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首页> 外文期刊>British Journal of Cancer >High dose cytosine arabinoside in the initial treatment of adults with acute lymphoblastic leukaemia
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High dose cytosine arabinoside in the initial treatment of adults with acute lymphoblastic leukaemia

机译:大剂量胞嘧啶阿拉伯糖苷在成人急性淋巴细胞白血病的初始治疗中

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In a study conducted at St Bartholomew's Hospital between 1972 and 1982, using moderately intensive therapy (OPAL/HEAV'D), a low blast count at presentation (less than 10 x 10(9) 1(-1)) and common ALL (C-ALL) phenotype correlated favourably with duration of remission. Fifty-four patients (age range 15-57, median 32) subsequently received a modification of the previous treatment programme which included high-dose ara-C 2 g m-2 b.d. for 6 days as cycle 3 (OPAL + HD ARA-C). CR was achieved in 36/54 (67%) patients, response correlating favourably with younger age (15-30 years vs 31-57 years, P = 0.02). Three patients died in CR. Overall, there was no difference in survival or remission duration between patients who received high dose ara-C and those in the control group. However, in contrast to the early results, there was a reversal in the relevance of the prognostic factors with a trend in favour of high blast count (greater than 10 x 10(9) 1(-1)) and T-cell phenotype in terms of remission duration. Moreover, comparison of duration of remission for the previously defined prognostic groups according to therapy suggests that the prognosis of patients with 'high risk' disease (T, B, null ALL or high blast count) is improved with more intensive therapy. In contrast, those with 'low risk' disease (C-ALL and low blast count) have a better prognosis with less intensive therapy. These observations confirm those of others and allow for individualization of therapy on the basis of pre-treatment variables.
机译:在1972年至1982年之间于圣巴塞洛缪医院进行的一项研究中,采用中度深层治疗(OPAL / HEAV'D),呈现时的爆炸次数低(少于10 x 10(9)1(-1))和常见ALL( C-ALL)表型与缓解时间有利地相关。 54名患者(年龄范围15-57,中位数32)随后接受了先前治疗方案的修改,其中包括大剂量ara-C 2 g m-2b.d。周期3(OPAL + HD ARA-C)持续6天。在36/54(67%)的患者中获得了CR,其应答与年龄较小(15-30岁对31-57岁,P = 0.02)相关。 3例患者死于CR。总体而言,接受高剂量ara-C的患者与对照组之间的生存或缓解时间无差异。然而,与早期结果相反,预后因素的相关性有所逆转,倾向于高胚盘计数(大于10 x 10(9)1(-1))和T细胞表型。缓解期的条款。此外,根据治疗方案对先前定义的预后组的缓解时间进行比较,结果表明,通过加强治疗可以改善“高风险”疾病(T,B,无效ALL或高母细胞计数)患者的预后。相比之下,那些“低风险”疾病(C-ALL和低胚泡计数)的患者预后较差,但预后较好。这些观察结果证实了其他观点,并允许根据治疗前变量对治疗进行个体化。

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