Ixabepilone and Liposomal Doxorubicin in Advanced Ovarian Cancer

Completed · Phase 1/Phase 2

Conditions studied: Fallopian Tube Cancer, Female Reproductive Cancer, Recurrent Breast Cancer, Recurrent Ovarian Epithelial Cancer, Stage III Ovarian Epithelial Cancer, Stage IV Breast Cancer, Stage IV Ovarian Epithelial Cancer

In brief

This trial is studying the side effects and best dose of ixabepilone when given together with pegylated liposomal doxorubicin hydrochloride and to see how well they work in treating women with advanced ovarian epithelial, primary peritoneal cavity, or fallopian tube cancer or metastatic breast cancer. Drugs used in chemotherapy, such as ixabepilone and pegylated liposomal doxorubicin hydrochloride, 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.

Key facts

Study ID

NCT00182767

Run by

National Cancer Institute (NCI)

People needed

45

Starts

2006-01-01

Expected to finish

2014-05-01

Last updated by the study team

2016-03-10

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Histologically or cytologically confirmed diagnosis of 1 of the following: advanced ovarian epithelial, primary peritoneal cavity, or fallopian tube cancer (phase I and II) or metastatic breast cancer (phase I only).
• Platinum- and taxane-resistant disease, defined as a disease-free interval of < 6 months after completion of platinum- and taxane-based chemotherapy. Disease progression during the regimen (phase II) or previously treated with >= 2 prior regimens for metastatic breast cancer, including 1 taxane-based regimen in the adjuvant or metastatic setting (phase I).
• Meets 1 of the following criteria: Previously treated with a standard course of taxane- and platinum-based chemotherapy for ovarian epithelial, primary peritoneal cavity, or fallopian tube cancer, that is platinum-refractory or -sensitive disease (phase I );
• Measurable or evaluable disease, meeting 1 of the following criteria: unidimensionally measurable lesion, known disease and CA 125 > 50 U/mL on 2 occasions >= 1 week apart or known disease and CA 27-29, CA 15-3, or CA 125 > 50 U/mL on 2 occasions >= 1 week apart (for breast cancer patients)
• ECOG 0-2 or Karnofsky 60-100%
• At least 3 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered.
• At least 1 week since prior chemotherapy if given on a daily or weekly schedule and recovered.
• At least 3 weeks since prior radiotherapy and recovered.
• Recovered for more than 4 weeks from all adverse events related to prior agents.
• Normal organ function including:
• Normal bilirubin
• WBC >= 3,000/mm3
• Absolute neutrophil count >= 1,500/mm3
• Platelet count >= 100,000/mm3
• AST and ALT =< 2.5 times upper limit of normal (ULN)
• Creatinine =< 1.5 times ULN or Creatinine clearance ≥ 60 mL/min

You may not qualify if…

• No other concurrent investigational agents.
• No concurrent combination antiretroviral therapy for HIV-positive patients.
• No other concurrent anticancer therapy.
• Has received a previous chemotherapy regimen for this cancer that included drugs such as docetaxel or paclitaxel.
• Life expectancy of more than 3 months
• No symptomatic congestive heart failure
• No unstable angina pectoris
• No cardiac arrhythmia
• Not pregnant or nursing
• Fertile patients must use effective contraception
• No history of allergic reaction attributed to compounds of similar chemical or biological composition to Cremophor® or study drugs
• No neuropathy >= grade 2
• No ongoing or active infection
• No psychiatric illness or social situation that would preclude study compliance.
• No other uncontrolled illness.
• No active brain metastases, including any of the following: evidence of cerebral edema by CT scan or MRI, evidence of disease progression on prior imaging studies, requirement for steroids or clinical symptoms of brain metastasis.

Where it is running

• University of Connecticut — Farmington, Connecticut, United States
• Women's Cancer Care Associates LLC — Albany, New York, United States
• Weill Medical College of Cornell University — New York, New York, United States
• Albert Einstein College of Medicine — The Bronx, New York, United States
• Montefiore Medical Center - Moses Campus — The Bronx, New York, United States

Full record on ClinicalTrials.gov

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