Trimodality therapy for atypical teratoid/rhabdoid tumor is associated with improved overall survival: A surveillance, epidemiology, and end results analysis

Background Atypical teratoid/rhabdoid tumors (AT/RTs) are rare aggressive central nervous system tumors. The use of radiation therapy (RT) remains controversial, especially for patients younger than three years of age. The purpose of the current investigation is to robustly analyze the impact of RT...

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Veröffentlicht in:Pediatric blood & cancer 2019-12, Vol.66 (12), p.e27969-n/a
Hauptverfasser: Quinn, Thomas J., Almahariq, Muayad F., Siddiqui, Zaid A., Thompson, Andrew B., Hamstra, Daniel A., Kabolizadeh, Peyman, Gowans, Kate L., Chen, Peter Y.
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Sprache:eng
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Zusammenfassung:Background Atypical teratoid/rhabdoid tumors (AT/RTs) are rare aggressive central nervous system tumors. The use of radiation therapy (RT) remains controversial, especially for patients younger than three years of age. The purpose of the current investigation is to robustly analyze the impact of RT among pediatric AT/RT patients using the Surveillance, Epidemiology, and End Results (SEER) database. Methods SEER 18 Custom Data registries were queried for AT/RT (ICD‐0‐3 9508/3). A total of 190 pediatric AT/RT patients were identified, of whom 102 underwent surgery + chemotherapy and 88 underwent trimodality therapy. Univariate and multivariable analyses using Kaplan‐Meier and Cox proportional hazards regression modeling were performed. Propensity‐score matched analysis with inverse probability of treatment weighting was performed to account for indication bias. The landmark method was used to account for immortal time bias. Results The majority of patients were
ISSN:1545-5009
1545-5017
DOI:10.1002/pbc.27969