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Characterization of recurrence patterns and outcomes of medulloblastoma in adults: The University of Texas MD Anderson Cancer Center experience.
Gregory, Timothy A; Mastall, Maximilian; Lin, Heather; Hess, Kenneth R; Yuan, Ying; Martin-Bejarano Garcia, Manuela; Fuller, Gregory N; Alfaro, Kristin D; Gule-Monroe, Maria K; Huse, Jason T; Khatua, Soumen; Rao, Ganesh; Sandberg, David I; Wefel, Jeffrey S; Yeboa, Debra N; Paulino, Arnold C; McGovern, Susan L; Zaky, Wafik; Mahajan, Anita; Suki, Dima; Weathers, Shiao-Pei; Harrison, Rebecca A; de Groot, John F; Puduvalli, Vinay K; Penas-Prado, Marta; Majd, Nazanin K.
Affiliation
  • Gregory TA; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Mastall M; Department of Neurology, Clinical Neuroscience and Brain Tumor Center, University Hospital Zurich, Zurich, Switzerland.
  • Lin H; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Hess KR; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Yuan Y; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Martin-Bejarano Garcia M; Health Research Institute, Hospital Clinico San Carlos, Madrid, Spain.
  • Fuller GN; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Alfaro KD; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Gule-Monroe MK; Department of Neuroradiology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Huse JT; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Khatua S; Department of Pediatric Neuro-Oncology, Mayo Clinic, Rochester, Minnesota, USA.
  • Rao G; Department of Neurosurgery, Baylor College of Medicine, Houston, Texas, USA.
  • Sandberg DI; Department of Pediatric Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Wefel JS; Department of Neuropsychology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Yeboa DN; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Paulino AC; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • McGovern SL; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Zaky W; Department of Pediatric Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Mahajan A; Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota, USA.
  • Suki D; Department of Pediatric Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Weathers SP; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Harrison RA; Department of Neuro-Oncology, BC Cancer Agency Vancouver Centre, Vancouver, British Columbia, Canada.
  • de Groot JF; Brain Tumor Center, UCSF Medical Center, San Francisco, California, USA.
  • Puduvalli VK; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Penas-Prado M; Neuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
  • Majd NK; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Neurooncol Adv ; 5(1): vdad032, 2023.
Article in En | MEDLINE | ID: mdl-37114244
ABSTRACT

Background:

Medulloblastoma in adults is rare and treatment decisions are largely driven from pediatric literature. We sought to characterize recurrent medulloblastoma in adults.

Methods:

From a single-institution dataset of 200 adult patients diagnosed with medulloblastoma during 1978-2017, those with recurrence were analyzed for clinical features, treatment, and outcome.

Results:

Of the 200 patients, 82 (41%) with median age of 29 years (18-59) had recurrence after a median follow-up time of 8.4 years (95% CI = 7.1, 10.3). Of these, 30 (37%) were standard-risk, 31 (38%) were high-risk, and 21 (26%) had unknown-risk diseases at the time of initial diagnosis. Forty-eight (58%) presented with recurrence outside the posterior fossa, of whom 35 (43%) had distant recurrence only. Median Progression-free survival (PFS) and OS from initial surgery were 33.5 and 62.4 months, respectively. Neither PFS nor OS from initial diagnosis differed between the standard-risk and high-risk groups in those who experience recurrence (P = .505 and .463, respectively). Median OS from first recurrence was 20.3 months, also with no difference between the standard-risk and high-risk groups (P = .518). Recurrences were treated with combinations of re-resection (20 patients; 25%), systemic chemotherapy (61 patients; 76%), radiation (29 patients; 36%), stem cell transplant (6 patients; 8%), and intrathecal chemotherapy (4 patients; 5%). Patients who received radiation at recurrence had better OS (32.9 months) than those who did not (19.2 months) (P = .034).

Conclusions:

Recurrent medulloblastoma in adults has a poor prognosis irrespective of initial risk stratification. Recurrence commonly arises outside the posterior fossa years after initial diagnosis.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Neurooncol Adv Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Neurooncol Adv Year: 2023 Type: Article Affiliation country: United States