Department of Radiology and Nuclear Medicine, VU University Medical Center, Amsterdam, The Netherlands.
Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Int J Radiat Oncol Biol Phys. 2018 Jun 1;101(2):406-410. doi: 10.1016/j.ijrobp.2018.02.005. Epub 2018 Feb 13.
To investigate the predictive value of [F]-fluoromethylcholine positron emission tomography/computed tomography (PET/CT)-derived parameters on progression-free survival (PFS) in oligometastatic prostate cancer patients treated with stereotactic body radiation therapy (SBRT).
In [F]-fluoromethylcholine PET/CT scans of 40 consecutive patients with ≤4 metachronous metastases treated with SBRT we retrospectively measured the number of metastases, standardized uptake values (SUV, SUV, SUV), metabolically active tumor volume (MATV), and total lesion choline uptake. Partial-volume correction was applied using the iterative deconvolution Lucy-Richardson algorithm.
Thirty-seven lymph node and 13 bone metastases were treated with SBRT. Thirty-three patients (82.5%) had 1 lesion, 4 (10%) had 2 lesions, and 3 (7.5%) had 3 lesions. After a median follow-up of 32.6 months (interquartile range, 35.5 months), the median PFS was 11.5 months (95% confidence interval 8.4-14.6 months). Having more than a single metastasis was a significant prognostic factor (hazard ratio 2.74; P = .03), and there was a trend in risk of progression for large MATV (hazard ratio 1.86; P = .10). No SUV or total lesion choline uptake was significantly predictive for PFS, regardless of partial-volume correction. All PET semiquantitative parameters were significantly correlated with each other (P ≤ .013).
The number of choline-avid metastases was a significant prognostic factor for progression after [F]-fluormethylcholine PET/CT-guided SBRT for recurrent oligometastatic prostate cancer, and there seemed to be a trend in risk of progression for patients with large MATVs. The lesional level of [F]-fluoromethylcholine uptake was not prognostic for progression.
研究氟甲基胆碱正电子发射断层扫描/计算机断层扫描(PET/CT)衍生参数对接受立体定向体部放射治疗(SBRT)治疗的寡转移性前列腺癌患者无进展生存期(PFS)的预测价值。
对 40 例接受 SBRT 治疗的≤4 个异时性转移的连续患者的氟甲基胆碱 PET/CT 扫描进行回顾性分析,我们测量了转移灶数量、标准摄取值(SUV、SUV、SUV)、代谢活跃肿瘤体积(MATV)和总病灶胆碱摄取。使用迭代去卷积 Lucy-Richardson 算法进行部分容积校正。
37 个淋巴结转移和 13 个骨转移接受 SBRT 治疗。33 例(82.5%)患者有 1 个病灶,4 例(10%)患者有 2 个病灶,3 例(7.5%)患者有 3 个病灶。中位随访时间为 32.6 个月(四分位间距,35.5 个月),中位 PFS 为 11.5 个月(95%置信区间 8.4-14.6 个月)。有多个转移灶是显著的预后因素(风险比 2.74;P=.03),并且 MATV 较大的进展风险有趋势(风险比 1.86;P=.10)。无论是否进行部分容积校正,SUV 或总病灶胆碱摄取均与 PFS 无显著相关性。所有 PET 半定量参数之间均显著相关(P≤.013)。
氟甲基胆碱 PET/CT 引导下 SBRT 治疗复发性寡转移性前列腺癌后,胆碱摄取转移灶数量是进展的显著预后因素,而 MATV 较大的患者进展风险似乎有趋势。病灶水平的氟甲基胆碱摄取与进展无相关性。