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Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)

INTRODUCTION: Despite the implementation of new therapeutic agents, management of relapsed multiple myeloma (MM) remains a challenge. Salvage autologous hematopoietic cell transplant (AHCT) remains a valid therapeutic option for eligible patients who achieve prolonged response after a first AHCT. Ho...

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Autores principales: van de Wyngaert, Zoe, Malard, Florent, Hulin, Cyrille, Caillot, Denis, Mariette, Clara, Facon, Thierry, Touzeau, Cyrille, Perrot, Aurore, Moreau, Philippe, Hebraud, Benjamin, Kanouni, Tarik, Heshmati, Farhad, Lebon, Delphine, Mohty, Mohamad, Chabannon, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924840/
https://www.ncbi.nlm.nih.gov/pubmed/36781774
http://dx.doi.org/10.1007/s44228-023-00030-0
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author van de Wyngaert, Zoe
Malard, Florent
Hulin, Cyrille
Caillot, Denis
Mariette, Clara
Facon, Thierry
Touzeau, Cyrille
Perrot, Aurore
Moreau, Philippe
Hebraud, Benjamin
Kanouni, Tarik
Heshmati, Farhad
Lebon, Delphine
Mohty, Mohamad
Chabannon, Christian
author_facet van de Wyngaert, Zoe
Malard, Florent
Hulin, Cyrille
Caillot, Denis
Mariette, Clara
Facon, Thierry
Touzeau, Cyrille
Perrot, Aurore
Moreau, Philippe
Hebraud, Benjamin
Kanouni, Tarik
Heshmati, Farhad
Lebon, Delphine
Mohty, Mohamad
Chabannon, Christian
author_sort van de Wyngaert, Zoe
collection PubMed
description INTRODUCTION: Despite the implementation of new therapeutic agents, management of relapsed multiple myeloma (MM) remains a challenge. Salvage autologous hematopoietic cell transplant (AHCT) remains a valid therapeutic option for eligible patients who achieve prolonged response after a first AHCT. However, a second graft is not always available, and these patients may need a second mobilization. PATIENTS AND METHODS: This prospective, non-interventional, multicenter study aimed to collect data on the feasibility of salvage AHCT using a plerixafor-based hematopoietic cell mobilization in relapsed MM, according to the plerixafor label in France. Adult patients with relapsed MM eligible for a second AHCT and mobilized using granulocyte- colony stimulating factor (G-CSF) and plerixafor were included. RESULTS: Of the 23 patients, 17 achieved a successful hematopoietic cell mobilization and 13 were able to proceed to a second AHCT. Median age was 62.9 years (min–max 51–71). Ten patients (77%) were male. Eleven (85%) received AHCT as a third-line treatment or more. Median time between first and second AHCT was 5.4 years (range, 2.6–16.3). Among 18 evaluable patients, mobilization was successful for 17 (94%) of them [95% CI 84–100], with no reported side effects. Among the 13 patients who underwent salvage AHCT, the median time to engraftment was 14 days (min–max 11–29). One-year progression-free and overall survival were 88.9% [95% CI 43.3–98.4] and 100%, respectively. CONCLUSION: This study demonstrated that plerixafor allows safe and efficient mobilization in relapsed MM patients who are candidates for a salvage AHCT. TRIAL REGISTRATION: NCT02439476 Registered 8 May 2015, https://clinicaltrials.gov/ct2/show/NCT02439476.
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spelling pubmed-99248402023-02-14 Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03) van de Wyngaert, Zoe Malard, Florent Hulin, Cyrille Caillot, Denis Mariette, Clara Facon, Thierry Touzeau, Cyrille Perrot, Aurore Moreau, Philippe Hebraud, Benjamin Kanouni, Tarik Heshmati, Farhad Lebon, Delphine Mohty, Mohamad Chabannon, Christian Clin Hematol Int Research Article INTRODUCTION: Despite the implementation of new therapeutic agents, management of relapsed multiple myeloma (MM) remains a challenge. Salvage autologous hematopoietic cell transplant (AHCT) remains a valid therapeutic option for eligible patients who achieve prolonged response after a first AHCT. However, a second graft is not always available, and these patients may need a second mobilization. PATIENTS AND METHODS: This prospective, non-interventional, multicenter study aimed to collect data on the feasibility of salvage AHCT using a plerixafor-based hematopoietic cell mobilization in relapsed MM, according to the plerixafor label in France. Adult patients with relapsed MM eligible for a second AHCT and mobilized using granulocyte- colony stimulating factor (G-CSF) and plerixafor were included. RESULTS: Of the 23 patients, 17 achieved a successful hematopoietic cell mobilization and 13 were able to proceed to a second AHCT. Median age was 62.9 years (min–max 51–71). Ten patients (77%) were male. Eleven (85%) received AHCT as a third-line treatment or more. Median time between first and second AHCT was 5.4 years (range, 2.6–16.3). Among 18 evaluable patients, mobilization was successful for 17 (94%) of them [95% CI 84–100], with no reported side effects. Among the 13 patients who underwent salvage AHCT, the median time to engraftment was 14 days (min–max 11–29). One-year progression-free and overall survival were 88.9% [95% CI 43.3–98.4] and 100%, respectively. CONCLUSION: This study demonstrated that plerixafor allows safe and efficient mobilization in relapsed MM patients who are candidates for a salvage AHCT. TRIAL REGISTRATION: NCT02439476 Registered 8 May 2015, https://clinicaltrials.gov/ct2/show/NCT02439476. Springer Netherlands 2023-02-12 /pmc/articles/PMC9924840/ /pubmed/36781774 http://dx.doi.org/10.1007/s44228-023-00030-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
van de Wyngaert, Zoe
Malard, Florent
Hulin, Cyrille
Caillot, Denis
Mariette, Clara
Facon, Thierry
Touzeau, Cyrille
Perrot, Aurore
Moreau, Philippe
Hebraud, Benjamin
Kanouni, Tarik
Heshmati, Farhad
Lebon, Delphine
Mohty, Mohamad
Chabannon, Christian
Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)
title Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)
title_full Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)
title_fullStr Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)
title_full_unstemmed Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)
title_short Non-interventional Study Evaluating the Mobilization of Stem Cells by Plerixafor Before Salvage Autologous Stem Cell Transplant in Relapsed Multiple Myeloma (IFM-2015-03)
title_sort non-interventional study evaluating the mobilization of stem cells by plerixafor before salvage autologous stem cell transplant in relapsed multiple myeloma (ifm-2015-03)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924840/
https://www.ncbi.nlm.nih.gov/pubmed/36781774
http://dx.doi.org/10.1007/s44228-023-00030-0
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