Carboplatin and Gemcitabine in Treating Patients With Locally Advanced or Metastatic Breast Cancer

NCT ID: NCT00470249

Last Updated: 2021-02-01

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 5 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-07-15
• Study Completion Date: 2008-11-03

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as carboplatin and gemcitabine, 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.

PURPOSE: This phase II trial is studying how well giving carboplatin together with gemcitabine works in treating patients with locally advanced or metastatic breast cancer.

Detailed Description

OBJECTIVES:

Primary

• Determine the overall response rate in patients with anthracycline- and taxane-resistant locally advanced or metastatic breast cancer treated with dose-dense carboplatin and gemcitabine hydrochloride.

Secondary

• Determine the overall toxicity of this regimen in these patients.
• Determine the overall survival of patients treated with this regimen.
• Determine the time to disease progression in patients treated with this regimen.
• Determine the duration of response in patients treated with this regimen.
• Determine the time to treatment failure in patients treated with this regimen.

OUTLINE: This is a nonrandomized, open-label study.

Patients receive carboplatin IV over 30 minutes on day 1 and gemcitabine hydrochloride IV over 150 minutes on day 2. Treatment repeats every 14 days for up to 9 courses in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed periodically for 2 years.

PROJECTED ACCRUAL: A total of 35 patients will be accrued for this study.

Conditions

Breast Cancer

Study Design

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

Study Groups

Patients with (HER-2)-negative and anthracycline- and taxane-resistant

Patients with human epidermal growth factor 2 (HER-2)-negative locally advanced or metastatic breast cancer that was anthracycline- and taxane-resistant

Group Type: EXPERIMENTAL

Carboplatin

Intervention Type: DRUG

At a dose equivalent to an area under the concentration-time curve of 4.5 mg/ml.min on day 1 of every 2-week cycle

Gemcitabine Hydrochloride

Intervention Type: DRUG

1500 mg/m2 on day 2 of every 2-week cycle

Interventions

Carboplatin

At a dose equivalent to an area under the concentration-time curve of 4.5 mg/ml.min on day 1 of every 2-week cycle

Intervention Type: DRUG

Gemcitabine Hydrochloride

1500 mg/m2 on day 2 of every 2-week cycle

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• DISEASE CHARACTERISTICS: histologically confirmed breast cancer, locally advanced or metastatic disease, recurrent or refractory disease, histological or cytological confirmation required for recurrence in a solitary site
• Must have received prior anthracycline and taxane as neoadjuvant, adjuvant, or metastatic therapy
• At least 1 measurable site of disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques or ≥ 10 mm by spiral CT scan
• Palpable disease allowed, Lesions that have been irradiated in the advanced setting cannot be included as sites of measurable disease
• No nonmeasurable disease only, including the following:
• Bone lesions
• Leptomeningeal disease
• Ascites
• Pleural or pericardial effusion
• Inflammatory breast disease
• Lymphangitic pulmonary disease
• Abdominal masses that are not confirmed and followed by imaging techniques
• Cystic lesions
• No HER2-positive disease, defined as 3+ by IHC OR positive by FISH or chromogenic in situ hybridization
• Hormone receptor status not specified
• PATIENT CHARACTERISTICS:
• Male or female, Menopausal status not specified, ECOG performance status 0-1, Estimated life expectancy ≥ 12 weeks, Not pregnant or nursing, fertile patients must use effective contraception during and for 3 months after completion of study therapy
• ANC ≥ 1,500/mm³
• Platelet count ≥ 100,000/mm³
• Hemoglobin ≥ 9 g/dL
• ALT or AST < 2.5 times upper limit of normal (ULN)
• Bilirubin normal
• Alkaline phosphatase ≤ 2.5 times ULN
• Creatinine ≤ 1.25 times ULN OR creatinine clearance > 40 mL/min
• Calcium ≤ 1.2 times ULN
• No concurrent serious medical or psychiatric illness, including any serious active infection incompatible with the study
• No other primary malignancy except carcinoma in situ of the cervix, adequately treated nonmelanomatous skin cancer, or any other malignancy previously treated ≥ 5 years ago with no evidence of recurrence
• No peripheral neuropathy ≥ grade 2
• PRIOR CONCURRENT THERAPY (See Disease Characteristics):
• Recovered from prior chemotherapy
• Prior hormonal therapy or immunotherapy allowed
• Antitumoral hormonal therapy must be discontinued prior to study entry
• More than 4 weeks since prior radiotherapy and recovered
• No prior radiotherapy to the whole pelvis or to ≥ 25% of the bone marrow
• No prior gemcitabine hydrochloride, cisplatin, or carboplatin
• No other cytotoxic chemotherapy for 21 days before and for 14 days after completion of study therapy
• More than 30 days since prior treatment with a drug (not including study drug) that has not received regulatory approval for any indication at the time of study entry
• Bisphosphonate therapy may not be initiated or discontinued within 4 weeks of study entry
• No more than 1 prior course of chemotherapy for metastatic disease
• Prior chemotherapy in the adjuvant setting allowed
• Concurrent palliative radiotherapy to existing painful lesions (soft tissue or bone) allowed
• New bone pain requiring radiotherapy > 4 weeks after first study treatment considered disease progression
• New pain in a soft tissue lesion without other objective changes may be irradiated provided ≥ 1 other site of nonirradiated measurable disease exists
• No other concurrent anticancer treatment
• No concurrent tamoxifen citrate, aromatase inhibitors, or progestagens

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

Sponsors

University of Southampton

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Nicholas Murray, MD

Role: STUDY_CHAIR

University Hospital Southampton NHS Foundation Trust

Locations

Royal Bournemouth Hospital

Bournemouth, England, United Kingdom

Portsmouth Oncology Centre at Saint Mary's Hospital

Portsmouth, England, United Kingdom

Southampton General Hospital

Southampton, England, United Kingdom

Countries

United Kingdom

Related Links

https://f1000research.com/articles/9-4

Publication of the results

Other Identifiers

2005-005164-83

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CDR0000542627

Identifier Type: -

Identifier Source: org_study_id