Palbociclib drug combined with the standard treatment improved survival rate in women suffering from hormone receptor-positive metastatic breast cancer.

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The FDA has approved palbociclib drug for patients with HR-positive, HER2-negative metastatic breast cancer who experienced disease progression after undergoing hormone therapy.
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Palbociclib is a novel oral drug that inhibits enzymes important in cell division called cyclin-dependent kinase (CDK) 4/6. An international clinical trial called PALOMA-3 evaluated palbociclib in 521 women with HR-positive metastatic breast cancer who had relapsed or progressed after prior hormone therapy.
The trial participants were randomized to receive either palbociclib and fulvestrant (a standard treatment) or a placebo and fulvestrant.In a previous analysis of PALOMA-3 led by Cristofanilli and published in The Lancet Oncology, palbociclib and fulvestrant were found to be associated with a significant improvement in progression-free survival, compared to fulvestrant alone.
The findings led to FDA approval of palbociclib for patients with HR-positive, HER2-negative metastatic breast cancer who experienced disease progression following hormone therapy.The current study, published in the New England Journal of Medicine, reported overall survival outcomes for participants in PALOMA-3. It is the first to report overall survival data from a phase III trial testing a CDK4/6 inhibitor in this patient population, said Cristofanilli.
Investigators found palbociclib led to a clinically meaningful improvement in overall survival; median overall survival was 34.9 months in the palbociclib and fulvestrant group, compared to 28 months in the control group. The benefit was even greater in patients with sensitivity to prior hormone therapy.
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