NewYork-Presbyterian Hospital/Weill Cornell Medical Center is the first and only hospital in the five boroughs of New York City to offer women with early stage breast cancer INTRABEAM radiotherapy, an innovative radiation treatment delivered in a single dose at the time of surgery.
Women with early stage breast cancer often have breast-conserving surgery, otherwise known as a lumpectomy, to remove a cancerous tumor. Lumpectomy is followed by a regimen of daily doses of radiation therapy to the entire breast, generally lasting six to seven consecutive weeks.
"INTRABEAM Radiotherapy may be an effective alternative to a six to seven week regimen following surgery for select patients because it allows us to precisely target any remaining cancer cells right inside the tumor bed, where the tumor is most likely to recur," says Dr. Mary Katherine Hayes, clinical director of Radiation Oncology at NewYork-Presbyterian Hospital/Weill Cornell Medical Center and associate professor of Clinical Radiology and Radiation Oncology at Weill Cornell Medical College.
Immediately following removal of the tumor, while the patient is still on the operating table, the INTRABEAM applicator's small, cylindrical tip is placed inside the tumor cavity to deliver a superficial dose of radiation for 20-30 minutes, while limiting exposure to healthy surrounding tissue and organs. After the applicator is removed, the surgical incision is closed.
"Our ability to use this radiation technique in such a timely manner may add to its effectiveness since the area in need of treatment can be directly visualized at the moment the tumor is removed," say Dr. Alexander J. Swistel, attending breast surgeon at the Iris Cantor Women's Health Center at NewYork-Presbyterian/Weill Cornell Medical Center and associate professor of clinical surgery at Weill Cornell Medical College.
This alternative to conventional full-breast radiation therapy is in step with the hospital's longstanding practice of tailoring partial breast cancer treatments to a growing number of patients with a small, early stage tumor. Eliminating an additional 6-7 weeks of radiation therapy is particularly convenient for patients who do not live in close proximity to a hospital or an established radiation therapy facility.
A 10-year randomized phase 3 clinical trial of intraoperative therapy for breast cancer found that for selected patients, single dose radiotherapy delivered at the time of surgery yielded the same results as conventional full breast radiation delivered over several weeks. The TARGIT-A Trial, published in The Lancet in July 2010, studied only the INTRABEAM system and was the largest randomized clinical trial conducted in this field, more than two thousand women in multiple countries were enrolled.
While INTRABEAM is limited to a select group of patients with a very small tumor, if tissue samples removed during surgery prove more aggressive than preliminary tests revealed, the patient will still be able to undergo conventional full-breast radiation. However, the patient would not need to undergo the final five-day phase of conventional treatment, known as boost therapy, which targets the tumor bed with external radiation.
The above story is based on materials provided by NewYork-Presbyterian Hospital/Columbia University Medical Center and NewYork-Presbyterian Hospital/W. Note: Materials may be edited for content and length.
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