Despite progress, viagra 40mg genetic profiling of tumors has a long way to go
Genetic tests for cancer have come a long way since they first entered the clinic in 1995. Back then, store mutations in two genes—known as BRCA1 and BRCA2—hinted at the crucial role that genetics can play in treatment decisions. Women carrying one of those mutations (and having a family history of breast or ovarian cancer) were much more likely than the general population to develop tumors in their breasts or ovaries. Then, stuff as now, some of these women opted to have their breasts and ovaries removed before any malignant growths could arise.
In the intervening decades, researchers have come to recognize that most cancers are driven largely by abnormalities in genes. Genetic analysis of tumors has, therefore, become standard practice for many malignancies—such as breast, lung and colon cancer—because the information may help guide therapy. Clinicians have amassed a modest arsenal of drugs able to counteract some of the most common mutations.
Yet many patients learn that their cancers have mutations for which no drug exists. In fact, the roles many of these genetic changes play in cancer growth are poorly understood. Complex analyses of DNA done across a range of cancer types have revealed a landscape rife with genetic mutations, and very little of this encyclopedic information is helping doctors to make treatment decisions. To date, the U.S. Food and Drug Administration has approved just 29 tests for specific mutations that can directly influence therapy.
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