Multiple Myeloma Clinical Trial
Official title:
Analysis of Data Collected in the European Group for Blood and Marrow Transplantation (EBMT) Registry on a Cohort of Patients Receiving Plerixafor
In the European Union (EU), plerixafor is indicated in combination with granulocyte colony
stimulating factor (G-CSF) to enhance mobilisation of haematopoietic stem cells (HSCs) to
the peripheral blood (PB) for collection and subsequent autologous transplantation in
patients with lymphoma and multiple myeloma (MM) whose cells mobilise poorly.
This is a clinical outcome analysis of a prospectively defined cohort of patients with data
reported retrospectively to the European Group for Blood and Marrow Transplantation (EBMT)
who have lymphoma or multiple myeloma (MM), whose cells mobilize poorly, and who have
undergone autologous haematopoietic stem cell (HSC) transplantation during the years 2008 up
to and including 2012.
The EBMT is a non-profit, scientific society representing more than 600 transplant centers
mainly in Europe. The EBMT promotes all activity aiming to improve stem cell transplantation
or cellular therapy, which includes registering all the activity relating to stem cell
transplants. Data are entered, managed, and maintained in a central database with internet
access; each EBMT center is represented in this database.
The analysis of data from a well established registry like the EBMT registry allows for
follow up of a large number of patients who are representative of the patient population
receiving plerixafor.
n/a
Observational Model: Cohort, Time Perspective: Retrospective
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