Maintenance Chemotherapy in Patients With High-Risk Rhabdomyosarcoma: Long-Term Survival Analysis of the European Paediatric Soft Tissue Sarcoma Study Group RMS 2005 Trial.

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-06-01 Epub Date: 2025-03-07 DOI:10.1200/JCO-24-02850
Gianni Bisogno, Julia Chisholm, Raquel Hladun, Gian Luca De Salvo, Florent Guerin, Michela Casanova, Henry Mandeville, Rita Alaggio, Beatrice Coppadoro, Daniel Orbach, Andrea Ferrari, Rick van Rijn, Anne-Sophie Defachelles, Myriam Ben-Arush, Heidi Glosli, Maja Cesen, Johannes H M Merks, Véronique Minard-Colin
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引用次数: 0

Abstract

The European Paediatric Soft Tissue Sarcoma Study Group (EpSSG) RMS 2005 trial evaluated maintenance chemotherapy in high-risk rhabdomyosarcoma (RMS). Patients were randomly assigned to either discontinue treatment (standard arm) or receive six 28-day cycles of vinorelbine (25 mg/m2) once per day on days 1, 8, and 15, plus once daily low-dose cyclophosphamide (25 mg/m2; experimental arm). Initial results showed improved overall survival (OS), but disease-free survival (DFS) improvement was not statistically significant. This report presents mature survival outcomes after extended follow-up. Between April 2006 and December 2016, 186 patients were enrolled in the standard arm and 185 in the experimental arm. After a median follow-up of 122.1 months from diagnosis and 114 months from random assignment, recurrence, progression, or death occurred in 103 patients (61 standard arm, 42 experimental arm). The 10-year DFS was 66.5% (95% CI, 59 to 74) in the standard arm versus 77.1% (95% CI, 70.3 to 82.5) in the experimental arm (P = .025). Corresponding 10-year OS rates were 70.8% (95% CI, 63.3 to 77.0) and 82.9% (95% CI, 76.6 to 87.7; P = .0099). Long-term results of the RMS2005 trial confirm the survival benefit of maintenance chemotherapy with vinorelbine and low-dose cyclophosphamide for patients with high-risk RMS.

高危横纹肌肉瘤患者的维持化疗:欧洲儿科软组织肉瘤研究小组RMS 2005试验的长期生存分析
欧洲儿科软组织肉瘤研究组(EpSSG) 2005年RMS试验评估了高危横纹肌肉瘤(RMS)的维持化疗。患者被随机分配到停止治疗(标准组)或接受6个28天周期的长春瑞滨(25mg /m2),每天1次,第1、8和15天,加上每天1次低剂量环磷酰胺(25mg /m2;实验机构)。初步结果显示总生存期(OS)改善,但无病生存期(DFS)改善无统计学意义。本报告介绍了延长随访后的成熟生存结果。在2006年4月至2016年12月期间,186名患者入组标准组,185名入组实验组。在诊断后122.1个月和随机分配后114个月的中位随访后,103例患者出现复发、进展或死亡(61例标准组,42例实验组)。标准组的10年DFS为66.5% (95% CI, 59 - 74),而实验组的10年DFS为77.1% (95% CI, 70.3 - 82.5) (P = 0.025)。相应的10年OS率分别为70.8% (95% CI, 63.3 - 77.0)和82.9% (95% CI, 76.6 - 87.7;P = .0099)。RMS2005试验的长期结果证实了长春瑞滨和低剂量环磷酰胺维持化疗对高危RMS患者的生存益处。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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