Docetaxel With or Without Phenoxodiol in Treating Patients With Recurrent Advanced Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cavity Cancer

NCT ID: NCT00303888

Last Updated: 2018-01-17

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-05-31
• Study Completion Date: 2009-10-31

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Phenoxodiol may help docetaxel work better by making tumor cells more sensitive to the drug.

PURPOSE: This randomized phase I/II trial is studying the side effects of docetaxel when given together with either phenoxodiol or placebo and to see how well it works in treating patients with recurrent advanced ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cavity cancer.

Detailed Description

OBJECTIVES:

Primary

• Determine the safety and tolerability of combination therapy comprising phenoxodiol and docetaxel in patients with recurrent or persistent advanced ovarian epithelial, fallopian tube, or primary peritoneal cavity cancer.

Secondary

• Determine the effect of phenoxodiol on the toxicity of docetaxel using a weekly treatment regimen.
• Determine if combination therapy comprising phenoxodiol and docetaxel is more efficacious than docetaxel therapy alone.
• Determine if combination therapy comprising phenoxodiol and docetaxel affects blood levels of either drug.
• Determine phenotypic differences in the tumor cells of "responders" and "non-responders."

OUTLINE: This is a randomized, placebo-controlled, double-blind study. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive docetaxel IV over 1 hour on days 1, 8, and 15 and oral placebo three times daily on days 1-21.
• Arm II: Patients receive oral phenoxodiol three times daily on days 1-21 and docetaxel as in arm I.

Treatment in both arms repeats every 4 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed monthly for 6 months, every 3 months for 1 year, and then annually thereafter.

PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.

3/31/2017 NOTE

This study was terminated 10/2009 due to lack of enrollment. The study never progressed to Phase 2.

Conditions

Fallopian Tube Cancer; Ovarian Cancer; Primary Peritoneal Cavity Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Arm I

Patients receive docetaxel IV over 1 hour on days 1, 8, and 15 and oral placebo three times daily on days 1-21.

Group Type: EXPERIMENTAL

docetaxel

Intervention Type: DRUG

Given IV

placebo

Intervention Type: OTHER

Given orally

Arm II

Patients receive oral phenoxodiol three times daily on days 1-21 and docetaxel IV over 1 hour on days 1, 8, and 15.

Group Type: EXPERIMENTAL

docetaxel

Intervention Type: DRUG

Given IV

idronoxil

Intervention Type: DRUG

Given orally

Interventions

docetaxel

Given IV

Intervention Type: DRUG

idronoxil

Given orally

Intervention Type: DRUG

placebo

Given orally

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Received platinum and taxane combination chemotherapy as first-line treatment with disease recurrence > 6 months after conclusion of therapy

• No demonstrated refractoriness or resistance to weekly docetaxel
• Meets 1 of the following criteria:

• Doubling of blood levels of CA125 in the past 6 months and CA125 levels ≥ 2 times upper limit of normal (ULN)
• Measurable disease defined as ≥ 1 lesion ≥ 20 mm by conventional techniques or ≥ 10 mm by spiral CT scan
• No active CNS metastases

• Prior CNS metastases allowed provided they were treated with radiation therapy and disease has been stable for 4 weeks

PATIENT CHARACTERISTICS:

• Karnofsky performance score ≥ 60%
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for 3 months after completion of study treatment
• Life expectancy ≥ 3 months
• Creatinine ≤ 1.5 mg/dL
• Transaminases ≤ 3 times upper limit of normal (ULN)
• Bilirubin normal
• Platelet count > 100,000/mm^3
• WBC > 3,000/mm^3
• Neutrophil count > 1,500/mm^3
• Hemoglobin ≥ 8.0 g/dL
• Peripheral neuropathy ≤ grade 1
• Relative proportions of AST, ALT, and alkaline phosphatase according 1 to the following criteria:

• Alkaline phosphatase (AP) normal AND AST/ALT ≤ 5 times ULN
• AP ≤ 2.5 times ULN AND AST/ALT ≤ 1.5 times ULN
• AP ≤ 5 times ULN AND AST/ALT normal
• No active infection
• No concurrent severe and/or uncontrolled medical disease (e.g., uncontrolled diabetes, hypertension, ischemic heart disease, or congestive heart failure)
• No history of chronic active hepatitis or cirrhosis
• No history of severe hypersensitivity to docetaxel or other drugs formulated with polysorbate 80

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• No investigational agents within 4 weeks prior to study entry
• Recovered from prior antineoplastic therapy
• No other concurrent investigational drugs
• No other concurrent chemotherapy, radiotherapy, immunotherapy, or hormonal antitumor therapy

• Concurrent localized radiation therapy allowed for control of local disease complications (e.g., bone metastases) that do not represent a general progression of the disease status
• No concurrent grapefruit or grapefruit juice
• No concurrent amifostine

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 120 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Yale University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Thomas J. Rutherford, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

Yale Cancer Center

New Haven, Connecticut, United States

Countries

United States

Other Identifiers

YALE-HIC-27640

Identifier Type: -

Identifier Source: secondary_id

YALE-012705

Identifier Type: -

Identifier Source: secondary_id

0504027640

Identifier Type: -

Identifier Source: org_study_id