Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group

Cash Thomas; McIlvaine Elizabeth; Krailo Mark D.; Lessnick Stephen L.; Lawlor Elizabeth R.; Laack Nadia; Sorger Joel; Marina Neyssa; Grier Holcombe E.; Granowetter Linda; Womer Richard B.; DuBois Steven G.

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Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group

机译：骨骼外和骨骼局限性尤因肉瘤患者的临床特征和结局比较：儿童肿瘤学组的一份报告

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BackgroundThe prognostic significance of having extraskeletal (EES) versus skeletal Ewing sarcoma (ES) in the setting of modern chemotherapy protocols is unknown. The purpose of this study was to compare the clinical characteristics, biologic features, and outcomes for patients with EES and skeletal ES.

机译：背景在现代化学治疗方案中，骨骼外（EES）与骨骼尤文氏肉瘤（ES）的预后意义尚不清楚。这项研究的目的是比较EES和骨骼ES患者的临床特征，生物学特征和结局。

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《Pediatric blood & cancer》 |2016年第10期|共9页
作者
Cash Thomas; McIlvaine Elizabeth; Krailo Mark D.; Lessnick Stephen L.; Lawlor Elizabeth R.; Laack Nadia; Sorger Joel; Marina Neyssa; Grier Holcombe E.; Granowetter Linda; Womer Richard B.; DuBois Steven G.;
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正文语种 eng
中图分类儿科学;
关键词
extraosseous; extraskeletal Ewing sarcoma; gene expression; gene profiling; prognosis; soft-tissue Ewing sarcoma;

机译：骨外;骨骼外尤文氏肉瘤;基因表达;基因分析;预后;软组织尤文氏肉瘤;

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1. Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group [J] . Cash Thomas, McIlvaine Elizabeth, Krailo Mark D., Pediatric blood & cancer . 2016,第10期

机译：骨骼外和骨骼局限性尤因肉瘤患者的临床特征和结局比较：儿童肿瘤学组的一份报告
2. Impact of Two Measures of Micrometastatic Disease on Clinical Outcomes in Patients with Newly Diagnosed Ewing Sarcoma: A Report from the Children's Oncology Group [J] . Vo Kieuhoa T., Edwards Jeremy V., Epling C. Lorrie, Clinical cancer research: an official journal of the American Association for Cancer Research . 2016,第14期

机译：两种微转移疾病措施对新诊断尤因肉瘤患者临床结局的影响：儿童肿瘤学组的报告
3. Comparison of Epidemiology, Clinical Features, and Outcomes of Patients with Reported Ewing Sarcoma and PNET over 40 Years Justifies Current WHO Classification and Treatment Approaches [J] . Kevin Campbell, David Shulman, Katherine A. Janeway, Sarcoma . 2018,第1期

机译：报告的40年来尤因肉瘤和PNET患者的流行病学，临床特征和结果的比较证明了当前的WHO分类和治疗方法是合理的
4. Electronic Patient Reported Outcomes in Paediatric Oncology - Applying Mobile and Near Field Communication Technology [C] . Katharina DUREGGER, Dieter HAYN, Michael NITZLNADER, eHealth Conference . 2016

机译：电子患者报告儿科肿瘤的结果 - 应用移动和近场通信技术
5. BMI-1 expression inversely correlates with differentiation but not clinical outcome or CDKN2a expression in Ewing sarcoma family of tumors. [D] . van Doorninck, John Anthony. 2009

机译：BMI-1表达与尤因肉瘤家族中的分化呈负相关，但与临床结局或CDKN2a表达无关。
6. Comparison of Clinical Features and Outcomes in Patients with Extraskeletal Versus Skeletal Localized Ewing Sarcoma: A Report from the Children’s Oncology Group [O] . Thomas Cash, Elizabeth McIlvaine, Mark D. Krailo, -1

机译：骨骼外和骨骼局限性尤文肉瘤患者的临床特征和结果比较：儿童肿瘤学组的一份报告
7. Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children’s Oncology Group [O] . Cash, Thomas, McIlvaine, Elizabeth, Krailo, Mark D., 2016

机译：骨骼外与骨骼局部尤文肉瘤患者的临床特征和结果比较：来自儿童肿瘤学组的报告

Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group

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