Literature DB >> 33713387

Defibrotide in hematopoietic stem cell transplantation: A multicenter survey study of the Spanish Hematopoietic Stem Cell Transplantation Group (GETH).

Marta González Vicent1, Cristina Díaz de Heredia2, Jesús González de Pablo1, Blanca Molina1, Alexandra Regueiro3, Antonio Pérez Martinez4, Pilar Palomo5, Lucía López Corral6, Estefanía García7, José María Fernández8, Ariadna Pérez9, María José Jiménez10, Manuel Guerreiro8, Carlos Vallejo11, Ana Isabel Gallardo12, Oriana López13, Ana Benito12, Julia Marsal14, Mónica Duarte15, Leyre Bento16, Isabel Badell17, Alexandra Pedraza18, Ana Jiménez Ubieto19, Pedro González20, Ignacio Gómez Centurión21, Lissette Costilla22, Cristina Beléndez21, Albert Esquirol17, Ildefonso Espigado23, Esperanza Lavilla24, Miguel Ángel Díaz1.   

Abstract

BACKGROUND: Defibrotide is approved in European Union for the treatment of severe sinusoidal obstruction syndrome (SOS) after HSCT. However, it has also been used for SOS prophylaxis, moderate SOS and in other complications such as transplant-associated thrombotic microangiopathy (TAM). The objective of this study was to evaluate current uses, effectiveness and safety of defibrotide in patients with HSCT.
METHODS: This multicenter, retrospective study included patients treated with defibrotide for any indication at 28 HSCT centers of the Grupo Español de Trasplante Hematopoyetico (GETH) including the pediatric subgroup Grupo Español de Trasplante de Medula en Niños (GETMON).
RESULTS: Three hundred and eighty eight patients treated with defibrotide between January 2011 and December 2018 were included. 253 patients were children, and 135 patients were adults. In total, 332 transplants were allogeneic, and the remainder were autologous. Main indications for defibrotide use were severe/very severe SOS in 173 patients, SOS prophylaxis in 135 patients, moderate SOS in 41 patients, TAM in six patients and suspected SOS in 33 patients. Overall survival (OS) at day +100 in the SOS prophylaxis group was 89% (95% CI, 87%-91%). In the group of patients with moderate and severe/very severe SOS, the OS at day +100 was 80% (95% CI, 74%-86%) and 62% (95% CI, 59%-65%), respectively (P = .0015). With a longer follow-up, median of 2 years (4 months-7 years), OS was 63% (95% CI, 59%-67%) in the SOS prophylaxis patients. OS for patients with moderate and severe/very severe SOS groups was 53% (95% CI, 47%-61%) and 26% (95% CI, 22%-30%), respectively (P = .006). 191 patients died, and SOS was the main cause of death in 23 patients (12%).
CONCLUSIONS: Defibrotide has an acceptable safety profile with an improved response in severe/very severe SOS compared with historical controls, mainly in pediatric patients. Use of defibrotide for prophylaxis may improve prognosis of patients at high risk of complications due to endothelial damage such as those who receive a second transplant. SOS has an important impact on the HSCT long-term survival, as can be concluded from our study.
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  defibrotide; hematopoietic transplantation; sinusoidal obstruction syndrome

Year:  2021        PMID: 33713387     DOI: 10.1111/ejh.13618

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  1 in total

1.  T-Cell Depleted Haploidentical Transplantation in Children With Hematological Malignancies: A Comparison Between CD3+/CD19+ and TCRαβ+/CD19+ Depletion Platforms.

Authors:  Marta Gonzalez-Vicent; Blanca Molina; Ivan Lopez; Josune Zubicaray; Julia Ruiz; Jose Luis Vicario; Elena Sebastián; June Iriondo; Ana Castillo; Lorea Abad; Manuel Ramirez; Julian Sevilla; Miguel A Diaz
Journal:  Front Oncol       Date:  2022-06-20       Impact factor: 5.738

  1 in total

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