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The
21-gene assay and its impact on breast cancer treatment
Joseph Ragaz, MD, FRCPC
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Every year, many Canadians are receiving adjuvant chemotherapy
for breast cancer that may not be required. Like many therapies
given to large unselected populations, it is evident that some individuals
benefit a great deal, some less, and some not at all. There is increasing
evidence that the recently developed 21-gene assay test1,2,3 can
identify breast cancer patients considered for adjuvant chemotherapy
who will not benefit from this treatment.
In the US, the 21-gene assay test was approved by the US Food and
Drug Administration (FDA) in 2005. Since 2007, this test has become
routine for node-negative breast cancer patients whose tumours test
positive for hormone receptors and who are candidates for adjuvant
chemotherapy.4,5 The cost-benefit analyses in the US project substantial
quality of life and cost benefits due to avoided chemotherapy.
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here (pdf format)
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