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改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析

OBJECTIVE: To analyze the therapeutic effect of a modified LMB89 Group C regimen in the treatment of pediatric high-risk Burkitt lymphoma. METHODS: The clinical data of 172 children with newly diagnosed high-risk Burkitt lymphoma from January 2007 to April 2017 were retrospectively analyzed. All the...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342876/
https://www.ncbi.nlm.nih.gov/pubmed/31495128
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.08.002
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description OBJECTIVE: To analyze the therapeutic effect of a modified LMB89 Group C regimen in the treatment of pediatric high-risk Burkitt lymphoma. METHODS: The clinical data of 172 children with newly diagnosed high-risk Burkitt lymphoma from January 2007 to April 2017 were retrospectively analyzed. All the cases were treated with the modified LMB89 Group C regimen. RESULTS: The median age of the patients was 6 (1–14) years. The sex ratio was 5.1∶1, 144 boys (83.7%) and 28 girls (16.3%). According to St. Jude staging classification, 2 patients (1.2%) were in stage Ⅱ, 54 (31.4%) in stage Ⅲ and 116 (67.4%) in stage Ⅳ. Of them, 46 patients (26.7%) had mature B cell acute lymphoblastic leukemia (B-ALL), and 52 patients had central nervous system (CNS) involvement. According to risk group, the patients can be divided into group C1 (CNS1, without testicles/ovaries involvement, n=65), group C2 (CNS2, testicles/ovaries involvement, n=55) and group C3 (CNS3, n=52). A total of 145 patients received rituximab combined with chemotherapy during the treatment, 10 patients suffered from progressive disease and died, and 5 patients relapsed. Treatment-related mortality was 2.9%. With a median follow-up of 36.0 (0.5–119.0) months, 3-year overall survival (OS) rate was (88.9±2.4) % and event free survival (EFS) rate was (87.9±2.6) % for all patients. 3-year EFS rates were (96.9±2.1) %, (90.9±3.9) % and (73.4±6.5) % for Group C1, C2 and C3 respectively, and that of Group C3 was significantly lower than that of Group C1 (χ(2)=12.939, P=0.001) and Group C2 (χ(2)=6.302, P=0.036). The 3-year EFS rates were (79.3±6.8) % and (44.4±16.6) % for patients in group C3 treated with chemotherapy combined with rituximab and chemotherapy alone (χ(2)=5.972, P=0.015). Multivariable Cox regression analysis showed that Stage Ⅳ (including B-ALL), residual diseases in mid-term evaluation were independent unfavorable prognostic factors[HR=4.241 (95%CI 1.163–27.332), P=0.026; HR=32.184 (95%CI 11.441–99.996), P<0.001]. CONCLUSION: The modified LMB89 Group C regimen has ideal effect for the children with high-risk Burkitt lymphoma.
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spelling pubmed-73428762020-07-16 改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To analyze the therapeutic effect of a modified LMB89 Group C regimen in the treatment of pediatric high-risk Burkitt lymphoma. METHODS: The clinical data of 172 children with newly diagnosed high-risk Burkitt lymphoma from January 2007 to April 2017 were retrospectively analyzed. All the cases were treated with the modified LMB89 Group C regimen. RESULTS: The median age of the patients was 6 (1–14) years. The sex ratio was 5.1∶1, 144 boys (83.7%) and 28 girls (16.3%). According to St. Jude staging classification, 2 patients (1.2%) were in stage Ⅱ, 54 (31.4%) in stage Ⅲ and 116 (67.4%) in stage Ⅳ. Of them, 46 patients (26.7%) had mature B cell acute lymphoblastic leukemia (B-ALL), and 52 patients had central nervous system (CNS) involvement. According to risk group, the patients can be divided into group C1 (CNS1, without testicles/ovaries involvement, n=65), group C2 (CNS2, testicles/ovaries involvement, n=55) and group C3 (CNS3, n=52). A total of 145 patients received rituximab combined with chemotherapy during the treatment, 10 patients suffered from progressive disease and died, and 5 patients relapsed. Treatment-related mortality was 2.9%. With a median follow-up of 36.0 (0.5–119.0) months, 3-year overall survival (OS) rate was (88.9±2.4) % and event free survival (EFS) rate was (87.9±2.6) % for all patients. 3-year EFS rates were (96.9±2.1) %, (90.9±3.9) % and (73.4±6.5) % for Group C1, C2 and C3 respectively, and that of Group C3 was significantly lower than that of Group C1 (χ(2)=12.939, P=0.001) and Group C2 (χ(2)=6.302, P=0.036). The 3-year EFS rates were (79.3±6.8) % and (44.4±16.6) % for patients in group C3 treated with chemotherapy combined with rituximab and chemotherapy alone (χ(2)=5.972, P=0.015). Multivariable Cox regression analysis showed that Stage Ⅳ (including B-ALL), residual diseases in mid-term evaluation were independent unfavorable prognostic factors[HR=4.241 (95%CI 1.163–27.332), P=0.026; HR=32.184 (95%CI 11.441–99.996), P<0.001]. CONCLUSION: The modified LMB89 Group C regimen has ideal effect for the children with high-risk Burkitt lymphoma. Editorial office of Chinese Journal of Hematology 2019-08 /pmc/articles/PMC7342876/ /pubmed/31495128 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.08.002 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析
title 改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析
title_full 改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析
title_fullStr 改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析
title_full_unstemmed 改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析
title_short 改良LMB 89 C组方案治疗儿童高危伯基特淋巴瘤172例临床分析
title_sort 改良lmb 89 c组方案治疗儿童高危伯基特淋巴瘤172例临床分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342876/
https://www.ncbi.nlm.nih.gov/pubmed/31495128
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.08.002
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