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伴有 dic(9;20)(p11;q13) 的儿童 B 细胞前体急性淋巴细胞白血病经柏林-法兰克福-慕尼黑(BFM)方案治疗,其中包含强化诱导和诱导后巩固治疗的预后相关性。

Prognostic relevance of dic(9;20)(p11;q13) in childhood B-cell precursor acute lymphoblastic leukaemia treated with Berlin-Frankfurt-Münster (BFM) protocols containing an intensive induction and post-induction consolidation therapy.

机构信息

Department of Paediatric Haematology and Oncology, St Anna Children's Hospital, Vienna, Austria.

出版信息

Br J Haematol. 2010 Apr;149(1):93-100. doi: 10.1111/j.1365-2141.2009.08059.x. Epub 2010 Jan 13.

Abstract

The presence of a dicentric chromosome dic(9;20) has been reported to have an unfavourable prognosis in children with B-cell precursor acute lymphoblastic leukaemia (BCP-ALL). As outcome may be influenced by type and composition of treatment, we analyzed 19 BCP-ALL patients with dic(9;20) who have been treated with ALL-BFM (Berlin-Frankfurt-Münster) protocols that included a 4-drug induction and subsequent consolidation therapy. All patients were good responders to prednisone and in complete remission after induction therapy. Eight patients had no molecular disease after induction and another eight patients had levels < or =10(-4) after consolidation therapy. After a median follow-up of 3.4 years, probabilities of 5-year event-free and overall survival were 75 +/- 11% and 94 +/- 6%, respectively. Of note, there was a tendency for extramedullary disease in case of relapse (two of three relapses with central nervous system involvement). In conclusion, in the context of ALL-BFM protocols dic(9;20)-positivity appeared to have a favourable prognosis, which could be due to a dose- and time-intensified induction and induction consolidation therapy. Given that in vitro studies have shown high cellular sensitivity of dic(9;20)-positive leukemic blasts to l-asparaginase and cytarabine, it is reasonable to speculate that both drugs, as given early during BFM-like induction and consolidation therapy, may have contributed to this good outcome.

摘要

存在双着丝粒染色体 dic(9;20) 已被报道与儿童 B 细胞前体急性淋巴细胞白血病 (BCP-ALL) 的不良预后有关。由于治疗的类型和组成可能会影响结果,我们分析了 19 例接受 ALL-BFM(柏林-法兰克福-明斯特)方案治疗的 BCP-ALL 患者,该方案包括 4 种药物诱导和随后的巩固治疗。所有患者对泼尼松均有良好反应,诱导治疗后完全缓解。8 例患者诱导后无分子疾病,另 8 例患者巩固治疗后水平 < 或 =10(-4)。中位随访 3.4 年后,5 年无事件生存率和总生存率分别为 75 +/- 11%和 94 +/- 6%。值得注意的是,在复发时存在骨髓外疾病的趋势(3 例复发中有 2 例伴有中枢神经系统受累)。总之,在 ALL-BFM 方案中,dic(9;20)-阳性似乎具有良好的预后,这可能是由于诱导和诱导巩固治疗的剂量和时间强化。鉴于体外研究表明 dic(9;20)-阳性白血病细胞对 L-天冬酰胺酶和阿糖胞苷具有高细胞敏感性,因此可以合理地推测,这两种药物在 BFM 样诱导和巩固治疗早期使用,可能对这种良好的结果有贡献。

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