Recurrent pediatric infratentorial ependymomas: a systematic review and meta-analysis on outcomes and molecular classification

Author:

Montgomery Eric Y.1,Thirunavu Vineeth2,Pagadala Manasa2,Shlobin Nathan A.2,Plant-Fox Ashley S.3,Lam Sandi24,DeCuypere Michael24

Affiliation:

1. University of Texas Southwestern Medical Center, Dallas, Texas;

2. Division of Pediatric Neurosurgery, Ann and Robert H. Lurie Children’s Hospital of Chicago, Illinois;

3. Division of Hematology, Oncology, Neuro-Oncology, and Stem Cell Transplantation, Ann and Robert H. Lurie Children’s Hospital of Chicago, Illinois; and

4. Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois

Abstract

OBJECTIVE The aim of this study was to summarize the prognosis of recurrent infratentorial ependymomas based on treatment and molecular characterization. METHODS Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, the authors searched the PubMed, Scopus, Embase, and Ovid databases for studies on recurrent infratentorial ependymomas in patients younger than 25 years of age. Exclusion criteria included case series of fewer than 5 patients and studies that did not provide time-dependent survival data. RESULTS The authors’ database search yielded 482 unique articles, of which 18 were included in the final analysis. There were 479 recurrent infratentorial pediatric ependymomas reported; 53.4% were WHO grade II and 46.6% were WHO grade III tumors. The overall mortality for recurrent infratentorial pediatric ependymomas was 49.1% (226/460). The pooled mean survival was 30.2 months after recurrence (95% CI 22.4–38.0 months). Gross-total resection (GTR) was achieved in 243 (59.0%) patients at initial presentation. The mean survival postrecurrence for those who received initial GTR was 42.3 months (95% CI 35.7–47.6 months) versus 26.0 months (95% CI 9.6–44.6 months) for those who received subtotal resection (STR) (p = 0.032). There was no difference in the mean survival between patients who received GTR (49.3 months, 95% CI 32.3–66.3 months) versus those who received STR (41.4 months, 95% CI 11.6–71.2 months) for their recurrent tumor (p = 0.610). In the studies that included molecular classification data, there were 169 (83.3%) posterior fossa group A (PFA) tumors and 34 (16.7%) posterior fossa group B (PFB) tumors, with 28 tumors harboring a 1q gain. PFA tumors demonstrated worse mean postprogression patient survival (24.7 months, 95% CI 15.3–34.0 months) compared with PFB tumors (48.0 months, 95% CI 32.8–63.2 months) (p = 0.0073). The average postrecurrence survival for patients with 1q+ tumors was 14.7 months. CONCLUSIONS The overall mortality rate for recurrent infratentorial ependymomas was found to be 49.1%, with a pooled mean survival of 30.2 months in the included sample population. More than 80% of recurrent infratentorial ependymomas were of the PFA molecular subtype, and both PFA tumors and those with 1q gain demonstrated worse prognosis after recurrence.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference46 articles.

1. Pediatric ependymoma;Vitanza NA,2016

2. Comparison of epidemiology, treatments, and outcomes in pediatric versus adult ependymoma;Elsamadicy AA,2020

3. A systematic review and meta-analysis of outcomes in pediatric, recurrent ependymoma;Byer L,2019

4. Delineation of two clinically and molecularly distinct subgroups of posterior fossa ependymoma;Witt H,2011

5. A prognostic gene expression signature in infratentorial ependymoma;Wani K,2012

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1. The role of surgery in recurrent ependymomas;Journal of Neurosurgery: Pediatrics;2023-09-01

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