Suppr超能文献

[改良B-NHL-BFM-90方案治疗儿童及青少年间变性T细胞淋巴瘤的疗效]

[Efficacy of modified B-NHL-BFM-90 protocol on anaplastic T-cell lymphoma in children and adolescents].

作者信息

Sun Xiao-Fei, Zhen Zi-Jun, Xiang Xiao-Juan, Ling Jia-Yu, Peng Rou-Jun, Xia Yi, Zheng Lei, Luo Wen-Biao, Lin Hui, Guan Zhong-Zhen

机构信息

State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, China.

出版信息

Ai Zheng. 2009 May;28(5):506-10.

Abstract

BACKGROUND AND OBJECTIVE

Anaplastic T-cell lymphoma in children and adolescents is an aggressive malignant non-Hodgkin's lymphoma (NHL). The optimal treatment regimen needs to be investigated. This study was to evaluate the efficacy of modified B-NHL-BFM-90 protocol on anaplastic T-cell lymphoma in children and adolescents.

METHODS

From October 2002 to January 2008, 18 untreated anaplastic T-cell lymphoma patients aged less than 16 years were enrolled, and treated with modified B-NHL-BFM-90 protocol including cyclophosphamide, vincristine, ifosfamide, etoposide, adriamycin, HD-methotrexate, vindesine, dexamethasone, cytarabine/HD-cytarabine. Intrathecal injection was given every course.

RESULTS

Of the 18 patients, 15 (83.3%) achieved complete remission (CR), and three (16.7%) achieved partial remission (PR). The patients were followed up for 4-68 months (median, 31 months). The 3-year event-free survival (EFS) rates were (87.4+/-8.4)% for all patients, 100% for stage II patients, and (85.1+/-9.7)% for stage III/IV patients; 100% for low risk group, (88.9+/-10.5)% for moderate risk group, and (80.0+/-17.9)% for high risk group. Most patients suffered from grade 3-4 myelosuppression and recovered after active support care. One patient with stage IV disease received autologous peripheral blood stem cell transplantation (PBSCT) after CR and was still alive. Two patients had tumor relapsed and died at three and five months after off treatment, respectively.

CONCLUSIONS

Modified B-NHL-BFM-90 protocol, with tolerable toxicity, is an effective treatment regimen for anaplastic T-cell lymphoma in children and adolescents. It should be used in experienced cancer centers and hematological units.

摘要

背景与目的

儿童和青少年间变性T细胞淋巴瘤是一种侵袭性恶性非霍奇金淋巴瘤(NHL)。需要研究最佳治疗方案。本研究旨在评估改良的B-NHL-BFM-90方案治疗儿童和青少年间变性T细胞淋巴瘤的疗效。

方法

2002年10月至2008年1月,纳入18例年龄小于16岁的未经治疗的间变性T细胞淋巴瘤患者,采用改良的B-NHL-BFM-90方案进行治疗,该方案包括环磷酰胺、长春新碱、异环磷酰胺、依托泊苷、阿霉素、大剂量甲氨蝶呤、长春地辛、地塞米松、阿糖胞苷/大剂量阿糖胞苷。每疗程均给予鞘内注射。

结果

18例患者中,15例(83.3%)达到完全缓解(CR),3例(16.7%)达到部分缓解(PR)。患者随访4 - 68个月(中位时间31个月)。所有患者的3年无事件生存率(EFS)为(87.4±8.4)%,Ⅱ期患者为100%,Ⅲ/Ⅳ期患者为(85.1±9.7)%;低危组为100%,中危组为(88.9±10.5)%,高危组为(80.0±17.9)%。大多数患者出现3 - 4级骨髓抑制,经积极支持治疗后恢复。1例Ⅳ期患者在CR后接受了自体外周血干细胞移植(PBSCT),目前仍然存活。2例患者分别在停止治疗后3个月和5个月肿瘤复发死亡。

结论

改良的B-NHL-BFM-90方案毒性可耐受,是治疗儿童和青少年间变性T细胞淋巴瘤的有效治疗方案。应在有经验的癌症中心和血液科使用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验