Treatment differences and long-term outcomes in adults and children with Ewing sarcoma

IF 2.4 3区 医学 Q3 ONCOLOGY
Omar I. Hajjaj , Lauren Corke , Caron Strahlendorf , Sarah Nicole Hamilton , Xiaolan Feng , Christine E. Simmons
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Abstract

Introduction

Ewing sarcoma is an aggressive malignancy primarily affecting children and adolescents. Limited research is available on treatment practices, clinical course, and survival in adults.

Methods

A multi-institution retrospective cohort study of all adults (>18 years) and children (≤18 years) with Ewing sarcoma treated in British Columbia, Canada between January 01, 2000 and December 31, 2018.

Results

One-hundred seven individuals (66 adults, 41 children) were included in the analysis. 5-year OS was 58 % in adults and 75 % in children. For individuals with local disease, 5-year OS was 74 % in adults and 84 % in children. Adult status was associated with impaired PFS (HR, 1.8; 95 % CI, 1.0 – 3.1, p=0.04) and OS (HR, 1.8; 95 % CI, 0.9 – 3.5; p=0.088). A Charlson Comorbidity Index (CCI) ≥3 was associated with impaired survival in adults and children (HR, 3.9, 95 % CI, 2.0 – 7.5; p=<0.001); baseline CCIs were not significantly different between groups. Most adults (61/66; 92 %) and all children (41/41; 100 %) received systemic treatment with no significant difference in mean lines of therapy, treatment modalities or agents. Most children received interval-compressed chemotherapy (35/41; 85 %) compared to adults (19/61; 29 %; p=<0.001). Interval-compression was not significantly associated with improved survival in adults with local disease (HR, 0.51; 95 % CI 0.1 – 2.3; p=0.373). Children more often initiated treatment within 28 days of diagnosis (31/33; 94 %) compared to adults (41/64; 64 %, p=0.001). Treatment within 28 days was associated with improved survival in the entire cohort (HR, 2.04 95 % CI, 1.1 – 3.9; p = 0.03). This association was preserved in subanalysis of individuals with local disease (HR, 5.4; 95 % CI, 1.9 – 15; p = 0.001) and only adults (HR, 5.3, 95 % CI, 1.7 – 17; p = 0.005).

Discussion

Survival for adults with Ewing sarcoma is inferior to children despite similarities in presentation, tumour characteristics and treatments. Further studies on the value of interval-compression in adults are required. Timely initation of treatment should be a priority for this disease.

成人和儿童尤文肉瘤患者的治疗差异和长期疗效。
简介尤文肉瘤是一种侵袭性恶性肿瘤,主要影响儿童和青少年。有关成人治疗方法、临床过程和存活率的研究十分有限:对2000年1月1日至2018年12月31日期间在加拿大不列颠哥伦比亚省接受治疗的所有成人(大于18岁)和儿童(小于18岁)尤文肉瘤患者进行多机构回顾性队列研究:177人(66名成人,41名儿童)被纳入分析。成人的5年生存率为58%,儿童为75%。对于患有局部疾病的患者,5年生存率成人为74%,儿童为84%。成人患者的 PFS(HR,1.8;95 % CI,1.0 - 3.1,p=0.04)和 OS(HR,1.8;95 % CI,0.9 - 3.5;p=0.088)受损。Charlson合并症指数(CCI)≥3与成人和儿童的生存率下降有关(HR,3.9;95 % CI,2.0 - 7.5;p=讨论:尽管表现、肿瘤特征和治疗方法相似,但成人尤文肉瘤患者的生存率却低于儿童患者。需要进一步研究间期压缩对成人的价值。及时开始治疗应是这种疾病的首要任务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Epidemiology
Cancer Epidemiology 医学-肿瘤学
CiteScore
4.50
自引率
3.80%
发文量
200
审稿时长
39 days
期刊介绍: Cancer Epidemiology is dedicated to increasing understanding about cancer causes, prevention and control. The scope of the journal embraces all aspects of cancer epidemiology including: • Descriptive epidemiology • Studies of risk factors for disease initiation, development and prognosis • Screening and early detection • Prevention and control • Methodological issues The journal publishes original research articles (full length and short reports), systematic reviews and meta-analyses, editorials, commentaries and letters to the editor commenting on previously published research.
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