Management of pilomyxoid astrocytomas: our experience

Hitoshi Tsugu1, Shinya Oshiro, Fumio Yanai

  • 1Department of Neurosurgery, Fukuoka University Faculty of Medicine, Jonan-ku, Fukuoka 814-0180, Japan. h-tsugu@fukuoka-u.ac.jp

Abstract

Insights

Pilomyxoid astrocytoma (PMA) treatment involves chemotherapy, often with cisplatin (CDDP)/carboplatin (CBDCA) and etoposide. Continued chemotherapy, even with new drug combinations, shows promise for tumor regression in recurrent cases.

Area of Science:

  • Pediatric Oncology
  • Neuro-oncology
  • Clinical Research

Background:

  • Pilomyxoid astrocytoma (PMA) presents a higher risk of recurrence and cerebrospinal fluid (CSF) dissemination compared to pilocytic astrocytoma (PA).
  • This study focuses on the treatment strategies for pediatric PMA patients.

Observation:

  • A cohort of 5 patients (2 male, 3 female; ages 3 months to 11 years) diagnosed between 1992 and 2007 were analyzed.
  • Initial radiographic examination revealed CSF dissemination in three patients.
  • All patients underwent chemotherapy, with cisplatin (CDDP)/carboplatin (CBDCA) and etoposide being the most frequent initial combinations.

Findings:

  • Four out of five patients demonstrated significant tumor regression following chemotherapy.
  • One patient experienced tumor progression and died 22 months post-diagnosis.
  • Treatment adjustments, including changing or adding drugs, were made when initial chemotherapy proved ineffective.

Implications:

  • Chemotherapy demonstrates a positive impact on PMA treatment outcomes, even in cases with initial ineffectiveness.
  • Continued CDDP/CBDCA-based chemotherapy, incorporating novel drug combinations, is recommended for managing PMA.
  • Further research with larger patient cohorts is warranted to solidify these findings.

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