Gaynor J J, Tan C C, Casper E S, Collin C F, Friedrich C, Shiu M, Hajdu S I, Brennan M F
Department of Epidemiology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.
J Clin Oncol. 1992 Aug;10(8):1317-29. doi: 10.1200/JCO.1992.10.8.1317.
The prognostic value of factors used in clinicopathologic staging of localized soft tissue sarcoma (STS) of the extremity were analyzed comprehensively.
Four hundred twenty-three patients with STS that was confined to the extremity were admitted to Memorial Sloan-Kettering Cancer Center from 1968 to 1978. Cox models for the hazards rates of tumor mortality, development of a distant metastasis, strictly local recurrence, and postmetastasis survival were developed. Tests of changes in the prognostic value of the important variables over time were performed, as well as an analysis of the effect of a local recurrence on the hazard rate of distant metastasis.
Three unfavorable characteristics contained independent prognostic value for the rates of distant metastasis and tumor mortality: high grade (P less than .00001), deep location (P less than .0002), and size greater than or equal to 5 cm (P less than .007). Their Cox model coefficients did not differ significantly (P greater than or equal to .65); thus, a staging scheme based on the risk of ever developing a distant metastasis would assign equal prognostic weights to grade, depth, and size. The tumor grade effect during the initial 18 months was much larger in magnitude than those for depth and size, and its effect disappeared beyond that time (P = .0003). Thus, a staging scheme based on the risk of early metastatic spread would assign a distinctly larger prognostic weight to grade and lesser but equal weights to depth and size. There was no local recurrence effect on the rate of distant metastasis in the high-risk group (high grade, deep, and greater than or equal to 5 cm; P = .75), but there was a significant association among the remaining groups combined (P = .0039). The magnitude of this association actually increased according to the number of favorable characteristics presented (P = .0024).
The refinement of clinicopathologic staging may depend on the choice of outcome variable: ultimate prognosis versus early metastatic spread. Additionally, the observed local recurrence effect may be explained by a tendency for some patients to acquire one or more unfavorable risk factors at the time of local recurrence.
全面分析用于肢体局限性软组织肉瘤(STS)临床病理分期的因素的预后价值。
1968年至1978年,423例局限于肢体的STS患者被收入纪念斯隆凯特琳癌症中心。建立了肿瘤死亡率、远处转移发生、严格局部复发以及转移后生存的风险率的Cox模型。对重要变量的预后价值随时间的变化进行了检验,并分析了局部复发对远处转移风险率的影响。
三个不良特征对远处转移率和肿瘤死亡率具有独立的预后价值:高分级(P<0.00001)、深部位置(P<0.0002)以及大小大于或等于5 cm(P<0.007)。它们的Cox模型系数无显著差异(P≥0.65);因此,基于发生远处转移风险的分期方案会给分级、深度和大小赋予相等的预后权重。在最初18个月期间,肿瘤分级的影响程度远大于深度和大小的影响程度,且超过该时间后其影响消失(P = 0.0003)。因此,基于早期转移扩散风险的分期方案会给分级赋予明显更大的预后权重,给深度和大小赋予较小但相等的权重。在高危组(高分级、深部且大于或等于5 cm;P = 0.75)中,局部复发对远处转移率没有影响,但在其余合并组中有显著关联(P = 0.0039)。这种关联的程度实际上根据呈现的有利特征数量而增加(P = 0.0024)。
临床病理分期的细化可能取决于结局变量的选择:最终预后与早期转移扩散。此外,观察到的局部复发影响可能是由于一些患者在局部复发时倾向于获得一个或多个不良风险因素来解释。