Oral Etoposide for Relapsed or Refractory Ewing Sarcoma in Adolescent and Adult Patients.

Q2 Medicine
Sarcoma Pub Date : 2024-12-13 eCollection Date: 2024-01-01 DOI:10.1155/sarc/8247342
Louise Kostos, Victoria Rayson, Jayesh Desai, Lisa Orme, Susie Bae, Anne Hamilton, Stephen J Luen, Jeremy Lewin
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引用次数: 0

Abstract

Prognosis remains poor for patients with relapsed or refractory Ewing sarcoma, with limited treatment options after first-line therapy. Oral etoposide has efficacy in the paediatric setting; however, data are limited in adults. A retrospective analysis was conducted on 33 patients with relapsed or refractory Ewing sarcoma who completed at least one cycle of oral etoposide at the Peter MacCallum Cancer Centre from 2005 to 2020. The median age at diagnosis and first relapse was 21 and 23 years, respectively. All patients had prior exposure to intravenous etoposide. Nine patients (27%) had stable disease for at least 6 months, and six patients (18%) had a partial response. The clinical benefit rate was 45%. The median PFS was 3.6 months (95% CI: 1.7-5.5), and OS was 8.5 months (95% CI: 4.1-13.0). Despite prior exposure, oral etoposide demonstrated antitumour activity and durable responses in the relapsed or refractory setting for adult patients with Ewing sarcoma.

口服依托泊苷治疗青少年和成人复发或难治性尤文氏肉瘤。
复发或难治性尤文氏肉瘤患者的预后仍然很差,一线治疗后的治疗选择有限。口服依托泊苷对儿科有效;然而,成人的数据有限。2005年至2020年,Peter MacCallum癌症中心对33例复发或难治性Ewing肉瘤患者进行了回顾性分析,这些患者至少完成了一个周期的口服依托泊苷。确诊和首次复发的中位年龄分别为21岁和23岁。所有患者均曾静脉注射依托泊苷。9名患者(27%)病情稳定至少6个月,6名患者(18%)部分缓解。临床获益率为45%。中位PFS为3.6个月(95% CI: 1.7-5.5), OS为8.5个月(95% CI: 4.1-13.0)。尽管先前暴露,口服依托泊苷在复发或难治性成年尤文氏肉瘤患者中显示出抗肿瘤活性和持久的反应。
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
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.
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