From the Departments of Nuclear Medicine.
Oncology.
Clin Nucl Med. 2023 Sep 1;48(9):775-780. doi: 10.1097/RLU.0000000000004763. Epub 2023 Jun 29.
The aim of this study was to evaluate the prognostic value of 68 Ga-labeled prostate-specific membrane antigen (PSMA) PET/CT in metastatic castration-resistant prostate cancer patients receiving second-line chemotherapy with cabazitaxel.
All patients with metastatic castration-resistant prostate cancer who underwent a PSMA PET/CT within 8 weeks before initiating the cabazitaxel treatment were retrospectively evaluated. The whole-body PSMA total tumor volume (PSMA-TV) was measured for each patient. Other factors such as prostate-specific antigen, hemoglobin, lactate dehydrogenase, and alkaline phosphatase were recorded. A log-rank cutoff finder was used to define the PSMA-TV optimal cutoff. Survival analyses were performed using Cox regression and Kaplan-Meier methods.
In total, 32 patients were included, receiving a median of 6 cycles of cabazitaxel (range, 2-10). After a median follow-up of 12 months, 28 patients presented disease progression, and 18 died. Baseline PSMA-TV presented a significant association with progression-free survival (PFS) and overall survival (OS; P = 0.035 and P = 0.002, respectively). Optimal PSMA-TV cutoffs were 515 mL for PFS and 473 mL for OS. Patients with low volume presented longer PFS and OS than those with high volume: median PFS, 21 versus 12 weeks, respectively (hazard ratio, 0.33; P = 0.017); and median OS, 24 versus 8.5 months, respectively (hazard ratio, 0.21; P = 0.002). On the multivariable analyses, PSMA-TV remained an independent predictor of OS ( P = 0.016).
Our results show that total tumor volume measured on PSMA PET/CT is a prognostic biomarker in patients treated with cabazitaxel. High PSMA-TV before treatment initiation is associated with shorter PFS and OS.
本研究旨在评估 68Ga 标记的前列腺特异性膜抗原(PSMA)PET/CT 在接受卡巴他赛二线化疗的转移性去势抵抗性前列腺癌(mCRPC)患者中的预后价值。
回顾性评估了所有在开始卡巴他赛治疗前 8 周内行 PSMA PET/CT 的 mCRPC 患者。为每位患者测量全身 PSMA 总肿瘤体积(PSMA-TV)。记录前列腺特异性抗原、血红蛋白、乳酸脱氢酶和碱性磷酸酶等其他因素。使用对数秩检验确定 PSMA-TV 的最佳截断值。使用 Cox 回归和 Kaplan-Meier 方法进行生存分析。
共纳入 32 例患者,接受中位数为 6 周期卡巴他赛(范围 2-10)治疗。中位随访 12 个月后,28 例患者出现疾病进展,18 例患者死亡。基线 PSMA-TV 与无进展生存期(PFS)和总生存期(OS)显著相关(P = 0.035 和 P = 0.002)。最佳 PSMA-TV 截断值分别为 515mL 用于 PFS 和 473mL 用于 OS。低体积组的 PFS 和 OS 均长于高体积组:中位 PFS 分别为 21 周和 12 周(风险比,0.33;P = 0.017);中位 OS 分别为 24 个月和 8.5 个月(风险比,0.21;P = 0.002)。多变量分析显示,PSMA-TV 仍然是 OS 的独立预测因子(P = 0.016)。
我们的研究结果表明,PSMA PET/CT 上测量的总肿瘤体积是接受卡巴他赛治疗的患者的预后生物标志物。治疗前 PSMA-TV 较高与较短的 PFS 和 OS 相关。