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Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization

BACKGROUND: When used for hematopoietic stem cell mobilization, plerixafor was originally recommended to be administered 11 hours prior to apheresis based on the peak effect of 10 to 14 hours translating into an administration time of 10 to 11 pm. Reports of post-plerixafor anaphylactic reactions ma...

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Autores principales: El Rahi, Cynthia, Cox, James Eldin, May, Romelia, Carrum, George, Anyadike, Gloria Obi, Scholoff, Audrey, Kamble, Rammurti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120178/
https://www.ncbi.nlm.nih.gov/pubmed/30186032
http://dx.doi.org/10.1177/1179545X18792253
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author El Rahi, Cynthia
Cox, James Eldin
May, Romelia
Carrum, George
Anyadike, Gloria Obi
Scholoff, Audrey
Kamble, Rammurti
author_facet El Rahi, Cynthia
Cox, James Eldin
May, Romelia
Carrum, George
Anyadike, Gloria Obi
Scholoff, Audrey
Kamble, Rammurti
author_sort El Rahi, Cynthia
collection PubMed
description BACKGROUND: When used for hematopoietic stem cell mobilization, plerixafor was originally recommended to be administered 11 hours prior to apheresis based on the peak effect of 10 to 14 hours translating into an administration time of 10 to 11 pm. Reports of post-plerixafor anaphylactic reactions mandated labeling change by the Food and Drug Administration with recommendation of monitoring patients after administration. Based on data suggesting sustained plerixafor activity at 18 hours, we changed our administration time to 4 pm at our center. OBJECTIVE: The objective of this study is to compare the stem cell collection efficiency before and after the practice change at our institution. METHODS: A retrospective chart review for patients with multiple myeloma, Hodgkin lymphoma, and non-Hodgkin lymphoma who received a plerixafor-containing mobilization regimen was conducted. The primary end point was the percentage of patients achieving the minimal CD34(+) cell goal in ⩽2 apheresis days. The secondary end points included the percentage of patients achieving the preferred CD34(+) cell goal in ⩽2 apheresis days, days of apheresis, total CD34(+) cells Collected, and engraftment time. RESULTS: A total of 208 patients (4 pm group n = 68, 10 pm group n = 140) with multiple myeloma (n = 112), Hodgkin lymphoma (n = 10), and non-Hodgkin lymphoma (n = 86) were included in the analysis. About 91% and 89% (P = .804) of the patients in the 4 and 10 pm groups, respectively, collected minimum cell dose. Preferred CD34(+) cell goal was achieved in 57% and 53% of patients in the 4 and 10 pm groups, respectively. CONCLUSIONS: Late afternoon administration of plerixafor provides efficient stem cell mobilization.
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spelling pubmed-61201782018-09-05 Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization El Rahi, Cynthia Cox, James Eldin May, Romelia Carrum, George Anyadike, Gloria Obi Scholoff, Audrey Kamble, Rammurti Clin Med Insights Blood Disord Original Research BACKGROUND: When used for hematopoietic stem cell mobilization, plerixafor was originally recommended to be administered 11 hours prior to apheresis based on the peak effect of 10 to 14 hours translating into an administration time of 10 to 11 pm. Reports of post-plerixafor anaphylactic reactions mandated labeling change by the Food and Drug Administration with recommendation of monitoring patients after administration. Based on data suggesting sustained plerixafor activity at 18 hours, we changed our administration time to 4 pm at our center. OBJECTIVE: The objective of this study is to compare the stem cell collection efficiency before and after the practice change at our institution. METHODS: A retrospective chart review for patients with multiple myeloma, Hodgkin lymphoma, and non-Hodgkin lymphoma who received a plerixafor-containing mobilization regimen was conducted. The primary end point was the percentage of patients achieving the minimal CD34(+) cell goal in ⩽2 apheresis days. The secondary end points included the percentage of patients achieving the preferred CD34(+) cell goal in ⩽2 apheresis days, days of apheresis, total CD34(+) cells Collected, and engraftment time. RESULTS: A total of 208 patients (4 pm group n = 68, 10 pm group n = 140) with multiple myeloma (n = 112), Hodgkin lymphoma (n = 10), and non-Hodgkin lymphoma (n = 86) were included in the analysis. About 91% and 89% (P = .804) of the patients in the 4 and 10 pm groups, respectively, collected minimum cell dose. Preferred CD34(+) cell goal was achieved in 57% and 53% of patients in the 4 and 10 pm groups, respectively. CONCLUSIONS: Late afternoon administration of plerixafor provides efficient stem cell mobilization. SAGE Publications 2018-08-30 /pmc/articles/PMC6120178/ /pubmed/30186032 http://dx.doi.org/10.1177/1179545X18792253 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
El Rahi, Cynthia
Cox, James Eldin
May, Romelia
Carrum, George
Anyadike, Gloria Obi
Scholoff, Audrey
Kamble, Rammurti
Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization
title Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization
title_full Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization
title_fullStr Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization
title_full_unstemmed Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization
title_short Efficacy of Afternoon Plerixafor Administration for Stem Cell Mobilization
title_sort efficacy of afternoon plerixafor administration for stem cell mobilization
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120178/
https://www.ncbi.nlm.nih.gov/pubmed/30186032
http://dx.doi.org/10.1177/1179545X18792253
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