Bamias Aristotle, Basdanis George, Xanthakis Ioannis, Pavlidis Nicholas, Fountzilas George
Dept of Clinical Therapeutics, Medical School, University of Athens, Greece.
Int J Gastrointest Cancer. 2005;36(1):29-38. doi: 10.1385/IJGC:36:1:029.
Although the TNM system is useful in predicting survival in resected colorectal cancer, heterogeneity within the same stages regarding prognosis exists. We are presenting a pooled analysis of prognostic factors from two randomized studies of adjuvant treatment conducted by the Hellenic Cooperative Oncology Group.
Patients with stage II or III colon (n = 279) or rectal (n = 220) cancer were included in this analysis. Following surgery, patients received: 5-fluorouracil/leucovorin (5-FU/LV) (n = 135), 5-FU/LV and interferon Alfa-2a (IFNA-2a) (n = 138), 5-FU/LV and pelvic chemoradiotherapy (n = 106), and pelvic chemoradiotherapy alone (n = 108).
Median follow up was 92 mo. The number of involved lymph nodes (LNs), tumor differentiation, and the presence of regional implants were independent prognostic factors for both OS and TTP, while nerve invasion was only significant for TTP. Patients were stratified into three prognostic groups (low-risk: no LNs and grade 1/2; high-risk: > 3 LNs and grade 3/4; intermediate-risk: remaining patients) with distinct differences in 5-yr survival (84.7% vs 57.6% vs 32.4%) and 5-yr TTP (81.2% vs 54.5% vs 28.6%).
The combination of clinicopathological prognostic factors can be more informative than the traditional TNM staging system. Such stratification may be necessary in randomized trials and could be useful in deciding the most appropriate adjuvant treatment strategies.
尽管TNM系统有助于预测接受手术切除的结直肠癌患者的生存率,但相同分期患者的预后存在异质性。我们对希腊合作肿瘤学组进行的两项辅助治疗随机研究中的预后因素进行了汇总分析。
本分析纳入了II期或III期结肠癌(n = 279)或直肠癌(n = 220)患者。术后,患者接受以下治疗:5-氟尿嘧啶/亚叶酸(5-FU/LV)(n = 135)、5-FU/LV联合干扰素α-2a(IFNA-2a)(n = 138)、5-FU/LV联合盆腔放化疗(n = 106)以及单纯盆腔放化疗(n = 108)。
中位随访时间为92个月。受累淋巴结数量、肿瘤分化程度以及区域种植转移的存在是总生存期(OS)和无进展生存期(TTP)的独立预后因素,而神经侵犯仅对TTP有显著影响。患者被分为三个预后组(低风险:无淋巴结转移且1/2级;高风险:> 3个淋巴结转移且3/4级;中风险:其余患者),5年生存率(84.7%对57.6%对32.4%)和5年TTP(81.2%对54.5%对28.6%)存在明显差异。
临床病理预后因素的组合可能比传统的TNM分期系统提供更多信息。这种分层在随机试验中可能是必要的,并且有助于确定最合适的辅助治疗策略。