Mount Vernon Center for Cancer Treatment, Northwood, United Kingdom.
Cancer. 2013 Feb 15;119(4):748-55. doi: 10.1002/cncr.27825. Epub 2012 Sep 25.
Only 2 prospective studies have previously reported prognostic factors for anal cancer, European Organization for Research and Treatment of Cancer trial 22861 (EORTC 22861) and Radiation Therapy Oncology Group trial 98-11 (RTOG 98-11). Both of those trials reported that clinically positive lymph nodes and male sex predicted poorer overall survival (OS). The EORTC 22861 trial indicated that the same factors were prognostic for locoregional control. In the current report, the authors investigated potential prognostic factors from the first United Kingdom Coordinating Committee on Cancer Research Anal Cancer Trial (ACT I), in which patients were randomized to receive either radiotherapy alone or chemoradiation (CRT) with concurrent 5-fluorouracil/mitomycin C.
In the ACT I trial, associations between several baseline characteristics and 3 endpoints were investigated: locoregional failure (LRF), anal cancer death (ACD), and OS. The analyses were restricted to 292 patients who received CRT, which subsequently became standard treatment. A score was derived using multivariable Cox regression to identify the set of factors that, together, had the best prognostic performance. This score was then validated with a large, independent prospective trial (the ACT II trial).
Palpable, clinically positive lymph nodes were associated with LRF (P = .012), a greater risk of ACD (P = .031), and decreased OS (P = .006) in multivariable analyses. Men had worse outcomes than women for LRF (P = .036), ACD (P = .039), and OS (P = .008). On average, a lower hemoglobin level had an adverse effect on ACD (P = .008), and a higher white blood cell count had an adverse effect on OS (P = .001). However, external validation of the score was poor for LRF (area under the curve [AUC] = 54%) but was better for ACD (AUC = 67%) and OS (AUC = 63%).
The results from this analysis of the ACT I trial supported evidence for palpable lymph nodes and male sex as prognostic factors for LRF and OS, and lower hemoglobin levels and a higher white blood cell count were identified as prognostic factors for ACD and OS, respectively.
仅有两项前瞻性研究曾报道过肛门癌的预后因素,分别为欧洲癌症研究与治疗组织试验 22861(EORTC 22861)和放射治疗肿瘤学组试验 98-11(RTOG 98-11)。这两项试验均报告称,临床阳性淋巴结和男性性别预示着总体生存率(OS)更差。EORTC 22861 试验表明,同样的因素对局部区域控制具有预后意义。在当前的报告中,作者研究了英国癌症研究协调委员会肛门癌试验(ACT I)中的潜在预后因素,其中患者被随机分配接受单独放疗或放化疗(CRT)联合氟尿嘧啶/丝裂霉素 C。
在 ACT I 试验中,作者研究了几个基线特征与 3 个终点之间的关联:局部区域失败(LRF)、肛门癌死亡(ACD)和 OS。分析仅限于接受 CRT 的 292 名患者,该疗法随后成为标准治疗。使用多变量 Cox 回归得出一个评分,以确定一组具有最佳预后性能的因素。该评分随后在一项大型独立前瞻性试验(ACT II 试验)中得到验证。
触诊阳性的临床淋巴结与 LRF(P=.012)、更大的 ACD 风险(P=.031)和 OS 降低(P=.006)相关,这在多变量分析中得到了证实。男性在 LRF(P=.036)、ACD(P=.039)和 OS(P=.008)方面的预后比女性更差。平均而言,较低的血红蛋白水平对 ACD 有不利影响(P=.008),较高的白细胞计数对 OS 有不利影响(P=.001)。然而,评分的外部验证对于 LRF 较差(曲线下面积[AUC]为 54%),但对于 ACD(AUC=67%)和 OS(AUC=63%)更好。
对 ACT I 试验的分析结果支持了触诊淋巴结和男性性别作为 LRF 和 OS 的预后因素的证据,并且较低的血红蛋白水平和较高的白细胞计数分别被确定为 ACD 和 OS 的预后因素。