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利妥昔单抗联合改良NHL-BFM-90方案治疗儿童及青少年伯基特淋巴瘤的长期临床结局

[Long-term clinical outcome of children and adolescents with Burkitt's lymphoma treated with rituximab combined with modified NHL-BFM-90 regimen].

作者信息

Li Y X, Yin Q S, Ai H, Mi R H, Zhang L N, Li Y F, Wei X D, Song Y P

机构信息

Department of Medicine, the First People's Hospital of Zhengzhou, Zhengzhou 450000.

Department of Hematology, Henan Cancer Hospital, the Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2019 Feb 26;99(8):605-610. doi: 10.3760/cma.j.issn.0376-2491.2019.08.008.

Abstract

To evaluate the efficacy and safety of rituximab combined with the modified NHL-BFM-90 protocol in childhood and adolescence with Burkitts lymphoma (BL). A retrospective analysis of 67 untreated childhood and adolescence patients with BL was made. All patients were treated with the modified NHL-BFM-90 protocol with or without rituximab. The 64 patients (95.52%) achieved complete remission (CR), 3 patients (4.48%) partial remission (PR), and the overall response rate (CR+PR) was 100%. 67 patients were followed up for a median of 44 (3-89) months. The 3 and 5-year overall survival (OS) were 92.54% and 88.98%, respectively. The 3 and 5-year progression-free survival (PFS) were all 90.34%. The 5-year OS were 100%,91.7% and 80.0% in low risk, moderate risk and high risk group, respectively, and the difference was statistically significant (=0.048). Of the 67 patients, 55 patients (82.09%) were treated with rituximab plus chemotherapy. Compared with the 5-year OS and PFS of 74.3% and 78.6% in the chemotherapy group, the 5-year OS and PFS in the rituximab plus chemotherapy group were 95.2% and 95.5%, respectively, and the difference was statistically significant ( value was 0.021, and 0.036, respectively). Major toxicity was myelosuppression and mucositis. No treatment related death was found. Rituximab combined with the modified NHL-BFM-90 protocol was highly effective for children and adolescents with BL, and significantly improved long-term survival.

摘要

评估利妥昔单抗联合改良的NHL-BFM-90方案治疗儿童和青少年伯基特淋巴瘤(BL)的疗效和安全性。对67例未经治疗的儿童和青少年BL患者进行回顾性分析。所有患者均接受改良的NHL-BFM-90方案治疗,部分患者联合使用利妥昔单抗。64例患者(95.52%)达到完全缓解(CR),3例患者(4.48%)部分缓解(PR),总缓解率(CR+PR)为100%。67例患者中位随访44(3-89)个月。3年和5年总生存率(OS)分别为92.54%和88.98%。3年和5年无进展生存率(PFS)均为90.34%。低危、中危和高危组的5年OS分别为100%、91.7%和80.0%,差异有统计学意义(P=0.048)。67例患者中,55例(82.09%)接受利妥昔单抗联合化疗。与化疗组5年OS和PFS分别为74.3%和78.6%相比,利妥昔单抗联合化疗组5年OS和PFS分别为95.2%和95.5%,差异有统计学意义(P值分别为0.021和0.036)。主要毒性为骨髓抑制和黏膜炎。未发现与治疗相关的死亡。利妥昔单抗联合改良的NHL-BFM-90方案对儿童和青少年BL患者疗效显著,显著提高了长期生存率。

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