Outcome for young children newly diagnosed with ependymoma, treated with intensive induction chemotherapy followed by myeloablative chemotherapy and autologous stem cell rescue Journal Article


Authors: Zacharoulis, S.; Levy, A.; Chi, S. N.; Gardner, S.; Rosenblum, M.; Miller, D. C.; Dunkel, I.; Diez, B.; Sposto, R.; Ji, L.; Asgharzadeh, S.; Hukin, J.; Belasco, J.; Dubowy, R.; Kellie, S.; Termuhlen, A.; Finlay, J.
Article Title: Outcome for young children newly diagnosed with ependymoma, treated with intensive induction chemotherapy followed by myeloablative chemotherapy and autologous stem cell rescue
Abstract: Background:. The purpose of this study is to investigate the efficacy of an intensive chemotherapy induction regimen followed by myeloablative chemotherapy and autologous hematopoietic stem cell rescue (AHSCR) in children with newly diagnosed ependymoma. Patients and Methods:. Twenty-nine children less than 10 years of age at diagnosis of ependymoma were enrolled on the "Head Start" studies. Twenty-four patients with localized disease received an induction regimen including five cycles of chemotherapy (cisplatin, vincristine, etoposide cyclophosphamide, and high dose methotrexate for patients with metastatic disease). Following induction, individuals without evidence of disease proceeded to marrow-ablative chemotherapy (thiotepa, carboplatin, and etoposide) with AHSCR. Results:. The estimated 5-year event free survival (EFS) and overall survival (OS) from diagnosis were 12% (±6%) and 38% (±10%), respectively. The toxic mortality amongst this group of 29 patients was 10.3%. Younger age (less than 18 months at diagnosis) was the only statistically significant prognostic factor. The estimated 5-year OS rate for the five patients with metastatic disease at presentation was 80% (±18%). Overall, radiation-free survival at 5 years from diagnosis was 8% (±5%). Conclusions:. The use of an intensive induction chemotherapy regimen including myeloablative chemotherapy followed by AHSCR in newly diagnosed young children with ependymoma is not superior to other previously reported chemotherapeutic strategies. © 2006 Wiley-Liss, Inc.
Keywords: cancer chemotherapy; child; clinical article; preschool child; school child; treatment outcome; treatment response; child, preschool; disease-free survival; antibiotic agent; mortality; cisplatin; area under the curve; disease free survival; combined modality therapy; chemotherapy; methotrexate; drug megadose; outcome assessment; brain neoplasms; follow-up studies; carboplatin; metastasis; multiple cycle treatment; neoplasm recurrence, local; etoposide; antineoplastic combined chemotherapy protocols; cyclophosphamide; vincristine; patient monitoring; hematopoietic stem cell transplantation; transplantation; thiotepa; febrile neutropenia; drug fatality; statistical significance; infant; ependymoma; granulocyte colony stimulating factor; transplantation, autologous; autologous hematopoietic stem cell transplantation; thrombocyte transfusion; cns tumors
Journal Title: Pediatric Blood and Cancer
Volume: 49
Issue: 1
ISSN: 1545-5009
Publisher: Wiley Periodicals, Inc  
Date Published: 2007-07-01
Start Page: 34
End Page: 40
Language: English
DOI: 10.1002/pbc.20935
PUBMED: 16874765
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 27" - "Export Date: 17 November 2011" - "CODEN: PBCEA" - "Source: Scopus"
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  1. Ira J Dunkel
    371 Dunkel
  2. Marc Rosenblum
    424 Rosenblum