Phase 2 Study of Twice Weekly VELCADE and CAELYX in Patients With Ovarian Cancer Failing Platinum Containing Regimens

NCT ID: NCT00610792

Last Updated: 2009-07-14

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Total Enrollment: 91 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-07-31

Brief Summary

This a Phase 2, multicenter open label, uncontrolled 2-step design. Patients will be arranged in two groups based upon the response to their last platinum containing therapy. The two groups are, 1) Platinum Resistant Patients: patients with progressive disease while on platinum containing therapy or stable disease after at least 4 cycles; patients relapsing following an objective response while still receiving treatment; patients relapsing after an objective response within 6 months from the discontinuation of the last chemotherapy and 2) Platinum-Sensitive Patients: patients who relapsed following an objective response after 6 months from the discontinuation of platinum containing chemotherapy. All patients will receive pyridoxine at least 200mg by mouth daily beginning approximately one week prior to the initiation of the combination chemotherapy and it will continue up to the end of the last treatment cycle.

Conditions

Ovarian Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

Group Type: EXPERIMENTAL

bortezomib

Intervention Type: DRUG

1.3 mg/m2 on Days 1, 4, 8 \& 11 every 3 weeks (1 cycle = 21 days) for up to six cycles

pegylated liposomal doxorubicin

Intervention Type: DRUG

30 mg/m2 on Day 1 every 3 weeks (1 cycle = 21 days) for up to six cycles

Interventions

bortezomib

1.3 mg/m2 on Days 1, 4, 8 \& 11 every 3 weeks (1 cycle = 21 days) for up to six cycles

Intervention Type: DRUG

pegylated liposomal doxorubicin

30 mg/m2 on Day 1 every 3 weeks (1 cycle = 21 days) for up to six cycles

Intervention Type: DRUG

Other Intervention Names

VELCADE; CAELYX

Eligibility Criteria

Inclusion Criteria

• Histologically/cytologically confirmed diagnosis of ovarian carcinoma of epithelial origin, primary tubal or peritoneal carcinoma;
• Progressive or recurrent disease
• The following patient types based upon the disease measurability may enroll in this study and will be considered for efficacy evaluation.

Patients may have measurable disease strictly following the RECIST guidelines. CA125 levels must be obtained according to the Rustin guidelines to enable a complete evaluation of response/progressive disease according to the GCIG guidelines. Patients may enter with a solitary measurable lesion which has not been confirmed by histology/cytology. These patients will be considered evaluable for response according to a modified RECIST which will not require the histological/cytological confirmation of the lesion. CA125 levels must be obtained according to the Rustin guidelines to enable a complete evaluation of progressive disease according to the GCIG guidelines. Patients with non-measurable disease will be considered evaluable for response provided CA125 data has been collected according to the Rustin guidelines and a complete evaluation of response/progressive disease according to the GCIG guidelines maybe conducted.

• Numbers of prior chemotherapy(s): maximum 2 prior chemotherapies. Reintroduction of a platinum at relapse, after an initial response lasting > 6 months is considered 1 chemotherapy regimen only.
• ECOG performance status grade 0 or 1
• Age ≥ 18 and ≤ 75 yrs
• Adequate hematological, liver and renal function (hemoglobin ≥ 9 g/dL, absolute neutrophil count (ANC) ≥ 1.50 x 109/L; platelets ≥ 100 x 109/L, bilirubin within UNL; alkaline phosphatase ≤ 1.5 x UNL; ALT, AST ≤ UNL or ≤ 2.5 x UNL in case of liver metastases; albumin ≥ 2.5 g/dL; creatinine ≤ UNL
• Life expectancy of at least 3 months
• Prior anthracycline limited to doxorubicin equivalent of 280mg/m2 with progression free interval of at least 12 months for patients who have been pre-treated with CAELYX
• LVEF must be within normal limits
• Signed and dated informed consent

Exclusion Criteria

• Chemotherapy, hormonal, radiation or immunotherapy or participation in any investigational drug study within 4 weeks of study entry
• Pre-existing peripheral neuropathy > Grade 1
• Presence of cirrhosis or active or chronic hepatitis
• Presence of serious cardiac (congestive heart failure, angina pectoris, myocardial infarction within one year prior to study entry, uncontrolled hypertension or arrhythmia), neurological or psychiatric disorder
• Presence of uncontrolled intercurrent illness or any condition which in the judgment of the Investigator would place the subject at undue risk or interfere with the results of the study
• Symptomatic brain metastases or leptomeningeal disease
• Pregnancy or lactation or unwillingness to use adequate method of birth control
• Active infection
• Known history of allergy to mannitol, boron or liposomally formulated drugs.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Millennium Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Millennium Pharmaceuticals, Inc.

Principal Investigators

Medical Monitor

Role: STUDY_DIRECTOR

Millennium Pharmaceuticals, Inc.

Locations

Division of Gynecologic Oncology, Università Catholica Sacre Cuore

Campbasso, , Italy

Istituto Europeo di Oncologia (IEO)

Milan, , Italy

Istituto Nazionale dei Tumori

Milan, , Italy

Dept. Procreational Medicine, Università di Pisa

Pisa, , Italy

Kantonsspital St. Gallen

Sankt Gallen, CH, Switzerland

Gynecologic Oncology Unit

Ospedale Sant' Anna, Turin, Switzerland

Istituto Oncologico della Svizzera Italiana

Bellinzona, , Switzerland

Countries

Italy; Switzerland

Other Identifiers

S043VELC02

Identifier Type: -

Identifier Source: secondary_id

26866138-OVC-2001

Identifier Type: -

Identifier Source: org_study_id