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Neoadjuvant Chemotherapy With Myocet/Taxotere/Herceptin for HER2 Positive Breast Cancer Patients

Phase 1
Completed
Conditions
Breast Cancer
Interventions
Registration Number
NCT00129896
Lead Sponsor
Spanish Breast Cancer Research Group
Brief Summary

This is an open-label study to assess the efficacy and tolerability of the combination Myocet®/Taxotere®/Herceptin® as primary treatment for HER2 positive breast cancer patients. HER2 status will be confirmed centrally by fluorescence in situ hybridization (FISH).

Phase I: Initial doses will be:

Myocet: 50-60 mg/m² day 1 every 3 weeks; Taxotere 60-75 mg/m² day 1 every 3 weeks; and Herceptin (4) 2 mg/kg weekly.

Sample size will depend on the number of patients recruited during dose escalation. Three patients must be recruited in each dose level. If one out of three experiences a dose-limiting toxicity (DLT), 3 more patients must be recruited in the same dose level. Considering that there are 4 dose levels to be tested, the estimated number of patients is 9 to 24. Patients receiving the recommended dose (RD) will be incorporated into phase II of the study.

Detailed Description

Phase II: The average pathological complete response rate reported in other trials is around 11%. The investigators expect to achieve an increase of 14% on this rate; that is, they expect a pathological response rate of 25%. With a= 0.05 and β=0.2, 18 patients are initially needed. If at least 3 pathological complete responses are achieved, recruitment will continue to up to 53 patients. At least 10 pathological complete responses are needed to probe the hypothesis. Considering a 10% post-randomization drop-out rate, a total of 59 patients must be recruited for the trial.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
73
Inclusion Criteria
  • Written informed consent.
  • Breast cancer stages II and IIIA with histological diagnoses by true-cut.
  • Breast cancer tumours overexpressing HER2neu, centrally confirmed by FISH.
  • No evidence of metastasis: bilateral mammography, thorax x-ray, computed tomography (CT)-scan or abdominal echography and bone scintigraphy.
  • Estrogen and progesterone hormone receptor status, determined before study registration.
  • Age >= 18 years old.
  • Performance status (Karnofsky index) >= 80.
  • Adequate cardiac function by LVEF in the previous 14 days.
  • Hematology: neutrophils >= 2.0 x10^9/l; platelets >= 100 x10^9/l; hemoglobin >= 10 g/dl.
  • Adequate hepatic function: total bilirubin <= 1x upper normal limit (UNL); SGOT and SGPT <= 2.5xUNL; alkaline phosphatase <= 2.5xUNL.
  • Adequate renal function: creatinine <= 1xUNL; creatinine clearance >= 60 ml/min.
  • Patients able to comply with study treatment and follow-up.
  • Negative pregnancy test in the previous 14 days.
  • Adequate contraceptive method during the study and up to 3 months after definitive surgery.
Exclusion Criteria
  • HER2neu negative tumours.
  • Prior systemic therapy for breast cancer.
  • Prior treatment with anthracyclines or taxanes (paclitaxel, docetaxel) for any previous malignancy.
  • Prior radiotherapy for breast cancer.
  • Bilateral invasive breast cancer.
  • Pregnant or lactating women.
  • Previous grade >= 2 motor or sensorial neurotoxicity (National Cancer Institute Common Toxicity Criteria [NCI CTC]).
  • Other serious comorbidities: congestive heart failure or unstable angina; prior history of myocardial infarction in previous year; uncontrolled hypertension (HT); high risk arrhythmias; history of significant neurological or psychiatric disorders; uncontrolled active infection; active peptic ulcer; unstable diabetes mellitus; dyspnea at rest; or chronic therapy with oxygen.
  • Previous or current history of neoplasms different from breast cancer, except for skin carcinoma, cervical in situ carcinoma, or any other tumor curatively treated and without recurrence in the last 10 years; ductal in situ carcinoma in the same breast; lobular in situ carcinoma.
  • Chronic treatment with corticosteroids.
  • Contraindications for administration of corticosteroids, anthracyclines, docetaxel, trastuzumab or egg derivates.
  • Concomitant treatment with other therapy for cancer.
  • Males.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Myocet+Taxotere+HerceptinHerceptinMyocet 50 mg/m2; Taxotere 60 mg/m2; Herceptín 4 mg/Kg (first dose) and in the following cycles 2 mg/Kg
Myocet+Taxotere+HerceptinMyocetMyocet 50 mg/m2; Taxotere 60 mg/m2; Herceptín 4 mg/Kg (first dose) and in the following cycles 2 mg/Kg
Myocet+Taxotere+HerceptinTaxotereMyocet 50 mg/m2; Taxotere 60 mg/m2; Herceptín 4 mg/Kg (first dose) and in the following cycles 2 mg/Kg
Primary Outcome Measures
NameTimeMethod
Tolerability (Phase I): Recommended Doses of the combination treatmentup to 24 months since last patient included in the Phase I

Recommended Doses of the combination treatment

Efficacy (Phase II): Percentage (%) pathological Complete Response achieved according to Miller and Payne Criteriaup to 24 months since last patient included in the Phase II

% pathological Complete Response achieved according to Miller and Payne Criteria

Secondary Outcome Measures
NameTimeMethod
Clinical response ratesup to 6 months since last patient treatment

Clinical responses evaluated by radiological imaging

Potential cardiac toxicityup to 12 months since last patient included

Left ventricular ejection fraction \[LVEF\] by multiple-gated acquisition \[MUGA\])

Surgery type (conservative surgery versus mastectomy)up to 7 months since last patient treatment

% conservative or mastectomy surgery

Post-surgery node statusup to 7 months since last patient treatment

according to Miller and Payne Criteria

Safety: Adverse Events evaluated according to NCI CTC v2.024 months since last patient included

Adverse Events evaluated according to NCI CTC v2.0

Molecular changes in blood and tissue exams24 months

Different biomarkers evaluated

Trial Locations

Locations (16)

Hospital Universitario Virgen de los Lirios

🇪🇸

Alcoy, Alicante, Spain

Hospital Universitario Germans Trias i Pujol

🇪🇸

Badalona, Barcelona, Spain

Consorci Sanitari de Terrassa

🇪🇸

Terrassa, Barcelona, Spain

Althaia-Xarxa Assistencial de Manresa

🇪🇸

Manresa, Barcelona, Spain

Corporació Sanitaria Parc Taulí

🇪🇸

Sabadell, Barcelona, Spain

Hospital de la Ribera

🇪🇸

Alzira, Valencia, Spain

Onkologikoa

🇪🇸

Donostia-San Sebastian, Guipúzcoa, Spain

Hospital Infanta Cristina

🇪🇸

Badajoz, Spain

Complejo Hospitalario Universitario A Coruña

🇪🇸

A Coruña, Spain

Hospital Clinic i Provincial

🇪🇸

Barcelona, Spain

Complejo Hospitalario de Jaén

🇪🇸

Jaén, Spain

Hospital Universitario Miguel Servet

🇪🇸

Zaragoza, Spain

Hospital Clínico Universitario Virgen de la Victoria

🇪🇸

Málaga, Spain

Hospital Universitario La Fe

🇪🇸

Valencia, Spain

Hospital Universitario Lucus Augusti

🇪🇸

Lugo, Spain

Instituto Valenciano de Oncología

🇪🇸

Valencia, Spain

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