Aschele Carlo, Debernardis Domizia, Lonardi Sara, Bandelloni Roberto, Casazza Stefania, Monfardini Silvio, Gallo Luigi
Department of Medical Oncology, E.O. Ospedali Galliera, Genova, Italy.
J Clin Oncol. 2004 Sep 15;22(18):3758-65. doi: 10.1200/JCO.2004.08.066.
To determine whether deleted in colon cancer (DCC) protein expression in colorectal cancer (CRC) metastases could predict outcome to palliative fluorouracil (FU)-based chemotherapy and to assess whether it is similar to that observed in the corresponding primary tumors.
DCC protein expression was assessed immunohistochemically on archival specimens of CRC metastases from 42 patients homogeneously treated by methotrexate-modulated bolus FU alternated to 6-S-leucovorin-modulated infused FU and was retrospectively correlated with patient characteristics and clinical outcome. In a subset analysis, DCC immunoreactivity was compared between metastatic CRC and the corresponding primary tumors and regional lymph node metastases.
Positive immunoreactivity for DCC was found in 45% of patients. Eighteen (78%) of 23 patients for whom multiple samples were available displayed a similar pattern of expression in distant metastases and primary tumors. The median survival time was 14.3 months in patients without DCC expression and 21.4 months in patients with DCC-positive tumors (log-rank test, P =.04); the 2-year survival rates were 8.5% and 42.5%, respectively. Response rates to chemotherapy were not significantly different between the two groups. By multivariate analysis, DCC protein expression maintained its prognostic value and showed to be the single best predictor of survival, with a relative risk of 2.16.
Our results indicate that expression of the DCC protein in CRC metastases is similar to that observed in the corresponding primary tumors and represents a dominant predictor of survival in patients with unresectable, advanced CRC who are undergoing palliative FU-based chemotherapy.
确定结直肠癌(CRC)转移灶中结肠癌缺失(DCC)蛋白表达是否可预测基于氟尿嘧啶(FU)的姑息化疗疗效,并评估其是否与相应原发性肿瘤中的情况相似。
对42例接受甲氨蝶呤调节的大剂量FU与6-S-亚叶酸调节的静脉输注FU交替治疗的CRC转移灶存档标本进行免疫组化评估DCC蛋白表达,并回顾性分析其与患者特征及临床结局的相关性。在亚组分析中,比较转移性CRC与相应原发性肿瘤及区域淋巴结转移灶之间的DCC免疫反应性。
45%的患者DCC免疫反应性呈阳性。在有多个样本的23例患者中,18例(78%)在远处转移灶和原发性肿瘤中表现出相似的表达模式。DCC表达阴性的患者中位生存时间为14.3个月,DCC阳性肿瘤患者为21.4个月(对数秩检验,P = 0.04);2年生存率分别为8.5%和42.5%。两组化疗反应率无显著差异。多因素分析显示,DCC蛋白表达保持其预后价值,是生存的最佳单一预测指标,相对风险为2.16。
我们的结果表明,CRC转移灶中DCC蛋白表达与相应原发性肿瘤中的情况相似,是接受基于FU的姑息化疗的不可切除晚期CRC患者生存的主要预测指标。