Go Se-Il, Lee Min Jeong, Lee Won Sup, Choi Hye Jung, Lee Un Seok, Kim Rock Bum, Kang Myoung Hee, Kim Hoon-Gu, Lee Gyeong-Won, Kang Jung Hun, Lee Jeong-Hee, Kim Sun Joo
From the Department of Internal Medicine, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju, Korea (S-IG, MJL, WSL, HJC, USL, MHK, H-GK, G-WL, JHK); Department of Preventive Medicine and Environmental Health Center, Gyeongsang National University School of Medicine, Jinju, Korea (RBK), Department of Pathology, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju, Korea (JHL); and Department of Laboratory Medicine, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju, Korea (SJK).
Medicine (Baltimore). 2015 Jul;94(30):e951. doi: 10.1097/MD.0000000000000951.
Systemic activation of hemostasis and thrombosis has been implicated in tumor progression and metastasis. D-dimer has been used as an indicator for the thrombosis. Here, we investigated the role of the activation of coagulation in patients with metastatic gastric cancer by measuring D-dimer level.We conducted an observation study of 46 metastatic gastric cancer patients who received palliative chemotherapy (CTx). D-dimer levels were assessed before CTx and at the first response evaluation after CTx.The overall survival (OS) of patients with pretreatment D-dimer levels <1.5 μg/mL was significantly longer than that of patients with D-dimer levels ≥1.5 μg/mL (22.0 vs 7.9 months, P = 0.019). At the first response evaluation, the mean level of D-dimer was significantly decreased by 2.11 μg/mL in patients either with partial response or stable disease (P = 0.011) whereas the mean level of D-dimer, although the difference did not reach statistical significance, was increased by 2.46 μg/mL in patients with progressive disease. In addition, the OS of patients with D-dimer levels <1.0 μg/mL at the first response evaluation was significantly longer than that of patients with D-dimer levels ≥1.0 μg/mL (22.0 vs 7.0 months, P = 0.009). The lower D-dimer levels (<1.0 μg/mL) at the first response evaluation after CTx was independent predictive factor for better survival in multivariate analysis (P = 0.037).This study suggests that D-dimer levels may serve as a biomarker for response to CTx and OS in patients with metastatic gastric cancer.
止血和血栓形成的全身激活与肿瘤进展和转移有关。D-二聚体已被用作血栓形成的指标。在此,我们通过测量D-二聚体水平来研究凝血激活在转移性胃癌患者中的作用。我们对46例接受姑息化疗(CTx)的转移性胃癌患者进行了观察性研究。在CTx前和CTx后的首次疗效评估时评估D-二聚体水平。预处理D-二聚体水平<1.5μg/mL的患者的总生存期(OS)显著长于D-二聚体水平≥1.5μg/mL的患者(22.0对7.9个月,P = 0.019)。在首次疗效评估时,部分缓解或病情稳定的患者的D-二聚体平均水平显著降低2.11μg/mL(P = 0.011),而病情进展的患者的D-二聚体平均水平虽未达到统计学显著性差异,但升高了2.46μg/mL。此外,首次疗效评估时D-二聚体水平<1.0μg/mL的患者的OS显著长于D-二聚体水平≥1.0μg/mL的患者(22.0对7.0个月,P = 0.009)。在多变量分析中,CTx后首次疗效评估时较低的D-二聚体水平(<1.0μg/mL)是更好生存的独立预测因素(P = 0.037)。本研究表明,D-二聚体水平可能作为转移性胃癌患者对CTx反应和OS的生物标志物。