Department of Nuclear Medicine, Catholic Kwandong University College of Medicine, International St. Mary's Hospital, Simgokro 100 Gil 25, Seo-gu, Incheon, 22711, Republic of Korea.
Division of Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, 23-20 Byeongmyeong-dong, Dongnam-gu, Cheonan, Chungcheongnam-do, 31151, Republic of Korea.
Lung Cancer. 2018 Apr;118:41-47. doi: 10.1016/j.lungcan.2018.01.020. Epub 2018 Feb 3.
We investigated whether F-fluorodeoxyglucse (FDG) uptake of bone marrow (BM) on positron emission tomography/computed tomography (PET/CT) has implications for predicting clinical outcomes in patients with small cell lung cancer (SCLC).
We retrospectively enrolled 70 SCLC patients who underwent FDG PET/CT prior to treatment. On PET/CT, maximum FDG uptake of all tumor lesions (Tmax), coefficient of variation (COV) of FDG uptake of primary tumor, and mean FDG uptake of BM (BM SUV) were measured. The relationships of BM SUV with PET/CT parameters of SCLC and serum markers were evaluated. Univariate and multivariate analyses were performed to assess the significance of BM SUV for predicting progression-free survival (PFS) and overall survival (OS).
BM SUV had significant positive correlations with Tmax, COV of primary tumor, white blood cell count, and serum C-reactive protein level (p < .05). On univariate analysis, BM SUV showed significant association with only PFS (p = .006). On multivariate analysis, Veterans Administration Lung Cancer Study Group (VALSG) stage, N stage, M stage, Tmax, and BM SUV were independent prognostic factors for PFS (p < .05) and, for OS, VALSG stage and M stage were independent prognostic factors (p < .05). Among patients with limited disease, patients with high FDG uptake of BM had significantly worse PFS than did those with low FDG uptake of BM (p < .05), but, there was no significant difference in PFS between patients with extensive disease and patients with limited disease and high FDG uptake of BM (p > .05).
FDG uptake of BM was an independent predictor of disease progression in SCLC patients. Patients with limited disease and high FDG uptake of BM had similar PFS to those with extensive disease.
我们研究了正电子发射断层扫描/计算机断层扫描(PET/CT)上骨髓(BM)的 F-氟脱氧葡萄糖(FDG)摄取是否与小细胞肺癌(SCLC)患者的临床结局相关。
我们回顾性纳入了 70 例在治疗前接受 FDG PET/CT 的 SCLC 患者。在 PET/CT 上,测量了所有肿瘤病变的最大 FDG 摄取量(Tmax)、原发肿瘤 FDG 摄取的变异系数(COV)和 BM 的平均 FDG 摄取量(BM SUV)。评估了 BM SUV 与 SCLC 的 PET/CT 参数和血清标志物的关系。进行了单因素和多因素分析,以评估 BM SUV 对预测无进展生存期(PFS)和总生存期(OS)的意义。
BM SUV 与 Tmax、原发肿瘤 COV、白细胞计数和血清 C 反应蛋白水平呈显著正相关(p<.05)。单因素分析显示,仅 BM SUV 与 PFS 显著相关(p=0.006)。多因素分析显示,退伍军人管理局肺癌研究组(VALSG)分期、N 分期、M 分期、Tmax 和 BM SUV 是 PFS 的独立预后因素(p<.05),而对于 OS,VALSG 分期和 M 分期是独立的预后因素(p<.05)。在局限期患者中,BM FDG 摄取高的患者的 PFS 明显差于 BM FDG 摄取低的患者(p<.05),但广泛期患者与局限期患者和 BM FDG 摄取高的患者的 PFS 无显著差异(p>.05)。
BM 的 FDG 摄取是 SCLC 患者疾病进展的独立预测因子。局限期且 FDG 摄取高的患者的 PFS 与广泛期患者相似。