Breast Cancer Clinical Trial

Evaluate The Accuracy Of Breast MRI Biopsy In Diagnosing A Complete Tumor Response For Some Women Following Neoadjuvant Chemotherapy For Breast Cancer

Summary

The purpose of this study is to test the ability of a breast MRI biopsy to accurately diagnose a complete tumor response to the neoadjuvant chemotherapy (NAC) that the patient just finished. Numerous studies have shown that MRI has the highest accuracy for diagnosing a complete tumor response. The investigator wants to see if in a certain group of women who's breast cancer is no longer visible on the post-treatment MRI that the biopsy specimens from a MRI guided biopsy will accurately diagnose a complete tumor response to treatment which may in the future make breast surgery unnecessary in some women.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Women age 18 years or older
Confirmed histologic diagnosis of operable HER2 overexpressing (ER<10%, PR<10%, and HER2 2+ or FISH amplified) OR triple negative (ER<10%, PR<10%, and HER2 0/1+ or 2+/FISH not amplified) OR ER positive invasive ductal or invasive lobular breast cancer including MSKCC pathology confirmation
Operable breast cancer treated with NAC undergoing either breast conservation or total Mastectomy who have had a post-NAC clinical bilateral breast MRI demonstrating a complete imaging response, which is defined as no residual tumor enhancement.
No indication of distant metastases (M0)
Tumor site amenable to MRI guided biopsy as determined by the radiologist
Definitive surgery being performed at MSKCC within within 0-60 days of completing NAC
ECOG performance status score of 0 to ≤ 2 and or KPS performance status score of 80% to 100%
Women of childbearing potential (WOCBP) must not be pregnant.
Women must not be breastfeeding
Willing and able to provide informed consent and adhere to the study visit schedule and plan as specified in this protocol

Exclusion Criteria:

Medical history and concurrent disease:

Prior history of treated breast cancer
Any underlying medical or psychiatric conditions, which in the opinion of the investigator, will make performing the study intervention hazardous or obscure the interpretation of the results

Prohibited Treatments and/or Therapies:

Prior history of breast cancer surgery and/or radiotherapy.

Study is for people with:

Breast Cancer

Estimated Enrollment:

45

Study ID:

NCT03289195

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 7 Locations for this study

See Locations Near You

Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
Basking Ridge New Jersey, 07920, United States More Info
Elizabeth Sutton, MD
Contact
646-888-5455
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Middletown New Jersey, 07748, United States More Info
Elizabeth Sutton, MD
Contact
646-888-5455
Memorial Sloan Kettering Bergen (All Protocol Activities)
Montvale New Jersey, 07645, United States More Info
Elizabeth Sutton, PhD
Contact
646-888-5455
Memorial Sloan Kettering Suffolk-Commack (All Protocol Activities)
Commack New York, 11725, United States More Info
Elizabeth Sutton, MD
Contact
646-888-5455
Memorial Sloan Kettering Westchester (All Protocol Activities)
Harrison New York, 10604, United States More Info
Elizabeth Sutton, MD
Contact
646-888-5455
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York New York, 10065, United States More Info
Elizabeth Sutton, MD
Contact
646-888-5455
Mahmoud El-Tamer
Contact
646-888-4755
Memorial Sloan Kettering Nassau (All Protocol Activities)
Rockville Centre New York, 11570, United States More Info
Elizabeth Sutton, MD
Contact
646-888-5455

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

45

Study ID:

NCT03289195

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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