Excellent outcome of young children with nodular desmoplastic medulloblastoma treated on "Head Start" III: a multi-institutional, prospective clinical trial.


Journal

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

Informations de publication

Date de publication:
18 12 2020
Historique:
pubmed: 19 4 2020
medline: 23 3 2021
entrez: 19 4 2020
Statut: ppublish

Résumé

"Head Start" III, was a prospective clinical trial using intensive induction followed by myeloablative chemotherapy and autologous hematopoietic cell rescue (AuHCR) to either avoid or reduce the dose/volume of irradiation in young children with medulloblastoma. Following surgery, patients received 5 cycles of induction followed by myeloablative chemotherapy using carboplatin, thiotepa, and etoposide with AuHCR. Irradiation was reserved for children >6 years old at diagnosis or with residual tumor post-induction. Between 2003 and 2009, 92 children <10 years old with medulloblastoma were enrolled. Five-year event-free survival (EFS) and overall survival (OS) rates (±SE) were 46 ± 5% and 62 ± 5% for all patients, 61 ± 8% and 77 ± 7% for localized medulloblastoma, and 35 ± 7% and 52 ± 7% for disseminated patients. Nodular/desmoplastic (ND) medulloblastoma patients had 5-year EFS and OS (±SE) rates of 89 ± 6% and 89 ± 6% compared with 26 ± 6% and 53 ± 7% for classic and 38 ± 13% and 46 ± 14% for large-cell/anaplastic (LCA) medulloblastoma, respectively. In multivariate Cox regression analysis, histology was the only significant independent predictor of EFS after adjusting for stage, extent of resection, regimen, age, and sex (P <0.0001). Five-year irradiation-free EFS was 78 ± 8% for ND and 21 ± 5% for classic/LCA medulloblastoma patients. Myelosuppression was the most common toxicity, with 2 toxic deaths. Twenty-four survivors completed neurocognitive evaluation at a mean of 4.9 years post-diagnosis. IQ and memory scores were within average range overall, whereas processing speed and adaptive functioning were low-average. We report excellent survival and preservation of mean IQ and memory for young children with ND medulloblastoma using high-dose chemotherapy, with most patients surviving without irradiation.

Sections du résumé

BACKGROUND
"Head Start" III, was a prospective clinical trial using intensive induction followed by myeloablative chemotherapy and autologous hematopoietic cell rescue (AuHCR) to either avoid or reduce the dose/volume of irradiation in young children with medulloblastoma.
METHODS
Following surgery, patients received 5 cycles of induction followed by myeloablative chemotherapy using carboplatin, thiotepa, and etoposide with AuHCR. Irradiation was reserved for children >6 years old at diagnosis or with residual tumor post-induction.
RESULTS
Between 2003 and 2009, 92 children <10 years old with medulloblastoma were enrolled. Five-year event-free survival (EFS) and overall survival (OS) rates (±SE) were 46 ± 5% and 62 ± 5% for all patients, 61 ± 8% and 77 ± 7% for localized medulloblastoma, and 35 ± 7% and 52 ± 7% for disseminated patients. Nodular/desmoplastic (ND) medulloblastoma patients had 5-year EFS and OS (±SE) rates of 89 ± 6% and 89 ± 6% compared with 26 ± 6% and 53 ± 7% for classic and 38 ± 13% and 46 ± 14% for large-cell/anaplastic (LCA) medulloblastoma, respectively. In multivariate Cox regression analysis, histology was the only significant independent predictor of EFS after adjusting for stage, extent of resection, regimen, age, and sex (P <0.0001). Five-year irradiation-free EFS was 78 ± 8% for ND and 21 ± 5% for classic/LCA medulloblastoma patients. Myelosuppression was the most common toxicity, with 2 toxic deaths. Twenty-four survivors completed neurocognitive evaluation at a mean of 4.9 years post-diagnosis. IQ and memory scores were within average range overall, whereas processing speed and adaptive functioning were low-average.
CONCLUSION
We report excellent survival and preservation of mean IQ and memory for young children with ND medulloblastoma using high-dose chemotherapy, with most patients surviving without irradiation.

Identifiants

pubmed: 32304218
pii: 5821791
doi: 10.1093/neuonc/noaa102
pmc: PMC7746930
doi:

Substances chimiques

Carboplatin BG3F62OND5

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1862-1872

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014089
Pays : United States

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

Girish Dhall (G)

Division of Pediatric Hematology-Oncology, University of Alabama Birmingham, Birmingham, Alabama, USA.

Sharon H O'Neil (SH)

Division of Neurology and The Saban Research Institute, Children's Hospital Los Angeles (CHLA), Los Angeles, California, USA.

Lingyun Ji (L)

Department of Preventive Medicine, Keck School of Medicine at the University of Southern California, Los Angeles, California, USA.

Kelley Haley (K)

Division of Hematology-Oncology CHLA, Los Angeles, California, USA.

Ashley M Whitaker (AM)

Division of Hematology-Oncology CHLA, Los Angeles, California, USA.

Marvin D Nelson (MD)

Department of Radiology CHLA, Los Angeles, California, USA.

Floyd Gilles (F)

Department of Pathology CHLA, Los Angeles, California, USA.

Sharon L Gardner (SL)

Division of Pediatric Hematology-Oncology, NYU Medical Center, New York, New York, USA.

Jeffrey C Allen (JC)

Division of Pediatric Hematology-Oncology, NYU Medical Center, New York, New York, USA.

Albert S Cornelius (AS)

Division of Pediatric Hematology-Oncology, Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA.

Kamnesh Pradhan (K)

Division of Pediatric Hematology-Oncology, Riley Hospital for Children, Indianapolis, Indiana, USA.

James H Garvin (JH)

Division of Pediatric Hematology-Oncology, New York Presbyterian Hospital, New York, New York, USA.

Randal S Olshefski (RS)

Division of Pediatric Hematology-Oncology, Nationwide Children's Hospital, Columbus, Ohio, USA.

Juliette Hukin (J)

Division of Pediatric Hematology-Oncology, British Columbia Children's Hospital, Vancouver, British Columbia, Canada.

Melanie Comito (M)

Division of Pediatric Hematology-Oncology, Penn State Hershey Children's Hospital, Hershey, Pennsylvania, USA.

Stewart Goldman (S)

Division of Pediatric Hematology-Oncology, Lurie Children's Hospital, Chicago, Illinois, USA.

Mark P Atlas (MP)

Division of Pediatric Hematology-Oncology, Children's Medical Center of New York, New York, New York, USA.

Andrew W Walter (AW)

Division of Pediatric Hematology-Oncology, Alfred I. duPont Hospital for Children, Wilmington, Delaware, USA.

Stephen Sands (S)

Departments of Psychiatry and Behavioral Sciences and Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Richard Sposto (R)

Division of Hematology-Oncology CHLA, Los Angeles, California, USA.

Jonathan L Finlay (JL)

Division of Pediatric Hematology-Oncology, Nationwide Children's Hospital, Columbus, Ohio, USA.

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