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CNS-3 status remains an independent adverse prognosis factor in children with acute lymphoblastic leukemia (ALL) treated without cranial irradiation: Results of EORTC Children Leukemia Group study 58951

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  • معلومة اضافية
    • Contributors:
      Département Pédiatrie CHRU Montpellier; Pôle Femme Mère Enfant CHRU Montpellier; Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier)-Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier); Université de Montpellier (UM); EORTC Headquarters Brussels, Belgium; Ghent University Hospital; Children's University Hospital Queen Fabiola Bruxelles, Belgium; Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille); Centre Hospitalier Universitaire de Toulouse (CHU Toulouse); Unité d'Hémato-Immunologie pédiatrique Hôpital Robert Debré, Paris; Service d'Immuno-hématologie pédiatrique Hôpital Robert Debré, Paris; Hôpital Robert Debré-Hôpital Robert Debré; University Hospital Gasthuisberg Leuven; Hôpital de Hautepierre Strasbourg; Instituto Português de Oncologia do Porto / Portuguese Oncology Institute of Porto (IPO Porto); Hôpital JeanMinjoz; Hôpital Américain; Hôpital universitaire Robert Debré Reims (CHU Reims); Hôpital Cimiez Nice (CHU); Unité d'hémato-immuno-oncologie pédiatrique CHU Caen; Université de Caen Normandie (UNICAEN); Normandie Université (NU)-Normandie Université (NU)-CHU Caen; Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN); Centre hospitalier universitaire de Poitiers = Poitiers University Hospital (CHU de Poitiers La Milétrie ); Centre Hospitalier Universitaire CHU Grenoble (CHUGA); Antwerp University Hospital Edegem (UZA); Service de chirurgie pédiatrique CHR de la Citadelle; Hôpital de la Citadelle (CHR); Département de génétique Robert Debré; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP Hôpital universitaire Robert-Debré Paris; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP); Hématopoïèse normale et pathologique : émergence, environnement et recherche translationnelle Paris ((UMR_S1131 / U1131)); Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité); Institut Universitaire d'Hématologie (IUH); Université Paris Diderot - Paris 7 (UPD7); Centre Hospitalier Universitaire de Nice (CHU Nice); Institut d'hématologie et d'oncologie pédiatrique CHU - HCL (IHOPe); Hospices Civils de Lyon (HCL); Université Claude Bernard Lyon 1 (UCBL); Université de Lyon
    • بيانات النشر:
      HAL CCSD
      Elsevier
    • الموضوع:
      2021
    • Collection:
      HAL Lyon 1 (University Claude Bernard Lyon 1)
    • نبذة مختصرة :
      International audience ; To evaluate the prognostic significance of initial central nervous system (CNS) involvement of children with acute lymphoblastic leukemia (ALL) enrolled in the EORTC 58951 trial.Patients and methods: From 1998 to 2008, 1930 ALL patients were included in the randomized EORTC 58951 trial. Overall treatment intensity was adjusted according to known prognostic factors including the level of minimal residual disease after induction treatment. CNS-directed therapy comprised four to 11 courses of i.v. methotrexate (5g/m2), and 10 to 19 intrathecal chemotherapy injections, depending on risk group and CNS status. Cranial irradiation was omitted for all patients.Results: The overall 8-year event-free survival (EFS) and overall survival (OS) rates were 81.3% and 88.1%, respectively. In the CNS-1, TPL+, CNS-2, and CNS-3 groups, the 8-year EFS rates were 82.1%, 77.1%, 78.3%, and 57.4%, respectively. Multivariable analysis indicated that initial CNS-3 status, but not CNS-2 or TLP+, was an independent adverse predictor of outcome. The 8-year incidence of isolated CNS relapse was 1.7% and of isolated or combined CNS relapse it was 3.7%. NCI high-risk group, male sex, CNS-2 and CNS-3 status were independent predictors for a higher incidence of any CNS relapse.Conclusions: CNS-3 status remains associated with poor prognosis and requires intensification of both systemic and CNS-directed therapy. This trial was registered at https://clinicaltrials.gov/under/NCT00003728.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/34034929; hal-03653879; https://hal.umontpellier.fr/hal-03653879; https://hal.umontpellier.fr/hal-03653879/document; https://hal.umontpellier.fr/hal-03653879/file/S0929693X21000890.pdf; PII: S0929-693X(21)00089-0; PUBMED: 34034929
    • الرقم المعرف:
      10.1016/j.arcped.2021.04.009
    • Rights:
      http://creativecommons.org/licenses/by-nc/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.FAF2B823