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Efficacy of High-Dose Chemotherapy and Three-Dimensional Conformal Radiation for Atypical Teratoid/Rhabdoid Tumor: A Report From the Children's Oncology Group Trial ACNS0333.
Reddy, Alyssa T; Strother, Douglas R; Judkins, Alexander R; Burger, Peter C; Pollack, Ian F; Krailo, Mark D; Buxton, Allen B; Williams-Hughes, Chris; Fouladi, Maryam; Mahajan, Anita; Merchant, Thomas E; Ho, Ben; Mazewski, Claire M; Lewis, Victor A; Gajjar, Amar; Vezina, Louis-Gilbert; Booth, Timothy N; Parsons, Kerry W; Poss, Vicky L; Zhou, Tianni; Biegel, Jaclyn A; Huang, Annie.
Afiliação
  • Reddy AT; Departments of Neurology and Pediatrics, University of California San Francisco, San Francisco, CA.
  • Strother DR; Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Judkins AR; Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles; Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Burger PC; Department of Pathology, Johns Hopkins University, Baltimore, MD.
  • Pollack IF; Department Neurosurgery, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA.
  • Krailo MD; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Buxton AB; Children's Oncology Group, Monrovia, CA.
  • Williams-Hughes C; Children's Oncology Group, Monrovia, CA.
  • Fouladi M; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
  • Mahajan A; Department of Radiation Oncology, Mayo Clinic, Rochester, MN.
  • Merchant TE; Department of Radiation Oncology, St Jude Children's Research Hospital, Memphis, TN.
  • Ho B; Department of Cell Biology, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Mazewski CM; Aflac Cancer & Blood Disorders Center, Children's Healthcare of Atlanta; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Lewis VA; Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Gajjar A; Department of Oncology, St Jude Children's Research Hospital, Memphis, TN.
  • Vezina LG; Department of Radiology, The George Washington University School Medicine and Health Sciences, Washington, DC.
  • Booth TN; Department of Radiology, University of Texas Southwestern, Dallas, TX.
  • Parsons KW; AstraZeneca Pharmaceuticals, Cambridge, UK.
  • Poss VL; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL.
  • Zhou T; Department of Mathematics and Statistics, California State University at Long Beach, Long Beach, CA.
  • Biegel JA; Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles; Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Huang A; Department of Pediatrics, Hospital for Sick Children, Arthur and Sonia Labatt Brain Tumour Research Centre, Toronto, Ontario, Canada.
J Clin Oncol ; 38(11): 1175-1185, 2020 04 10.
Article em En | MEDLINE | ID: mdl-32105509
PURPOSE: Atypical teratoid/rhabdoid tumor (AT/RT) is an aggressive, early-childhood brain tumor without standard effective treatment. To our knowledge, we conducted the first AT/RT-specific cooperative group trial, ACNS0333, to examine the efficacy and safety of intensive postoperative chemotherapy and focal radiation to treat AT/RT. PATIENTS AND METHODS: Patients from birth to 22 years of age with AT/RT were eligible. After surgery, they received 2 courses of multiagent chemotherapy, followed by 3 courses of high-dose chemotherapy with peripheral blood stem cell rescue and involved-field radiation therapy. Timing of radiation was based on patient age and disease location and extent. Central testing of tumor and blood for SMARCB1 status was mandated. Tumor molecular subclassification was performed retrospectively. The primary analysis was event-free survival (EFS) for patients < 36 months of age compared with a cooperative groups' historical cohort. Although accrual was based on the therapeutic question, potential prognostic factors, including age, tumor location, M stage, surgical resection, order of therapy, germline status, and molecular subtype, were explored. RESULTS: Of 65 evaluable patients, 54 were < 36 months of age. ACNS0333 therapy significantly reduced the risk of EFS events in patients < 36 months of age compared with the historical cohort (P < .0005; hazard rate, 0.43; 95% CI, 0.28 to 0.66). Four-year EFS and overall survival for the entire cohort were 37% (95% CI, 25% to 49%) and 43% (95% CI, 31% to 55%), respectively. Timing of radiation did not affect survival, and 91% of relapses occurred by 2 years from enrollment. Treatment-related deaths occurred in 4 patients. CONCLUSION: The ACNS0333 regimen dramatically improved survival compared with historical therapies for patients with AT/RT. Clinical characteristics and molecular subgrouping suggest prognostic differences. ACNS0333 results lay a foundation on which to build future studies and incorporate testing of new therapeutic agents.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Teratoma / Protocolos de Quimioterapia Combinada Antineoplásica / Tumor Rabdoide / Radioterapia Conformacional Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Clin Oncol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Teratoma / Protocolos de Quimioterapia Combinada Antineoplásica / Tumor Rabdoide / Radioterapia Conformacional Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Clin Oncol Ano de publicação: 2020 Tipo de documento: Article