涂梅峰, 郑文, 张运涛, 王小沛, 宋玉琴, 谢彦, 林宁晶, 平凌燕, 应志涛, 刘卫平, 邓丽娟, 张晨, 朱军. 氟达拉滨联合化疗治疗20例初治边缘区淋巴瘤的临床观察[J]. 中国肿瘤临床, 2011, 38(5): 292-295 . DOI: 10.3969/j.issn.1000-8179.2011.05.013
引用本文: 涂梅峰, 郑文, 张运涛, 王小沛, 宋玉琴, 谢彦, 林宁晶, 平凌燕, 应志涛, 刘卫平, 邓丽娟, 张晨, 朱军. 氟达拉滨联合化疗治疗20例初治边缘区淋巴瘤的临床观察[J]. 中国肿瘤临床, 2011, 38(5): 292-295 . DOI: 10.3969/j.issn.1000-8179.2011.05.013

氟达拉滨联合化疗治疗20例初治边缘区淋巴瘤的临床观察

  • 摘要: 目的:探讨氟达拉滨联合化疗方案治疗初治边缘区B细胞淋巴瘤的疗效和不良反应。方法:2005年9月至2010年2月期间,收治经北京肿瘤医院确诊的初治边缘区B细胞淋巴瘤患者20例, 其中结外、 结和脾边缘区淋巴瘤分别为16例、3例和1例。治疗方法均采用含氟达拉滨的方案,其中采用FC方案 (氟达拉滨+环磷酰胺) 治疗14例,采用Rituximab (利妥昔单抗,R) -FC治疗6例。所有患者均接受1~6个周期化疗,平均完成为4.3个周期。结果:20例患者中达完全缓解者18例 (90%), 达部分缓解者2例 (10%), 总有效率 (完全缓解+部分缓解) 为100%。所有患者的1年和2年总生存率均为88%, 1年和2年无进展生存率均为88%, 1年和2年的无瘤生存率均为85%。全组共化疗86个周期, 主要不良反应为骨髓抑制和轻度胃肠道反应。51%周期发生白细胞下降, 其中9.3%周期发生Ⅲ/Ⅳ度白细胞减少; 6例 (30%) 患者出现血小板下降,年龄≥60岁患者中血小板下降发生率为66.7% (4/6), 而<60岁患者中血小板下降发生率为14.3% (2/14),P=0.037; 20%周期发生胃肠道反应; 8%周期发生轻度肝功能损伤; 1例 (5%) 患者合并肺部真菌感染。结论:氟达拉滨联合环磷酰胺对初治边缘区B细胞淋巴瘤的近期疗效较好, 不良反应可耐受, 远期疗效值得期待。

     

    Abstract: Efficacy of Fludarabine–based Combination Chemotherapy in 20 Patients UndergoingInitial Treatment of Marginal Zone B-cell LymphomaMeifeng TU, Wen ZHENG, Yuntao ZHANG, Xiaopei WANG, Yuqin SONG, Yan XIE, Ningjing LIN, Lingyan PING, Zhitao YING,Weiping LIU, Lijuan DENG, Chen ZHANG, Jun ZHUCorrespondence to: Jun ZHU, E-mail: zj@bjcancer.orgDepartment of Lymphoma, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking UniversitySchool of Clinical Oncology, Beijing Cancer Hospital, Beijing Institute for Cancer Research, Beijing 100142, ChinaAbstract Objective: To evaluate the efficacy and safety of fludarabine-based combination chemotherapy in 20 patients undergo-ing initial treatment for marginal zone B-cell lymphoma ( MZL ). Methods: Data of 20 patients with initial treatment of MZL in thestudy hospital between September 2005 and February 2010, including 16 with extranodal MZL, 3 with nodal MZL and 1 with splenicMZL, were reviewed in this study. A fludarabine-based regimen was administered in all patients. Specifically, 14 patients were treatedwith a FC regimen (Fludarabine and cyclophosphamide) while 6 were treated with R-FC ( Rituximab + FC ). On average the patients re-ceived 4.3 ( 1~6 ) therapeutic cycles. Results: Eighteen of the 20 patients ( 90 % ) achieved complete remission (CR) and the other 2 pa-tients ( 10 % ) achieved partial remission ( PR ). The total effective rate ( CR + PR ) was 100 % ( 20/20 ). In all 20 patients, the 1- and2-year overall survival rates were 88 %, the progression-free survival ( PFS ) rate was 88 % and the disease-free survival rate was 85 %.Myelosuppression and mild GI toxicity were the major side effects. The rates of leucopenia, nausea and vomiting and mild liver injurywere 51 % ( Ⅲ+Ⅳ 9.3 % ), 20%, and 8%, respectively. Six patients ( 30 % ) had thrombocytopenia; the incidence of thrombocytopeniawas 66.7% (4/6) in patients over 60 years old and 14.3% (2/14) in patients younger than 60 years old ( P = 0.037 ). Pulmonary fungal in-fection occurred in 1 patient ( 5 % ). Conclusion: The fludarabine-based chemotherapy regimen has shown a satisfactory therapeutic ef-fect on patients undergoing initial treatment for MZL, and the corresponding side effects can be well tolerated.Keywords Lymphoma; Marginal zone B-cell; Fludarabine; Combination chemotherapy

     

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