Suppr超能文献

日本儿童白血病研究协会(JACLS) NHL-98 方案治疗儿童 B 细胞非霍奇金淋巴瘤和成熟 B 细胞急性淋巴细胞白血病的结果。

Results of the Japan Association of Childhood Leukemia Study (JACLS) NHL-98 protocol for the treatment of B-cell non-Hodgkin lymphoma and mature B-cell acute lymphoblastic leukemia in childhood.

机构信息

Hiroshima Red Cross Hospital & Atomic-Bomb Survivors Hospital, Naka-ku, Hiroshima, Japan.

出版信息

Leuk Lymphoma. 2011 Feb;52(2):223-9. doi: 10.3109/10428194.2010.537794. Epub 2011 Jan 24.

Abstract

The Japan Association of Childhood Leukemia Study (JACLS) NHL-98 is a multicenter study designed to evaluate treatment outcomes in Japanese children with B-cell non-Hodgkin lymphoma (B-NHL) and mature B-cell acute lymphoblastic leukemia (B-ALL). The study was supported by a central pathology review system and used a new, standardized protocol with short, intensive treatment regimens. From April 1998 to May 2002, 69 patients with B-NHL and B-ALL up to 16 years of age were enrolled in the NHL-98 study. Treatment was stratified by risk group; patients with limited disease were in groups A and B, and those with extensive disease were in groups C and D. Patients in groups B, C, and D received consolidation phases with high-dose methotrexate (HDMTX) followed by other multi-agent chemotherapy. Patients in group A did not receive either MTX or etoposide. Only patients in group D received etoposide. The event-free survival rates were 100% in groups A and B, 75.1% in group C, and 66.2% in group D. Overall, patients with limited disease had favorable results. For patients with extensive disease, additional treatment options such as increased doses of anticancer drugs warrant further investigation.

摘要

日本儿童白血病研究协会(JACLS) NHL-98 是一项多中心研究,旨在评估日本儿童 B 细胞非霍奇金淋巴瘤(B-NHL)和成熟 B 细胞急性淋巴细胞白血病(B-ALL)的治疗结果。该研究得到了中央病理审查系统的支持,并使用了一种新的标准化方案,包括短而密集的治疗方案。1998 年 4 月至 2002 年 5 月,69 名年龄在 16 岁以下的 B-NHL 和 B-ALL 患者参加了 NHL-98 研究。治疗根据风险组分层;局限性疾病患者分为 A 组和 B 组,广泛性疾病患者分为 C 组和 D 组。B、C 和 D 组的患者接受高强度甲氨蝶呤(HDMTX)巩固阶段治疗,随后进行其他多药物化疗。A 组的患者未接受 MTX 或依托泊苷治疗。只有 D 组的患者接受依托泊苷治疗。A 组和 B 组的无事件生存率为 100%,C 组为 75.1%,D 组为 66.2%。总体而言,局限性疾病患者的结果良好。对于广泛性疾病患者,需要进一步研究增加抗癌药物剂量等额外治疗选择。

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