Pharmacokinetic and pharmacodynamic study of lenograstim for hematopoietic stem cell mobilization: a prospective randomized study for optimal apheresis.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
05 2019
Historique:
received: 13 12 2018
revised: 14 01 2019
accepted: 17 01 2019
pubmed: 30 3 2019
medline: 2 6 2020
entrez: 30 3 2019
Statut: ppublish

Résumé

This study evaluated the correlation between the pharmacokinetics and pharmacodynamics of granulocyte colony-stimulating factor (lenograstim) and the impact of initiation time of apheresis on stem cell mobilization in patients with multiple myeloma. Twenty-four patients with multiple myeloma were randomized into one of the two groups (early vs. late). Lenograstim at 10 μg/kg/day once daily was injected for at least 4 consecutive days. Apheresis was initiated 2 hours after the fourth dose of lenograstim in the early collection group and 16 hours after the fourth dose of lenograstim in the late collection group. Blood sampling for pharmacokinetics was performed within 30 minutes before, and 1, 2, 6, and 24 hours after the fourth dose of lenograstim. Overall, the two groups (early vs. late, n = 10 vs. 14) exhibited similar baseline characteristics including age, sex, subtype of myeloma, stage distribution, and myeloma-associated symptoms. No correlation was found between plasma lenograstim concentration and peripheral blood (PB) CD34+ cell counts or hematopoietic progenitor cells. In the late collection group, the median number of apheresis procedures for minimal collection was significantly lower (early vs. late: 2 vs. 1; p = 0.04) and there was a higher number of total collected PB CD34+ cells in a single session of apheresis (1.4 vs. 3.1; p = 0.06). There were no differences in median overall PB stem cell collection efficiency. Late collection positively impacted the number of apheresis procedures for minimal collection, with numerically improved PB stem cell collection efficiency at first apheresis in patients with multiple myeloma.

Sections du résumé

BACKGROUND
This study evaluated the correlation between the pharmacokinetics and pharmacodynamics of granulocyte colony-stimulating factor (lenograstim) and the impact of initiation time of apheresis on stem cell mobilization in patients with multiple myeloma.
STUDY DESIGN AND METHODS
Twenty-four patients with multiple myeloma were randomized into one of the two groups (early vs. late). Lenograstim at 10 μg/kg/day once daily was injected for at least 4 consecutive days. Apheresis was initiated 2 hours after the fourth dose of lenograstim in the early collection group and 16 hours after the fourth dose of lenograstim in the late collection group. Blood sampling for pharmacokinetics was performed within 30 minutes before, and 1, 2, 6, and 24 hours after the fourth dose of lenograstim.
RESULTS
Overall, the two groups (early vs. late, n = 10 vs. 14) exhibited similar baseline characteristics including age, sex, subtype of myeloma, stage distribution, and myeloma-associated symptoms. No correlation was found between plasma lenograstim concentration and peripheral blood (PB) CD34+ cell counts or hematopoietic progenitor cells. In the late collection group, the median number of apheresis procedures for minimal collection was significantly lower (early vs. late: 2 vs. 1; p = 0.04) and there was a higher number of total collected PB CD34+ cells in a single session of apheresis (1.4 vs. 3.1; p = 0.06). There were no differences in median overall PB stem cell collection efficiency.
CONCLUSION
Late collection positively impacted the number of apheresis procedures for minimal collection, with numerically improved PB stem cell collection efficiency at first apheresis in patients with multiple myeloma.

Identifiants

pubmed: 30924165
doi: 10.1111/trf.15265
doi:

Substances chimiques

Antigens, CD34 0
Lenograstim 6WS4C399GB

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1781-1788

Informations de copyright

© 2019 AABB.

Auteurs

Jihoon Kang (J)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Division of Hematology/Oncology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Jung Yong Hong (JY)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Dok Hyun Yoon (DH)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Jeong Eun Kim (JE)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Kyu-Pyo Kim (KP)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Shin Kim (S)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Kyoung Min Lee (KM)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Jung Sun Park (JS)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Ji Sung Lee (JS)

Clinical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, South Korea.

Cheolwon Suh (C)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

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Classifications MeSH