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采用含利妥昔单抗的基于BFM95方案治疗高肿瘤负荷的新诊断儿童成熟B细胞淋巴瘤/白血病的疗效改善:来自中国上海的报告

Improved Outcome of Newly Diagnosed Childhood Mature B-Cell Lymphoma/Leukemia With High Tumor Burden Treated With BFM95-based Protocol Combining Rituximab: A Report From Shanghai, China.

作者信息

Fu Yang, Wang Hongsheng, Zhai Xiaowen, Qian Xiaowen, Meng Jianhua, Miao Hui, Zhu Xiaohua, Yu Yi, Lu Fengjuan

机构信息

Department of Hematology and Oncology, National Children's Medical Center, Children's Hospital of Fudan University, Shanghai, China.

出版信息

J Pediatr Hematol Oncol. 2019 Apr;41(3):170-174. doi: 10.1097/MPH.0000000000001419.

Abstract

In this study we evaluated children with newly diagnosed advanced (stage III and stage IV) mature B-cell non-Hodgkin lymphoma (B-NHL) or mature B-cell acute leukemia (B-AL), who were treated with Berlin-Frankfurt-Münster (BFM)95-based protocol combined with rituximab (R+BFM95). Our study recruited 46 patients who were treated with BFM95 protocol combined with rituximab. There are 23 patients as the historical control treated with BFM90 protocol. Compared with patients treated with BFM90 protocol, the 5-year event-free survival (EFS) rate of patients under R+BFM95 was higher (83.7%±5.7% vs. 69.6%±9.6%; P=0.1062). Among subgroups of our patients, the 5-year EFS of patients with stage III was 87.3%±6.1% vs. 77.8%±9.8% (P=0.2998), stage IV/B-AL was 72.7%±13.4% versus 40.0%±21.9% (P=0.0878) between patients treated with R+BFM95 and BFM90, respectively. Among patients whose lactate dehydrogenase (LDH) level were <500 U/L at diagnosis, R+BFM95 protocol reached 100% survival, nevertheless the 5-year EFS of patients in this group was not statistically different from that of patients treated with BFM90 (92.3%±7.4%; P=0.2994). Among patients had LDH≥500 U/L at diagnosis, the 5-year EFS in R+BFM95 group was 77.2%±7.7% (32 patients) and significantly higher than that of BFM90 group (40.0%±15.5%, 10 patients; P=0.0048). We found that rituximab has improved the EFS of childhood B-NHL/B-AL with LDH≥500U/L. Our results require validation from future studies with large cohort.

摘要

在本研究中,我们评估了新诊断为晚期(III期和IV期)成熟B细胞非霍奇金淋巴瘤(B-NHL)或成熟B细胞急性白血病(B-AL)的儿童,他们接受了基于柏林-法兰克福-明斯特(BFM)95方案联合利妥昔单抗(R+BFM95)的治疗。我们的研究招募了46例接受BFM95方案联合利妥昔单抗治疗的患者。有23例患者作为接受BFM90方案治疗的历史对照。与接受BFM90方案治疗的患者相比,R+BFM95治疗的患者5年无事件生存率(EFS)更高(83.7%±5.7%对69.6%±9.6%;P=0.1062)。在我们患者的亚组中,III期患者的5年EFS在R+BFM95组与BFM90组分别为87.3%±6.1%对77.8%±9.8%(P=0.2998),IV期/B-AL患者为72.7%±13.4%对40.0%±21.9%(P=0.0878)。在诊断时乳酸脱氢酶(LDH)水平<500 U/L的患者中,R+BFM95方案的生存率达到100%,不过该组患者的5年EFS与接受BFM90治疗的患者无统计学差异(92.3%±7.4%;P=0.2994)。在诊断时LDH≥500 U/L的患者中,R+BFM95组的5年EFS为77.2%±7.7%(32例患者),显著高于BFM90组(40.0%±15.5%,10例患者;P=0.0048)。我们发现利妥昔单抗提高了LDH≥500U/L的儿童B-NHL/B-AL的EFS。我们的结果需要未来大样本队列研究的验证。

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