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首页> 外文期刊>Oncology letters >Metastatic extraskeletal Ewing's sarcoma treated with trabectedin: A case report
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Metastatic extraskeletal Ewing's sarcoma treated with trabectedin: A case report

机译:曲贝汀治疗转移性骨骼外尤文肉瘤:1例

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摘要

The Ewing's sarcoma family of tumors (ESFT) comprises a number of rare malignant tumors. Standard first-line treatment for patients with these tumors includes chemotherapy with a five-drug regimen of vincristine, doxorubicin (Adriamycin((R))) and cyclophosphamide, alternating with ifosfamide and etoposide (VAC/IE). In cases of inadequate response, there are a number of second-line regimens available. However, further treatment options are required for those patients with disease unresponsive to standard treatment. Trabectedin is a novel treatment option for patients with ESFT. The present study reports the case of a Caucasian 69-year-old female patient who presented with a soft tissue mass on the chest wall that had developed 7 months earlier. A computed tomography scan revealed a 9x8x7-cm mass on the anterior chest wall above the pectoral muscle. Histopathological evaluations and molecular analysis indicated that it was consistent with a metastatic extraskeletal Ewing's sarcoma. The patient was treated with an alternating VAC/IE regimen; however, an inadequate response was observed. The patient received second-line treatment with a gemcitabine and dacarbazine combination regimen, but the disease progressed. Subsequently, treatment with trabectedin (1.5 mg/m(2) as a 24-h continuous infusion every 3 weeks) was initiated. Trabectedin treatment resulted in long-lasting (18 months) progression-free survival. It is vital that novel drugs continue to being developed for patients with ESFT following progression subsequent to standard chemotherapy. The current report presents a case of a patient with metastatic, pre-treated Ewing's sarcoma achieving disease stabilization with trabectedin. Based on these results and the observed tolerability profile, trabectedin represents an alternative treatment for patients with ESFT. Further studies are required in order to determine the efficacy of trabectedin as monotherapy or in combination with other drugs. It is also important to identify which tumor subtypes, specific translocations and patient profiles will benefit the most from treatment with trabectedin.
机译:尤因氏肉瘤肿瘤家族(ESFT)包括许多罕见的恶性肿瘤。对于患有这些肿瘤的患者,标准的一线治疗方法包括用长春新碱,阿霉素(Adriamycin(R))和环磷酰胺五种方案联合异环磷酰胺和依托泊苷(VAC / IE)进行化疗。在反应不足的情况下,可以使用许多第二线治疗方案。但是,对于那些对标准治疗无反应的疾病患者,则需要进一步的治疗选择。 Trabectedin是ESFT患者的新型治疗选择。本研究报告了一名69岁白种人女性患者的病例,患者出现了7个月前发育的胸壁软组织肿块。计算机断层扫描显示在胸肌上方的前胸壁上有9x8x7-cm的肿块。组织病理学评估和分子分析表明,它与转移性骨骼外尤文氏肉瘤一致。该患者接受了交替的VAC / IE方案治疗;但是,观察到反应不足。该患者接受了吉西他滨和达卡巴嗪联合治疗的二线治疗,但疾病进展。随后,开始用trabectedin(每3周24小时连续输注1.5 mg / m(2))进行治疗。 Trabectedin治疗可导致长期(18个月)无进展生存期。在标准化学疗法后进展的情况下,继续为ESFT患者开发新药至关重要。本报告介绍了一例转移性,经过治疗的尤因氏肉瘤患者,使用特拉贝汀可达到疾病稳定的目的。基于这些结果和观察到的耐受性,曲贝汀代表了ESFT患者的另一种治疗方法。为了确定曲贝汀作为单药治疗或与其他药物联用的疗效,需要进行进一步的研究。识别哪种肿瘤​​亚型,特异性易位和患者概况也将从特拉贝汀治疗中受益最大,这一点也很重要。

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