Intravenous Busulfan, Dimethylacetamide and neurotoxicity after high-dose pretransplant conditioning chemotherapy

Author:

Ramdial Jeremy1,Nieto Yago2,Andersson Borje3ORCID,Chan Kok Hoe1,Petitto Gabriela Sanchez1,Valdez Benigno4

Affiliation:

1. M D Anderson Cancer Center

2. MD Anderson Cancer Center, University of Texas

3. University of Texas MD Anderson Cancer Center

4. MD Anderson

Abstract

Abstract Intravenous Busulfan-based (IV Bu-) conditioning regimens are widely used in stem cell transplant and have been demonstrated as more effective and safer than cyclophosphamide and total body irradiation. Despite its superiority concerns remain regarding toxicities, specifically, veno-occlusive disease/sinusoidal obstructive syndrome, reproductive toxicity and neurotoxicity. Some of these concerns do not relate to busulfan itself, but to its composite solvent vehicle including N,N‑dimethylacetamide (DMA). Herein, we report a case series of six patients who received high-dose IV Bu-based conditioning regimens, and who developed neurotoxicity with various neurological manifestations and outcomes, ranging from mild to fatal. This case series highlights the need for further studies to investigate the safety of IV Bu, especially in patients with an underlying organic brain disorder, who have been treated with immunoconjugates with a potential for central neurotoxicity, or who have received therapeutic brain irradiation.

Publisher

Research Square Platform LLC

Reference26 articles.

1. FDA Approval of NDA 20–954, February 4, 1999; Reviewer report on IV Busulfan.

2. Andersson BS, Valdez B.C., and Jones R.B. Pharmacologic Basis for High-dose Chemotherapy, in Thomas’ Hematopoietic Cell Transplantation. 4th Edition. Appelbaum FR, Forman SJ, Negrin RS, Blume KG (Eds.) John Wiley & Sons, Ltd. 2016; pp. 211–224

3. Center for International Blood and Marrow Transplantation Research, Website, 2022.

4. Intravenous versus oral busulfan as part of a busulfan/cyclophosphamide preparative regimen for allogeneic hematopoietic stem cell transplantation: decreased incidence of hepatic venoocclusive disease (HVOD), HVOD-related mortality, and overall 100-day mortality;Kashyap A;Biol Blood Marrow Transplant,2002

5. Phase II trial of high-dose Gemcitabine/Busulfan/Melphalan with autologous stem-cell transplantation for primary refractory or poor-risk relapsed Hodgkin’s Lymphoma;Nieto Y;Biol Blood Marrow Transplant,2018

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