Department I of Internal Medicine, German Hodgkin Study Group (GHSG), University Hospital Cologne.
Ann Oncol. 2013 Dec;24(12):3070-6. doi: 10.1093/annonc/mdt413. Epub 2013 Oct 22.
In early-stage Hodgkin's lymphoma (HL), treatment according to the early favorable or unfavorable subgroup is guided by staging definitions, which differ between various study groups worldwide. We analyzed risk factors used in different international staging systems and their impact on the outcome of early-stage HL patients.
In 1173 early-stage HL patients treated homogenously within the German Hodgkin Study Group (GHSG) trials HD10 and HD11, the impact of three staging systems developed and used by the GHSG, the European Organization for Research and Treatment of Cancer (EORTC), and the National Comprehensive Cancer Network (NCCN) in discriminating risk groups for progression-free survival (PFS) and overall survival (OS) was assessed and the relevance of their single risk factors was investigated.
All the three staging systems defined an unfavorable risk group out of early-stage patients of comparable size (56%, 55%, and 57%), having a significantly poorer PFS and OS as compared with the corresponding favorable group; 5-year differences between early favorable and early unfavorable in terms of PFS were 9.4% (HR 2.61, 95% CI 1.74-3.91), 6.7% (HR 2.10, 95% CI 1.41-3.13), and 8.6% (HR 2.14, 95% CI 1.45-3.16) with the GHSG, EORTC, and NCCN definition, respectively. Sensitivity was high for all systems (84%, 79%, and 83%); however, there was a low specificity with high rates of false-positive results (1-specificity 54%, 53%, and 55%, respectively). Models of high sensitivity included risk factors associated with large tumor burden and high tumor activity. Most risk factors for tumor-specific end points were also predictive of OS.
Differentiating between a favorable and an unfavorable risk group has significant impact on PFS and OS in early-stage HL patients in the modern treatment era. Risk-adapted treatment strategies using new risk factors with higher specificity are needed.
在早期霍奇金淋巴瘤(HL)中,根据早期预后良好或不良亚组进行治疗,其依据是分期定义,而这些定义在全球各个研究组之间有所不同。我们分析了不同国际分期系统中使用的风险因素及其对早期 HL 患者结局的影响。
在德国霍奇金研究组(GHSG)的 HD10 和 HD11 两项试验中,对 1173 例早期 HL 患者进行了均匀治疗,评估了 GHSG、欧洲癌症研究与治疗组织(EORTC)和美国国家综合癌症网络(NCCN)制定和使用的三种分期系统区分无进展生存(PFS)和总生存(OS)风险组的能力,并研究了其单个风险因素的相关性。
所有三种分期系统均从早期患者中定义了一个不良风险组(大小相当,分别为 56%、55%和 57%),与相应的有利组相比,PFS 和 OS 明显较差;在 PFS 方面,5 年早期有利与早期不利的差异分别为 9.4%(HR 2.61,95%CI 1.74-3.91)、6.7%(HR 2.10,95%CI 1.41-3.13)和 8.6%(HR 2.14,95%CI 1.45-3.16),分别与 GHSG、EORTC 和 NCCN 定义相关。所有系统的敏感性均较高(84%、79%和 83%);然而,特异性较低,假阳性率较高(1 特异性分别为 54%、53%和 55%)。高敏感性模型包括与大肿瘤负荷和高肿瘤活性相关的风险因素。大多数肿瘤特异性终点的风险因素也可预测 OS。
在现代治疗时代,早期 HL 患者中,区分预后良好和不良风险组对 PFS 和 OS 有显著影响。需要使用特异性更高的新风险因素制定风险适应治疗策略。