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Pathological perspectives in pilocytic astrocytomas: extent of resection as the sole critical factor for recurrence-free survival, and the challenge of evaluating conclusions derived from limited data

dc.contributor.coauthorCha, Soonmee
dc.contributor.coauthorPekmezci, Melike
dc.contributor.coauthorTihan, Tarik
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorBaygül, Arzu Eden
dc.contributor.kuauthorKulaç, İbrahim
dc.contributor.kuauthorSözmen, Banu Oflaz
dc.contributor.kuauthorYenidoğan, İrem
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-01-19T10:32:51Z
dc.date.issued2023
dc.description.abstractIntroduction: Pilocytic astrocytoma (PA) is one of the most common primary intracranial neoplasms in childhood with an overall favorable prognosis. Despite decades of experience, there are still diagnostic and treatment challenges and unresolved issues regarding risk factors associated with recurrence, most often due to conclusions of publications with limited data. We analyzed 499 patients with PA diagnosed in a single institution over 30 years in order to provide answers to some of the unresolved issues. Materials and Methods: We identified pilocytic astrocytomas diagnosed at the University of California, San Francisco, between 1989 and 2019, confirmed the diagnoses using the WHO 2021 essential and desirable criteria, and performed a retrospective review of the demographic and clinical features of the patients and the radiological, pathologic and molecular features of the tumors. Results: Among the patients identified from pathology archives, 499 cases fulfilled the inclusion criteria. Median age at presentation was 12 years (range 3.5 months – 73 years) and the median follow-up was 78.5 months. Tumors were predominantly located in the posterior fossa (52.6%). There were six deaths, but there were confounding factors that prevented a clear association of death to tumor progression. Extent of resection was the only significant factor for recurrence-free survival. Recurrence-free survival time was 321.0 months for gross total resection, compared to 160.9 months for subtotal resection (log rank, p <0.001). Conclusion: Multivariate analysis was able to identify extent of resection as the only significant variable to influence recurrence-free survival. We did not find a statistically significant association between age, NF1 status, tumor location, molecular alterations, and outcome. Smaller series with apparently significant results may have suffered from limited sample size, limited variables, acceptance of univariate analysis findings as well as a larger p value for biological significance. PA still remains a predominantly surgical disease and every attempt should be made to achieve gross total resection since this appears to be the most reliable predictor of recurrence-free survival. © 2023 The author(s).
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume4
dc.identifier.doi10.17879/freeneuropathology-2023-5116
dc.identifier.issn26994445
dc.identifier.quartileN/A
dc.identifier.scopus2-s2.0-85174960333
dc.identifier.urihttps://doi.org/10.17879/freeneuropathology-2023-5116
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26479
dc.keywordsAstrocytoma
dc.keywordsCircumscribed gliomas
dc.keywordsEntity
dc.keywordsGlioma
dc.keywordsJuvenile pilocytic astrocytoma
dc.keywordsPilocytic astrocytoma
dc.keywordsPiloid
dc.keywordsPilomyxoid
dc.keywordsTumor type
dc.language.isoeng
dc.publisherUniversity of Muenster
dc.relation.ispartofFree Neuropathology
dc.subjectMedicine
dc.titlePathological perspectives in pilocytic astrocytomas: extent of resection as the sole critical factor for recurrence-free survival, and the challenge of evaluating conclusions derived from limited data
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKulaç, İbrahim
local.contributor.kuauthorYenidoğan, İrem
local.contributor.kuauthorSözmen, Banu Oflaz
local.contributor.kuauthorBaygül, Arzu Eden
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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