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Phase II Study of Dose-Dense Doxurubicin and Cyclophosphamide (AC) Followed By Paclitaxel With Trastuzumab in HER2/ NEU-Amplified Breast Cancer: Feasibility

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status and phase

Completed
Phase 2

Conditions

Breast Cancer

Treatments

Drug: AC [Adriamycin (A) (also known as doxorubicin) and Cyclophosphamide (C)] Followed By Paclitaxel (P)

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

HER-2/neu (+) breast cancer is a more aggressive form of breast cancer. HER-2/neu is a protein that is overproduced by your tumor. It makes your cancer more aggressive. Standard treatments for this type of cancer will help some people, but there is a moderate to high chance that your cancer may come back.

The purpose of this study is to see if a new regimen will be effective in preventing cancer from coming back. This is a phase II trial. In this trial, patient get a drug regimen that has been tested in small groups of people to see what dose is safe. Researchers now wish to see how effective the drug is for HER-2/neu (+) breast cancer. The objective includes looking at short-term side effects and risks of the drug. All of the drugs on this regimen can affect the heart which can be a serious side effect. The drugs affect on heart function is a primary focus.

Enrollment

70 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adenocarcinoma breast cancer
  • ECOG performance status of 0 or 1
  • peripheral neuropathy less than or equal to 1
  • discontinued hormonal therapy as a chemoprevention while onstudy
  • LVEF by MUGA > 55%?
  • Absolute neutrophil count (ANC)> 1000/µL)
  • platelet count > 100,000/µL)
  • SGOT OR SGPT < 92.5 units/L

Exclusion criteria

  • Stage IV breast cancer
  • any chemotherapy, radiation therapy, immunotherapy, or biotherapy for a CURRENT breast cancer
  • pregnant or lactating patients
  • active second malignancy, other than adequately treated non-melanoma skin cancers or in situ cervical cancer
  • previous allergy/hypersensitivity to Doxorubicin, Cyclophosphamide, Paclitaxel, or other drugs formulated in Cremophor EL?
  • unstable angina, congestive heart failure, current use of digitalis, beta-blockers, or calcium blockers for therapy of congestive heart failure, arrhythmia requiring medical therapy, or a history of a myocardial infarction within 12 months
  • psychiatric illness that prevents her from understanding the nature of this study and complying with protocol requirements?
  • active, unresolved infections
  • sensitivity to E. coli derived proteins
  • prior chemotherapy with an anthracycline
  • prior Herceptin therapy

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

70 participants in 1 patient group

1
Experimental group
Description:
single arm study
Treatment:
Drug: AC [Adriamycin (A) (also known as doxorubicin) and Cyclophosphamide (C)] Followed By Paclitaxel (P)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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