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Phase 2 N=32 Treatment

Evaluate Trastuzumab Plus Standard Chemotherapy Given Before Surgery in Breast Cancer Patients With Low HER 2 Expression

Breast Cancer

Enrolled (actual)
32
Serious AEs
15.6%
Results posted
Apr 2018
Primary outcome: Primary: Pathologic Complete Response — 26 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
nab-paclitaxel (Drug); trastuzumab (Drug); Doxorubicin (Drug); cyclophosphamide (Drug); Growth Factor Support (Biological); Surgery (Procedure)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
University of Kansas Medical Center
Primary completion
May 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Pathologic Complete Response
26

Summary

The purpose of this study is to find out if there is a benefit of adding Herceptin (trastuzumab) to standard chemotherapy in this type of breast cancer.

Eligibility Criteria

Inclusion Criteria

  • Female patient ≥ 18 years of age
  • Histologically proven stage II or III adenocarcinoma of the breast
  • Must be candidate for neoadjuvant treatment (Tumor size ≥ 2 cm, T2, T3, T4 and/or clinical N1 or N2).
  • HER-2/neu 1+ or 2+ by immunohistochemistry
  • Must have operable tumor.
  • Performance status of 2 or better per SWOG criteria
  • LVEF ≥ 55% by echocardiogram performed within 4 weeks prior to treatment initiation
  • If patient of childbearing potential, pregnancy test is negative
  • Patients with reproductive potential must use an effective method to avoid pregnancy for the duration of the trial.
  • Adequate bone marrow function: ANC > 1500/mm3, platelet count > 100,000/mm3, and hemoglobin > 9 g/dL
  • Adequate kidney function: serum creatinine of 60 mL/min
  • Adequate hepatic function: transaminases 2.2)
  • Patients who have had prior endocrine therapy for > 4 weeks or chemotherapy for this breast cancer will be excluded.
  • Locally advanced, inoperable tumors will be excluded.
  • The presence of any other medical or psychiatric disorder that, in the opinion of the treating physician, would contraindicate the use of drugs in this protocol or place the subject at undue risk for treatment complications.
  • History of significant cardiac disease, cardiac risk factors or uncontrolled arrhythmias
  • Ejection fraction < 55%
  • Pregnancy or lactation
  • Patients with inadequate laboratory values (as defined above) are excluded from study.
  • Patients with NCI common toxicity criteria (CTC) grade 2 or greater peripheral neuropathy are excluded from study.
  • Patients with active infection are excluded from study.
  • Patients with concomitant or previous malignancies within the last 5 years, are excluded from the study. Exceptions include: adequately treated basal or squamous cell carcinoma of the skin, carcinoma in situ of the cervix, and ductal carcinoma in situ (DCIS).
  • Patients with emotional limitations are excluded from study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00944047). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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