Literature DB >> 20530974

FDA review summary: Mozobil in combination with granulocyte colony-stimulating factor to mobilize hematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation.

Michael Brave1, Ann Farrell, Sue Ching Lin, Terrance Ocheltree, Sarah Pope Miksinski, Shwu-Luan Lee, Haleh Saber, Jeanne Fourie, Christoffer Tornoe, Brian Booth, Weishi Yuan, Kun He, Robert Justice, Richard Pazdur.   

Abstract

PURPOSE: On December 15, 2008, the US Food and Drug Administration approved plerixafor (Mozobil; Genzyme Corp.), a new small-molecule inhibitor of the CXCR4 chemokine receptor, for use in combination with granulocyte colony-stimulating factor (G-CSF) to mobilize hematopoietic stem cells (HSC) to the peripheral blood for collection and subsequent autologous transplantation in patients with non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM). This summary reviews the database supporting this approval. EXPERIMENTAL
DESIGN: The safety and efficacy of plerixafor were demonstrated by 2 multicenter, randomized, placebo-controlled studies in patients with NHL and MM who were eligible for autologous HSC transplantation. The primary efficacy end points were the collection of > or = 5 x 10(6) CD34+ cells/kg from the peripheral blood in 4 or fewer apheresis sessions in patients with NHL or > or = 6 x 10(6) CD34+ cells/kg from the peripheral blood in 2 or fewer apheresis sessions in patients with MM.
RESULTS: The 2 randomized studies combined enrolled 600 patients (298 with NHL and 302 with MM). Fifty-nine percent of patients with NHL who were mobilized with G-CSF and plerixafor had peripheral blood HSC collections of > or = 5 x 10(6) CD34+ cells/kg in 4 or fewer apheresis sessions, compared with 20% of patients with NHL who were mobilized with G-CSF and placebo (p < 0.001). Seventy-two percent of patients with MM who were mobilized with Mozobil and G-CSF had peripheral blood HSC collections of > or = 6 x 10(6) CD34+ cells/kg in 2 or fewer apheresis sessions, compared with 34% of patients with MM who were mobilized with placebo and G-CSF (p < 0.001). Common adverse reactions included diarrhea, nausea, vomiting, flatulence, injection site reactions, fatigue, arthralgia, headache, dizziness, and insomnia.
CONCLUSIONS: This report describes the Food and Drug Administration review supporting the approval of plerixafor. Copyright 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20530974     DOI: 10.1159/000315736

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  38 in total

1.  The effective use of plerixafor as a real-time rescue strategy for patients poorly mobilizing autologous CD34(+) cells.

Authors:  Ajay K Gopal; Mehdi Karami; JoAl Mayor; Mylene Macebeo; Michael Linenberger; William I Bensinger; Leona Holmberg
Journal:  J Clin Apher       Date:  2012-02-02       Impact factor: 2.821

Review 2.  The pharmacology of regenerative medicine.

Authors:  George J Christ; Justin M Saul; Mark E Furth; Karl-Erik Andersson
Journal:  Pharmacol Rev       Date:  2013-07-01       Impact factor: 25.468

3.  A pilot study evaluating the safety and CD34+ cell mobilizing activity of escalating doses of plerixafor in healthy volunteers.

Authors:  Steven J Lemery; Matthew M Hsieh; Aleah Smith; Sheila Rao; Hanh M Khuu; Donohue Theresa; Jennifer M Viano; Lisa Cook; Rose Goodwin; Carol Boss; Gary Calandra; Nancy Geller; John Tisdale; Richard Childs
Journal:  Br J Haematol       Date:  2011-02-24       Impact factor: 6.998

4.  Mobilizing plasmacytoid dendritic cells.

Authors:  Edmund K Waller
Journal:  Blood       Date:  2017-05-11       Impact factor: 22.113

Review 5.  Hematopoietic Stem Cell Gene Therapy: Progress and Lessons Learned.

Authors:  Richard A Morgan; David Gray; Anastasia Lomova; Donald B Kohn
Journal:  Cell Stem Cell       Date:  2017-11-02       Impact factor: 24.633

6.  Association of chemokine and chemokine receptor expression with the invasion and metastasis of lung carcinoma.

Authors:  Yan Liu; Bing-Quan Wu; Hua Geng; Mei-Lin Xu; Hao-Hao Zhong
Journal:  Oncol Lett       Date:  2015-06-22       Impact factor: 2.967

7.  G-CSF supplementation with chemotherapy can promote revascularization and subsequent tumor regrowth: prevention by a CXCR4 antagonist.

Authors:  Tali Voloshin; Svetlana Gingis-Velitski; Rotem Bril; Liat Benayoun; Michal Munster; Chloe Milsom; Shan Man; Robert S Kerbel; Yuval Shaked
Journal:  Blood       Date:  2011-06-17       Impact factor: 22.113

Review 8.  Great promise of tissue-resident adult stem/progenitor cells in transplantation and cancer therapies.

Authors:  Murielle Mimeault; Surinder K Batra
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

9.  Initial assessment of the role of CXC chemokine receptor 4 after polytrauma.

Authors:  Harold H Bach; Vikas Saini; Todd A Baker; Abhishek Tripathi; Richard L Gamelli; Matthias Majetschak
Journal:  Mol Med       Date:  2012-09-25       Impact factor: 6.354

10.  Regulation of the thrombin/protease-activated receptor 1 axis by chemokine (CXC motif) receptor 4.

Authors:  Xianlong Gao; You-Hong Cheng; Garrett A Enten; Anthony J DeSantis; Vadim Gaponenko; Matthias Majetschak
Journal:  J Biol Chem       Date:  2020-08-24       Impact factor: 5.157

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