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Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma

STUDY DESIGN: Retrospective study. PURPOSE: To obtain information useful in establishing treatment guidelines by evaluating baseline clinical features and treatment outcomes of patients with spinal cord astrocytoma (SCA). OVERVIEW OF LITERATURE: The optimal management of SCA remains controversial, a...

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Autores principales: Seki, Toshitaka, Hida, Kazutoshi, Yano, Shunsuke, Aoyama, Takeshi, Koyanagi, Izumi, Sasamori, Toru, Hamauch, Shuji, Houkin, Kiyohiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995260/
https://www.ncbi.nlm.nih.gov/pubmed/27559457
http://dx.doi.org/10.4184/asj.2016.10.4.748
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author Seki, Toshitaka
Hida, Kazutoshi
Yano, Shunsuke
Aoyama, Takeshi
Koyanagi, Izumi
Sasamori, Toru
Hamauch, Shuji
Houkin, Kiyohiro
author_facet Seki, Toshitaka
Hida, Kazutoshi
Yano, Shunsuke
Aoyama, Takeshi
Koyanagi, Izumi
Sasamori, Toru
Hamauch, Shuji
Houkin, Kiyohiro
author_sort Seki, Toshitaka
collection PubMed
description STUDY DESIGN: Retrospective study. PURPOSE: To obtain information useful in establishing treatment guidelines by evaluating baseline clinical features and treatment outcomes of patients with spinal cord astrocytoma (SCA). OVERVIEW OF LITERATURE: The optimal management of SCA remains controversial, and there are no standard guidelines. METHODS: The study included 20 patients with low-grade and 13 with high-grade SCA surgically treated between 1989 and 2014. Patients were classified according to the extent of surgical resection. Survival was assessed using Kaplan–Meier plots and compared between groups by log-rank tests. Neurological status was defined by the modified McCormick scale and compared between groups by Mann–Whitney U tests. RESULTS: Surgical resection was performed for 19 of 20 low-grade (95%) and 10 of 13 high-grade (76.9%) SCA patients. Only nine patients (27.3%) underwent gross total resection, all of whom had low-grade SCA. Of all patients, 51.5% showed deteriorated neurological status compared to preoperative baseline. Median overall survival was significantly longer for low-grade SCA than that (91 months, 78% at 5 years vs. 15 months, 31% at 5 years; p=0.007). Low-grade SCA patients benefited from more aggressive resection, whereas high-grade SCA patients did not. Multivariate analysis revealed histology status (hazard ratio [HR], 0.30; 95% confidence interval [CI], 0.09–0.98; p<0.05) and postoperative neurological status (HR, 0.12; CI, 0.02–0.95; p<0.05) as independent predictors of longer overall survival. Adjuvant radiotherapy had no significant impact on survival rate. However, a trend for increased survival was observed with radiation cordotomy (RCT) in high-grade SCA patients. CONCLUSIONS: Aggressive resection for low-grade and RCT may prolong survival. Preservation of neurological status is an important treatment goal. Given the low incidence of SCA, establishing strong collaborative, interdisciplinary, and multi-institutional study groups is necessary to define optimal treatments.
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spelling pubmed-49952602016-08-24 Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma Seki, Toshitaka Hida, Kazutoshi Yano, Shunsuke Aoyama, Takeshi Koyanagi, Izumi Sasamori, Toru Hamauch, Shuji Houkin, Kiyohiro Asian Spine J Clinical Study STUDY DESIGN: Retrospective study. PURPOSE: To obtain information useful in establishing treatment guidelines by evaluating baseline clinical features and treatment outcomes of patients with spinal cord astrocytoma (SCA). OVERVIEW OF LITERATURE: The optimal management of SCA remains controversial, and there are no standard guidelines. METHODS: The study included 20 patients with low-grade and 13 with high-grade SCA surgically treated between 1989 and 2014. Patients were classified according to the extent of surgical resection. Survival was assessed using Kaplan–Meier plots and compared between groups by log-rank tests. Neurological status was defined by the modified McCormick scale and compared between groups by Mann–Whitney U tests. RESULTS: Surgical resection was performed for 19 of 20 low-grade (95%) and 10 of 13 high-grade (76.9%) SCA patients. Only nine patients (27.3%) underwent gross total resection, all of whom had low-grade SCA. Of all patients, 51.5% showed deteriorated neurological status compared to preoperative baseline. Median overall survival was significantly longer for low-grade SCA than that (91 months, 78% at 5 years vs. 15 months, 31% at 5 years; p=0.007). Low-grade SCA patients benefited from more aggressive resection, whereas high-grade SCA patients did not. Multivariate analysis revealed histology status (hazard ratio [HR], 0.30; 95% confidence interval [CI], 0.09–0.98; p<0.05) and postoperative neurological status (HR, 0.12; CI, 0.02–0.95; p<0.05) as independent predictors of longer overall survival. Adjuvant radiotherapy had no significant impact on survival rate. However, a trend for increased survival was observed with radiation cordotomy (RCT) in high-grade SCA patients. CONCLUSIONS: Aggressive resection for low-grade and RCT may prolong survival. Preservation of neurological status is an important treatment goal. Given the low incidence of SCA, establishing strong collaborative, interdisciplinary, and multi-institutional study groups is necessary to define optimal treatments. Korean Society of Spine Surgery 2016-08 2016-08-16 /pmc/articles/PMC4995260/ /pubmed/27559457 http://dx.doi.org/10.4184/asj.2016.10.4.748 Text en Copyright © 2016 by Korean Society of Spine Surgery http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Seki, Toshitaka
Hida, Kazutoshi
Yano, Shunsuke
Aoyama, Takeshi
Koyanagi, Izumi
Sasamori, Toru
Hamauch, Shuji
Houkin, Kiyohiro
Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma
title Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma
title_full Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma
title_fullStr Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma
title_full_unstemmed Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma
title_short Clinical Factors for Prognosis and Treatment Guidance of Spinal Cord Astrocytoma
title_sort clinical factors for prognosis and treatment guidance of spinal cord astrocytoma
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995260/
https://www.ncbi.nlm.nih.gov/pubmed/27559457
http://dx.doi.org/10.4184/asj.2016.10.4.748
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