Breast Cancer Clinical Trial

Multi-Beam Intensity-Modulated Radiation Therapy for Node-Positive Breast Cancer

Summary

This study is being performed to understand the safety of a new radiation treatment called "Multi-Beam Intensity Modulated Radiation Therapy" ( IMRT). Currently, the standard way of giving radiation is with "simplified" IMRT, which uses only 2 beams of radiation. "Multi-beam" IMRT works by using 6-12 small radiation beams to give a more "tailored" or "customized" radiation dose to the breast, chest wall, and the lymph nodes. At the same time, multi-beam IMRT may allow the dose to the heart, lungs, and nearby tissue to be lowered, especially when the internal mammary lymph nodes need to be targeted by radiation.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Female gender
Age ≥18 years
An invasive primary breast cancer of any histology arising from breast parenchyma
Patient must be status post mastectomy or partial mastectomy with an assessment of axillary nodes via sentinel lymph node biopsy and/or axillary lymph node dissection
Pathologic confirmation of metastatic disease in at least one regional lymph node. Regional lymph nodes are defined as the ipsilateral axillary lymph nodes, ipsilateral supraclavicular lymph nodes, and ipsilateral internal mammary lymph nodes. Thus, any T stage is allowed as long as the N stage is ≥1 and M stage is 0.
Patient signed study-specific consent form.

Exclusion Criteria:

Patients with distant metastasis.
Patients who are pregnant or breastfeeding.
Patients with psychiatric or addictive disorders that would preclude obtaining informed consent.
Time between initial diagnosis of breast cancer and start of radiation therapy exceeds 13 months.
Estimated life expectancy judged to be less than one year by patient's treating radiation oncologist.
Prior radiation therapy to the ipsilateral or contralateral breast or thorax.
Primary breast cancer is a lymphoma or sarcoma histology.
Patients with a history of non-skin malignancy <5 years prior to the diagnosis of breast cancer.
Patients requiring radiation to the bilateral breasts.

Study is for people with:

Breast Cancer

Estimated Enrollment:

116

Study ID:

NCT01127373

Recruitment Status:

Completed

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 6 Locations for this study

See Locations Near You

Memorial Sloan Kettering Basking Ridge (Follow Up Only)
Basking Ridge New Jersey, 07920, United States
Memoral Sloan Kettering Monmouth (Follow Up Only)
Middletown New Jersey, 07748, United States
Memorial Sloan Kettering Commack (Follow Up Only)
Commack New York, 11725, United States
Memorial Sloan Kettering Westchester (Follow Up Only)
Harrison New York, 10604, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
Memorial Sloan Kettering Rockville Centre (Follow Up Only)
Rockville Centre New York, , United States
Memorial Sloan Kettering Nassau (Follow Up Only)
Uniondale New York, 11553, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

116

Study ID:

NCT01127373

Recruitment Status:

Completed

Sponsor:


Memorial Sloan Kettering Cancer Center

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