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Second malignancies in young children with primary brain tumors following treatment with prolonged postoperative chemotherapy and delayed irradiation: a Pediatric Oncology Group study.

Publication ,  Journal Article
Duffner, PK; Krischer, JP; Horowitz, ME; Cohen, ME; Burger, PC; Friedman, HS; Kun, LE
Published in: Ann Neurol
September 1998

Between 1986 and 1990, the Pediatric Oncology Group conducted a study in which 198 children younger than 3 years of age with malignant brain tumors were treated with prolonged postoperative chemotherapy in an effort to delay irradiation and reduce long-term neurotoxicity. Children younger than 2 years of age received 24 months of chemotherapy followed by irradiation, and those between 2 and 3 years of age received 12 months of chemotherapy plus irradiation. Chemotherapy was given in 28-day cycles (AAB, AAB), with cycle A = vincristine (0.065 mg/kg) intravenously on days 1 and 8 and cyclophosphamide (65 mg/kg) intravenously on day 1, and cycle B = cisplatinum (4 mg/kg) intravenously on day 1 and etoposide (6.5 mg/kg) intravenously on days 3 and 4. Five of the 198 children developed second malignancies, with a cumulative risk at 8 years of 11.3% (95% confidence interval [CI], 0-39%). Four of the five second malignancies occurred in children younger than 2 years of age at diagnosis, with a cumulative risk at 8 years of 18.9% (CI, 0-70%). Initial diagnoses were choroid plexus carcinoma (2 children), ependymoma (1 child), desmoplastic infantile ganglioglioma (2 children), and medulloblastoma (1 child). Duration from diagnosis of initial tumor to second malignancy was 33, 35, 57, 66, and 92 months. Three children younger than 2 years of age developed lymphoproliferative disease, that is, myelodysplastic syndrome (2 children), both with monosomy 7 deletions, and acute myelogenous leukemia (1 child), after 24 to 26 cycles of chemotherapy, including 8 cycles of etoposide. Two of 3 received craniospinal irradiation (2,560/3,840 cGy) and (3,520/5,320 cGy). Time to second malignancy was 7 years 8 months, 4 years 9 months, and 2 years 9 months. Two children developed solid tumors, at 5 years 6 months and 2 years 11 months, respectively, after initiation of treatment. A sarcoma developed after 26 cycles of chemotherapy and no irradiation, and a meningioma developed after 12 cycles of chemotherapy and local craniospinal irradiation. Potential causative factors for this high rate of secondary malignancies include prolonged use of alkylating agents and etoposide with or without irradiation.

Duke Scholars

Published In

Ann Neurol

DOI

ISSN

0364-5134

Publication Date

September 1998

Volume

44

Issue

3

Start / End Page

313 / 316

Location

United States

Related Subject Headings

  • Risk Assessment
  • Radiotherapy, Adjuvant
  • Postoperative Period
  • Neurology & Neurosurgery
  • Neoplasms, Second Primary
  • Infant
  • Humans
  • Follow-Up Studies
  • Drug Administration Schedule
  • Child, Preschool
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Duffner, P. K., Krischer, J. P., Horowitz, M. E., Cohen, M. E., Burger, P. C., Friedman, H. S., & Kun, L. E. (1998). Second malignancies in young children with primary brain tumors following treatment with prolonged postoperative chemotherapy and delayed irradiation: a Pediatric Oncology Group study. Ann Neurol, 44(3), 313–316. https://doi.org/10.1002/ana.410440305
Duffner, P. K., J. P. Krischer, M. E. Horowitz, M. E. Cohen, P. C. Burger, H. S. Friedman, and L. E. Kun. “Second malignancies in young children with primary brain tumors following treatment with prolonged postoperative chemotherapy and delayed irradiation: a Pediatric Oncology Group study.Ann Neurol 44, no. 3 (September 1998): 313–16. https://doi.org/10.1002/ana.410440305.
Journal cover image

Published In

Ann Neurol

DOI

ISSN

0364-5134

Publication Date

September 1998

Volume

44

Issue

3

Start / End Page

313 / 316

Location

United States

Related Subject Headings

  • Risk Assessment
  • Radiotherapy, Adjuvant
  • Postoperative Period
  • Neurology & Neurosurgery
  • Neoplasms, Second Primary
  • Infant
  • Humans
  • Follow-Up Studies
  • Drug Administration Schedule
  • Child, Preschool