Lee Dong Soo, Park Kyung Ran, Kim Seung Joon, Chung Mi Joo, Lee Yun Hee, Chang Ji Hyun, Kang Jin Hyoung, Hong Sook Hee, Kim Myung Sin, Kim Yeon Sil
Department of Radiation Oncology, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Department of Radiation Oncology, School of Medicine, Ewha Womans University, Seoul, South Korea.
Tumour Biol. 2016 Jan;37(1):619-25. doi: 10.1007/s13277-015-3776-5. Epub 2015 Aug 4.
This study aimed to evaluate the clinical correlations between serum lactate dehydrogenase (LDH) levels and tumor characteristics and to investigate the prognostic impact of serum LDH levels in advanced non-small cell lung cancer (NSCLC). A total of 394 patients were included in the present study between June 2007 and January 2013. All eligible patients had serum LDH levels available before treatment, and whole-body metastatic extent was measured using whole-body metastatic scores, as determined by 18(F)-fludeoxyglucose positron emission tomography scans from 1 to 7 as the sum of each metastatic region. The diagnostic cutoff value for an abnormal serum LDH level was 450 IU/L. The median serum LDH level was 477 IU/L (range, 113-2850), and 224 (56.9 %) patients had abnormal serum LDH levels. The serum LDH levels showed no significant associations with age, gender, histology, tumor differentiation, and smoking history. However, the proportion of patients with abnormal serum LDH levels was statistically significantly higher in the high total metastatic score group (scores 3-7) than in the low total metastatic score group (scores 1-2) (65.3 vs 50.4 %, p = 0.001). In a multivariate survival analysis, age (p = 0.001), gender (p = 0.001), histology (p = 0.003), tumor differentiation (p = 0.001), Eastern Cooperative Oncology Group (ECOG) performance status (p = 0.001), LDH levels (p = 0.046), and treatment factors (p = 0.001) proved to be independent prognostic factors for survival outcomes. The results of this study suggest that the serum LDH levels at presentation may be significantly correlated with whole-body tumor extent and might independently but modestly prognosticate OS in stage IV NSCLC.
本研究旨在评估血清乳酸脱氢酶(LDH)水平与肿瘤特征之间的临床相关性,并探讨血清LDH水平对晚期非小细胞肺癌(NSCLC)预后的影响。2007年6月至2013年1月期间,共有394例患者纳入本研究。所有符合条件的患者在治疗前均有血清LDH水平数据,全身转移程度采用全身转移评分进行测量,该评分由18(F)-氟脱氧葡萄糖正电子发射断层扫描确定,范围为1至7分,为每个转移区域得分之和。血清LDH水平异常的诊断临界值为450 IU/L。血清LDH水平中位数为477 IU/L(范围为113 - 2850),224例(56.9%)患者血清LDH水平异常。血清LDH水平与年龄、性别、组织学类型、肿瘤分化程度及吸烟史均无显著相关性。然而,高全身转移评分组(评分3 - 7分)血清LDH水平异常的患者比例在统计学上显著高于低全身转移评分组(评分1 - 2分)(65.3%对50.4%,p = 0.001)。在多因素生存分析中,年龄(p = 0.001)、性别(p = 0.001)、组织学类型(p = 0.003)、肿瘤分化程度(p = 0.001)、东部肿瘤协作组(ECOG)体能状态(p = 0.001)、LDH水平(p = 0.046)及治疗因素(p = 0.001)被证明是生存结局的独立预后因素。本研究结果表明,就诊时的血清LDH水平可能与全身肿瘤范围显著相关,并且可能独立但适度地预测IV期NSCLC患者的总生存期。
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