Optimizing autologous stem cell collections for patients with multiple myeloma receiving G‐CSF and Plerixafor: A single center project

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Autores principales: Ayda Javanbakht, Stephanie Stringer, Hollie Anderson, Ellie Hamilton, Anisha Philip, Edmund K. Waller, Amelia A. Langston, Nisha Joseph, John D. Roback, Thomas Schneider, H. Cliff Sullivan, Jeanne E. Hendrickson
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Publicado: Wiley 2024
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author Ayda Javanbakht
Stephanie Stringer
Hollie Anderson
Ellie Hamilton
Anisha Philip
Edmund K. Waller
Amelia A. Langston
Nisha Joseph
John D. Roback
Thomas Schneider
H. Cliff Sullivan
Jeanne E. Hendrickson
author_facet Ayda Javanbakht
Stephanie Stringer
Hollie Anderson
Ellie Hamilton
Anisha Philip
Edmund K. Waller
Amelia A. Langston
Nisha Joseph
John D. Roback
Thomas Schneider
H. Cliff Sullivan
Jeanne E. Hendrickson
Ayda Javanbakht
Stephanie Stringer
Hollie Anderson
Ellie Hamilton
Anisha Philip
Edmund K. Waller
Amelia A. Langston
Nisha Joseph
John D. Roback
Thomas Schneider
H. Cliff Sullivan
Jeanne E. Hendrickson
collection Wiley Open Access
contents Optimizing autologous stem cell collections for patients with multiple myeloma receiving G‐CSF and Plerixafor: A single center project Ayda Javanbakht Stephanie Stringer Hollie Anderson Ellie Hamilton Anisha Philip Edmund K. Waller Amelia A. Langston Nisha Joseph John D. Roback Thomas Schneider H. Cliff Sullivan Jeanne E. Hendrickson Journal of Clinical Apheresis AbstractBackgroundIncreasing indications for cellular therapy collections have stressed our healthcare system, with autologous collections having a longer than desired wait time until apheresis collection. This quality improvement initiative was undertaken to accommodate more patients within existing resources.Study Design and MethodsPatients with multiple myeloma who underwent autologous peripheral blood stem cell collection from October 2022 to April 2023 were included. Demographic, mobilization, laboratory, and apheresis data were retrospectively collected from the medical record.ResultsThis cohort included 120 patients (49.2% male), with a median age of 60 years. All received G‐CSF and 95% received pre‐emptive Plerixafor approximately 18 hours pre‐collection. Most (79%) had collection goals of at least 8 × 106/kg CD34 cells, with 63% over 70 years old having this high collection goal (despite 20 years of institutional data showing <1% over 70 years old have a second transplant). With collection efficiencies of 55.9%, 44% of patients achieved their collection goal in a single day apheresis collection. A platelet count <150 × 103/μL on the day of collection was a predictor for poor mobilization; among 27 patients with a low baseline platelet count, 17 did not achieve the collection goal and 2 failed to collect a transplantable dose.ConclusionsWith minor collection goal adjustments, 15% of all collection appointments could have been avoided over this 6‐month period. Other strategies to accommodate more patients include mobilization modifications (Plerixafor timing or substituting a longer acting drug), utilizing platelet counts to predict mobilization, and modifying apheresis collection volumes or schedule templates. 10.1002/jca.22127 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/jca.22127
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spellingShingle Optimizing autologous stem cell collections for patients with multiple myeloma receiving G‐CSF and Plerixafor: A single center project
Ayda Javanbakht
Stephanie Stringer
Hollie Anderson
Ellie Hamilton
Anisha Philip
Edmund K. Waller
Amelia A. Langston
Nisha Joseph
John D. Roback
Thomas Schneider
H. Cliff Sullivan
Jeanne E. Hendrickson
Journal of Clinical Apheresis
Optimizing autologous stem cell collections for patients with multiple myeloma receiving G‐CSF and Plerixafor: A single center project Ayda Javanbakht Stephanie Stringer Hollie Anderson Ellie Hamilton Anisha Philip Edmund K. Waller Amelia A. Langston Nisha Joseph John D. Roback Thomas Schneider H. Cliff Sullivan Jeanne E. Hendrickson Journal of Clinical Apheresis AbstractBackgroundIncreasing indications for cellular therapy collections have stressed our healthcare system, with autologous collections having a longer than desired wait time until apheresis collection. This quality improvement initiative was undertaken to accommodate more patients within existing resources.Study Design and MethodsPatients with multiple myeloma who underwent autologous peripheral blood stem cell collection from October 2022 to April 2023 were included. Demographic, mobilization, laboratory, and apheresis data were retrospectively collected from the medical record.ResultsThis cohort included 120 patients (49.2% male), with a median age of 60 years. All received G‐CSF and 95% received pre‐emptive Plerixafor approximately 18 hours pre‐collection. Most (79%) had collection goals of at least 8 × 106/kg CD34 cells, with 63% over 70 years old having this high collection goal (despite 20 years of institutional data showing <1% over 70 years old have a second transplant). With collection efficiencies of 55.9%, 44% of patients achieved their collection goal in a single day apheresis collection. A platelet count <150 × 103/μL on the day of collection was a predictor for poor mobilization; among 27 patients with a low baseline platelet count, 17 did not achieve the collection goal and 2 failed to collect a transplantable dose.ConclusionsWith minor collection goal adjustments, 15% of all collection appointments could have been avoided over this 6‐month period. Other strategies to accommodate more patients include mobilization modifications (Plerixafor timing or substituting a longer acting drug), utilizing platelet counts to predict mobilization, and modifying apheresis collection volumes or schedule templates. 10.1002/jca.22127 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Optimizing autologous stem cell collections for patients with multiple myeloma receiving G‐CSF and Plerixafor: A single center project
topic Journal of Clinical Apheresis
url https://onlinelibrary.wiley.com/doi/10.1002/jca.22127