Cargando…

Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center

OBJECTIVE: To explore the histopathological characteristics of paired recurrent gliomas and their clinical significance. METHODS: Glioma patients who received both primary surgery and reoperation when recurrence at Sun Yat-sen University Cancer Center from June 2001 to June 2019 were enrolled. Clini...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Cong, Xi, Shaoyan, Chen, Yingshen, Guo, Chengcheng, Zhang, Ji, Yang, Qunying, Wang, Jian, Sai, Ke, Zeng, Jing, Wang, Jing, Zhang, Zhiqiang, Ke, Chao, Chen, Zhongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811748/
https://www.ncbi.nlm.nih.gov/pubmed/36597096
http://dx.doi.org/10.1186/s12885-022-10484-9
_version_ 1784863590547718144
author Li, Cong
Xi, Shaoyan
Chen, Yingshen
Guo, Chengcheng
Zhang, Ji
Yang, Qunying
Wang, Jian
Sai, Ke
Zeng, Jing
Wang, Jing
Zhang, Zhiqiang
Ke, Chao
Chen, Zhongping
author_facet Li, Cong
Xi, Shaoyan
Chen, Yingshen
Guo, Chengcheng
Zhang, Ji
Yang, Qunying
Wang, Jian
Sai, Ke
Zeng, Jing
Wang, Jing
Zhang, Zhiqiang
Ke, Chao
Chen, Zhongping
author_sort Li, Cong
collection PubMed
description OBJECTIVE: To explore the histopathological characteristics of paired recurrent gliomas and their clinical significance. METHODS: Glioma patients who received both primary surgery and reoperation when recurrence at Sun Yat-sen University Cancer Center from June 2001 to June 2019 were enrolled. Clinical and pathological characteristics were analyzed retrospectively, and histopathology of reoperation specimens was divided into three categories according to tumor cell activity and the degree of necrosis: active group, low-activity group, and necrosis group. RESULTS: A total of 89 patients were included in this study. The 2016 WHO grade of the first operation pathology and IDH1 status were related to survival time after the first operation, but there was no significant association with survival time after reoperation. The time interval between primary and reoperation was shorter for primary high-grade glioma and/or IDH1 wild-type tumor patients than for low-grade glioma and/or IDH1 mutant tumor patients (P < 0.001). Histopathological types of recurrent gliomas were analyzed, and 67 cases (75.3%) were classified into the active group, 14 (15.8%) into the low-activity group, and 8 (8.9%) into the necrosis group. The low-activity or necrosis group was associated with a higher radiotherapy dose and shorter operation interval. Further univariate and multivariate Cox survival analyses showed the histopathological patterns of recurrent gliomas to be related to survival time after reoperation. CONCLUSION: Primary WHO low grade or IDH1 mutant gliomas appeared survival benefit mainly on later recurrence, but was not a prognostic predictor following recurrence. Histopathological feature of recurrent glioma is related to previous treatment, including radiotherapy dosage and chemotherapy treatment, and is also an important independent prognostic factor for patients after reoperation.
format Online
Article
Text
id pubmed-9811748
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-98117482023-01-05 Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center Li, Cong Xi, Shaoyan Chen, Yingshen Guo, Chengcheng Zhang, Ji Yang, Qunying Wang, Jian Sai, Ke Zeng, Jing Wang, Jing Zhang, Zhiqiang Ke, Chao Chen, Zhongping BMC Cancer Research OBJECTIVE: To explore the histopathological characteristics of paired recurrent gliomas and their clinical significance. METHODS: Glioma patients who received both primary surgery and reoperation when recurrence at Sun Yat-sen University Cancer Center from June 2001 to June 2019 were enrolled. Clinical and pathological characteristics were analyzed retrospectively, and histopathology of reoperation specimens was divided into three categories according to tumor cell activity and the degree of necrosis: active group, low-activity group, and necrosis group. RESULTS: A total of 89 patients were included in this study. The 2016 WHO grade of the first operation pathology and IDH1 status were related to survival time after the first operation, but there was no significant association with survival time after reoperation. The time interval between primary and reoperation was shorter for primary high-grade glioma and/or IDH1 wild-type tumor patients than for low-grade glioma and/or IDH1 mutant tumor patients (P < 0.001). Histopathological types of recurrent gliomas were analyzed, and 67 cases (75.3%) were classified into the active group, 14 (15.8%) into the low-activity group, and 8 (8.9%) into the necrosis group. The low-activity or necrosis group was associated with a higher radiotherapy dose and shorter operation interval. Further univariate and multivariate Cox survival analyses showed the histopathological patterns of recurrent gliomas to be related to survival time after reoperation. CONCLUSION: Primary WHO low grade or IDH1 mutant gliomas appeared survival benefit mainly on later recurrence, but was not a prognostic predictor following recurrence. Histopathological feature of recurrent glioma is related to previous treatment, including radiotherapy dosage and chemotherapy treatment, and is also an important independent prognostic factor for patients after reoperation. BioMed Central 2023-01-03 /pmc/articles/PMC9811748/ /pubmed/36597096 http://dx.doi.org/10.1186/s12885-022-10484-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Cong
Xi, Shaoyan
Chen, Yingshen
Guo, Chengcheng
Zhang, Ji
Yang, Qunying
Wang, Jian
Sai, Ke
Zeng, Jing
Wang, Jing
Zhang, Zhiqiang
Ke, Chao
Chen, Zhongping
Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
title Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
title_full Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
title_fullStr Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
title_full_unstemmed Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
title_short Clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
title_sort clinical significance of histopathological features of paired recurrent gliomas: a cohort study from a single cancer center
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811748/
https://www.ncbi.nlm.nih.gov/pubmed/36597096
http://dx.doi.org/10.1186/s12885-022-10484-9
work_keys_str_mv AT licong clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT xishaoyan clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT chenyingshen clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT guochengcheng clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT zhangji clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT yangqunying clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT wangjian clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT saike clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT zengjing clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT wangjing clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT zhangzhiqiang clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT kechao clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter
AT chenzhongping clinicalsignificanceofhistopathologicalfeaturesofpairedrecurrentgliomasacohortstudyfromasinglecancercenter