Induction Chemotherapy and Conformal Radiation Therapy for Very Young Children With Nonmetastatic Medulloblastoma: Children's Oncology Group Study P9934

Author:

Ashley David M.1,Merchant Thomas E.1,Strother Douglas1,Zhou Tianni1,Duffner Patricia1,Burger Peter C.1,Miller Douglas C.1,Lyon Nancy1,Bonner Melanie J.1,Msall Michael1,Buxton Allen1,Geyer Russell1,Kun Larry E.1,Coleman Lee1,Pollack Ian F.1

Affiliation:

1. David M. Ashley, Deakin University, Geelong, Australia; David M. Ashley, Barwon Health, Geelong, Australia; Thomas E. Merchant, Larry E. Kun, St Jude Children's Research Hospital, Memphis, TN; Douglas Strother, University of Calgary and Alberta Children's Hospital, Calgary, Canada; Tianni Zhou, University of Southern California, Los Angeles, CA; Tianni Zhou, Allen Buxton, Statistics and Data Center Childrens' Oncology Group, Los Angeles, CA; Patricia Duffner, Hunter James Kelly Research Institute,...

Abstract

Purpose P9934 was a prospective trial of systemic chemotherapy, second surgery, and conformal radiation therapy (CRT) limited to the posterior fossa and primary site for children between 8 months and 3 years old with nonmetastatic medulloblastoma. The study was open from June 2000 until June 2006. Patients and Methods After initial surgery, children received four cycles of induction chemotherapy, followed by age- and response-adjusted CRT to the posterior fossa (18 or 23.4 Gy) and tumor bed (cumulative 50.4 or 54 Gy) and maintenance chemotherapy. Neurodevelopmental outcomes were evaluated and event-free survival (EFS) results were directly compared with a previous study of multiagent chemotherapy without irradiation (Pediatric Oncology Group [POG] trial 9233). Results Seventy-four patients met eligibility requirements. The 4-year EFS and overall survival probabilities were 50% ± 6% and 69% ± 5.5%, respectively, which compared favorably to the results from POG 9233. Analysis showed that the desmoplastic/nodular subtype was a favorable factor in predicting survival. Our 4-year EFS rate was 58% ± 8% for patients with desmoplasia. Whereas seven of 10 patients who had disease progression before CRT had primary-site failure, 15 of 19 patients who progressed after CRT had distant-site failure. Neurodevelopmental assessments did not show a decline in cognitive or motor function after protocol-directed chemotherapy and CRT. Conclusion The addition of CRT to postoperative chemotherapy in young children with nonmetastatic medulloblastoma increased event-free survival compared with the use of postoperative chemotherapy alone. Future studies will use histopathologic typing (desmoplastic/nodular versus nondesmoplastic/nodular) to stratify patients for therapy by risk of relapse.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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