Primary central nervous system tumor treatment and survival in the United States, 2004–2015

Introduction Brain tumor treatment and survival information is generally limited in large-scale cancer datasets. We provide a clinical investigation of current patterns of care and survival estimates for central nervous system (CNS) tumors treated in the United States. Methods We analyzed the Nation...

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Veröffentlicht in:Journal of neuro-oncology 2019-08, Vol.144 (1), p.179-191
Hauptverfasser: Garcia, Catherine R., Slone, Stacey A., Dolecek, Therese A., Huang, Bin, Neltner, Janna H., Villano, John L.
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container_issue 1
container_start_page 179
container_title Journal of neuro-oncology
container_volume 144
creator Garcia, Catherine R.
Slone, Stacey A.
Dolecek, Therese A.
Huang, Bin
Neltner, Janna H.
Villano, John L.
description Introduction Brain tumor treatment and survival information is generally limited in large-scale cancer datasets. We provide a clinical investigation of current patterns of care and survival estimates for central nervous system (CNS) tumors treated in the United States. Methods We analyzed the National Cancer Database from 2004–2015 for all patients with diagnosis of primary CNS tumors. We describe patient demographics, treatment modality, and analyzed survival estimates. Results 512,168 patient tumor records were examined. The most common histology was meningioma (43.6%), followed by glioblastoma (22.0%), and nerve sheath tumors (10.6%). Patients had a median age of 60 years, with a female (57.9%), white (85.0%), and non-Hispanic (87.8%) predominance. Tumors were reported as World Health Organization (WHO) grade I for 55.9% of the patients, grade II for 5.9%, grade III for 4.4%, grade IV for 24.3%, and grade unknown or not applicable for 9.4%. Overall, 56% underwent surgical procedures, 30.4% received radiation, and 20.6% received chemotherapy. Radiation plus chemotherapy and surgery was the most common treatment modality in high-grade tumors (40.5% in WHO grade III and 49.3% in WHO grade IV), while surgery only or watchful waiting was preferred in low-grade tumors. Older age, male gender, non-Hispanic origin, higher number of comorbidities, and lower socioeconomic status were identified as risk factors for mortality. Conclusions Our analysis provides long-term survival estimates and initial treatment decisions for patients with CNS tumors in hospitals throughout the United States. Age, comorbidities, gender, ethnicity, and socioeconomic characteristics were determinants of survival.
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We provide a clinical investigation of current patterns of care and survival estimates for central nervous system (CNS) tumors treated in the United States. Methods We analyzed the National Cancer Database from 2004–2015 for all patients with diagnosis of primary CNS tumors. We describe patient demographics, treatment modality, and analyzed survival estimates. Results 512,168 patient tumor records were examined. The most common histology was meningioma (43.6%), followed by glioblastoma (22.0%), and nerve sheath tumors (10.6%). Patients had a median age of 60 years, with a female (57.9%), white (85.0%), and non-Hispanic (87.8%) predominance. Tumors were reported as World Health Organization (WHO) grade I for 55.9% of the patients, grade II for 5.9%, grade III for 4.4%, grade IV for 24.3%, and grade unknown or not applicable for 9.4%. Overall, 56% underwent surgical procedures, 30.4% received radiation, and 20.6% received chemotherapy. Radiation plus chemotherapy and surgery was the most common treatment modality in high-grade tumors (40.5% in WHO grade III and 49.3% in WHO grade IV), while surgery only or watchful waiting was preferred in low-grade tumors. Older age, male gender, non-Hispanic origin, higher number of comorbidities, and lower socioeconomic status were identified as risk factors for mortality. Conclusions Our analysis provides long-term survival estimates and initial treatment decisions for patients with CNS tumors in hospitals throughout the United States. Age, comorbidities, gender, ethnicity, and socioeconomic characteristics were determinants of survival.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-019-03218-8</identifier><identifier>PMID: 31254264</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adolescent ; Adult ; Age Factors ; Aged ; Brain cancer ; Brain tumors ; Case-Control Studies ; Central nervous system ; Central Nervous System Neoplasms - classification ; Central Nervous System Neoplasms - mortality ; Central Nervous System Neoplasms - pathology ; Central Nervous System Neoplasms - therapy ; Chemotherapy ; Child ; Child, Preschool ; Clinical Study ; Combined Modality Therapy ; Demography ; Female ; Follow-Up Studies ; Glioblastoma ; Humans ; Infant ; Infant, Newborn ; Male ; Medicine ; Medicine &amp; Public Health ; Meningioma ; Middle Aged ; Nervous system ; Neurology ; Oncology ; Patients ; Prognosis ; Risk factors ; Socioeconomic factors ; Surgery ; Survival ; Survival Rate ; Time Factors ; Tumors ; Young Adult</subject><ispartof>Journal of neuro-oncology, 2019-08, Vol.144 (1), p.179-191</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Journal of Neuro-Oncology is a copyright of Springer, (2019). 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We provide a clinical investigation of current patterns of care and survival estimates for central nervous system (CNS) tumors treated in the United States. Methods We analyzed the National Cancer Database from 2004–2015 for all patients with diagnosis of primary CNS tumors. We describe patient demographics, treatment modality, and analyzed survival estimates. Results 512,168 patient tumor records were examined. The most common histology was meningioma (43.6%), followed by glioblastoma (22.0%), and nerve sheath tumors (10.6%). Patients had a median age of 60 years, with a female (57.9%), white (85.0%), and non-Hispanic (87.8%) predominance. Tumors were reported as World Health Organization (WHO) grade I for 55.9% of the patients, grade II for 5.9%, grade III for 4.4%, grade IV for 24.3%, and grade unknown or not applicable for 9.4%. Overall, 56% underwent surgical procedures, 30.4% received radiation, and 20.6% received chemotherapy. Radiation plus chemotherapy and surgery was the most common treatment modality in high-grade tumors (40.5% in WHO grade III and 49.3% in WHO grade IV), while surgery only or watchful waiting was preferred in low-grade tumors. Older age, male gender, non-Hispanic origin, higher number of comorbidities, and lower socioeconomic status were identified as risk factors for mortality. Conclusions Our analysis provides long-term survival estimates and initial treatment decisions for patients with CNS tumors in hospitals throughout the United States. 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We provide a clinical investigation of current patterns of care and survival estimates for central nervous system (CNS) tumors treated in the United States. Methods We analyzed the National Cancer Database from 2004–2015 for all patients with diagnosis of primary CNS tumors. We describe patient demographics, treatment modality, and analyzed survival estimates. Results 512,168 patient tumor records were examined. The most common histology was meningioma (43.6%), followed by glioblastoma (22.0%), and nerve sheath tumors (10.6%). Patients had a median age of 60 years, with a female (57.9%), white (85.0%), and non-Hispanic (87.8%) predominance. Tumors were reported as World Health Organization (WHO) grade I for 55.9% of the patients, grade II for 5.9%, grade III for 4.4%, grade IV for 24.3%, and grade unknown or not applicable for 9.4%. Overall, 56% underwent surgical procedures, 30.4% received radiation, and 20.6% received chemotherapy. 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subjects Adolescent
Adult
Age Factors
Aged
Brain cancer
Brain tumors
Case-Control Studies
Central nervous system
Central Nervous System Neoplasms - classification
Central Nervous System Neoplasms - mortality
Central Nervous System Neoplasms - pathology
Central Nervous System Neoplasms - therapy
Chemotherapy
Child
Child, Preschool
Clinical Study
Combined Modality Therapy
Demography
Female
Follow-Up Studies
Glioblastoma
Humans
Infant
Infant, Newborn
Male
Medicine
Medicine & Public Health
Meningioma
Middle Aged
Nervous system
Neurology
Oncology
Patients
Prognosis
Risk factors
Socioeconomic factors
Surgery
Survival
Survival Rate
Time Factors
Tumors
Young Adult
title Primary central nervous system tumor treatment and survival in the United States, 2004–2015
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