Fischer-Valuck Benjamin W, Chen Ishita, Srivastava Amar J, Floberg John M, Rao Yuan James, King Allison A, Shinohara Eric T, Perkins Stephanie M
Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
Department of Pediatric Hematology and Oncology, Washington University School of Medicine, St. Louis, Missouri.
Cancer. 2017 Feb 15;123(4):682-687. doi: 10.1002/cncr.30405. Epub 2016 Nov 2.
Atypical teratoid rhabdoid tumors (ATRTs) are rare brain tumors that occur primarily in children under the age of 3 years. This report evaluates the treatment approach and survival outcomes in a large cohort of patients treated in the United States.
Using the National Cancer Database, the analysis included all ATRT patients aged 0 to 18 years who were diagnosed between 2004 and 2012 and had complete treatment data.
Three hundred sixty-one ATRT patients were evaluated. The 5-year overall survival (OS) rate was 29.9%, and it was significantly lower for children who were less than 3 years old (5-year OS, 27.7%) versus those who were 3 years old or older (5-year OS, 37.5%; P < .001). The best outcome was seen for patients with localized disease who received trimodality therapy (surgery, chemotherapy, and radiation therapy [RT]) with a 5-year OS rate of 46.8%. The utilization of trimodality therapy significantly increased during the study period (27.7% in 2004-2008 vs 45.1% in 2009-2012; P < .01), largely because of the increased use of RT. In a multivariate analysis, treatment that did not utilize trimodality therapy was associated with significantly worse OS (hazard ratio, 2.52; 95% confidence interval (1.82-3.51). Children aged 0 to 2 years were significantly less likely to receive trimodality therapy because of decreased utilization of RT in this age group.
The use of trimodality therapy significantly increased during the study period and was associated with improved outcomes. For patients with localized disease who received trimodality therapy, the OS rate at 5 years approached 50%. However, further research into the optimal management of children less than 3 years old is needed because of their significantly worse OS in comparison with older children. Cancer 2017;123:682-687. © 2016 American Cancer Society.
非典型畸胎样横纹肌样瘤(ATRT)是一种罕见的脑肿瘤,主要发生在3岁以下儿童。本报告评估了美国一大群接受治疗的患者的治疗方法和生存结果。
利用国家癌症数据库,分析纳入了2004年至2012年间诊断的所有0至18岁且有完整治疗数据的ATRT患者。
对361例ATRT患者进行了评估。5年总生存率(OS)为29.9%,3岁以下儿童(5年OS,27.7%)显著低于3岁及以上儿童(5年OS,37.5%;P<0.001)。局限性疾病患者接受三联疗法(手术、化疗和放疗[RT])的预后最佳,5年OS率为46.8%。在研究期间,三联疗法的使用显著增加(2004 - 2008年为27.7%,2009 - 2012年为45.1%;P<0.01),这主要是由于放疗使用的增加。在多变量分析中,未采用三联疗法的治疗与显著更差的OS相关(风险比,2.52;95%置信区间[1.82 - 3.51])。0至2岁儿童接受三联疗法的可能性显著更低,因为该年龄组放疗的使用减少。
在研究期间,三联疗法的使用显著增加且与改善的结果相关。对于接受三联疗法的局限性疾病患者,5年OS率接近50%。然而,由于3岁以下儿童与大龄儿童相比OS显著更差,因此需要对其最佳管理进行进一步研究。《癌症》2017年;123:682 - 687。©2016美国癌症协会