Carboplatin With or Without Decitabine in Treating Patients With Progressive, Advanced Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer

NCT ID: NCT00748527

Last Updated: 2013-07-10

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 134 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-07-31
• Study Completion Date: 2010-11-30

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as carboplatin and decitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. It is not yet known whether carboplatin is more effective with or without decitabine in treating patients with ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer.

PURPOSE: This randomized phase II trial is studying carboplatin and decitabine to see how well they work compared with carboplatin alone in treating patients with progressive, advanced ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer.

Detailed Description

OBJECTIVES:

Primary

• To compare the response rate in patients with progressive, advanced ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer who have methylated hMLH1 DNA in plasma treated with carboplatin with vs without decitabine.

Secondary

• To compare the response rate in all patients (regardless of methylation status) treated with these regimens.
• To compare the progression-free survival and overall survival of patients treated with these regimens.
• To compare the safety and tolerability of these regimens.
• To determine the feasibility of combining decitabine with carboplatin.
• To determine the incidence of hypersensitivity reactions to carboplatin.
• To study the relationship between peak plasma levels of decitabine and global or CpG island specific methylation.
• To study the relationship between global and gene specific methylation in peripheral blood mononuclear cells and response.

Tertiary

• To correlate the methylation status of genes associated with drug resistance detected in plasma DNA with response.
• To determine the sensitivity and specificity of methylation of genes associated with drug resistance detected in plasma DNA as a predictor of methylation status in tumor cells isolated from ascites or tumor biopsy.
• To study methylation and expression of genes in tumor cells isolated from ascites or tumor biopsy before and after treatment with decitabine and/or carboplatin.
• To investigate any correlation between methylation and expression of genes in surrogate tissues, body fluids, or tumor cells and response or progression-free survival.
• To examine markers of cell death in plasma.
• To compare the methylation in tumor taken at the time of presentation vs at the time of treatment.

OUTLINE: This is a multicenter study. Patients are stratified according to prior first-line treatment (platinum alone vs platinum and taxane vs platinum and other combination), WHO performance status (0 vs 1 vs 2), measurable disease criteria (RECIST criteria vs CA-125 criteria vs both), participating center, and the number of prior platinum-based regimens (1 vs 2). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive carboplatin IV over 30-60 minutes on day 1.
• Arm II: Patients receive decitabine IV over 6 hours on day 1 and carboplatin IV over 30-60 minutes on day 8.

In both arms, treatment repeats every 28 days for up to 8 courses in the absence of disease progression or unacceptable toxicity.

Patients undergo blood sample collection periodically for pharmacodynamic studies. Samples are assessed for methylation of hMLH1 by methylation-specific PCR; global DNA methylation by high performance liquid chromatography (HPLC) ; methylation of the MAGE-1A gene promoter by methylation-specific PCR or bisulfite pyrosequencing; and markers of apoptosis by ELISA. Pharmacokinetic studies of decitabine are also performed using blood samples from patients randomized to arm II. Ascitic fluid and/or tumor tissue samples may also be collected for pharmacodynamic studies.

After completion of study treatment, patients are followed at 28 days and then every 2 months thereafter.

Peer Reviewed and Funded or Endorsed by Cancer Research UK.

Conditions

Fallopian Tube Cancer; Ovarian Cancer; Peritoneal Cavity Cancer

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive carboplatin IV over 30-60 minutes on day 1.

Group Type: ACTIVE_COMPARATOR

carboplatin

Intervention Type: DRUG

Given IV

Arm II

Patients receive decitabine IV over 6 hours on day 1 and carboplatin IV over 30-60 minutes on day 8.

Group Type: EXPERIMENTAL

carboplatin

Intervention Type: DRUG

Given IV

decitabine

Intervention Type: DRUG

Given IV

Interventions

carboplatin

Given IV

Intervention Type: DRUG

decitabine

Given IV

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients with disease progression, as defined by GCIG guidelines, within 12 months after completion of their last treatment are eligible provided study treatment commences ≤ 14 months after the last prior treatment
• Measurable disease by RECIST criteria and/or CA-125 criteria

• Measurable lesions are defined as those that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 20 mm by conventional techniques (physical examination, CT scan, x-ray, or MRI) or as ≥ 10 mm by spiral CT scan
• Patients with evaluable disease by CA-125 criteria are eligible provided CA-125 is ≥ 2 times upper limit of normal (ULN) within 2 weeks prior to initiating study treatment
• Disease is not considered measurable if patient received prior mouse antibodies or if there has been medical and/or surgical interference with the peritoneum or pleura (e.g., paracentesis) within the past 28 days
• Ascites requiring therapeutic drainage allowed only if there is measurable disease by RECIST criteria

• Ascites that do not require therapeutic drainage allowed even if disease is evaluable by CA-125 criteria alone

PATIENT CHARACTERISTICS:

• WHO performance status 0-2
• Hemoglobin ≥ 10.0 g/dL
• WBC ≥ 3.0 x 10^9/L
• Neutrophil count ≥ 1.5 x 10^9/L
• Platelet count ≥ 100 x 10^9/L
• Bilirubin ≤ 30 μmol/L
• ALT and/or AST ≤ 2.5 times ULN (≤ 5 times ULN if due to tumor involvement of liver)
• EDTA/DTPA clearance ≥ 50 mL/min (uncorrected value)
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception for 4 weeks prior to, during, and for 6 months after completion of study treatment
• No known hepatitis B, hepatitis C, or HIV positivity
• No non-malignant systemic disease, including active uncontrolled infection, that would make the patient a high medical risk
• No other current malignancies, except adequately treated cone-biopsied in situ carcinoma of the cervix or basal cell or squamous cell carcinoma of the skin

• Patients who have undergone potentially curative therapy for a prior malignancy are eligible provided there is no evidence of disease for ≥ 5 years and the patient is deemed to be at low risk for recurrence
• No intolerance to carboplatin (with a dose of ≥ AUC 5), as defined by any of the following:

• Neutropenia or thrombocytopenia causing dose delay of > 4 days on more than 2 occasions
• Grade III or IV hypersensitivity reaction (not controlled by a desensitization regimen)
• Hospitalization for confirmed febrile neutropenia (fever ≥ 38°C)
• Requirement for platelet transfusion
• No other condition that, in the investigator's opinion, would not make the patient a good candidate for this study

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• Recovered from prior therapy (alopecia, grade 1 neuropathy, and certain grade 1 toxicities allowed)
• More than 28 days since prior maintenance therapy (e.g., erlotinib or bevacizumab)
• More than 4 weeks since prior radiotherapy, endocrine therapy, immunotherapy, chemotherapy, biological therapy, or investigational agents
• More than 4 weeks since prior major thoracic and/or abdominal surgery and recovered
• No other concurrent anti-cancer therapy, including radiotherapy or investigational drugs

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cancer Research UK

OTHER

Sponsor Role: lead

Principal Investigators

Stanley B. Kaye, MD, FRCP

Role: STUDY_CHAIR

Royal Marsden NHS Foundation Trust

Locations

Leeds Cancer Centre at St. James's University Hospital

Leeds, England, United Kingdom

Leicester Royal Infirmary

Leicester, England, United Kingdom

Saint Bartholomew's Hospital

London, England, United Kingdom

Royal Marsden - London

London, England, United Kingdom

Hammersmith Hospital

London, England, United Kingdom

Mount Vernon Cancer Centre at Mount Vernon Hospital

Northwood, England, United Kingdom

Royal Marsden - Surrey

Sutton, England, United Kingdom

Weston General Hospital

Weston-super-Mare, England, United Kingdom

Belfast City Hospital Trust Incorporating Belvoir Park Hospital

Belfast, Northern Ireland, United Kingdom

Edinburgh Cancer Centre at Western General Hospital

Edinburgh, Scotland, United Kingdom

Beatson West of Scotland Cancer Centre

Glasgow, Scotland, United Kingdom

Countries

United Kingdom

Other Identifiers

CDR0000613805

Identifier Type: REGISTRY

Identifier Source: secondary_id

EUDRACT-2006-002324-41

Identifier Type: -

Identifier Source: secondary_id

MGI-CRUK-PH2/051

Identifier Type: -

Identifier Source: secondary_id

CTA-21106/0219/001

Identifier Type: -

Identifier Source: secondary_id

CRUK-PH2/051

Identifier Type: -

Identifier Source: org_study_id

NCT00514124

Identifier Type: -

Identifier Source: nct_alias