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Posted by on Mar 7, 2013 in Colorectal cancer | 0 comments

In a nutshell

This article presents the results from the first human trial of PD 0332991, a new anti-cancer drug. The main objective of the study was to determine the safety and recommended dose for further testing. Results warrant further studies and revealed that neutropenia (low white cell count) was the main side effect.

Some background

Cells multiply by dividing themselves. CDK proteins are involved in controlling this cell division process. Some CDK proteins, notably CDK 4 and 6 found in cancer cells, can be blocked with highly specific drugs that may stop tumor growth.

PD 0332991 is currently investigated as a clinically useful CDK 4/6 blocker (inhibitor). Previous trials showed that it inhibits tumor growth in mice and that it may be used together with other chemotherapy drugs to lower toxicity.

Methods & findings

The study presented in this article was the first human trial of PD 0332991. 41 patients previously treated with other types of chemotherapy were included between 2004 – 2008. The main objective was to discover the maximum tolerated dose of the drug that may be used in subsequent trials. Results showed that a dose of 125 mg/m2 of PD 0332991, given daily in the first 21 days out of 28 (which represented a full cycle) was safe. The main adverse effect, that required stopping the drug, was neutropenia (low white cell count). Other adverse effects were: fatigue, nausea and diarrhea.

The bottom line

The authors recommended further testing (Phase II trials) with a 125 mg/m2 dose of PD 0332991.

The fine print

Despite showing significant promise, CDK 4/6 inhibitors still need thorough testing before becoming a standard of care. This was the first human trial of PD 0332991 and the drug was only given to a small number of patients with advanced disease.

Published By :

Clinical Cancer Research

Date :

Jun 18, 2013

Original Title :

Phase I, dose-escalation trial of the oral cyclin-dependent kinase 4/6 inhibitor PD 0332991, administered using a 21-day schedule in patients with advanced cancer

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