Cisplatin + RT for Triple Negative Breast Cancer

Status:	Active, not recruiting
Conditions:	Breast Cancer, Cancer
Therapuetic Areas:	Oncology
Healthy:	No
Age Range:	18 - Any
Updated:	11/21/2018
Start Date:	October 2012
End Date:	October 2023

A Phase I Dose-Escalation Study of Cisplatin and Radiation Therapy for Patients With Triple Negative Breast Cancer

This is a Phase I dose escalation study of cisplatin and concurrent radiation in patients
with ER negative, PR negative and HER2 negative breast cancer who have undergone
breast-conserving surgery or mastectomy.

Primary objective: To assess the safety, tolerability, and maximum tolerated dose (MTD) of
cisplatin when given concurrently with radiation therapy for participants with Stage II or
III breast cancer who have undergone breast conserving surgery or mastectomy

This is a phase I dose escalation study of cisplatin and radiation to determine the toxicity
of this combined treatment and establish an MTD.

Inclusion Criteria:

- Primary tumor is triple negative breast cancer

- Breast-conserving surgery or mastectomy with surgical excision of all gross disease
with negative surgical margins

- Pathologic or clinical stage II or III disease

- At least 3 week interval from last chemotherapy administration/breast surgery to
radiation (no more than 8 weeks)

Exclusion Criteria:

- Pregnant or breastfeeding

- Prior radiation to breast or ipsilateral regional nodes

- Ongoing therapy with other investigational agents

- Hormonal therapy

- Significant co-morbidity

- Pathologic complete response following preoperative chemotherapy

- Biopsy proven metastatic disease

We found this trial at

sites

Massachusetts General Hospital

185 Cambridge Street
Boston, Massachusetts 02114

617-724-5200