Predictors of Recurrence and Patterns of Initial Failure in Localized Ewing Sarcoma: A Contemporary 20-Year Experience.

Q2 Medicine Sarcoma Pub Date : 2021-04-17 eCollection Date: 2021-01-01 DOI:10.1155/2021/6681741
Gregory C Stachelek, John A Ligon, Jennifer Vogel, Adam S Levin, Nicolas J Llosa, Brian H Ladle, Christian F Meyer, Stephanie A Terezakis, Carol D Morris, Matthew M Ladra, Christine A Pratilas
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引用次数: 5

Abstract

Background: The majority of patients with localized Ewing sarcoma will remain disease-free long term, but for those who suffer recurrence, successful treatment remains a challenge. Identification of clinicopathologic factors predictive of recurrence could suggest areas for treatment optimization. We sought to describe our experience regarding predictors of recurrence and patterns of first failure in patients receiving modern systemic therapy for nonmetastatic Ewing sarcoma.

Methods: The medical records of pediatric and adult patients treated for localized Ewing sarcoma between 1999 and 2019 at Johns Hopkins Hospital were retrospectively analyzed. Local control was surgery, radiotherapy, or both. Recurrence-free survival (RFS) was calculated using the Kaplan-Meier method. Univariable and multivariable Cox proportional-hazards modeling was performed to obtain hazard ratios (HR) for recurrence.

Results: In 94 patients with initially localized disease, there were 21 recurrences: 4 local, 14 distant, and 3 combined. 5-year and 10-year RFS were 75.6% and 70.5%, respectively. On multivariable analysis including age at diagnosis and tumor size, <95% tumor necrosis following neoadjuvant chemotherapy (NAC; HR 14.3, p = 0.028) and radiological tumor size change during NAC (HR 1.04 per 1% decrease in size change, p = 0.032) were independent predictors of recurrence. Among patients experiencing distant recurrence, pulmonary metastases were present in 82% and were the only identifiable site of disease in 53%.

Conclusions: Poor pathologic or radiologic response to NAC is predictive of recurrence in patients with localized Ewing sarcoma. Suboptimal tumor size reduction following chemotherapy provides a means to risk-stratify patients who do not undergo definitive resection. Isolated pulmonary recurrence was a common event.

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局部尤文氏肉瘤复发和初始失败模式的预测因素:近20年的经验。
背景:大多数局部尤文氏肉瘤患者将长期无病,但对于那些复发的患者,成功的治疗仍然是一个挑战。确定预测复发的临床病理因素可以建议优化治疗的领域。我们试图描述我们在接受现代全身治疗的非转移性尤因肉瘤患者的复发预测因素和首次失败模式方面的经验。方法:回顾性分析美国约翰霍普金斯医院1999 - 2019年收治的局限性尤文氏肉瘤患儿和成人的病历。局部控制采用手术、放疗或两者兼而有之。采用Kaplan-Meier法计算无复发生存期(RFS)。采用单变量和多变量Cox比例风险模型获得复发的风险比(HR)。结果:94例最初为局部病变的患者中,21例复发:局部4例,远处14例,合并3例。5年和10年RFS分别为75.6%和70.5%。在多变量分析中,包括诊断年龄和肿瘤大小(p = 0.028)和NAC期间放射学上的肿瘤大小变化(大小变化每减少1%的HR为1.04,p = 0.032)是复发的独立预测因素。在远处复发的患者中,82%存在肺转移,53%是唯一可识别的疾病部位。结论:对NAC不良的病理或放射学反应可预测局部尤文氏肉瘤的复发。化疗后肿瘤大小的次优缩小为不接受最终切除的患者提供了一种风险分层的方法。孤立的肺部复发是常见的事件。
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来源期刊
Sarcoma
Sarcoma Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.00
自引率
0.00%
发文量
15
审稿时长
14 weeks
期刊介绍: Sarcoma is dedicated to publishing papers covering all aspects of connective tissue oncology research. It brings together work from scientists and clinicians carrying out a broad range of research in this field, including the basic sciences, molecular biology and pathology and the clinical sciences of epidemiology, surgery, radiotherapy and chemotherapy. High-quality papers concerning the entire range of bone and soft tissue sarcomas in both adults and children, including Kaposi"s sarcoma, are published as well as preclinical and animal studies. This journal provides a central forum for the description of advances in diagnosis, assessment and treatment of this rarely seen, but often mismanaged, group of patients.
期刊最新文献
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