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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.
Sirvent, N; Suciu, S; De Moerloose, B; Ferster, A; Mazingue, F; Plat, G; Yakouben, K; Uyttebroeck, A; Paillard, C; Costa, V; Simon, P; Pluchart, C; Poirée, M; Minckes, O; Millot, F; Freycon, C; Maes, P; Hoyoux, C; Cavé, H; Rohrlich, P; Bertrand, Y; Benoit, Y.
Afiliación
  • Sirvent N; Department of Pediatric Hematology-Oncology, CHU, Montpellier, France; University Montpellier, Montpellier, France. Electronic address: n-sirvent@chu-montpellier.fr.
  • Suciu S; EORTC Headquarters, Brussels, Belgium.
  • De Moerloose B; Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent University, Ghent, Belgium.
  • Ferster A; Department of Pediatric Hematology-Oncology, Children's University Hospital Queen Fabiola, Université Libre de Bruxelles (ULB), Brussels, Belgium.
  • Mazingue F; Department of Pediatric Hematology-Oncology, CHRU, Lille, France.
  • Plat G; Department of Pediatric Hematology-Oncology, CHU-Hôpital Purpan, Toulouse, France.
  • Yakouben K; Department of Pediatric Hematology, Robert-Debré Hospital, AP-HP, Paris, France.
  • Uyttebroeck A; Department of Pediatric Hematology-Oncology, University Hospital Gasthuisberg, Leuven, Belgium.
  • Paillard C; Department of Pediatric Hematology-Oncology, University Hospital Hautepierre, Strasbourg, France.
  • Costa V; Department of Pediatrics, Portuguese Oncology Institute, Porto, Portugal.
  • Simon P; Pediatric Hematology Unit, CHU Jean-Minjoz Hospital, Besançon, France.
  • Pluchart C; Department of Pediatric Hematology-Oncology, American Memorial Hospital, Reims, France.
  • Poirée M; Department of Pediatric Hematology-Oncology, CHU Nice, Nice, France.
  • Minckes O; Department of Pediatric Hematology-Oncology, CHU, Caen, France.
  • Millot F; Pediatric Oncology Unit, University Hospital, Poitiers, France.
  • Freycon C; Department of Pediatric Oncology, University Hospital, Grenoble, France.
  • Maes P; Department of Pediatrics, University Hospital Antwerp, Antwerp, Belgium.
  • Hoyoux C; Department of Pediatrics, CHR de la Citadelle, Liège, Belgium.
  • Cavé H; Department of Genetics, Assistance publique-Hôpitaux de Paris (AP-HP), Robert-Debré Hospital, Paris, France; INSERM UMR 1131, University Institute of Hematology, University Paris-Diderot, Paris Sorbonne Cité, Paris, France.
  • Rohrlich P; Department of Pediatric Hematology-Oncology, CHU Nice, Nice, France.
  • Bertrand Y; Institute of Pediatric Hematology and Oncology (IHOP), Hospices Civils de Lyon, University Lyon 1, Lyon, France.
  • Benoit Y; Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent University, Ghent, Belgium.
Arch Pediatr ; 28(5): 411-416, 2021 Jul.
Article en En | MEDLINE | ID: mdl-34034929
ABSTRACT

AIM:

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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sistema Nervioso Central / Valor Predictivo de las Pruebas / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Arch Pediatr Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sistema Nervioso Central / Valor Predictivo de las Pruebas / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Arch Pediatr Año: 2021 Tipo del documento: Article