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免疫化疗时代滤泡性淋巴瘤的化疗、化疗剂量强度与预后的关系:来自爱荷华大学/梅奥诊所淋巴瘤卓越研究专项分子流行病学资源项目的报告

Relationships between chemotherapy, chemotherapy dose intensity and outcomes of follicular lymphoma in the immunochemotherapy era: a report from the University of Iowa/Mayo Clinic Lymphoma Specialized Program of Research Excellence Molecular Epidemiology Resource.

作者信息

Wudhikarn Kitsada, Smith Brian J, Button Anna M, Habermann Thomas M, Thompson Carrie A, Rosenstein Lori J, Syrbu Sergei I, Weiner George J, Cerhan James R, Link Brian K

机构信息

a Department of Medicine , College of Medicine, University of Iowa , Iowa City , IA , USA.

b Department of Biostatistics , College of Public Health, University of Iowa , Iowa City , IA , USA.

出版信息

Leuk Lymphoma. 2015;56(8):2365-72. doi: 10.3109/10428194.2014.994206. Epub 2015 Feb 9.

Abstract

The optimal treatment of follicular lymphoma (FL) is not established. Rituximab's value potentially dilutes the impact of chemotherapy on FL. We reviewed 337 cases of FL treated initially with rituximab as monotherapy or with chemotherapy at the University of Iowa/Mayo Clinic from 2002 to 2009, investigating the association between chemotherapy delivery of cyclophosphamide or doxorubicin and survival. With median follow-up duration of 52.7 months, event-free survival (EFS) and overall survival (OS) were similar between the two groups, with a trend toward better EFS in the R-chemotherapy cohort (hazard ratio [HR]=1.24, p=0.28). In the R-chemotherapy group, increased total dose delivery and delivered dose intensity of doxorubicin were associated with improved EFS only in patients who did not receive R-maintenance (HR=0.81; p=0.02 and HR=0.94; p=0.04). Cyclophosphamide delivery was not associated with EFS. Thus, in the immunochemotherapy era, chemotherapy delivery strategy requires re-evaluation.

摘要

滤泡性淋巴瘤(FL)的最佳治疗方案尚未确定。利妥昔单抗的价值可能会削弱化疗对FL的疗效。我们回顾了2002年至2009年在爱荷华大学/梅奥诊所最初接受利妥昔单抗单药治疗或化疗的337例FL病例,研究环磷酰胺或阿霉素化疗给药与生存之间的关联。中位随访时间为52.7个月,两组的无事件生存期(EFS)和总生存期(OS)相似,R-化疗队列的EFS有改善趋势(风险比[HR]=1.24,p=0.28)。在R-化疗组中,仅在未接受R-维持治疗的患者中,阿霉素的总给药剂量增加和给药剂量强度增加与EFS改善相关(HR=0.81;p=0.02和HR=0.94;p=0.04)。环磷酰胺给药与EFS无关。因此,在免疫化疗时代,化疗给药策略需要重新评估。

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