A retrospective analysis of the risk factors affecting recurrence time in patients with recurrent glioblastoma

Renhua Huang(Second Affiliated Hospital of Soochow University), Tianwei Wang(Renji Hospital), Zhijun Liao(Shanghai International Medical Center), Zhenwei Wang(Renji Hospital), Ming Ye(Renji Hospital), Di Zhou(Shanghai Jiao Tong University), Huaying Xie(Shanghai Jiao Tong University), Yongrui Bai(Renji Hospital), Yongming Qiu(Shanghai Jiao Tong University), Yulong Liu(Soochow University)
Annals of Palliative Medicine
May 1, 2021
Cited by 16Open Access
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Abstract

BACKGROUND: This study explored the related factors that influence the recurrence time of glioblastomas (GBM). METHODS: A retrospective study of recurrent GBM patients with surgical resection was performed. Recurrence time was analyzed using Kaplan-Meier survival curves. The Cox regression model was used to investigate the possible factors associated with recurrence time. RESULTS: A total of 176 patients (113 males and 63 females) were enrolled in the study, with a median age of 57 years (range, 19-76 years). From this cohort, 18 patients (10.2%) had gross total resection (GTR), 53 patients (30.1%) had subtotal resection (STR), and 105 patients (59.7%) had partial resection (PR). Postoperatively, all patients received radiotherapy (RT), with 55.1% administered concurrent chemotherapy (CTh) and 59.7% administered adjuvant CTh. The median recurrence time was 10.0 months (range, 1.0-75.0 months). Patients with PR (P=0.004), gliomas that contacted the subventricular zone (SVZ) (P=0.004), isocitrate dehydrogenase 1 (IDH1) wild-type (P=0.048), telomerase reverse transcriptase (TERT) C228T wild-type (P=0.012), and positive glial fibrillary acidic protein (GFAP) expression (P=0.044) had a shortened time to recurrence. Cox regression analysis revealed that PR (P=0.036), SVZ contact (P=0.008), and TERT C228T wild type (P=0.023) were significantly associated with a shortened recurrence time. CONCLUSIONS: PR, tumor contacting the SVZ, and TERT C228T wild type were independent risk factors for tumor recurrence in patients with GBM.


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