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Relevance of clinical trials in acute myeloid leukaemia.

机译:急性髓细胞性白血病临床试验的相关性。

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Patients with newly diagnosed acute myeloid leukaemia (AML) are increasingly being enrolled in clinical trials sponsored by pharmaceutical companies or the National Cancer Institute. These trials routinely exclude patients who are less likely to respond (LLTR), e.g. those with Zubrod performance status >2 and levels of bilirubin or creatinine >/=2.0 mg/dL. Here we examine rates of enrollment of LLTR patients in clinical trials over the past 16 years. Overall, 2323 adults with newly diagnosed AML (excluding acute promyelocytic leukaemia) were registered on clinical trials from 1991 to 2006. LLTR patients constituted a significantly smaller proportion of the patients enrolled from 1999 to 2006 than from 1991 to 1998 (p < 0.0001, considering all patients and patients 60 years or older). While 54% of patients considered 'more likely to respond' (MLTR) (i.e. those with performance status <3, bilirubin <2.0 mg/dL and creatinine <2.0 mg/dL) were enrolled in these studies from 1999 to 2006, only 36% of LLTR patients were enrolled during this period (p < 0.0001). Our results suggest that newer clinical trials may be less applicable to LLTR patients than previous trials. There is a need for clinical trials specific to the LLTR population, the group most in need of novel therapies. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:新诊断为急性髓细胞性白血病(AML)的患者越来越多地参加由制药公司或美国国家癌症研究所赞助的临床试验。这些试验通常排除了不太可能发生反应(LLTR)的患者,例如Zubrod表现状态> 2且胆红素或肌酐水平> / = 2.0 mg / dL的患者。在这里,我们检查了过去16年中临床试验中LLTR患者的入选率。总体而言,从1991年至2006年,在临床试验中登记了2323名新近诊断为AML(不包括急性早幼粒细胞白血病)的成年人。从1999年至2006年,LLTR患者所占的比例明显低于1991年至1998年(p <0.0001,考虑到所有患者以及60岁以上的患者)。虽然从1999年到2006年,有54%的患者被认为“更有可能做出反应”(MLTR)(即,表现状态<3,胆红素<2.0 mg / dL和肌酐<2.0 mg / dL),但只有36%在此期间入组LLTR患者的百分比(p <0.0001)。我们的结果表明,较之以前的试验,较新的临床试验可能不适用于LLTR患者。需要针对LLTR人群(最需要新疗法的人群)进行特定的临床试验。版权所有(c)2008 John Wiley&Sons,Ltd.

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