cytological proof of epithelial ovarian cancer, and proven p53 mutated pathway by PCR/Sequencing. IHC will also be performed.
Measurable disease on a CT-scan or elevated Cancer Antigen (CA)-125 levels that can be monitored.
Patients previously received standard 1st line platinum therapy (combined with paclitaxel) for epithelial ovarian cancer, and showed recurrence on or within 3 months of this treatment.
Able and willing to voluntarily give written informed consent.
Able and willing to undergo blood sampling for pharmacokinetics and pharmacodynamics.
Life expectancy ≥ 3 months allowing adequate follow up of toxicity evaluation and anti-tumor activity.
Minimal acceptable safety laboratory values:
Absolute neutrophil count (ANC) of ≥ 1.5 x 109 /L (or 1500/m3).
Platelet count of ≥ 100 x 109 /L (or 100,000/mm3).
Hemoglobin ≥ 5.6 mmol/L (or 9.1 g/dl).
Hepatic function as defined by serum bilirubin ≤ 1.5 x ULN, ALAT and ASAT ≤ 2.5 x ULN, or ALAT and ASAT ≥ 5x ULN in case of liver metastases.
Renal function as defined by serum creatinine ≥ 1.5 x ULN or creatinine clearance ≥ 60 ml/min for patients with creatinine levels ≥ 1.5 x ULN (by Cockcroft-Gault formula).
WHO performance status of ≤ 2 on the Eastern Cooperative Oncology Group (ECOG) Performance Scale.
No radio- or chemotherapy within the last 4 weeks prior to study entry (palliative limited radiation for pain reduction is allowed)
Able and willing to swallow oral medication.
Able and willing to receive iv medication.
Negative pregnancy test (urine/serum) for female patients with childbearing potential.

Exclusion Criteria:

Symptomatic cerebral or leptomeningeal metastases.
Current participation or previous participation in a study with an investigational compound, or chemo- and/or radiotherapy within 28 days of receiving first dose of study medication. (Palliative limited radiation for pain reduction is allowed only between day 8 and day 21 of the study, and allowed to a limited area to palliate pain.
No prior radiation therapy to more than 30% of the bone marrow and patient must have recovered for at least 3 weeks from the hematologic toxicity of prior radiotherapy.
More than 1 prior cytotoxic chemotherapy regimen.
Prior stem cell or bone marrow transplant.
Unresolved (> grade 1) toxicities of previous chemotherapy, excluding alopecia.
Known hypersensitivity to the components of the combination study therapy or its analogs.
Patient has had prescription or non-prescription drugs or other products known to be metabolized by CYP3A4, or to inhibit or induce CYP3A4 that cannot be discontinued prior to Day 1 of dosing and withheld throughout the study until 2 days after the last dose of study medication
Bowel obstructions or motility disorders that may negatively affect oral drug absorption.
Patients with known alcoholism, drug addiction and/or a history of psychotic disorders who are not suitable for adequate follow up.
Women who are pregnant or breast feeding.
Fertile women who do not agree to use a reliable contraceptive method throughout the study.
Uncontrolled infectious disease or known Human Immunodeficiency Virus HIV-1 or HIV-2 type patients.
Patients with a known history of hepatitis B or C.
Neurological disease that may render a patient at increased risk for peripheral or central neurotoxicity.
Clinical history suggestive for Li Fraumeni syndrome.