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Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation
Sinusoidal Obstruction Syndrome (SOS) is a life threatening HSCT complication and it can rapidly evolve in Multiple Organ Dysfunction Syndrome, with a mortality exceeding 80%. Early treatment with defibrotide is the leading factor for efficacy. Its prophylactic use is recommended in the pediatric se...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240310/ https://www.ncbi.nlm.nih.gov/pubmed/35785209 http://dx.doi.org/10.3389/fonc.2022.933317 |
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author | Giglio, Fabio Xue, Elisabetta Greco, Raffaella Lazzari, Lorenzo Clerici, Daniela Teresa Lorentino, Francesca Mastaglio, Sara Marktel, Sarah Lupo-Stanghellini, Maria Teresa Marcatti, Magda Corti, Consuelo Bernardi, Massimo Piemontese, Simona Ciceri, Fabio Peccatori, Jacopo |
author_facet | Giglio, Fabio Xue, Elisabetta Greco, Raffaella Lazzari, Lorenzo Clerici, Daniela Teresa Lorentino, Francesca Mastaglio, Sara Marktel, Sarah Lupo-Stanghellini, Maria Teresa Marcatti, Magda Corti, Consuelo Bernardi, Massimo Piemontese, Simona Ciceri, Fabio Peccatori, Jacopo |
author_sort | Giglio, Fabio |
collection | PubMed |
description | Sinusoidal Obstruction Syndrome (SOS) is a life threatening HSCT complication and it can rapidly evolve in Multiple Organ Dysfunction Syndrome, with a mortality exceeding 80%. Early treatment with defibrotide is the leading factor for efficacy. Its prophylactic use is recommended in the pediatric setting, but its value isn’t validated for adults, although factors for individual risk assessment are debated. We here present a real-world experience of Defibrotide prophylaxis in adults at very high risk of SOS. We treated with prophylactic Defibrotide and Ursodeoxycholic Acid seven patients receiving allogeneic HSCT for high risk B-ALL, previously treated with single agent Inotuzomab-Ozogamicin. They all had other high risk factors for SOS such as previous hepatotoxicity, previous allo-HSCT, double alkylating conditioning. All patients received Treosulfan-Fludarabine conditioning, Thiotepa was added in 4 patients and 4GyTBI in 2 patients. GvHD prophylaxis included post-transplant cyclophosphamide, rapamycin and mycophenolate. Donor source was PBSC. Five patients received family MMRD transplant, 1 patient a MRD transplant and 1 patient a MUD transplant. Non-severe gastrointestinal bleeding occurred in two patients requiring defibrotide temporarily discontinuation. SOS occurred in 3/7 cases within 21 days after HSCT and no late-onset SOS were diagnosed. SOS caused death in all cases. All three patients were characterized by a common pattern of very high risk factors by prior HSCT, they all received a myeloablative conditioning with Treosulfan-Thiotepa and a MMRD transplant. Defibrotide prophylaxis apparently failed to protect against the development of SOS in those patients treated with a double alkylator-based conditioning regimen, while a possible efficacy for the other high-risk patients is debatable. |
format | Online Article Text |
id | pubmed-9240310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92403102022-06-30 Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation Giglio, Fabio Xue, Elisabetta Greco, Raffaella Lazzari, Lorenzo Clerici, Daniela Teresa Lorentino, Francesca Mastaglio, Sara Marktel, Sarah Lupo-Stanghellini, Maria Teresa Marcatti, Magda Corti, Consuelo Bernardi, Massimo Piemontese, Simona Ciceri, Fabio Peccatori, Jacopo Front Oncol Oncology Sinusoidal Obstruction Syndrome (SOS) is a life threatening HSCT complication and it can rapidly evolve in Multiple Organ Dysfunction Syndrome, with a mortality exceeding 80%. Early treatment with defibrotide is the leading factor for efficacy. Its prophylactic use is recommended in the pediatric setting, but its value isn’t validated for adults, although factors for individual risk assessment are debated. We here present a real-world experience of Defibrotide prophylaxis in adults at very high risk of SOS. We treated with prophylactic Defibrotide and Ursodeoxycholic Acid seven patients receiving allogeneic HSCT for high risk B-ALL, previously treated with single agent Inotuzomab-Ozogamicin. They all had other high risk factors for SOS such as previous hepatotoxicity, previous allo-HSCT, double alkylating conditioning. All patients received Treosulfan-Fludarabine conditioning, Thiotepa was added in 4 patients and 4GyTBI in 2 patients. GvHD prophylaxis included post-transplant cyclophosphamide, rapamycin and mycophenolate. Donor source was PBSC. Five patients received family MMRD transplant, 1 patient a MRD transplant and 1 patient a MUD transplant. Non-severe gastrointestinal bleeding occurred in two patients requiring defibrotide temporarily discontinuation. SOS occurred in 3/7 cases within 21 days after HSCT and no late-onset SOS were diagnosed. SOS caused death in all cases. All three patients were characterized by a common pattern of very high risk factors by prior HSCT, they all received a myeloablative conditioning with Treosulfan-Thiotepa and a MMRD transplant. Defibrotide prophylaxis apparently failed to protect against the development of SOS in those patients treated with a double alkylator-based conditioning regimen, while a possible efficacy for the other high-risk patients is debatable. Frontiers Media S.A. 2022-06-15 /pmc/articles/PMC9240310/ /pubmed/35785209 http://dx.doi.org/10.3389/fonc.2022.933317 Text en Copyright © 2022 Giglio, Xue, Greco, Lazzari, Clerici, Lorentino, Mastaglio, Marktel, Lupo-Stanghellini, Marcatti, Corti, Bernardi, Piemontese, Ciceri and Peccatori https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Giglio, Fabio Xue, Elisabetta Greco, Raffaella Lazzari, Lorenzo Clerici, Daniela Teresa Lorentino, Francesca Mastaglio, Sara Marktel, Sarah Lupo-Stanghellini, Maria Teresa Marcatti, Magda Corti, Consuelo Bernardi, Massimo Piemontese, Simona Ciceri, Fabio Peccatori, Jacopo Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation |
title | Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation |
title_full | Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation |
title_fullStr | Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation |
title_full_unstemmed | Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation |
title_short | Defibrotide Prophylaxis of Sinusoidal Obstruction Syndrome in Adults Treated With Inotuzumab Ozogamicin Prior to Hematopoietic Stem Cell Transplantation |
title_sort | defibrotide prophylaxis of sinusoidal obstruction syndrome in adults treated with inotuzumab ozogamicin prior to hematopoietic stem cell transplantation |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240310/ https://www.ncbi.nlm.nih.gov/pubmed/35785209 http://dx.doi.org/10.3389/fonc.2022.933317 |
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