Plerixafor
Autor: | Antona J. Wagstaff |
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Rok vydání: | 2009 |
Předmět: |
Oncology
Benzylamines Receptors CXCR4 medicine.medical_specialty medicine.medical_treatment Hematopoietic stem cell transplantation Cyclams Infusions Subcutaneous Heterocyclic Compounds Internal medicine medicine Humans Pharmacology (medical) Multiple myeloma business.industry Lymphoma Non-Hodgkin Plerixafor Hematopoietic Stem Cell Transplantation medicine.disease Hematopoietic Stem Cell Mobilization Lymphoma Non-Hodgkin's lymphoma Surgery Transplantation Regimen medicine.anatomical_structure Bone marrow Multiple Myeloma business medicine.drug |
Zdroj: | Drugs. 69:319-326 |
ISSN: | 0012-6667 |
DOI: | 10.2165/00003495-200969030-00007 |
Popis: | *The bicyclam plerixafor mobilizes haematopoietic stem cells (HSCs) from the bone marrow into the peripheral blood circulation and augments the effects of granulocyte colony-stimulating factor (G-CSF). *More patients requiring autologous HSC transplantation for non-Hodgkin's lymphoma or multiple myeloma in first or second remission achieved goal increases in mobilized CD34+ cells after subcutaneous plerixafor 240 microg/kg/day for up to four apheresis days in conjunction with a G-CSF treatment regimen than after placebo plus G-CSF. *Sufficient CD34+ cells for transplantation were collected earlier for recipients of plerixafor plus G-CSF (often after one apheresis) than for patients receiving placebo plus G-CSF. *Time to engraftment and durability of grafts after 12 months were similar for both plerixafor plus G-CSF and placebo plus G-CSF. *In a compassionate-use trial in patients with non-Hodgkin's lymphoma, multiple myeloma or Hodgkin's disease in whom prior mobilization attempts were unable to stimulate sufficient cells, therapy with the plerixafor/G-CSF combination regimen was successful in > or = 60% of patients. *Plerixafor appears to be generally well tolerated; most adverse effects in clinical trials were mild and transient. |
Databáze: | OpenAIRE |
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