CA19-9 level as a prognostic and predictive factor of bevacizumab efficacy in metastatic colorectal cancer patients undergoing oxaliplatin-based chemotherapy

被引:27
|
作者
Narita, Yukiya [1 ]
Taniguchi, Hiroya [1 ]
Komori, Azusa [1 ]
Nitta, Sohei [1 ]
Yamaguchi, Kazuhisa [1 ]
Kondo, Chihiro [1 ]
Nomura, Motoo [1 ]
Kadowaki, Shigenori [1 ]
Takahari, Daisuke [1 ]
Ura, Takashi [1 ]
Andoh, Masashi [1 ]
Muro, Kei [1 ]
机构
[1] Aichi Canc Ctr Hosp, Dept Clin Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
关键词
Bevacizumab; Carbohydrate antigen 19-9; Colorectal cancer; Predictive factor; Prognostic factor; PHASE-III; MUTATION STATUS; COMBINATION; FLUOROURACIL; LEUCOVORIN; THERAPY; HYPOXIA; TRIAL;
D O I
10.1007/s00280-013-2367-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:409 / 416
页数:8
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