Led by Dr Cynthia Ma, the study investigated 50 women with breast cancer treated with standard endocrine therapy in combination with Ibrance® prior to surgery. DiviTum® was used to measure cell proliferation rate in blood samples collected before and after 2 weeks of Ibrance® treatment. Results demonstrate a high ability of DiviTum® to identify each patient’s anti-proliferative effect of Ibrance®. The researchers conclude that DiviTum® can have a clinically useful role as an early indicator of treatment response to CDK 4/6 inhibitors such as Ibrance®.

“Our study provides the first clinical evidence of using DiviTum for measuring TK1 activity for early evaluation of the effect of palbociclib treatment in breast cancer. The results are very promising and support future studies of DiviTum to evaluate and identify patients for response to CDK 4/6 inhibitors,” says Dr Cynthia Ma, MD, PhD, Associate Professor of Medicine, Washington University School of Medicine, St Louis, US.

There are currently three approved CDK4/6 inhibitors (Ibrance® from Pfizer, Kisqali® from Novartis and Verzenio® from Lilly) with documented ability to prolong disease progression. Far from all patients benefit from therapy, and can experience severe side-effects from a treatment priced at $ 10,000 per month.

“These results correlating DiviTum to palbociclib efficacy are highly promising since there is no other blood based biomarker available for evaluating CDK 4/6 inhibitor efficacy today. CDK 4/6 inhibitors are very effective but also costly and far from all patients respond. It is therefore very important to provide new biomarkers in order to enable best possible treatments for patients and cost effectiveness for payers. These results support our aim to provide DiviTum as a standard tool for evaluating treatments in metastatic breast- and other cancers.” says Anders Rylander, CEO Biovica.

Link to the article: http://rdcu.be/y6zE