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低级别胶质瘤恶变的危险因素。

Risk Factors for Malignant Transformation of Low-Grade Glioma.

机构信息

Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio; Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Cleveland Clinic, Cleveland, Ohio.

Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

出版信息

Int J Radiat Oncol Biol Phys. 2018 Mar 15;100(4):965-971. doi: 10.1016/j.ijrobp.2017.12.258. Epub 2017 Dec 21.

Abstract

PURPOSE

The incidence, risk factors, and outcomes of low-grade glioma patients who undergo malignant transformation (MT) in the era of temozolomide are not well known. This study evaluates these factors in a large group of World Health Organization grade 2 glioma patients treated at a tertiary-care institution.

METHODS AND MATERIALS

Patient, tumor, and treatment factors were analyzed using an institutional review board-approved low-grade glioma database. Characteristics were compared using χ and Wilcoxon signed rank tests. Time to event was summarized using proportional hazards models. Univariate and multivariate survival analyses were performed.

RESULTS

Of a total of 599 patients, 124 underwent MT; 76 (61.3%) had biopsy-proven MT. The MT incidence was 21%, and the median time to MT was 56.4 months. The 5- and 10-year progression-free survival rates were 30.6% ± 4.2% and 4.8% ± 1.9%, respectively, for MT patients and 60% ± 2.4% and 38% ± 2.7%, respectively, for non-MT patients. The 5- and 10-year overall survival rates were 75% ± 4.0% and 46% ± 5.0%, respectively, for MT patients and 87% ± 1.7% and 78% ± 2.3%, respectively, for non-MT patients. On multivariate analysis, older age (P = .001), male sex (P = .004), multiple tumor locations (P = .004), chemotherapy alone (P = .012), and extent of resection (P = .045) remained significant predictors of MT.

CONCLUSIONS

MT affects survival. Risk factors include older age, male sex, multiple tumor locations, use of chemotherapy alone, and presence of residual disease. Our finding that initial interventions could affect the rate of MT is provocative, but these data should be validated using data from prospective trials. In addition to improving survival, future therapeutic efforts should focus on preventing MT.

摘要

目的

替莫唑胺时代低级别胶质瘤患者发生恶性转化(MT)的发生率、风险因素和结局尚不清楚。本研究评估了在一家三级医疗机构接受治疗的一大组世界卫生组织(WHO)2 级胶质瘤患者中的这些因素。

方法和材料

使用机构审查委员会批准的低级别胶质瘤数据库分析患者、肿瘤和治疗因素。使用 χ 和 Wilcoxon 符号秩检验比较特征。使用比例风险模型总结时间事件。进行单变量和多变量生存分析。

结果

总共 599 名患者中,有 124 名发生了 MT;76 例(61.3%)经活检证实为 MT。MT 发生率为 21%,MT 中位时间为 56.4 个月。MT 患者的 5 年和 10 年无进展生存率分别为 30.6%±4.2%和 4.8%±1.9%,而非 MT 患者分别为 60%±2.4%和 38%±2.7%。MT 患者的 5 年和 10 年总生存率分别为 75%±4.0%和 46%±5.0%,而非 MT 患者分别为 87%±1.7%和 78%±2.3%。多变量分析显示,年龄较大(P=.001)、男性(P=.004)、多个肿瘤部位(P=.004)、单独化疗(P=.012)和切除范围(P=.045)仍然是 MT 的显著预测因素。

结论

MT 影响生存。危险因素包括年龄较大、男性、多个肿瘤部位、单独化疗和存在残留疾病。我们发现初始干预可能会影响 MT 的发生率,这很有启发性,但这些数据应使用前瞻性试验的数据进行验证。除了提高生存率外,未来的治疗努力还应侧重于预防 MT。

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