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首页> 外文期刊>Pediatric blood & cancer >Outcome of childhood acute lymphoblastic leukemia with induction failure treated by the Japan Association of Childhood Leukemia study (JACLS) ALL F-protocol.
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Outcome of childhood acute lymphoblastic leukemia with induction failure treated by the Japan Association of Childhood Leukemia study (JACLS) ALL F-protocol.

机译:由日本儿童白血病协会研究(JACLS)ALL F协议治疗的儿童急性诱导淋巴细胞白血病急性发作的结果。

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BACKGROUND: Children with acute lymphoblastic leukemia (ALL) who fail to achieve complete remission (CR) after induction therapy (induction failure: IF) have a poor prognosis; however, there have been few prospective studies in patients with IF. PATIENTS AND METHODS: Between April 1997 and March 2005, 27 of 1,237 leukemic patients (2.2%) failed to achieve CR after four- or five-drug induction therapy. Twenty-three of these patients entered the F-protocol study, which mainly consisted of acute-myeloid-leukemia-oriented chemotherapy followed by scheduled hematopoietic cell transplantation (HCT). RESULTS: Seventeen (73.9%) of the 23 patients responded to re-induction chemotherapy with CR. Of note, 15 (93.8%) of 16 patients with Philadelphia-chromosome-negative (non-Ph(+)) ALL achieved CR; in contrast, only 2 (28.6%) of 7 Ph(+) patients achieved CR. Fourteen (82.4%) of 17 patients remained in CR (CCR) until their scheduled HCT, 12 of the 14 with CCR underwent HCT as scheduled, and 6 patients remain in first CR after a median of 78 months (range, 49-107 months). The 5-year overall survival (OS) rates of 16 patients with non-Ph(+) and 7 patients with Ph(+) were 43.8 +/- 12.4% and 14.3 +/- 13.2%, respectively (P = 0.012). The 5-year OS rate of the 17 patients who obtained CR by re-induction therapy and the 6 who did not were 47.1 +/- 12.1% and 0%, respectively (P < 0.001). CONCLUSION: Acute-myeloid-leukemia-oriented chemotherapy followed by scheduled HCT is a promising treatment strategy for non-Ph(+) ALL patients with IF.
机译:背景:急性淋巴细胞白血病(ALL)的儿童在诱导治疗(诱导失败:IF)后未能达到完全缓解(CR)的预后较差;但是,对IF患者的前瞻性研究很少。患者与方法:1997年4月至2005年3月,在4或5种药物诱导治疗后的1,237例白血病患者中,有27例(2.2%)未能达到CR。这些患者中有23名进入了F方案研究,该研究主要包括针对急性髓细胞白血病的化学疗法,然后进行预定的造血细胞移植(HCT)。结果:23例患者中有17例(73.9%)对CR的再诱导化疗有反应。值得注意的是,费城染色体阴性(非Ph(+))的16例患者中有15例(93.8%)均达到了CR;相反,在7名Ph(+)患者中,只有2(28.6%)名获得了CR。在计划的HCT之前,有17名患者中的14名(82.4%)处于CR(CCR)状态,在计划的HCT中有14名患者中的12名按计划进行了HCT,中位时间为78个月(49-107个月)后,有6名患者仍在首次CR中)。 16名非Ph(+)患者和7名Ph(+)患者的5年总生存率(OS)分别为43.8 +/- 12.4%和14.3 +/- 13.2%(P = 0.012)。通过再诱导治疗获得CR的17例患者和未获得CR的6例中5年OS发生率分别为47.1 +/- 12.1%和0%(P <0.001)。结论:急性髓细胞白血病定向化疗后计划行HCT是非Ph(+)ALL IF患者的有前途的治疗策略。

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