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Vorinostat and isotretinoin with chemotherapy in young children with embryonal brain tumors: A report from the Pediatric Brain Tumor Consortium (PBTC-026).
Leary, Sarah E S; Kilburn, Lindsay; Geyer, J Russell; Kocak, Mehmet; Huang, Jie; Smith, Kyle S; Hadley, Jennifer; Ermoian, Ralph; MacDonald, Tobey J; Goldman, Stewart; Phillips, Peter; Young Poussaint, Tina; Olson, James M; Ellison, David W; Dunkel, Ira J; Fouladi, Maryam; Onar-Thomas, Arzu; Northcott, Paul A.
Affiliation
  • Leary SES; Cancer and Blood Disorders Center, Seattle Children's Hospital, Seattle, Washington, USA.
  • Kilburn L; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Geyer JR; Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
  • Kocak M; Center for Cancer and Blood Disorders, Children's National Hospital, Washington, DC, USA.
  • Huang J; Cancer and Blood Disorders Center, Seattle Children's Hospital, Seattle, Washington, USA.
  • Smith KS; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Hadley J; Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
  • Ermoian R; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • MacDonald TJ; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Goldman S; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Phillips P; Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Young Poussaint T; Department of Radiation Oncology, University of Washington, Seattle, Washington, USA.
  • Olson JM; Aflac Cancer and Blood Disorders Center, Emory University, Atlanta, Georgia, USA.
  • Ellison DW; Department of Child Health, Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Dunkel IJ; Department of Pediatric Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Fouladi M; Department of Radiology, Boston Children's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.
  • Onar-Thomas A; Cancer and Blood Disorders Center, Seattle Children's Hospital, Seattle, Washington, USA.
  • Northcott PA; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Neuro Oncol ; 24(7): 1178-1190, 2022 07 01.
Article in En | MEDLINE | ID: mdl-34935967
ABSTRACT

BACKGROUND:

Embryonal tumors of the CNS are the most common malignant tumors occurring in the first years of life. This study evaluated the feasibility and safety of incorporating novel non-cytotoxic therapy with vorinostat and isotretinoin to an intensive cytotoxic chemotherapy backbone.

METHODS:

PBTC-026 was a prospective multi-institutional clinical trial for children <48 months of age with newly diagnosed embryonal tumors of the CNS. Treatment included three 21-day cycles of induction therapy with vorinostat and isotretinoin, cisplatin, vincristine, cyclophosphamide, and etoposide; three 28-day cycles of consolidation therapy with carboplatin and thiotepa followed by stem cell rescue; and twelve 28-day cycles of maintenance therapy with vorinostat and isotretinoin. Patients with M0 medulloblastoma (MB) received focal radiation following consolidation therapy. Molecular classification was by DNA methylation array.

RESULTS:

Thirty-one patients with median age of 26 months (range 6-46) received treatment on study; 19 (61%) were male. Diagnosis was MB in 20 and supratentorial CNS embryonal tumor in 11. 24/31 patients completed induction therapy within a pre-specified feasibility window of 98 days. Five-year progression-free survival (PFS) and overall survival (OS) for all 31 patients were 55 ± 15 and 61 ± 13, respectively. Five-year PFS was 42 ± 13 for group 3 MB (n = 12); 80 ± 25 for SHH MB (n = 5); 33 ± 19 for embryonal tumor with multilayered rosettes (ETMR, n = 6).

CONCLUSION:

It was safe and feasible to incorporate vorinostat and isotretinoin into an intensive chemotherapy regimen. Further study to define efficacy in this high-risk group of patients is warranted.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Cerebellar Neoplasms / Neuroectodermal Tumors, Primitive / Neoplasms, Germ Cell and Embryonal / Medulloblastoma Type of study: Clinical_trials / Observational_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Neuro Oncol Journal subject: NEOPLASIAS / NEUROLOGIA Year: 2022 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Cerebellar Neoplasms / Neuroectodermal Tumors, Primitive / Neoplasms, Germ Cell and Embryonal / Medulloblastoma Type of study: Clinical_trials / Observational_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Neuro Oncol Journal subject: NEOPLASIAS / NEUROLOGIA Year: 2022 Document type: Article Affiliation country: United States