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Clinical Trial Summary

To evaluate safety of 5 fraction accelerated partial brest irradiation in more convenient 5 fraction schedule.


Clinical Trial Description

The purpose of this study is to evaluate the rate of early and intermediate toxicity related to accelerated partial breast irradiation (APBI) delivered in a more convenient 5 fraction schedule using non-invasive image-guided breast brachytherapy (NIBB) (AccuBoost System) in women with resected, early stage breast cancer. Non-invasive image-guided breast brachytherapy (NIBB), using advanced image-guided radiation technology, has the potential to eliminate the disadvantages of the conventional APBI techniques. NIBB facilitates non-invasive partial breast irradiation without the use of catheters or implants. Yet by using breast immobilization and precise image-guidance, it reduces non-target breast tissue within the irradiated field compared with other non-invasive APBI techniques such as 3D-CRT. This has made NIBB an attractive approach to deliver APBI. We hypothesize that NIBB delivered in 5 treatments will be a more convenient, safe and effective modality to deliver partial breast irradiation. Anticipated advantages of NIBB protocol treatment include: - Convenient treatment schedule - Short course can allow for increased patient access to treatment - Non-invasive approach - Increased accuracy with precise targeting of lumpectomy cavity using advanced imaging - Reduced irradiation of non-target breast tissue - Reduced skin toxicity - No heart or lung radiation exposure - Reduced late skin or breast toxicity - High rate of good or excellent cosmetic outcome - High rate of ipsilateral breast tumor control comparable to other APBI techniques ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01961531
Study type Interventional
Source Brown University
Contact
Status Completed
Phase N/A
Start date July 24, 2014
Completion date November 30, 2021

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