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DA-EPOCH-R诱导化疗加自体移植巩固治疗双打击淋巴瘤的疗效

Outcomes of DA-EPOCH-R induction plus autologous transplant consolidation for double hit lymphoma.

作者信息

Chen Andy I, Leonard Jessica T, Okada Craig Y, Gay Nathan D, Chansky Kari, Fan Guang, Dunlap Jennifer B, Raess Philipp W, Braziel Rita M, Stentz Alex, Maziarz Richard T

机构信息

a Center for Hematologic Malignancies, Oregon Health & Science University , Portland , OR , USA.

b Cancer Research and Biostatistics , Seattle , WA , USA.

出版信息

Leuk Lymphoma. 2018 Aug;59(8):1884-1889. doi: 10.1080/10428194.2017.1406085. Epub 2017 Dec 3.

DOI:10.1080/10428194.2017.1406085
PMID:29199519
Abstract

High-grade B cell lymphoma with MYC and BCL2 rearrangements (double hit) has a poor prognosis with standard R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone). We report here a treatment algorithm of DA-EPOCH-R (dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, rituximab) followed by BEAM (carmustine, etoposide, cytarabine, melphalan) autologous transplant in 36 cases of previously untreated double hit lymphoma (DHL) from 2010 to 2015. A high risk International Prognostic Index (IPI) was present in 42% of cases. At median follow-up of 38 months, the 2-year progression free survival (PFS) and overall survival (OS) were 69% (95% CI 54-84%) and 71% (95% CI 56-86%). Eight cases were refractory to induction with 1-year OS 20%, and no factors were predictive for primary refractory disease. Of 28 responders, 17 proceeded to transplant while 11 were observed, primarily due to age and co-morbidities. By 24-week landmark analysis after diagnosis, the 2-year PFS and OS were both 94% (95% CI 83-100%) vs 79% (95% CI 52-100%) for transplant vs observation (p = .59 for both PFS and OS). There was no significant benefit to consolidative transplant in our series, and primary refractory DHL needs novel approaches.

摘要

伴有MYC和BCL2重排的高级别B细胞淋巴瘤(双打击)采用标准R-CHOP(利妥昔单抗、环磷酰胺、阿霉素、长春新碱、泼尼松)治疗时预后较差。我们在此报告了2010年至2015年间对36例初治双打击淋巴瘤(DHL)患者采用DA-EPOCH-R(剂量调整的依托泊苷、泼尼松、长春新碱、环磷酰胺、阿霉素、利妥昔单抗)方案治疗,随后进行BEAM(卡莫司汀、依托泊苷、阿糖胞苷、美法仑)自体移植的治疗方案。42%的病例存在高风险国际预后指数(IPI)。中位随访38个月时,2年无进展生存期(PFS)和总生存期(OS)分别为69%(95%可信区间54-84%)和71%(95%可信区间56-86%)。8例诱导治疗无效,1年总生存率为20%,且无因素可预测原发性难治性疾病。28例缓解者中,17例进行了移植,11例进行观察,主要原因是年龄和合并症。通过诊断后24周的标志性分析,移植组与观察组的2年PFS和OS分别为94%(95%可信区间83-100%)和79%(95%可信区间52-100%)(PFS和OS的P值均为0.59)。在我们的系列研究中,巩固性移植无显著益处,原发性难治性DHL需要新的治疗方法。

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