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SMILE 方案治疗自然杀伤/T 细胞淋巴瘤的疗效和安全性:亚洲淋巴瘤研究组的分析。

SMILE for natural killer/T-cell lymphoma: analysis of safety and efficacy from the Asia Lymphoma Study Group.

机构信息

Department of Medicine, Queen Mary Hospital, Hong Kong SAR, China.

出版信息

Blood. 2012 Oct 11;120(15):2973-80. doi: 10.1182/blood-2012-05-431460. Epub 2012 Aug 23.

Abstract

Natural killer/T-cell lymphoma is rare and aggressive, with poor outcome. Optimal treatment remains unclear. A novel regimen dexamethasone, methotrexate, ifosfamide, l-asparaginase, and etoposide (SMILE) showed promise in phase 1/2 studies with restrictive recruitment criteria. To define the general applicability of SMILE, 43 newly diagnosed and 44 relapsed/refractory patients (nasal, N = 60, nonnasal, N = 21; disseminated, N = 6; male, N = 59; female, N = 28) at a median age of 51 years (23-83 years) were treated. Poor-risk factors included stage III/IV disease (56%), international prognostic index of 3 to 5 (43%), and Korean prognostic scores of 3 to 4 (41%). A median of 3 (0-6; total = 315) courses of SMILE were administered. Significant toxicities included grade 3/4 neutropenia (N = 57; 5 sepsis-related deaths); grade 3/4 thrombocytopenia (N = 36); and nephrotoxicity (N = 15; 1 acute renal failure and death). Interim analysis after 2 to 3 cycles showed complete remission rate of 56%, partial remission rate of 22%, giving an overall response rate of 78%. On treatment completion, the overall-response rate became 81% (complete remission = 66%, partial remission = 15%). Response rates were similar for newly diagnosed or relapsed/refractory patients. At a median follow-up of 31 months (1-84 months), the 5-year overall survival was 50% and 4-year disease-free-survival was 64%. Multivariate analysis showed that international prognostic index was the most significant factor impacting on outcome and survivals.

摘要

自然杀伤细胞/T 细胞淋巴瘤较为罕见且侵袭性强,预后不良。最佳治疗方案仍不明确。一项新的方案(地塞米松、甲氨蝶呤、异环磷酰胺、左旋门冬酰胺酶和依托泊苷,即 SMILE)在纳入标准严格的 1/2 期研究中显示出良好的前景。为了明确 SMILE 方案的普遍适用性,我们对 43 例初诊和 44 例复发/难治性患者(鼻型,N=60;非鼻型,N=21;播散型,N=6;男性,N=59;女性,N=28)进行了治疗。这些患者的中位年龄为 51 岁(23-83 岁),具有以下不良预后因素:Ⅲ/Ⅳ期疾病(56%)、国际预后指数 3-5 分(43%)和韩国预后评分 3-4 分(41%)。中位接受 3 个周期(0-6 个周期;总周期数为 315 个)SMILE 治疗。主要毒性反应包括 3/4 级中性粒细胞减少(N=57;5 例与脓毒症相关的死亡)、3/4 级血小板减少(N=36)和肾毒性(N=15;1 例急性肾衰竭和死亡)。治疗 2-3 个周期后进行的中期分析显示,完全缓解率为 56%,部分缓解率为 22%,总缓解率为 78%。治疗结束时,总缓解率达到 81%(完全缓解率=66%,部分缓解率=15%)。新诊断和复发/难治性患者的缓解率相似。中位随访 31 个月(1-84 个月)时,5 年总生存率为 50%,4 年无疾病生存率为 64%。多因素分析显示,国际预后指数是影响预后和生存的最显著因素。

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