A Trial of Doxil and Multiday Vinorelbine in Patients With Metastatic Breast Cancer

NCT ID: NCT00159094

Last Updated: 2008-06-02

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-10-31

Brief Summary

This is a phase II trial of Doxil on day 1 and vinorelbine on days 1 and 2 in women with metastatic breast cancer. Administered every 28 days. A study to assess the safety and efficacy of Doxil and vinorelbine in metastatic breast cancer.

Detailed Description

PROTOCOL SUMMARY

Study design: Phase II trial of monthly Doxil® and vinorelbine on day 1 and 2 in women with metastatic breast cancer.

Treatment plan: Patients will continue therapy, until they have unacceptable toxicity or disease progression.

Primary endpoint: Response rate

Secondary endpoints: Time to progression, overall survival and toxicity.

Additional study objectives: Evaluation of treatment-related dyspnea, with measurement of pulse oximetry during and after drug administration, and rigorous study of patients who experience dyspnea. Palmar-plantar erythrodysesthesia (PPE) will be treated with one of 2 randomly assigned topical salves, measuring duration and severity of symptoms.

Eligibility: Women who have had prior chemotherapy in the adjuvant or metastatic setting, or both, up to 3 prior regimens. Patients having more than one prior regimen for metastatic disease must have a performance status of 0 or 1; others may have 0-2. No prior Doxil® or vinorelbine therapy. Patients are ineligible if prior anthracycline dose is greater than 400 mg/m2, or if they have primary anthracycline-refractory disease, with disease progression during treatment or with relapse/recurrence within 6 months after last dose of anthracycline. Patients must have normal neurologic, hematologic, renal and hepatic functional parameters. Asymptomatic brain metastases are permissible.

Treatment plan: Doxil® 40 mg/m2 IV infusion over 60 minutes on day 1 Vinorelbine 15 mg/m2 IV over 6 minutes on days 1 and 2 Dexamethasone 4 mg IV or 8 mg po (Doxil® pretreatment) Heparin 5000 U IV (Vinorelbine pretreatment) Pyridoxine (vitamin B6) 200 mg po qd Repeat every 28 days.

Supportive measures:

For anemia (hematocrit < 35): Procrit® 40,000 U q wk For neutropenia (ANC < 1,000/mm3 ): Prophylactic antibiotics (Cipro® or Septra®) For all cycles after neutropenic fever/infection or grade 3-4 stomatitis: Prophylactic Neulasta® 6 mg SQ on day 3 (This intervention may be adopted for all patients, all cycles, if 2 of the first 4 patients enrolled need it.) For PPE: randomize between 2 topical salves and document duration and severity of sx

Dose adjustments: Subsequent cycles are given on day 29 or after recovery or to grade 0-1 toxicity, with no more than 3 weeks delay. Reduce dose of both drugs by 25% if grade 3 or 4 stomatitis or palmar-plantar or grade 4 thrombocytopenia. Reduce dose of Doxil® ONLY by 50-75% if abnormal bilirubin, alkaline phosphatase and/or ALT, AST (appendix 14.3)

Conditions

Metastatic Breast Cancer

Study Design

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

Interventions

Doxil and Vinorelbine

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients must be informed of the investigational nature of this study and must give and sign informed consent in compliance with federal and institutional guidelines.
• Women 18 years or older with biopsy proven advanced breast cancer.
• Patients with reproductive potential must use an adequate contraceptive method (e.g., abstinence, intrauterine device, oral contraceptives, barrier device with spermicide, or surgical sterilization) during treatment and for three months after completing treatment.
• Performance status (PS) 0-2 (ECOG). PS must be 0-1 if patient has had more than one prior regimen for metastatic disease or more than 2 prior regimens, including adjuvant and metastatic.
• Measurable disease by RECIST criteria, with baseline staging completed within 14 days of registration.
• At least two weeks post surgery and three weeks from completion of irradiation and recovered from toxicities associated with these treatments.
• Psychological, family, social and geographical conditions allowing weekly medical follow up during chemotherapy are required.
• Preregistration blood work must include complete blood counts with differential, and blood chemistries including serum bilirubin, GGT, LDH, SGOT, SGPT, alkaline phosphatase, creatinine, and tumor markers, CEA and CA 27-29. Patients must have:

• Absolute neutrophil count (ANC) >1,500/mm3
• Platelet count >100,000/mm3
• Hemoglobin > 8.0 g/dl
• Serum creatinine < 2.5 mg/dl (< 200 mol/L)
• Serum bilirubin < the upper limit of normal (ULN)
• SGOT and SGPT or AST and ALT < 2.0 x ULN
• Alkaline phosphatase < 2.0 x ULN, except if attributed to tumor
• Life expectancy > than 12 week.

Exclusion Criteria

• Prior Doxil® or vinorelbine
• Cumulative anthracycline dose exceeding 400 mg/m2 anthracycline
• Primary anthracycline refractory disease, ie. disease progression during treatment or relapse/recurrence within 6 months after last dose of anthracycline
• If PS 0-1, more than 3 prior chemotherapy regimens, including adjuvant and metastatic
• If PS 2, more than 1 prior regimen for metastatic disease or more than 2 prior chemotherapy regimens, including adjuvant and metastatic
• Hormone therapy including aromatase inhibitors within 2 weeks of baseline
• Pregnant or lactating women. Women of reproductive potential must have a negative pregnancy test and must agree to use an effective contraceptive method
• Prior history of cardiac disease, with New York Heart Association Class II or greater, or clinical evidence of congestive heart failure
• Symptomatic brain metastasis
• Past medical history of severe hypersensitivity reaction to conventional formulation of doxorubicin HCL or the components of Doxil® or vinorelbine

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

Sponsors

Ortho Biotech, Inc.

INDUSTRY

Sponsor Role: collaborator

Hematology Oncology Consultants

OTHER

Sponsor Role: lead

Principal Investigators

Leslie R Laufman, MD

Role: PRINCIPAL_INVESTIGATOR

Hematology Oncology Consultants, Inc

Locations

Hematology Oncology Consultants, Inc

Columbus, Ohio, United States

Site Status: RECRUITING

Hematology Oncology Consultants, Inc

Newark, Ohio, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Leslie R Laufman, MD

Role: CONTACT

Phone: 614-846-0044

Email: email@hoci.org

Facility Contacts

Debbie Conover, RN

Role: primary

Heather Meek

Role: primary

Other Identifiers

DO03-21-005

Identifier Type: -

Identifier Source: org_study_id