Liu Yongping, Ling Yang, Qi Qiufeng, Tang Yexin, Xu Jianzhong, Tong Zhou, Sheng Guifeng, Yang Quanliang, Pan Yaodong
Clinical Oncology Laboratory, and.
Exp Ther Med. 2011 Nov;2(6):1177-1181. doi: 10.3892/etm.2011.338. Epub 2011 Aug 17.
Serum thymidine kinase 1 (STK1) is a reliable proliferation marker in most solid tumors, including gastric cancer. The aim of this study was to evaluate whether STK1 levels are related to the tumor response to chemotherapy and survival in advanced gastric cancer. The results showed that the average STK1 level in patients with gastric cancer (5.57±3.07 pM) was significantly higher than that in the healthy controls (1.12±0.57) (P<0.001). Among the 84 patients, the average STK1 level (6.02±3.12) in the 56 patients who did not undergo surgery was higher than the level (4.68±2.78) in the 28 patients who received surgery (P=0.049). The STK1 value correlated with clinical stage, ECOG PS and serum CEA levels (P<0.001, P=0.001 and P=0.004, respectively), but not with age and gender. The average STK1 levels after 1,2 and 4 cycles of chemotherapy did not significantly decrease in the total patients, when compared to the levels prior to chemotherapy. Yet, after 2 cycles of chemotherapy, the average level of STK1 was significantly decreased in patients who achieved an objective response (OR) (CR, PR or no recurrence). Particularly after 1 cycle of chemotherapy, the average level of STK1 in patients who achieved OR started to decline, while in most of the patients with disease progression or recurrence, the STK1 level started to increase. In patients receiving palliative chemotherapy or receiving adjuvant chemotherapy, a significant difference in the median PFS (median PFS, not defined vs. 4 months, P<0.001) or RFS (median RFS, not defined vs. 5 months, P<0.001) was noted between patients with decreased STK1 levels and patients with increased STK1 levels during the first 2 months of chemotherapy. The log-rank test showed that patients with decreased STK1 levels had a trend of a longer OS in the palliative chemotherapy group. Our results suggest that serum TK1 levels correlate with clinical stage, ECOG PS and serum CEA levels in patients with gastric cancer, and changes in STK1 levels during the first 2 months of chemotherapy may be more important for evaluating chemotherapy response, predicting PFS and RFS than baseline values of STK1 in patients with advanced gastric cancer.
血清胸苷激酶1(STK1)是包括胃癌在内的大多数实体瘤中一种可靠的增殖标志物。本研究旨在评估STK1水平是否与晚期胃癌的化疗反应及生存情况相关。结果显示,胃癌患者的STK1平均水平(5.57±3.07 pM)显著高于健康对照组(1.12±0.57)(P<0.001)。在84例患者中,56例未接受手术患者的STK1平均水平(6.02±3.12)高于28例接受手术患者的水平(4.68±2.78)(P=0.049)。STK1值与临床分期、美国东部肿瘤协作组体能状态(ECOG PS)及血清癌胚抗原(CEA)水平相关(分别为P<0.001、P=0.001和P=0.004),但与年龄和性别无关。与化疗前水平相比,化疗1、2和4周期后,所有患者的STK1平均水平均未显著下降。然而,化疗2周期后,达到客观缓解(OR)(完全缓解、部分缓解或无复发)的患者中,STK1平均水平显著下降。尤其是化疗1周期后,达到OR的患者中STK1平均水平开始下降,而在大多数疾病进展或复发的患者中,STK1水平开始升高。在接受姑息化疗或辅助化疗的患者中,化疗前2个月内STK1水平下降的患者与STK1水平升高的患者相比,无进展生存期(PFS)中位数(未定义vs. 4个月,P<0.001)或复发-free生存期(RFS)中位数(未定义vs. 5个月,P<0.001)存在显著差异。对数秩检验显示,姑息化疗组中STK1水平下降的患者总生存期(OS)有延长趋势。我们的结果表明,胃癌患者血清TK1水平与临床分期、ECOG PS及血清CEA水平相关,化疗前2个月内STK1水平的变化对于评估晚期胃癌患者的化疗反应、预测PFS和RFS可能比STK1的基线值更重要。