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首页> 外文期刊>International journal of hematology >High-dose methotrexate, etoposide, dexamethasone and pegaspargase (MEDA) combination chemotherapy is effective for advanced and relapsed/refractory extranodal natural killer/T cell lymphoma: a retrospective study
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High-dose methotrexate, etoposide, dexamethasone and pegaspargase (MEDA) combination chemotherapy is effective for advanced and relapsed/refractory extranodal natural killer/T cell lymphoma: a retrospective study

机译:回顾性研究表明,大剂量甲氨蝶呤,依托泊苷,地塞米松和培加斯加酶(MEDA)联合化疗可有效治疗晚期和复发/难治性结外自然杀伤/ T细胞淋巴瘤。

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摘要

Extranodal natural killer/T cell lymphoma, nasal type (ENK/TCL), is an aggressive and rare hematological malignancy. Patients with advanced and relapsed/refractory disease have very poor outcomes. In this study, we retrospectively assessed the efficacy and safety of MEDA regimen (methotrexate, etoposide, dexamethasone and pegaspargase) in the treatment of advanced and relapsed/refractory ENK/TCL patients. Thirteen patients received a total of 55 cycles of MEDA, with a median of four cycles. At the completion of treatment, the overall response rate was 76.9 %, with a complete response rate of 61.5 %. The 1-year overall survival rate was 69.2 %, and 1-year progression-free survival was 61.5 %. Treatment-related toxicity was monitored in all patients. Grade 3/4 neutropenia occurred in 46.2 % of patients. Serious infections happened in two cases (15.4 %). Grade 3/4 thrombocytopenia occurred in 30.8 % of patients, and 23.1 % received platelet transfusion. Grade 3/4 anemia was observed in 23.1 % of patients. Hepatotoxicity and low fibrinogen were common, but mild. These results show that MEDA regimen is very effective with tolerable adverse effects in the treatment of advanced and relapsed/refractory ENK/TCL. Further prospective trials are expected to validate the efficacy of MEDA in an expanded number of patients.
机译:鼻外型自然杀伤/ T细胞淋巴瘤(ENK / TCL)是一种侵袭性且罕见的血液系统恶性肿瘤。患有晚期和复发/难治性疾病的患者预后很差。在这项研究中,我们回顾性评估了MEDA方案(甲氨蝶呤,依托泊苷,地塞米松和培加aspargase)在晚期和复发/难治性ENK / TCL患者中的疗效和安全性。 13位患者共接受了55个MEDA周期,中位值为4个周期。治疗完成后,总缓解率为76.9%,完全缓解率为61.5%。 1年总生存率为69.2%,1年无进展生存率为61.5%。在所有患者中监测与治疗相关的毒性。 3/4级中性粒细胞减少症发生在46.2%的患者中。 2例(15.4%)发生严重感染。 30.8%的患者发生3/4级血小板减少症,接受血小板输注的比例为23.1%。在23.1%的患者中观察到3/4级贫血。肝毒性和低纤维蛋白原是常见的,但较轻。这些结果表明,MEDA方案在晚期和复发/难治性ENK / TCL的治疗中非常有效,并且具有可耐受的不良反应。预期将进行进一步的前瞻性试验,以验证MEDA在更多患者中的疗效。

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