In 2012, the CADTH Common Drug Review (CDR) examined the evidence on plerixafor, consisting of two randomized controlled trials, and issued a “do not list” recommendation based on the exclusion of the subpopulation of interest from the included studies (i.e. predicted poor or proven poor mobilizers). This Rapid Response report aims to identify and review the clinical and cost-effectiveness of plerixafor in patients who are failing stem cell mobilization. Guidelines associated with the use of plerixafor in patients failing stem cell mobilization will also be examined.
Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic reviews. The intent is to provide a list of sources of the best evidence on the topic that the Canadian Agency for Drugs and Technologies in Health (CADTH) could identify using all reasonable efforts within the time allowed. Rapid responses should be considered along with other types of information and health care considerations. The information included in this response is not intended to replace professional medical advice, nor should it be construed as a recommendation for or against the use of a particular health technology. Readers are also cautioned that a lack of good quality evidence does not necessarily mean a lack of effectiveness particularly in the case of new and emerging health technologies, for which little information can be found, but which may in future prove to be effective. While CADTH has taken care in the preparation of the report to ensure that its contents are accurate, complete and up to date, CADTH does not make any guarantee to that effect. CADTH is not liable for any loss or damages resulting from use of the information in the report.