The treatment arms were well matched for both baseline quality of life and treatment characteristics. Using a questionnaire designed to assess the quality of life of breast cancer patients, participants self-reported their overall well-being prior to treatment and six months after completing their therapy. Physicians assessed patient toxicities weekly during treatment and six months after completing radiation.

The researchers found that compared to the CF-WBI cohort, those randomized to HF-WBI experienced less acute toxicity during treatment, including: breast pain, dermatitis, skin darkening and fatigue. At six month follow up, toxicities were generally similar between the HF-WBI and CF-WBI patients, although the HF-WBI patients were noted to have less fatigue, and better ability to care for their family, compared to those treated with CF-WBI.


"Patients who received the shorter course reported less difficulty in caring for their families' needs. This is a major priority for women undergoing breast cancer radiation," says Shaitelman. "Most are busy working mothers, working inside or outside the home, and are juggling a number of priorities. It's paramount that we address this need."

The findings provide some of the first data to show a benefit with the shorter course of treatment - not just an alternative for patients, says Benjamin Smith, M.D., associate professor, Radiation Oncology, MD Anderson.

"This study fills in a missing piece in the literature," says Smith, the study's corresponding author. No longer do I regard the shorter course of treatment as just an option for patients, but rather the preferred starting point for discussion with patients if they need whole breast radiation."

Tumor control outcomes continue to be followed; to date no meaningful difference in survival has been found, say the researchers. Also, data like this and other studies are substantive enough that Smith feels it would be worthwhile for organizations like ASTRO and NCCN to consider expanding recommendations for patients to receive HF-WBI.

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Patients were enrolled at MD Anderson, the institution's Houston area locations, Orlando Health (formerly MD Anderson Orlando) in Orlando, Florida, and Banner MD Anderson in Gilbert, Arizona. The study was funded by a Career Development Aware from the Conquer Cancer Foundation of the American Society of Clinical Oncology, the Breast Cancer Research Foundation, grant RP140020 from the Cancer Prevention and Research Institute of Texas, the Center for Radiation Oncology Research at The University of Texas MD Anderson Cancer Center, a philanthropic gift from Ann and Clarence Cazalot, and grant P30CA016672 form the National Cancer Institute at the National Institutes of Health funding of the Biostatistics Resource Group. Neither Shaitelman nor Smith report any related conflicts.

In addition to Shaitelman and Smith, other authors include: from MD Anderson, Thomas A. Buchholz, M.D., Pamela J. Schlembach, M.D., Isidora Arzu, M.D., Ph.D., Elizabeth S. Bloom, M.D., Gregory M. Chronowski, M.D., Karen E. Hoffman, M.D., George H. Perkins, M.D., Valerie Reed, M.D., Shalin Shah, M.D., Michael C. Stauder, M.D., Eric A. Strom, M.D., Welela Tereffe, M.D., Wendy A. Woodward, M.D., Ph.D., Diana Amaya, Tanisha Davis, William Guerra, Lois Hamblin, all of Radiation Oncology. Also on the study from MD Anderson: Alastair M. Thompson, M.D., Kelly K. Hunt, M.D., both Breast Surgical Oncology; Gabriel Hortobagyi, M.D., Breast Medical Oncology, Donald Baumann, M.D., Plastic Surgery. Additional authors include: Joe Ensor, Ph.D., Houston Methodist Research Institute; Matthew Ballo, M.D., The University of Tennessee Health Science Center; Daniel Buchholz, M.D., Tomas Dvorak, M.D., Patrick Kelly, M.D., Ph.D., UF Health Cancer Center; Michelle Ludwig, M.D., Ph.D., Baylor College of Medicine; and Emily Grade, M.D., Banner MD Anderson Cancer Center.

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