Incidence and survival of gliomatosis cerebri: a population-based cancer registration study

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:2998090 7 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Incidence and survival of gliomatosis cerebri: a population-based cancer registration study
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Gliomatosis cerebri (GC) comprises a rare widespread infiltrating growth pattern of diffuse gliomas. We explored the incidence patterns and survival rates of GC in a population-based registration sample from the Surveillance, Epidemiology and End, Results database (1973–2012). GC cases (n = 176) were identified based on their International Classification of Diseases in Oncology (ICD-O-3) morphology code (9381). We calculated age-adjusted incidence rates (AIR) and evaluated temporal trends. Survival was assessed with Kaplan–Meier curves and Cox regression models. The annual AIR of GC was 0.1/million. We noted increasing trends in the preceding registration years (1973–2002; annually, + 7%) and a tendency of clinical/radiological approaches to substitute the gold-standard histological assessment for diagnosis. GC was diagnosed in the entire age spectrum (range 1–98 years), but higher incidence rates (0.43/million) were noted among the elderly (≥ 65 years). A slight male preponderance was identified (male-to-female ratio: 1.4). Median overall survival was 9 months with a 5 year survival rate of 18%. Increasing age, primary tumor location not restricted to the cerebral hemispheres and rural residence at diagnosis were identified as negative prognostic factors, whereas receipt of radiotherapy, surgical treatment, race and method of diagnosis were not associated with outcome. This first comprehensive overview of GC epidemiology exemplifies the rarity of the disease, provides evidence for male preponderance and increased incidence among the elderly and shows lower survival rates compared to the published single center reports. Expansion of registration to histological and molecular characteristics would allow emergence of clinical prognostic factors at the population level. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
Έτος δημοσίευσης:
2018
Συγγραφείς:
Georgakis, M.K.
Spinos, D.
Pourtsidis, A.
Psyrri, A.
Panourias, I.G.
Sgouros, S.
Petridou, E.T.
Περιοδικό:
Journal of Neuro-Oncology
Εκδότης:
Springer New York LLC
Τόμος:
138
Αριθμός / τεύχος:
2
Σελίδες:
341-349
Λέξεις-κλειδιά:
adolescent; adult; age distribution; aged; Article; cancer diagnosis; cancer incidence; cancer radiotherapy; cancer registry; cancer surgery; cancer survival; child; factual database; female; gliomatosis cerebri; gliosis; histopathology; human; ICD-O-3; major clinical study; male; middle aged; newborn; overall survival; population research; rural area; school child; sex difference; survival rate; survival time; trend study; tumor localization; young adult; cancer registry; central nervous system tumor; follow up; incidence; infant; neuroepithelioma; preschool child; prognosis; survival analysis; very elderly, Adolescent; Adult; Aged; Aged, 80 and over; Central Nervous System Neoplasms; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Incidence; Infant; Male; Middle Aged; Neoplasms, Neuroepithelial; Prognosis; SEER Program; Survival Analysis; Survival Rate; Young Adult
Επίσημο URL (Εκδότης):
DOI:
10.1007/s11060-018-2802-z
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