The addition of rituximab to CHOP chemotherapy improves overall and failure-free survival for follicular grade 3 lymphoma

The addition of rituximab to CHOP chemotherapy improves overall and failure-free survival for follicular grade 3 lymphoma
复制标题

DOI:
10.1093/annonc/mdm511
复制
发表时间:
2008-03-01
期刊:
影响因子:
50.5
通讯作者:
Fayad, L. E.
Fayad, L. E.
中科院分区:
医学1区
文献类型:
--
作者:
Overman, M. J.;Feng, L.;Fayad, L. E.

文献摘要

被引文献

相似文献

背景资料:利妥昔单抗蒽环类药物为基础的治疗滤泡性淋巴瘤3级的好处还没有studyed.Patients和方法:我们回顾性分析了45例滤泡性淋巴瘤3级谁与利妥昔单抗和环磷酰胺,多柔比星,长春新碱和泼尼松(CHOP)的组合治疗在得克萨斯大学医学博士安德森癌症中心的记录。反应率,无失败生存期(FFS),总生存期(OS)进行了估计和历史比较CHOP只治疗patients.Results:国际预后指数(IPI)分布为47%低,36%低中间,13%高中间,4%高风险。完全缓解率为96%。45名患者中有44人仍然活着。存活患者的中位随访时间为3.5年。根据IPI,低风险患者组的3年FFS率为80% [95%置信区间(CI)64%-100%],低-中等风险患者组为81%(95% CI 64%-100%),高-中等/高风险患者组为50%(95% CI 25%-100%)。在CHOP基础上加用利妥昔单抗可改善5年FFS,71%(95% CI 58%至87%)与44%相比(95% CI 36%至55%),P值为0.019,5年OS为98%(95% CI 93%~ 100%)与75%(95% CI 67%~ 84%)比较,P值为0.0034。结论:CHOP方案加用利妥昔单抗有效率高,早期生存率高。尽管使用利妥昔单抗,低风险患者仍然表现出高失败率。
Background: The benefit of adding rituximab to anthracycline-based therapy for follicular lymphoma grade 3 has not been studied.Patients and methods: We retrospectively reviewed the records of 45 patients with follicular grade 3 lymphoma who were treated with rituximab and the combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) at The University of Texas MD Anderson Cancer Center. Response rate, failure-free survival (FFS), and overall survival (OS) were estimated and a historical comparison to CHOP-only-treated patients was made.Results: The International Prognostic Index (IPI) distribution was 47% low, 36% low intermediate, 13% high intermediate, and 4% high risk. The complete response rate was 96%. Forty-four of 45 patients are still alive. Median follow-up for the alive patients is 3.5 years. The 3-year FFS rate according to the IPI was 80% [95% confidence interval (CI) 64% to 100%] in low, 81% in low intermediate (95% CI 64% to 100%), and 50% (95% CI 25% to 100%) in high-intermediate/high-risk patient group. The addition of rituximab to CHOP improved both 5-year FFS, 71% (95% CI 58% to 87%) compared with 44% (95% CI 36% to 55%) with P value of 0.019, and 5-year OS, 98% (95% CI 93% to 100%) compared with 75% (95% CI 67% to 84%) with P value of 0.0034.Conclusion: The addition of rituximab to CHOP provided a high response rate and excellent early survival. Poor-risk patients continue to demonstrate a high rate of failure despite the use of rituximab.