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决定儿童低级别胶质瘤成年幸存者长期预后的临床和治疗因素:一项基于人群的研究。

Clinical and treatment factors determining long-term outcomes for adult survivors of childhood low-grade glioma: A population-based study.

作者信息

Krishnatry Rahul, Zhukova Nataliya, Guerreiro Stucklin Ana S, Pole Jason D, Mistry Matthew, Fried Iris, Ramaswamy Vijay, Bartels Ute, Huang Annie, Laperriere Normand, Dirks Peter, Nathan Paul C, Greenberg Mark, Malkin David, Hawkins Cynthia, Bandopadhayay Pratiti, Kieran Mark W, Manley Peter E, Bouffet Eric, Tabori Uri

机构信息

Division of Hematology/Oncology, University of Toronto, Toronto, Canada.

Labatt Brain Tumor Research Centre, University of Toronto, Toronto, Canada.

出版信息

Cancer. 2016 Apr 15;122(8):1261-9. doi: 10.1002/cncr.29907. Epub 2016 Mar 10.

Abstract

BACKGROUND

The determinants of outcomes for adult survivors of pediatric low-grade glioma (PLGG) are largely unknown.

METHODS

This study collected population-based follow-up information for all PLGG patients diagnosed in Ontario, Canada from 1985 to 2012 (n = 1202) and determined factors affecting survival. The impact of upfront radiation treatment on overall survival (OS) was determined for a cohort of Ontario patients and an independent reference cohort from the Surveillance, Epidemiology, and End Results database.

RESULTS

At a median follow-up of 12.73 years (range, 0.02-33 years), only 93 deaths (7.7%) were recorded, and the 20-year OS rate was 90.1% ± 1.1%. Children with neurofibromatosis type 1 had excellent survival and no tumor-related deaths during adulthood. Adverse risk factors included pleomorphic xanthoastrocytoma (P < .001) and a thalamic location (P < .001). For patients with unresectable tumors surviving more than 5 years after the diagnosis, upfront radiotherapy was associated with an approximately 3-fold increased risk of overall late deaths (hazard ratio [HR], 3.3; 95% confidence interval [CI], 1.6-6.6; P = .001) and an approximately 4-fold increased risk of tumor-related deaths (HR, 4.4; 95% CI, 1.3-14.6; P = .013). In a multivariate analysis, radiotherapy was the most significant factor associated with late all-cause deaths (HR, 3.0; 95% CI, 1.3-7.0; P = .012) and tumor-related deaths (HR, 4.4; 95% CI, 1.3-14.6; P = 0.014). A similar association between radiotherapy and late deaths was observed in the independent reference cohort (P < .001). In contrast to early deaths, late mortality was associated not with PLGG progression but rather with tumor transformation and non-oncological causes.

CONCLUSIONS

The course of PLGG is associated with excellent long-term survival, but this is hampered by increased delayed mortality in patients receiving upfront radiotherapy. These observations should be considered when treatment options are being weighed for these patients.

摘要

背景

小儿低度恶性胶质瘤(PLGG)成年幸存者预后的决定因素很大程度上尚不清楚。

方法

本研究收集了1985年至2012年在加拿大安大略省诊断的所有PLGG患者(n = 1202)基于人群的随访信息,并确定了影响生存的因素。对于一组安大略省患者以及来自监测、流行病学和最终结果数据库的独立参考队列,确定了 upfront 放疗对总生存期(OS)的影响。

结果

在中位随访12.73年(范围0.02 - 33年)时,仅记录到93例死亡(7.7%),20年总生存率为90.1% ± 1.1%。1型神经纤维瘤病患儿成年期生存良好且无肿瘤相关死亡。不良风险因素包括多形性黄色星形细胞瘤(P <.001)和丘脑部位(P <.001)。对于诊断后存活超过5年的不可切除肿瘤患者, upfront 放疗与总体晚期死亡风险增加约3倍相关(风险比[HR],3.3;95%置信区间[CI],1.6 - 6.6;P =.001)以及肿瘤相关死亡风险增加约4倍相关(HR,4.4;95% CI,1.3 - 14.6;P =.013)。在多变量分析中,放疗是与晚期全因死亡(HR,3.0;95% CI,1.3 - 7.0;P =.012)和肿瘤相关死亡(HR,4.4;95% CI,1.3 - 14.6;P = 0.014)相关的最显著因素。在独立参考队列中也观察到放疗与晚期死亡之间存在类似关联(P <.001)。与早期死亡不同,晚期死亡率与PLGG进展无关,而是与肿瘤转化和非肿瘤原因有关。

结论

PLGG病程与良好的长期生存相关,但接受 upfront 放疗患者的延迟死亡率增加阻碍了这一点。在为这些患者权衡治疗方案时应考虑这些观察结果。

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