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Changes in serum thymidine kinase 1 levels during chemotherapy correlate with objective response in patients with advanced gastric cancer

机译:晚期胃癌患者化疗期间血清胸苷激酶1水平的变化与客观反应相关

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摘要

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.
机译:血清胸苷激酶1(STK1)是包括胃癌在内的大多数实体瘤的可靠增殖标志物。这项研究的目的是评估STK1水平是否与晚期胃癌对化疗的肿瘤反应和生存率有关。结果显示,胃癌患者的平均STK1水平(5.57±3.07 pM)显着高于健康对照组(1.12±0.57)(P <0.001)。在这84例患者中,未进行手术的56例患者的平均STK1水平(6.02±3.12)高于接受手术的28例患者的水平(4.68±2.78)(P = 0.049)。 STK1值与临床分期,ECOG PS和血清CEA水平相关(分别为P <0.001,P = 0.001和P = 0.004),而与年龄和性别无关。与化疗前的水平相比,总化疗患者在1,2和4周期化疗后的平均STK1水平没有明显降低。然而,经过2个疗程的化疗后,达到客观反应(OR)(CR,PR或无复发)的患者STK1的平均水平显着降低。特别是经过1个周期的化疗后,达到OR的患者的平均STK1水平开始下降,而在大多数疾病进展或复发的患者中,STK1的水平开始升高。在接受姑息性化疗或辅助化疗的患者中,中位PFS(中位PFS,未定义为4个月,P <0.001)或RFS(中位RFS,未定义为5个月,P <0.001)有显着差异。在化疗的前2个月中,STK1水平降低的患者与STK1水平升高的患者之间的关系被注意到。对数秩检验表明,姑息化疗组中STK1水平降低的患者有OS更长的趋势。我们的结果表明,胃癌患者的血清TK1水平与临床分期,ECOG PS和血清CEA水平相关,在化疗的前两个月中STK1水平的变化可能对评估化疗反应,预测PFS和RFS更为重要。晚期胃癌患者STK1的基线值。

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