Zhang Jiao, Yao Yan-Hong, Li Bao-Guo, Yang Qing, Zhang Peng-Yu, Wang Hai-Tao
1] Department of Interventional Oncology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin, China [2] Research Group of Evidence-based Clinical Oncology, Tianjin, China [3] Tianjin Key Laboratory of Cancer Prevention and Therapy, Tianjin, China.
1] Department of Interventional Oncology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin, China [2] Tianjin Key Laboratory of Cancer Prevention and Therapy, Tianjin, China.
Sci Rep. 2015 Apr 22;5:9800. doi: 10.1038/srep09800.
Although most studies have reported that high serum lactate dehydrogenase (LDH) levels are associated with poor prognosis in several malignancies, the consistency and magnitude of the impact of LDH are unclear. We conducted the first comprehensive meta-analysis of the prognostic relevance of LDH in solid tumors. Overall survival (OS) was the primary outcome; progression-free survival (PFS) and disease-free survival (DFS) were secondary outcomes. We identified a total of 68 eligible studies that included 31,857 patients. High LDH was associated with a HR for OS of 1.48 (95% CI = 1.43 to 1.53; P < 0.00001; I(2) = 93%), an effect observed in all disease subgroups, sites, stages and cutoff of LDH. HRs for PFS and DFS were 1.70 (95% CI = 1.44 to 2.01; P < 0.00001; I(2) = 13%) and 1.86(95% CI = 1.15 to 3.01; P = 0.01; I(2) = 88%), respectively. Analysis of LDH as a continuous variable showed poorer OS with increasing LDH (HR 2.11; 95% CI = 1.35 to 3.28). Sensitivity analyses showed there was no association between LDH cutoff and reported HR for OS. High LDH is associated with an adverse prognosis in many solid tumors and its additional prognostic and predictive value for clinical decision-making warrants further investigation.
尽管大多数研究报告称,高血清乳酸脱氢酶(LDH)水平与多种恶性肿瘤的预后不良相关,但LDH影响的一致性和程度尚不清楚。我们首次对LDH在实体瘤中的预后相关性进行了全面的荟萃分析。总生存期(OS)是主要结局;无进展生存期(PFS)和无病生存期(DFS)是次要结局。我们共纳入了68项符合条件的研究,涉及31,857例患者。高LDH与OS的风险比(HR)为1.48(95%置信区间[CI]=1.43至1.53;P<0.00001;I²=93%),在所有疾病亚组、部位、分期和LDH临界值中均观察到这一效应。PFS和DFS的HR分别为1.70(95%CI=1.44至2.01;P<0.00001;I²=13%)和1.86(95%CI=1.15至3.01;P=0.01;I²=88%)。将LDH作为连续变量进行分析显示,随着LDH升高,OS更差(HR 2.11;95%CI=1.35至3.28)。敏感性分析显示,LDH临界值与报告的OS的HR之间无关联。高LDH与许多实体瘤的不良预后相关,其对临床决策的额外预后和预测价值值得进一步研究。