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鞘内化疗的早期强化治疗几乎可消除急性淋巴细胞白血病患儿的中枢神经系统复发。

Early intensification of intrathecal chemotherapy virtually eliminates central nervous system relapse in children with acute lymphoblastic leukemia.

作者信息

Pui C H, Mahmoud H H, Rivera G K, Hancock M L, Sandlund J T, Behm F G, Head D R, Relling M V, Ribeiro R C, Rubnitz J E, Kun L E, Evans W E

机构信息

Department of Hematology-Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105-0318, USA.

出版信息

Blood. 1998 Jul 15;92(2):411-5.

PMID:9657739
Abstract

Central nervous system (CNS) relapse has been an obstacle to uniformly successful treatment of childhood acute lymphoblastic leukemia (ALL) for many years. We therefore intensified intrathecal chemotherapy (simultaneously administered methotrexate, hydrocortisone, and cytarabine) for 165 consecutive children with newly diagnosed ALL enrolled in Total Therapy Study XIIIA from December 1991 to August 1994. The 64 patients (39%) who had 1 or more blast cells in cytocentrifuged preparations of cerebrospinal fluid at diagnosis, with or without associated higher-risk features, received additional doses of intrathecal chemotherapy during remission induction and the first year of continuation treatment. Patients with higher-risk leukemia, regardless of cerebrospinal fluid findings, also received additional doses of intrathecal chemotherapy during the first year of continuation treatment. Cranial irradiation was reserved for patients with higher-risk leukemia (22% of the total). The 5-year cumulative risk of an isolated CNS relapse among all 165 patients was 1.2% (95% confidence interval, 0% to 2.9%), whereas that of any CNS relapse was 3.2% (0. 4% to 6.0%). The probability of surviving for 5 years without an adverse event of any type was 80.2% +/- 9.2% (SE). Our results suggest that early intensification of intrathecal chemotherapy will reduce the risk of CNS relapse to a very low level in children with ALL, securing a higher event-free survival rate overall.

摘要

多年来,中枢神经系统(CNS)复发一直是儿童急性淋巴细胞白血病(ALL)全面成功治疗的障碍。因此,我们对1991年12月至1994年8月参加总治疗研究XIIIA的165例新诊断的ALL患儿强化了鞘内化疗(同时给予甲氨蝶呤、氢化可的松和阿糖胞苷)。64例(39%)在诊断时脑脊液细胞离心涂片中有1个或更多原始细胞的患者,无论有无相关高危特征,在缓解诱导期和继续治疗的第一年接受了额外剂量的鞘内化疗。高危白血病患者,无论脑脊液检查结果如何,在继续治疗的第一年也接受了额外剂量的鞘内化疗。颅脑照射仅用于高危白血病患者(占总数的22%)。165例患者中孤立性CNS复发的5年累积风险为1.2%(95%置信区间,0%至2.9%),而任何CNS复发的风险为3.2%(0.4%至6.0%)。5年无任何不良事件存活的概率为80.2%±9.2%(SE)。我们的结果表明,早期强化鞘内化疗将使ALL患儿CNS复发风险降至极低水平,总体上确保更高的无事件生存率。

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