Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase II trial PNET HR+5.


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
01 07 2021
Historique:
pubmed: 31 12 2020
medline: 5 8 2021
entrez: 30 12 2020
Statut: ppublish

Résumé

High-risk medulloblastoma is defined by the presence of metastatic disease and/or incomplete resection and/or unfavorable histopathology and/or tumors with MYC amplification. We aimed to assess the 3-year progression-free survival (PFS) and define the molecular characteristics associated with PFS in patients aged 5-19 years with newly diagnosed high-risk medulloblastoma treated according to the phase II trial PNET HR+5. All children received postoperative induction chemotherapy (etoposide and carboplatin), followed by 2 high-dose thiotepa courses (600 mg/m2) with hematological stem cell support. At the latest 45 days after the last stem cell rescue, patients received risk-adapted craniospinal radiation therapy. Maintenance treatment with temozolomide was planned to start between 1-3 months after the end of radiotherapy. The primary endpoint was PFS. Outcome and safety analyses were per protocol (all patients who received at least one dose of induction chemotherapy). Fifty-one patients (median age, 8 y; range, 5-19) were enrolled. The median follow-up was 7.1 years (range: 3.4-9.0). The 3 and 5-year PFS with their 95% confidence intervals (95% CI) were 78% (65-88) and 76% (63-86), and the 3 and 5-year OS were 84% (72-92) and 76% (63-86), respectively. Medulloblastoma subtype was a statistically significant prognostic factor (P-value = 0.039) with large-cell/anaplastic being of worse prognosis, as well as a molecular subgroup (P-value = 0.012) with sonic hedgehog (SHH) and group 3 being of worse prognosis than wingless (WNT) and group 4. Therapy was well tolerated. This treatment based on high-dose chemotherapy and conventional radiotherapy resulted in a high survival rate in children with newly diagnosed high-risk medulloblastoma.

Sections du résumé

BACKGROUND
High-risk medulloblastoma is defined by the presence of metastatic disease and/or incomplete resection and/or unfavorable histopathology and/or tumors with MYC amplification. We aimed to assess the 3-year progression-free survival (PFS) and define the molecular characteristics associated with PFS in patients aged 5-19 years with newly diagnosed high-risk medulloblastoma treated according to the phase II trial PNET HR+5.
METHODS
All children received postoperative induction chemotherapy (etoposide and carboplatin), followed by 2 high-dose thiotepa courses (600 mg/m2) with hematological stem cell support. At the latest 45 days after the last stem cell rescue, patients received risk-adapted craniospinal radiation therapy. Maintenance treatment with temozolomide was planned to start between 1-3 months after the end of radiotherapy. The primary endpoint was PFS. Outcome and safety analyses were per protocol (all patients who received at least one dose of induction chemotherapy).
RESULTS
Fifty-one patients (median age, 8 y; range, 5-19) were enrolled. The median follow-up was 7.1 years (range: 3.4-9.0). The 3 and 5-year PFS with their 95% confidence intervals (95% CI) were 78% (65-88) and 76% (63-86), and the 3 and 5-year OS were 84% (72-92) and 76% (63-86), respectively. Medulloblastoma subtype was a statistically significant prognostic factor (P-value = 0.039) with large-cell/anaplastic being of worse prognosis, as well as a molecular subgroup (P-value = 0.012) with sonic hedgehog (SHH) and group 3 being of worse prognosis than wingless (WNT) and group 4. Therapy was well tolerated.
CONCLUSIONS
This treatment based on high-dose chemotherapy and conventional radiotherapy resulted in a high survival rate in children with newly diagnosed high-risk medulloblastoma.

Identifiants

pubmed: 33377141
pii: 6055191
doi: 10.1093/neuonc/noaa301
pmc: PMC8248855
doi:

Substances chimiques

Hedgehog Proteins 0

Types de publication

Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1163-1172

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Christelle Dufour (C)

Department of Pediatric and Adolescent Oncology, Gustave Roussy, Villejuif, France.

Stephanie Foulon (S)

Department of Biostatistics and Epidemiology, Gustave Roussy, University Paris-Saclay, Villejuif, France.
Oncostat U1018, Inserm, University Paris-Saclay, labeled Ligue Contre le Cancer, Villejuif, France.

Anne Geoffray (A)

Department of Pediatric Imaging, Fondation Lenval Children's Hospital, Nice, France.

Julien Masliah-Planchon (J)

INSERM U830, Laboratory of Translational Research in Pediatric Oncology, SIREDO Pediatric Oncology Center, Curie Institute, Paris, France.

Dominique Figarella-Branger (D)

Aix-Marseille Univ, APHM, CNRS, INP, Inst Neurophysiopathol, CHU Timone, Service d'Anatomie Pathologique et de Neuropathologie, Marseille, France.

Valerie Bernier-Chastagner (V)

Department of Radiotherapy, Alexis Vautrin Cancer Center, Vandoeuvre-les-Nancy, France.

Laetitia Padovani (L)

Department of Radiotherapy, CHU La Timone, AP-HM, Marseille, France.

Léa Guerrini-Rousseau (L)

Department of Pediatric and Adolescent Oncology, Gustave Roussy, Villejuif, France.

Cecile Faure-Conter (C)

Department of Pediatry, Institut d'Hématologie et d'Oncologie pédiatrique, Lyon, France.

Celine Icher (C)

Department of pediatrics, Bordeaux university hospital, Bordeaux, France.

Anne-Isabelle Bertozzi (AI)

Department of Pediatric Onco-hematology, CHU Toulouse, Toulouse, France.

Pierre Leblond (P)

Pediatric Oncology Unit, Oscar Lambret Comprehensive Cancer Center, Lille, France.

Tasnime Akbaraly (T)

Department of Pediatric Hematology-Oncology, Centre Hospitalo-Universitaire de Montpellier, Montpellier, France.

Franck Bourdeaut (F)

SIREDO Pediatric Oncology Center, Curie Institute, Paris, France.

Nicolas André (N)

Department of Pediatric Hematology and Oncology, La Timone Children's Hospital, Marseille, France.
SMARTc Unit, Centre de Recherche en Cancerologie de Marseille Inserm U1068 Aix Marseille Univ, MarseilleFrance.

Celine Chappé (C)

Department of Pediatric Oncology, Rennes University Hospital, Rennes, France.

Pascale Schneider (P)

Pediatric Hemato-Oncology Department, University Hospital, Rouen, Rouen, France.

Emilie De Carli (E)

Department of Pediatric Oncology, University Hospital, Angers, France.

Pascal Chastagner (P)

Department of Pediatric Oncology, Children's Hospital, Nancy, France.

Claire Berger (C)

Department of Pediatric Hematology and Oncology Unit, University Hospital of Saint-Étienne, Saint-Étienne, France.

Julien Lejeune (J)

Pediatric Onco-Hematology Unit, University Hospital of Tours, Tours, France.

Christine Soler (C)

Hematology Department, Hôpital l'Archet, CHU de Nice, Nice, France.

Natacha Entz-Werlé (N)

Pediatric Onco-Hematology Unit, CHU of Strasbourg, Strasbourg, France.

Marie-Bernadette Delisle (MB)

Departments of Pathology, Toulouse University Hospital, Toulouse III University, Toulouse, France.

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