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RTHP-16. PATTERNS OF TREATMENT AND OUTCOMES OF 1p19q CO-DELETED GLIOMAS

机译:RTHP-16。 1p19q共删除胶质瘤的治疗方式和结果

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摘要

Molecular markers are redefining classification of lower grade gliomas and ushering in a paradigm shift in their management. Our objective was to evaluate histologic grade on patterns of care and treatment outcomes for 1p19q co-deleted gliomas. We evaluated 737 patients in the National Cancer Database diagnosed with 1p19q co-deleted gliomas from 2004 through 2012 and treated with surgery followed by radiation therapy (RT), chemotherapy (CT), or combined-modality therapy. Patients with grade II tumors were more likely to receive surgery only than those with grade III tumors (58.1% vs. 14.8%, p<0.001), whereas those with grade III tumors were more likely to receive combined-modality therapy (52.2% vs. 6.1%, p<0.001). Among 472 patients with available follow-up, grade predicted overall survival, with an 8% difference at 2 years (98.2% grade II vs. 90.6% grade III, p<0.001). In a Cox multivariable proportional hazards model adjusting for patient and treatment factors, age (>59 yrs vs. <40 yrs; hazard ratio [HR] 15.66, 95% confidence interval [CI] 3.68–66.61, p<0.001), grade (III vs. II; HR 5.84, 95% CI 1.91–17.81, p=0.001), and histology (oligodendroglioma vs. other; HR 0.23, 95% CI 0.10–0.53, p=0.001) were associated with survival. Outcomes after surgery alone were different for grade II and grade III tumors (99.3% grade II vs. 75.7% grade III survival at 2 years, p<0.001), but the addition of post-operative therapy closed the gap between grades. Longer follow-up and additional molecular characterization is needed to further determine the influence of tumor grade in the management of type I 1p19q co-deleted glioma.
机译:分子标记物正在重新定义低级神经胶质瘤的分类,并在其管理中带来范式转变。我们的目标是评估1p19q共删除的神经胶质瘤的治疗模式和治疗结果的组织学等级。我们评估了2004年至2012年在国家癌症数据库中诊断为1p19q共缺失神经胶质瘤的737例患者,并对其进行了放射治疗(RT),化学疗法(CT)或联合疗法治疗。具有II级肿瘤的患者比仅具有III级肿瘤的患者更有可能接受手术治疗(58.1%vs. 14.8%,p <0.001),而具有III级肿瘤的患者更有可能接受联合治疗(52.2%vs. 6.1%,p <0.001)。在472名接受随访的患者中,等级预测了总生存期,两年后差异为8%(II级为98.2%,III级为90.6%,p <0.001)。在针对患者和治疗因素进行调整的Cox多变量比例风险模型中,年龄(> 59岁vs. <40岁;风险比[HR] 15.66,95%置信区间[CI] 3.68-66.61,p <0.001),等级( III vs. II; HR 5.84,95%CI 1.91-17.81,p = 0.001)和组织学(少突胶质细胞瘤与其他; HR 0.23,95%CI 0.10-0.53,p = 0.001)与生存率相关。 II级和III级肿瘤单独手术后的结果是不同的(II级99.3%vs. 2年时III。75%的生存率,p <0.001),但是增加术后治疗缩小了2级之间的差距。需要更长的随访和额外的分子表征来进一步确定肿瘤分级对I型1p19q共缺失神经胶质瘤的治疗的影响。

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