gms | German Medical Science

73. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
Joint Meeting mit der Griechischen Gesellschaft für Neurochirurgie

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

29.05. - 01.06.2022, Köln

Why do long-term survivors of childhood medulloblastoma die? A meta-analysis on cause-specific late mortality

Was sind die Todesursachen von Langzeitüberlebenden nach kindlichem Medulloblastom? Eine Meta-Analyse der ursachenspezifischen Mortalität

Meeting Abstract

  • presenting/speaker Hendrik-Jan Mijderwijk - Universitätsklinikum Düsseldorf, Klinik für Neurochirurgie, Düsseldorf, Deutschland
  • Daniel Hänggi - Universitätsklinikum Düsseldorf, Klinik für Neurochirurgie, Düsseldorf, Deutschland
  • Christopher Munoz-Bendix - Universitätsklinikum Düsseldorf, Klinik für Neurochirurgie, Düsseldorf, Deutschland
  • Thomas Beez - Universitätsklinikum Düsseldorf, Klinik für Neurochirurgie, Düsseldorf, Deutschland

Deutsche Gesellschaft für Neurochirurgie. 73. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), Joint Meeting mit der Griechischen Gesellschaft für Neurochirurgie. Köln, 29.05.-01.06.2022. Düsseldorf: German Medical Science GMS Publishing House; 2022. DocV057

doi: 10.3205/22dgnc063, urn:nbn:de:0183-22dgnc0630

Published: May 25, 2022

© 2022 Mijderwijk et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

Text

Objective: Long-term survival in children suffering from medulloblastoma is commonly evaluated with analysis reporting on all-cause mortality. There is a paucity on analyses that report on cause-specific mortality in these patients. Yet, this is highly relevant regarding duration of follow-up and imaging surveillance. We performed a proportional meta-analysis on cause-specific mortality in long-term childhood medulloblastoma survivors.

Methods: A comprehensive systematic literature search was performed on Medline, Embase, Web of Science, Cochrane and Google Scholar. Children suffering from medulloblastoma surviving at least 5 years after diagnosis were labelled as long-term survivors and eligible for inclusion in the analysis accordingly. Cause-specific mortality was divided into 1) recurrence or progression of medulloblastoma; 2) subsequent neoplasms; 3) other health-related causes not a result of medulloblastoma; 4) and miscellaneous causes (accidents, suicide, unknown causes). Analysis on the pooled data were performed using JBI SUMARI.

Results: Of the 344 identified studies, 4 studies reported on cause-specific mortality in long-term childhood medulloblastoma survivors. Cause-specific mortality data among 1917 patients was available. The pooled proportion of the random effects models equaled 0.121 (95% CI 0.103 – 0.141) for death related to recurrence or progression of medulloblastoma, 0.033 (95% CI 0.020 – 0.047) for death related to subsequent neoplasms, 0.034 (95% CI 0.002 – 0.097) for other health-related causes of death, and 0.018 (95% CI 0.000 – 0.065) for miscellaneous causes of death (Forrest plots, Figure 1 [Fig. 1] and Figure 2 [Fig. 2]).

Conclusion: This meta-analysis shows that circa 12% of long-term medulloblastoma survivors may die from tumor recurrence or progression. Death resulting from subsequent neoplasms or other (health-related) causes of death was less common, each <5%. To reduce late mortality, life-long guidance and personalized follow-up including imaging surveillance by health care professionals seems indicated.