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Hematopoietic stem cell transplantation for isolated extramedullary relapse of acute lymphoblastic leukemia in children

  • Maria Gabelli
  • , Marco Zecca
  • , Chiara Messina
  • , Elisa Carraro
  • , Barbara Buldini
  • , Attilio Maria Rovelli
  • , Franca Fagioli
  • , Alice Bertaina
  • , Edoardo Lanino
  • , Claudio Favre
  • , Marco Rabusin
  • , Arcangelo Prete
  • , Mimmo Ripaldi
  • , Walter Barberi
  • , Fulvio Porta
  • , Maurizio Caniglia
  • , Stella Santarone
  • , Paolo D’Angelo
  • , Giuseppe Basso
  • , Franco Locatelli
  • University of Padua
  • IRCCS Fondazione Policlinico San Matteo - Pavia
  • Azienda Ospedaliera San Gerardo Monza
  • Ospedale Infantile Regina Margherita
  • IRCCS Ospedale pediatrico Bambino Gesù - Roma
  • IRCCS Istituto Giannina Gaslini - Genova
  • Azienda Ospedaliero Universitaria Meyer
  • I.R.C.C.S. Materno Infantile Burlo Garofalo
  • Alma Mater Studiorum University of Bologna
  • Azienda Ospedaliera Santobono Pausillipon
  • University of Rome La Sapienza
  • Spedali Civili Di Brescia
  • University Hospital of Perugia
  • Ospedale di Pescara
  • Di Cristina e Benfratelli

Research output: Contribution to journalArticle

Abstract

Relapse of acute lymphoblastic leukemia (ALL) may occur in extramedullary sites, mainly central nervous system (CNS) and testis. Optimal post-remissional treatment for isolated extramedullary relapse (IEMR) is still controversial. We collected data of children treated with hematopoietic stem cell transplantation (HSCT) for ALL IEMR from 1990 to 2015 in Italy. Among 281 patients, 167 had a relapse confined to CNS, 73 to testis, 14 to mediastinum, and 27 to other organs. Ninety-seven patients underwent autologous HSCT, 79 received allogeneic HSCT from a matched family donor, 75 from a matched unrelated donor, and 30 from an HLA-haploidentical donor. The 10-year overall survival was 56% and was not influenced by gender, ALL blast immune-phenotype, age, site of relapse, duration of first remission, and type of HSCT. In multivariable analysis, the only prognostic factors were disease status at HSCT and year of transplantation. Patients transplanted in third or subsequent complete remission (CR) had a risk of death 2.3 times greater than those in CR2. Children treated after 2000 had half the risk of death than those treated before that year. Our results suggest that both autologous and allogeneic HSCT may be considered for the treatment of pediatric ALL IEMR after the achievement of CR2.
Original languageEnglish
Pages (from-to)275-283
Number of pages9
JournalBone Marrow Transplantation
Volume54
DOIs
Publication statusPublished - 2019

Keywords

  • ALL
  • HSCT

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