ReSPOND联盟中IDH1-野生型胶质母细胞瘤患者的性别差异。

Sree Gongala, Jose A Garcia, Nisha Korakavi, Nirav Patil, Hamed Akbari, Andrew Sloan, Jill S Barnholtz-Sloan, Jessie Sun, Brent Griffith, Laila M Poisson, Thomas C Booth, Rajan Jain, Suyash Mohan, MacLean P Nasralla, Spyridon Bakas, Charit Tippareddy, Josep Puig, Joshua D Palmer, Wenyin Shi, Rivka R Colen, Aristeidis Sotiras, Sung Soo Ahn, Yae Won Park, Christos Davatzikos, Chaitra Badve
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引用次数: 0

摘要

背景:目的:研究胶质母细胞瘤、异柠檬酸脱氢酶-1野生型(IDH1-WT)、4级患者在分子、临床和放射学肿瘤参数以及生存结果方面的性别差异:从胶质母细胞瘤精准肿瘤学放射组学特征联盟(ReSPOND)获得了1832例胶质母细胞瘤IDH1-WT患者的回顾性数据,这些数据包含全面的肿瘤参数信息。对缺失值进行了数据估算。通过非参数检验评估肿瘤参数的性别差异,如年龄、分子参数、术前 KPS 评分、肿瘤体积、震中和侧位。利用术前磁共振成像图生成空间图谱,以直观显示肿瘤特征。生存时间分析通过对数秩检验和 Cox 比例危险分析进行:GBM的女性确诊年龄中位数为64岁,而男性为61.9岁(FDR = 0.003)。男性的卡诺夫斯基表现评分(80分以上)高于女性(女性为60.4%,男性为69.7%,FDR = 0.044)。女性增强区(16.7 立方厘米,男性 20.6 立方厘米,FDR = 0.001)、坏死核心区(6.18 立方厘米,男性 7.76 立方厘米,FDR = 0.001)和水肿区(46.9 立方厘米,男性 59.2 立方厘米,FDR = 0.0001)的肿瘤体积较小。在所有人群中,右颞叶是最常见的肿瘤中心。男性更常累及右侧和左侧颞叶。生存结果和死亡率无明显差异。年龄越大、O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子未甲基化以及接受次全切除术会增加男性和女性的死亡风险:我们的研究表明,IDH1-WT 4级胶质母细胞瘤患者的临床和放射学肿瘤参数存在明显的性别差异。性别不是影响生存结果的独立预后因素,影响患者预后的肿瘤参数在男性和女性中是相同的:缩写:IDH1-WT=异柠檬酸脱氢酶-1野生型;MGMTp=O6-甲基鸟嘌呤-DNA-甲基转移酶启动子;KPS=卡诺夫斯基表现评分;EOR=切除范围;WHO=世界卫生组织;FDR=错误发现率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex-Specific Differences in Patients with IDH1-Wild-Type Grade 4 Glioma in the ReSPOND Consortium.

Background and purpose: Understanding sex-based differences in patients with glioblastoma is necessary for accurate personalized treatment planning to improve patient outcomes. Our purpose was to investigate sex-specific differences in molecular, clinical, and radiologic tumor parameters, as well as survival outcomes in patients with glioblastoma, isocitrate dehydrogenase-1 wild-type (IDH1-WT), grade 4.

Materials and methods: Retrospective data of 1832 patients with glioblastoma, IDH1-WT with comprehensive information on tumor parameters was acquired from the Radiomics Signatures for Precision Oncology in Glioblastoma consortium. Data imputation was performed for missing values. Sex-based differences in tumor parameters, such as age, molecular parameters, preoperative Karnofsky performance score (KPS), tumor volumes, epicenter, and laterality were assessed through nonparametric tests. Spatial atlases were generated by using preoperative MRI maps to visualize tumor characteristics. Survival time analysis was performed through log-rank tests and Cox proportional hazard analyses.

Results: Glioblastoma was diagnosed at a median age of 64 years in women compared with 61.9 years in men (false discovery rate [FDR] = 0.003). Men had a higher KPS (above 80) as compared with women (60.4% women versus 69.7% men, FDR = 0.044). Women had lower tumor volumes in enhancing (16.7 cm3 versus 20.6 cm3 in men, FDR = 0.001), necrotic core (6.18 cm3 versus 7.76 cm3 in men, FDR = 0.001), and edema regions (46.9 cm3 versus 59.2 cm3 in men, FDR = 0.0001). The right temporal region was the most common tumor epicenter in the overall population. Right as well as left temporal lobes were more frequently involved in men. There were no sex-specific differences in survival outcomes and mortality ratios. Higher age, unmethylated O6-methylguanine-DNA-methyltransferase promoter and undergoing subtotal resection increased the mortality risk in both men and women.

Conclusions: Our study demonstrates significant sex-based differences in clinical and radiologic tumor parameters of patients with glioblastoma. Sex is not an independent prognostic factor for survival outcomes and the tumor parameters influencing patient outcomes are identical for men and women.

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