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Clinical Trials/NCT01172223
NCT01172223
Completed
Phase 1

Phase I/II Trial of Primary Chemotherapy With Non-pegylated Liposomal Doxorubicin, Paclitaxel and Lapatinib in Patients With HER2-positive Early

Prof Dirk Elling1 site in 1 country81 target enrollmentSeptember 2007

Overview

Phase
Phase 1
Intervention
Myocet (Non-pegylated liposomal doxorubicin (NPLD))
Conditions
Breast Cancer
Sponsor
Prof Dirk Elling
Enrollment
81
Locations
1
Primary Endpoint
Determine the optimal doses for NPLD, paclitaxel and lapatinib (phase I)
Status
Completed
Last Updated
9 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 2007
End Date
December 2013
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Prof Dirk Elling
Responsible Party
Sponsor Investigator
Principal Investigator

Prof Dirk Elling

Professor

Sana-Klinikum Lichtenberg

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

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

Arms & Interventions

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)

Intervention: Myocet (Non-pegylated liposomal doxorubicin (NPLD))

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)

Intervention: Paclitaxel

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)

Intervention: Lapatinib (GW572016, Tykerb)

Outcomes

Primary Outcomes

Determine the optimal doses for NPLD, paclitaxel and lapatinib (phase I)

Time Frame: every 3 weeks

Evaluate the pathological response to NPLD, paclitaxel and lapatinib (phase II)

Time Frame: every 6 weeks

Study Sites (1)

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