A Pilot Study Omitting Radiation in the Treatment of Children with Newly Diagnosed Wnt-Activated Medulloblastoma

Author:

Cohen Kenneth J.1ORCID,Munjapara Vasu1ORCID,Aguilera Dolly2ORCID,Castellino Robert C.2ORCID,Stapleton Stacie L.3ORCID,Landi Daniel4ORCID,Ashley David M.5ORCID,Rodriguez Fausto J.6ORCID,Hawkins Cynthia7ORCID,Yang Edward8ORCID,London Wendy9ORCID,Chi Susan9ORCID,Bandopadhayay Pratiti910ORCID

Affiliation:

1. 1The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland.

2. 2Department of Pediatrics, Aflac Cancer & Blood Disorders Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, Georgia.

3. 3Cancer and Blood Disorders Institute, Johns Hopkins All Children's Hospital, St. Petersburg, Florida.

4. 4Department of Pediatrics, The Preston Robert Tisch Brain Tumor Center at Duke University Medical Center, Duke University Medical Center, Durham, North Carolina.

5. 5Department of Surgery, The Preston Robert Tisch Brain Tumor Center at Duke University Medical Center, Duke University Medical Center, Durham, North Carolina.

6. 6Department of Pathology & Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California.

7. 7Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, The University of Toronto, Toronto, Canada.

8. 8Department of Radiology, Boston Children's Hospital, Boston, Massachusetts.

9. 9Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.

10. 10Department of Pediatrics, Harvard Medical School, Broad Institute of MIT and Harvard, Boston, Massachusetts.

Abstract

Abstract Purpose: Treatment of wingless (WNT)-activated medulloblastoma (WNT+MB) with surgery, irradiation (XRT), and chemotherapy results in excellent outcomes. We studied the efficacy of therapy de-intensification by omitting XRT entirely in children with WNT+MB. Patients and Methods: Tumors were molecularly screened to confirm the diagnosis of WNT+MB. Eligible children were treated within 31 days following surgery with nine cycles of adjuvant chemotherapy per ACNS0331. No XRT was planned. The primary endpoint was the occurrence of relapse, progression, or death in the absence of XRT within the first two years after study enrollment. Four events in the first 10 evaluable patients would result in early study closure. Results: Fourteen children were prescreened, and nine met the protocol definition of WNT+MB. Six of the nine eligible patients consented to protocol therapy, and five completed planned protocol therapy. The first two children enrolled relapsed shortly after therapy completion with local and leptomeningeal recurrences. The study was closed early due to safety concerns. Both children are surviving after XRT and additional chemotherapy. A third child relapsed at completion of therapy but died of progressive disease 35 months from diagnosis. Two children finished treatment but immediately received post-treatment XRT to guard against early relapse. The final child's treatment was aborted in favor of a high-dose therapy/stem cell rescue approach. Although OS at 5 years is 83%, no child received only planned protocol therapy, with all receiving eventual XRT and/or alternative therapy. Conclusions: Radiotherapy is required to effectively treat children with WNT-altered medulloblastoma. See related commentary by Gottardo and Gajjar, p. 4996

Funder

Matthew Larson Foundation for Pediatric Brain Tumors

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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