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利妥昔单抗联合高剂量治疗和自体外周血干细胞移植治疗侵袭性B细胞淋巴瘤的多中心前瞻性研究
引用本文:石远凯,杨晟,韩晓红,马军,任汉云,岑溪南,周淑芸,王椿,姜文奇,黄慧强,王健民,朱军,陈虎,韩明哲,黄河,沈晓梅,刘鹏,何小慧.利妥昔单抗联合高剂量治疗和自体外周血干细胞移植治疗侵袭性B细胞淋巴瘤的多中心前瞻性研究[J].中华肿瘤杂志,2009,31(8).
作者姓名:石远凯  杨晟  韩晓红  马军  任汉云  岑溪南  周淑芸  王椿  姜文奇  黄慧强  王健民  朱军  陈虎  韩明哲  黄河  沈晓梅  刘鹏  何小慧
作者单位:1. 北京协和医学院肿瘤医院内科,中国医学科学院,100021
2. 哈尔滨血液病肿瘤研究所血液科
3. 北京医科大学附属第一医院血液科
4. 第一军医大学南方医院血液科
5. 上海第一人民医院血液科
6. 中山大学肿瘤中心内科
7. 第二军医大学长海医院血液内科
8. 北京肿瘤医院内科
9. 解放军第三0七医院移植科
10. 中国医学科学院血液病研究所造血干细胞移植科
11. 浙江大学第一医院血液科
12. 云南省第一医院血液科
基金项目:首都医学发展科研基金支持项目 
摘    要:目的 探讨在高剂量治疗联合自体外周血干细胞移植的基础上,加用利妥昔单抗治疗侵袭性B细胞淋巴瘤的可行性和疗效.方法 12个癌症研究中心共入组28例侵袭性B细胞淋巴瘤患者,其中22例为新诊断患者,6例为复发患者.每例患者共接受4次利妥昔单抗静脉输注,即在外周血干细胞动员化疗的前1天、动员化疗的第7天、干细胞回输的前1天和回输后的第8天各给予1次,每次375 mg/m2,共1500 mg/m2结果 高剂量治疗后,所有患者均达到完全缓解.中位随访37个月时,全组患者的4年总生存率和无进展生存率分别为75.0%和70.3%,新诊断患者的4年总生存率和无进展生存率均为72.7%.全组患者对利妥昔单抗治疗的耐受性较好,不良反应多为1、2度.结论 在高剂量治疗联合自体造血干细胞移植的基础上加入利妥昔单抗治疗侵袭性B细胞淋巴瘤是可行的,并且可能使患者的生存获益.

关 键 词:非霍奇金淋巴瘤  外周血干细胞移植  利妥昔单抗  化学疗法

A prospective multtcenter study of rituximab combined with high-dose chemotherapy and autologousperipheral blood stem cell transplantation for aggressive B-cell lymphoma
SHI Yuan-kai,YANG Sheng,HAN Xiao-hong,MA Jun,REN Han-yun,CEN Xi-nan,ZHOU Shu-yun,WANG Chun,JIANG Wen-qi,HUANG Hui-qiang,WANG Jian-ming,ZHU Jun,CHEN Hu,HAN Ming-zhe,HUANG He,SHEN Xiao-mei,LIU Peng,HE Xiao-hui.A prospective multtcenter study of rituximab combined with high-dose chemotherapy and autologousperipheral blood stem cell transplantation for aggressive B-cell lymphoma[J].Chinese Journal of Oncology,2009,31(8).
Authors:SHI Yuan-kai  YANG Sheng  HAN Xiao-hong  MA Jun  REN Han-yun  CEN Xi-nan  ZHOU Shu-yun  WANG Chun  JIANG Wen-qi  HUANG Hui-qiang  WANG Jian-ming  ZHU Jun  CHEN Hu  HAN Ming-zhe  HUANG He  SHEN Xiao-mei  LIU Peng  HE Xiao-hui
Abstract:Objective To investigate the feasibility and efficacy of rituximab combined with high-dose chemotherapy supported by autologous peripheral blood stem cell transplantation (ASCT) in patients with aggressive B-cell non-Hodgkin lymphoma (NHL). Methods Twenty-eight patients with aggressive B-cell NHL (22 newly diagnosed, 6 relapsed) were enrolled in this study. The high-dose chemotherapy included CHOP regimen ( CTX + ADM + VCR + PDN) for the newly diagnosed patients and DICE ( DEX + IFO + DDP + VP-16) or EPOCH ( VP-16 + PDN + VCR + CTX + ADM) for the relapsed patients. Each patient received infusion of rituximab at a dose of 375 mg/m2 for four times, on D1 before and on D7 peripheral blood stem cell mobilization, and on DI before and D8 after stem cell reinfusion. Results Complete remission was achieved in all patients after high dose chemotherapy and ASCT. At a median follow-up of 37 months, the estimated overall 4-year survival and progression-free survival rate for all patients were 75.0% and 70.3%, respectively, while both were 72.7% for the previously untreated patients. The therapy was generally well tolerated with few side-effects attributable to rituximab. Conclusion These results suggest that adding rituximab to high-dose chemotherapy with peripheral blood stem cell transplantation is feasible and may be beneficial for patients with aggressive B-cell non-Hodgkin lymphoma.
Keywords:Non-Hodgkin lymphoma  Peripheral blood stem cell transplantation  autolngous  Rituximab  Chemotherapy
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