Lacombe F, Arnoulet C, Maynadié M, Lippert E, Luquet I, Pigneux A, Vey N, Casasnovas O, Witz F, Béné M C
Hematology Laboratory, CHU Bordeaux, Hôpital Haut Levêque, Pessac, France.
Leukemia. 2009 Feb;23(2):350-7. doi: 10.1038/leu.2008.296. Epub 2008 Nov 6.
An early appreciation of treatment efficacy could be very useful in acute myeloblastic leukemia (AML), and a prognostic value has been suggested for the morphological assessment of decrease in blasts during induction therapy. More sensitive, multiparametric flow cytometry (FCM) can detect far lower blast counts, allowing for a precise and reliable calculation of blast cell decrease rate (BDR). Such a multiparametric FCM four-colours/single-tube protocol, combining CD11b, CD45-ECD and CD16-PC5, was applied to peripheral blood samples from 130 AML patients, collected daily during induction chemotherapy. Normalized blast cell percentages were used to calculate the relevant decrease slopes. Slope thresholds (<-25, -25 to -15 and >-15), or the time required to reach 90% depletion of the peripheral blast load (<5, 5 or >5 days), was strongly associated with the achievement of complete remission (P<0.0001). Log-rank test and Cox model showed that they also carried high statistical significance (P<0.0001) for disease-free survival. The prognostic value of cytogenetic features, confirmed in this series, was refined by BDR, which allowed to discriminate between good- and poor-risk patients among those with intermediate or normal karyotypes. This simple FCM protocol allows for an accurate prognostic sequential approach adapted to the determination of decrease in peripheral blast cells during induction chemotherapy.
早期评估治疗效果对急性髓细胞白血病(AML)可能非常有用,并且有人提出诱导治疗期间原始细胞减少的形态学评估具有预后价值。更灵敏的多参数流式细胞术(FCM)能够检测到低得多的原始细胞计数,从而可以精确可靠地计算原始细胞减少率(BDR)。这种结合了CD11b、CD45-ECD和CD16-PC5的多参数FCM四色/单管方案应用于130例AML患者诱导化疗期间每日采集的外周血样本。使用标准化的原始细胞百分比来计算相关的减少斜率。斜率阈值(<-25、-25至-15和>-15),或达到外周原始细胞负荷减少90%(<5、5或>5天)所需的时间,与完全缓解的实现密切相关(P<0.0001)。对数秩检验和Cox模型表明,它们对无病生存也具有高度统计学意义(P<0.0001)。本系列中证实的细胞遗传学特征的预后价值通过BDR得到了完善,BDR能够区分核型为中等或正常的患者中的低危和高危患者。这种简单的FCM方案允许采用一种准确的预后序贯方法,以适应诱导化疗期间外周原始细胞减少的测定。