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Women's Health Homepage

Hypofractionated whole-breast radiotherapy best for early-stage breast cancer patients under 50 Study supports higher dose, shorter form treatment

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Rhonda Engebretson ASRT member selected for FDA Mammography Quality Assurance Committee

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The TMIST study will determine if 3-D
mammograms reduce a woman's risk of
developing life-threatening cancer
than 2-D mammograms

Researchers to assess benefits of 3-D mammo versus 2-D

by John Fischer , Staff Reporter
A new study could determine if 3-D mammography reduces a woman’s risk of developing life-threatening breast cancer more than 2-D.

The ECOG-ACRIN Cancer Research Group (ECOG-ACRIN) and the National Cancer Institute (NCI) have developed the Tomosynthesis Mammographic Imaging Screening Trial (TMIST) to compare the two types of digital mammography in breast cancer screenings. ECOG-ACRIN will lead the study.

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“The information related to detecting life-threatening cancers is important because it gets to the purpose and essence of cancer screening,” Dr. Worta McCaskill-Stevens, M.D., M.S., chief of the Community Oncology and Prevention Trials Research Group at NCI, told HCB News. ”Another important aspect is that TMIST will compare the benefits and harms between 2-D and 3-D.”

3-D mammography is likely to detect more findings that require follow-ups and lead to more procedures and treatments than 2-D. It is unknown whether 3-D is better able to reduce a woman’s risk of developing an advanced, life-threatening form of cancer.

The trial will follow 165,000 women between 45 and 74 who are planning to undergo routine mammograms. Researchers will use the findings to determine the best course of action for screening women, as well as how to help women make informed decisions regarding screenings.

Participants will each be assigned to undergo either 3-D or 2-D mammogram screenings. Most will be screened annually. Postmenopausal women who show no high risk factors will be screened every two years. The study will also take into account diversity, basing participants on geographic location sites, race and ethnicity.

Data from each mammogram will be collected and evaluated, including imaging that shows no signs, suspicion or diagnosis of breast cancer. Follow-ups for imaging and biopsies will be reported. All participants will be checked for breast cancer status, treatment and outcomes from the time each starts the trial through at least 2025. Women who are diagnosed with breast cancer during any part of the study will continue to be a part of it and receive treatment.

All participants are encouraged to voluntarily submit blood samples and a swab of buccal cells from inside the mouth as part of TMIST’s effort to create a biorepository for future genetic markers for breast cancer. This will enable doctors and women to determine the best methods for screenings and evaluate risk factors of individual patients for developing diseases.

Tissue will also be collected from women who undergo biopsies as part of follow-ups for mammogram findings, allowing TMIST researchers to study the biology of screen-detected abnormalities and to evaluate the overdiagnosis of breast cancer from screenings.
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