Clinical outcomes and patterns of failure in pineoblastoma: A 30-year, single-institution retrospective review

Benjamin Farnia, Pamela K. Allen, Paul D. Brown, Soumen Khatua, Nicholas B. Levine, Jing Li, Marta Penas-Prado, Anita Mahajan, Amol J. Ghia

Research output: Contribution to journalReview articlepeer-review

36 Scopus citations

Abstract

Objective To update outcomes and assess prognostic factors in the modern, multimodality treatment of patients with pineoblastoma.

Methods The medical records of patients with pineoblastoma evaluated at the M.D. Anderson Cancer Center between 1982 and 2012 were reviewed retrospectively.

Results Thirty-one patients with medical records suitable for review were identified. The majority of patients were female (67.7%) with a median age at diagnosis of 18.2 years (range, 0.3-52.8 years). Twenty-one patients underwent surgical resection, recorded as gross total (n = 9) or subtotal (n = 12) resections. Thirty patients received radiation with photon-based therapy (n = 16), proton-based therapy (n = 13), or radiosurgery (n = 1) to a median craniospinal irradiation dose of 36 Gy (range, 23.4-40 Gy) and a median focal dose of 54 Gy (range, 40-58.4 Gy). Twenty-eight patients received chemotherapy before (n = 10), during (n = 10), and after (n = 22) radiation. Median overall survival was 8.7 years for the entire cohort, with 2-, 5-, and 10- year actuarial rates of 89.5%, 69.4%, and 48.6%, respectively. Median disease-free survival was 10 years with 2-, 5-, and 10- year actuarial rates of 84.3%, 62.6%, and 55.7%, respectively. Univariate analysis failed to correlate age, sex, or extent of surgical resection with disease-free or overall survival.

Conclusions Modern, multimodality treatment of pineoblastoma yields a high rate of overall survival, with acceptable short- and long-term toxicity. A greater M-stage at presentation and development of disease recurrence correlate with worse overall survival. Patients who received focal radiation initially experienced a greater rate of disease recurrence compared with those treated to the craniospinal axis.

Original languageEnglish (US)
Pages (from-to)1232-1241
Number of pages10
JournalWorld Neurosurgery
Volume82
Issue number6
DOIs
StatePublished - Dec 1 2014

Keywords

  • Combined modality
  • MIB-1
  • Neurosurgery
  • PNET
  • Pineal-parenchymal tumors
  • Pineoblastoma
  • Radiation
  • Radiosurgery
  • Retinoblastoma
  • Supratentorial

ASJC Scopus subject areas

  • Surgery
  • Clinical Neurology

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