特发性骨肉瘤患者用trofosfamide维持治疗-单中心经验。

A. Raciborska, K. Bilska, C. Rodríguez-Galindo
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引用次数: 3

摘要

背景:尤文氏肉瘤患者预后不佳。使用trofosfamide维持治疗已被提议作为治疗相同儿科恶性肿瘤的有效方案。我们试图评估trofosfamide对高危原发性骨尤文氏肉瘤患者的治疗方案。材料与方法15例原发性骨尤文氏肉瘤患者接受trofosfamide (750 mg/m2,口服,第1-10天)治疗,每28天一次。所有患者均有标准的肿瘤成像和实验室评估。所有的毒性都被记录下来。结果共给药90个周期(中位5个周期/例)。9例患者保持完全缓解,而6例患者在治疗期间出现疾病进展,中位进展时间为7.9个月(范围1.8至4.6)。11例患者(73.3%)存活,其中9例无疾病证据,中位随访时间为3.9年(7.4 - 7.6年)。在trofosfamide治疗开始时,所有活动性疾病患者均死亡。没有明显的毒性。结论对原发性骨尤文氏肉瘤患者应用trofosfamide治疗具有良好的耐受性,并可维持疗效。需要进一步的研究来更好地确定该方案在这些患者的前期管理中的使用。
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Maintenance treatment with trofosfamide in patients with primary bone ewing sarcoma - single center experience.
BACKGROUND Patients with Ewing sarcoma have a dismal outcome. Maintenance treatment with trofosfamide has been proposed as an effective regimen for same paediatric malignancies. AIM We sought to evaluate the schedule of trofosfamide for patients with high-risk primary bone Ewing sarcoma. MATERIALS AND METHODS Fifteen patients with primary bone Ewing sarcoma received treatment with trofosfamide (750 mg/m2 p.o. days 1-10) every 28 days. All patients hod standard tumour imaging and laboratory evaluation. All toxicities were documented. RESULTS A tatal of 90 cycles (median 5 cycles/patient) were administered. A complete response was maintained in nine patients, while six patients had disease progression during treatment Median time to progression was 7.9 months (range 1.8 to 4.6). Eleven patients (73.3%) are alive including nine with no evidence of disease with a median follow-up of 3.9 years (range 7.4 to 7.6). All patients with active disease at the start of the trofosfamide treatment died. There were no significant toxicities. CONCLUSIONS Treatment with trofosfamide is well-tolerated and could have a role to maintain response in patients with primary bone Ewing sarcoma. Further studies are needed to better define the use of this regimen in the upfrront management of those patients.
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Medycyna wieku rozwojowego
Medycyna wieku rozwojowego Medicine-Medicine (all)
CiteScore
0.90
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0.00%
发文量
53
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