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Prognostic Implication of the Absolute Lymphocyte to Absolute Monocyte Count Ratio in Patients With Classical Hodgkin Lymphoma Treated With Doxorubicin Bleomycin Vinblastine and Dacarbazine or Equivalent Regimens

机译:阿霉素博来霉素长春碱和达卡巴嗪或同等疗法治疗经典霍奇金淋巴瘤患者绝对淋巴细胞与绝对单核细胞计数比的预后意义

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摘要

Low absolute lymphocyte count (ALC) to absolute monocyte count (AMC) ratio (ALC/AMC) is an independent prognostic factor in Hodgkin lymphoma (HL), but different cutoffs (1.1, 1.5, and 2.9) have been applied. We aimed to validate the prognostic significance of ALC/AMC in 537 homogenously treated (doxorubicin, bleomycin, vinblastine, and dacarbazine or equivalents ± radiotherapy) classical HL patients at various cutoffs. The median ALC/AMC was 2.24 (0.44–20.50). The median AMC was 0.653 × 109/L (0.050–2.070). Lower ALC/AMC was associated with established markers of adverse prognosis. In total, 477 (89%), 418 (78%), and 189 (35%) patients had an ALC/AMC ratio of ≥1.1, ≥1.5, and ≥2.9; respectively; 20% had monocytosis (≥0.9 × 109/L). Ten-year time to progression (TTP) was 77% versus 55% for patients with ALC/AMC ≥1.1 and <1.1 (p = .0002), 76% versus 68% for ALC/AMC ≥1.5 and <1.5 (p = .049), 77% versus 73% for ALC/AMC ≥2.9 and <2.9 (p = .35), and 79% versus 70% for ALC/AMC ≥2.24 and <2.24 (p = .08), respectively. In stages ΙΑ/ΙΙΑ and in patients ≥60 years old, ALC/AMC had no significant effect on TTP. In advanced stages, ALC/AMC was significant only at the cutoff of 1.1 (10-year TTP 67% vs. 48%; p = .016). In younger, advanced-stage patients, the differences were more pronounced. In multivariate analysis of TTP, ALC/AMC < 1.1 (p = .007) and stage IV (p < .001) were independent prognostic factors; ALC/AMC was independent of International Prognostic Score in another model. ALC/AMC was more predictive of overall survival than TTP. At the cutoff of 1.1, ALC/AMC had independent prognostic value in multivariate analysis. However, the prognostically inferior group comprised only 11% of patients. Further research is needed prior to the widespread use of this promising marker.
机译:低的绝对淋巴细胞计数(ALC)与绝对单核细胞计数(AMC)之比(ALC / AMC)是霍奇金淋巴瘤(HL)的独立预后因素,但已应用了不同的临界值(1.1、1.5和2.9)。我们旨在验证ALC / AMC在537例不同水平的均一治疗(阿霉素,博来霉素,长春碱和达卡巴嗪或等效±放射治疗)的经典HL患者中的预后意义。 ALC / AMC中位数为2.24(0.44-20.50)。中值AMC为0.653×10 9 / L(0.050–2.070)。较低的ALC / AMC与不良预后的确定指标相关。总共有477(89%),418(78%)和189(35%)患者的ALC / AMC比值≥1.1,≥1.5和≥2.9;分别; 20%有单核细胞增多症(≥0.9×10 9 / L)。十年进展时间(TTP)为77%,而ALC / AMC≥1.1和<1.1的患者为55%(p = .0002),ALC / AMC≥1.5和<1.5的患者为76%对68%(p = ALC / AMC≥2.9和<2.9(<= 0.35)分别为77%和73%(p = .35),而ALC / AMC≥2.24和<2.24(p = .08)分别为79%和70%。在IIIA / IIIA期和≥60岁的患者中,ALC / AMC对TTP没有显着影响。在晚期阶段,ALC / AMC仅在临界值1.1时才有意义(10年期TTP为67%对48%; p = .016)。在较年轻的晚期患者中,差异更为明显。在TTP的多变量分析中,ALC / AMC <1.1(p = .007)和IV期(p <.001)是独立的预后因素。在另一个模型中,ALC / AMC独立于国际预后评分。 ALC / AMC比TTP更能预测整体存活率。截止到1.1,ALC / AMC在多变量分析中具有独立的预后价值。但是,预后较差的组仅占11%的患者。在广泛使用这种有前途的标记之前,需要进一步的研究。

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