Primary Chemotherapy in Patients With HER2-positive Early Breast Cancer

NCT ID: NCT01172223

Last Updated: 2016-11-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 81 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-09-30
• Study Completion Date: 2013-12-31

Brief Summary

Open-label, multicenter phase I/II trial. Patients with HER2-positive (overexpressing or amplified), invasive breast cancer with T1c N1-2 or T2 N0-2 disease will be treated with

• Non-pegylated liposomal doxorubicin (NPLD; Myocet, 60 mg/m^2 i.v. day 1 q3 weeks),
• Paclitaxel (175 mg/m^2 i.v. day 1 q3 weeks), and
• Lapatinib (GW572016, Tykerb, 750-1500 mg/d orally daily until the day of the definitive surgery) Treatment is planned for 6 cycles unless there is evidence of unacceptable toxicity, disease progression or inadequate efficacy (defined as a decrease in tumor size <25% after 4 courses measured by ultrasound or MR-mammography), or if the patient requested to be released.

Detailed Description

Breast cancer is the most common malignancy affecting females in northern Europe and North America, corresponding to an age-corrected annual incidence of 100 to 120 per 100000 females. Approximately 30-40% of all patients treated with curative intent will develop metastatic disease. Perioperative systemic treatment has made a major impact on relapse-free and overall survival of women with early-stage breast cancer [ , ] with therapeutic strategies being based on the endocrine responsiveness and the estimated risk of relapse defined by tumor size, axillary lymph node involvement, histologic and nuclear grade, lymphatic and/or vascular invasion, HER2/neu-overexpression and age [ ]. Perioperative therapy has traditionally been administered postoperatively, but chemotherapy is increasingly utilized in the preoperative setting as it can significantly improve the rate of breast conserving surgery, and new regimens can be evaluated rapidly and more precisely.

Conditions

Breast Cancer

Keywords

HER2-positive; early breast cancer

Study Design

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

Study Groups

LAPADO

Non-pegylated liposomal doxorubicin (NPLD; Myocet, 60 mg/m2 i.v. day 1 q3 weeks), Paclitaxel (175 mg/m2 i.v. day 1 q3 weeks), and Lapatinib (GW572016, Tykerb, 750-1500 mg/d orally daily until the day of the definitive surgery)

Group Type: EXPERIMENTAL

Myocet (Non-pegylated liposomal doxorubicin (NPLD))

Intervention Type: DRUG

60 mg/m\^2 i.v. day 1 q3 weeks

Paclitaxel

Intervention Type: DRUG

175 mg/m\^2 i.v. day 1 q3 weeks

Lapatinib (GW572016, Tykerb)

Intervention Type: DRUG

750-1500 mg/d orally daily until the day of the definitive surgery

Interventions

Myocet (Non-pegylated liposomal doxorubicin (NPLD))

60 mg/m\^2 i.v. day 1 q3 weeks

Intervention Type: DRUG

Paclitaxel

175 mg/m\^2 i.v. day 1 q3 weeks

Intervention Type: DRUG

Lapatinib (GW572016, Tykerb)

750-1500 mg/d orally daily until the day of the definitive surgery

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed breast cancer
• T1c N1-2 or T2 N0-2 disease
• HER2-positive tumours with 3+ intensity on immunohistochemical staining for HER2 or amplification of the HER2 gene on fluorescence in situ hybridization (FISH)
• No prior systemic treatment regimens for breast cancer
• Adequate hematologic function (ANC 1500 cells/µl, platelet count 100000/µl, and hemoglobin 8g/dl).
• Serum creatinine concentration < 1.5 times the upper limit of normal (ULN) and/or creatinine clearance >60 ml/min
• Bilirubin level < 1.5 X ULN
• Normal cardiac function with a left ventricular ejection fraction of at least 50% (as assessed by quantitative echocardiogram or MUGA scan)
• Karnofsky performance status 80%
• Age 18 years
• If the patient is of childbearing potential, she agrees to: comply with effective contraceptive measures, has been using adequate contraception since the last menses, will use adequate contraception during the study, and has a negative pregnancy test within one week of study entry
• Written informed consent prior to admission to this study

Exclusion Criteria

• Male patients
• Inflammatory or bilateral breast cancer
• Evidence of distant metastases
• Previous systemic or local treatment for breast cancer (including surgery, radiotherapy, cytotoxic and endocrine treatments)
• Past or current history of other neoplasms, except for
• Curatively treated non-melanoma skin cancer
• Adequately treated in situ carcinoma of the cervix
• Other cancer curatively treated and with no evidence of disease for at least 5 years
• Significant cardiac disease, including angina pectoris, severe cardiac arrhythmia requiring medication, severe conduction abnormalities, clinically significant valvular disease, cardiomegaly, ventricular hypertrophy, poorly uncontrolled hypertension (resting diastolic blood pressure >115 mmHg), prior myocardial infarction, CHF, or other cardiomyopathy
• Preexisting sensoric or motor polyneuropathy Grade 2 according to NCI CTC
• Serious intercurrent medical or psychiatric illness, including serious active infection
• Concurrent treatment with other experimental drugs. Participation in another clinical trial with any investigational drug within 30 days prior to study entry.
• Detained persons or prisoners
• Pregnant or nursing women

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

Sponsors

Prof Dirk Elling

OTHER

Sponsor Role: lead

Responsible Party

Prof Dirk Elling

Professor

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Dirk Elling

Role: PRINCIPAL_INVESTIGATOR

Sana Klinikum Lichtenberg, Berlin

Locations

Sana Klinikum Lichtenberg

Berlin, , Germany

Countries

Germany

Other Identifiers

2007-000924-42

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

LAPADO-Study

Identifier Type: -

Identifier Source: org_study_id