Phase II Study of Nonmetastatic Desmoplastic Medulloblastoma in Children Younger Than 4 Years of Age: A Report of the Children's Oncology Group (ACNS1221).


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 01 2020
Historique:
pubmed: 28 11 2019
medline: 1 7 2020
entrez: 28 11 2019
Statut: ppublish

Résumé

Nodular desmoplastic medulloblastoma (ND) and medulloblastoma with extensive nodularity (MBEN) have been associated with a more favorable outcome in younger children. However, treatment-related neurotoxicity remains a significant concern in this vulnerable group of patients. ACNS1221 was a prospective single-arm trial of conventional chemotherapy for nonmetastatic ND and MBEN based on a modified HIT SKK 2000 regimen excluding intraventricular methotrexate, aiming to achieve similar outcome (2-year progression-free survival [PFS] ≥ 90%) with reduced treatment-related neurotoxicity. Secondary objectives included feasibility of timely central pathology review and evaluation of tumor molecular profile. Twenty-five eligible patients (15 males and 10 females; median age, 18.7 months) were enrolled. Eighteen patients had ND and 7 had MBEN histology. Three patients had residual disease at baseline. The study closed early because of a higher than expected relapse rate. Twelve patients experienced relapse-local (n= 6), distant (n = 3), and combined (n = 3)-at a median of 9.8 months from diagnosis (range, 8.9-13.7 months), and 2 patients died of disease. Two-year PFS and overall survival rates were 52% (95% CI, 32.4% to 71.6%) and 92% (95% CI, 80.8% to 100.0%) respectively. Patients older than 12 months of age ( The proposed modified regimen of conventional systemic chemotherapy without serial intraventricular methotrexate injection failed to achieve the targeted 2-year PFS of 90%. With this cohort, we prospectively confirmed the existence of two SHH subgroups and observed a trend toward worse outcome for SHH-I patients.

Identifiants

pubmed: 31774708
doi: 10.1200/JCO.19.00845
pmc: PMC6968798
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

223-231

Subventions

Organisme : NCI NIH HHS
ID : U10 CA098413
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS102669
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : K08 CA155764
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States

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Auteurs

Lucie Lafay-Cousin (L)

Children's Hospital, Calgary, Alberta, Canada.

Eric Bouffet (E)

Hospital for Sick Children, Toronto, Ontario, Canada.

Douglas Strother (D)

Children's Hospital, Calgary, Alberta, Canada.

Vasilisa Rudneva (V)

St Jude Children's Research Hospital, Memphis, TN.

Cynthia Hawkins (C)

Hospital for Sick Children, Toronto, Ontario, Canada.

Charles Eberhart (C)

Johns Hopkins University, Baltimore, MD.

Craig Horbinski (C)

Northwestern University, Chicago, IL.

Linda Heier (L)

New York-Presbyterian Hospital/Weill Cornell Medical Center, New York, NY.

Mark Souweidane (M)

Memorial Sloan Kettering Cancer Center, New York, NY.

Chris Williams-Hughes (C)

Children's Oncology Group, Littleton, CO.

Arzu Onar-Thomas (A)

St Jude Children's Research Hospital, Memphis, TN.

Catherine A Billups (CA)

St Jude Children's Research Hospital, Memphis, TN.

Maryam Fouladi (M)

Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

Paul Northcott (P)

St Jude Children's Research Hospital, Memphis, TN.

Giles Robinson (G)

St Jude Children's Research Hospital, Memphis, TN.

Amar Gajjar (A)

St Jude Children's Research Hospital, Memphis, TN.

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