Jeong Shin Young, Kim Seong-Jang, Pak Kyoungjune, Lee Sang-Woo, Ahn Byeong-Cheol, Lee Jaetae
Department of Nuclear Medicine, School of Medicine, Kyungpook National University.
Department of Nuclear Medicine, Kyungpook National University Hospital, Daegu.
Medicine (Baltimore). 2018 Oct;97(43):e12859. doi: 10.1097/MD.0000000000012859.
Several studies have reported the prognostic value of F-fluorodeoxyglucose (F-FDG) bone marrow uptake (BMU) measured by F-FDG positron emission tomography (F-FDG PET) in various cancers. We performed a meta-analysis to evaluate the prognostic value of F-FDG BMU in patients with solid tumors.
Systematic searches of MEDLINE and Embase databases were performed using the keywords "F-FDG," "bone marrow," and "prognosis." All published human studies of the prognostic value of F-FDG BMU in patients with solid tumors were searched. The primary outcome was event-free survival (EFS), and the secondary endpoint was overall survival (OS); both of these were extracted directly from each study. The effects of F-FDG BMU on survival were assessed by using hazard ratios (HRs).
Ten studies with 1197 patients (8 studies reporting EFS in 1096 patients and 7 studies reporting OS in 836 patients) were included. In the EFS analysis, the combined HR was 1.75 (95% confidence interval [CI]: 1.45-2.11, P < .00001) in the random effects model (I = 51%, P = .05). The combined HR of OS was 1.40 (95% CI: 1.13-1.73, P = .002) in the random effects model (I = 52%, P = .05).
This meta-analysis has demonstrated that patients with a low level of F-FDG BMU have better EFS and OS than those with a high level of F-FDG BMU. Based on our results, we suggest that F-FDG BMU could be used as a biomarker for stratifying the risk of tumor progression in patients with solid tumors.
多项研究报告了通过氟脱氧葡萄糖(F-FDG)正电子发射断层扫描(F-FDG PET)测量的F-FDG骨髓摄取(BMU)在各种癌症中的预后价值。我们进行了一项荟萃分析,以评估F-FDG BMU在实体瘤患者中的预后价值。
使用关键词“F-FDG”、“骨髓”和“预后”对MEDLINE和Embase数据库进行系统检索。检索了所有已发表的关于F-FDG BMU在实体瘤患者中预后价值的人体研究。主要结局是无事件生存期(EFS),次要终点是总生存期(OS);这两者均直接从每项研究中提取。使用风险比(HRs)评估F-FDG BMU对生存的影响。
纳入了10项研究,共1197例患者(8项研究报告了1096例患者的EFS,7项研究报告了836例患者的OS)。在EFS分析中,随机效应模型的合并HR为1.75(95%置信区间[CI]:1.45-2.11,P<0.00001)(I=51%,P=0.05)。随机效应模型中OS的合并HR为1.40(95%CI:1.13-1.73,P=0.002)(I=52%,P=0.05)。
这项荟萃分析表明,F-FDG BMU水平低的患者比F-FDG BMU水平高的患者具有更好的EFS和OS。基于我们的结果,我们建议F-FDG BMU可作为实体瘤患者肿瘤进展风险分层的生物标志物。