Department of Clinical Oncology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya, Aichi, 464-8681, Japan,
Cancer Chemother Pharmacol. 2014 Feb;73(2):409-16. doi: 10.1007/s00280-013-2367-7. Epub 2013 Dec 10.
The prognostic and predictive values of carbohydrate antigen 19-9 (CA19-9) levels in metastatic colorectal cancer (mCRC) remain unclear. We reviewed all mCRC patients at a single institution to evaluate the relationship between CA19-9 levels and survival.
Two hundred and fifty-two patients underwent first-line chemotherapy using oxaliplatin-based regimens between April 2005 and December 2009. The relationship between baseline CA19-9 levels and survival was analyzed. Moreover, we evaluated the relationship between baseline CA19-9 levels and clinicopathological factors.
One hundred and fifty patients had elevated baseline CA19-9 levels (elevated group), and 79 patients had normal baseline CA19-9 (normal group) levels. Both KRAS and BRAF mutation rates were higher in the elevated group than in the normal group. Elevated CA19-9 level was a poor prognostic factor compared with normal CA19-9 levels (P = 0.0021). In the elevated group, the median survival time with bevacizumab was significantly longer with bevacizumab than without it (median OS, 27.8 vs. 15.3 months, P = 0.0019). However, the median survival time was not different with or without bevacizumab in the normal group (median OS, 36.5 vs. 38.0 months, P = 0.9515).
Our results suggest that baseline CA19-9 level is an independent prognostic factor in mCRC patients, and it correlated with the KRAS/BRAF mutation status. Bevacizumab exhibits clinical activity only for high CA19-9 levels in mCRC.
肿瘤相关抗原 19-9(CA19-9)水平在转移性结直肠癌(mCRC)中的预后和预测价值尚不清楚。我们回顾了单一机构的所有 mCRC 患者,以评估 CA19-9 水平与生存之间的关系。
252 例患者于 2005 年 4 月至 2009 年 12 月期间接受了一线奥沙利铂为基础的化疗方案。分析了基线 CA19-9 水平与生存之间的关系。此外,我们还评估了基线 CA19-9 水平与临床病理因素之间的关系。
150 例患者基线 CA19-9 水平升高(升高组),79 例患者基线 CA19-9 水平正常(正常组)。升高组 KRAS 和 BRAF 突变率均高于正常组。与正常 CA19-9 水平相比,升高的 CA19-9 水平是预后不良的因素(P=0.0021)。在升高组中,与无贝伐珠单抗治疗相比,贝伐珠单抗治疗的中位总生存期明显延长(中位 OS,27.8 个月 vs. 15.3 个月,P=0.0019)。然而,在正常组中,有无贝伐珠单抗治疗的中位总生存期无差异(中位 OS,36.5 个月 vs. 38.0 个月,P=0.9515)。
我们的结果表明,基线 CA19-9 水平是 mCRC 患者的独立预后因素,与 KRAS/BRAF 突变状态相关。贝伐珠单抗仅对 mCRC 中高 CA19-9 水平有临床活性。