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Improved outcome in high-risk childhood acute lymphoblastic leukemia defined by prednisone-poor response treated with double Berlin-Frankfurt-Muenster protocol II

  • Maurizio Aricò*
  • , Maria Grazia Valsecchi
  • , Valentino Conter
  • , Carmelo Rizzari
  • , Andrea Pession
  • , Chiara Messina
  • , Elena Barisone
  • , Vincenzo Poggi
  • , Giulio De Rossi
  • , Franco Locatelli
  • , Maria Concetta Micalizzi
  • , Giuseppe Basso
  • , Giuseppe Masera
  • *Autore corrispondente per questo lavoro
  • University of Bologna
  • IRCCS Fondazione Policlinico San Matteo - Pavia
  • University of Turin
  • Ospedale dei Bambini G. di Cristina
  • IRCCS Istituto Giannina Gaslini - Genova
  • IRCCS Ospedale pediatrico Bambino Gesù - Roma
  • University of Milan - Bicocca

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

One hundred ninety-eight children and adolescents were entered in the Associazione Italiana di Ematologia ed Oncologia Pediatrica (AIEOP)-ALL95 study for high-risk acute lymphoblastic leukemia (ALL). Inclusion criteria were poor response to initial prednisone/intrathecal methotrexate (prednisone-poor response [Pi resistance to induction therapy, translocation t(9;22), infants with the t(4;11), or CD10(-) ALL. The event-free survival (EFS) rate at 4 years was 56.5% (SE, 3.9%) for the entire group. The overall EFS rate in the current study was significantly better (P =.002) than that obtained in a comparable group of patients treated in the early 1990s in the AIEOP-ALL91 study. In particular, patients with PPR had a 4-year EFS of 61.1% (SE, 4.4%) versus 42.8% (SE, 5.4%) in the ALL 91 study (P =.008). Among PPR patients, those who were PPR-only(60.11% that is, they achieved CR and were negative for t(9;22) and t(4;11) translocations-had the best outcomes with this intensive treatment, even when additional adverse features (hyperleukocytosis, T phenotype) were present (4-year EFS, 70.1%; SE, 4.7%.). We attribute this improvement to the replacement of 6 alternating blocks of non-crossresistant drugs with an 8-drug reinduction regimen (Berlin-Frankfurt-Muenster [BFM] protocol 11), repeated twice, in the context of a standard BFM-type intensive chemotherapy for high-risk ALL. This modified therapy may lead to high cure rates for patients defined as at high risk for Intrinsic resistance to corticosteroids only. (Blood. 2002;100:420-426). (C) 2002 by The American Society of Hematology.
Lingua originaleInglese
pagine (da-a)420-426
Numero di pagine7
RivistaBlood
Volume100
Numero di pubblicazione2
DOI
Stato di pubblicazionePubblicato - 2002

OSS delle Nazioni Unite

Questo processo contribuisce al raggiungimento dei seguenti obiettivi di sviluppo sostenibile

  1. SDG 3 - Salute e benessere
    SDG 3 Salute e benessere

All Science Journal Classification (ASJC) codes

  • Biochimica
  • Immunologia
  • Ematologia
  • Biologia Cellulare

Keywords

  • Precursor Cell Lymphoblastic Leukemia-Lymphoma

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