Onal Cem, Guler Ozan Cem, Torun Nese, Oymak Ezgi, Reyhan Mehmet
Department of Radiation Oncology, Baskent University Faculty of Medicine, Adana Dr. Turgut Noyan Research and Treatment Center, Adana, 01120, Turkey.
Department of Radiation Oncology, Baskent University Faculty of Medicine, Ankara, Turkey.
Eur J Nucl Med Mol Imaging. 2023 Oct;50(12):3755-3764. doi: 10.1007/s00259-023-06321-1. Epub 2023 Jul 5.
We examined the prognostic significance of early changes in primary tumor SUV measured with Gallium-68-labeled prostate-specific membrane antigen positron emission tomography ([Ga]Ga-PSMA-11-PET/CT) and serum PSA values after neoadjuvant androgen deprivation treatment (nADT) in high-risk prostate cancer (PCa) patients treated with definitive radiotherapy (RT).
The clinical data and SUV parameters of 71 PCa patients were reviewed retrospectively. The serum PSA and primary tumor SUV values were calculated before and after the start of ADT. Using univariable and multivariable analyses, the prognostic factors predicting biochemical disease free survival (bDFS) and prostate cancer specific survival (PCSS) were investigated. In addition, logistic regression analysis was used to identify predictors of biochemical failure (BF).
All but one patient responded with a 98.8% reduction in serum PSA (21.8 ng/mL vs. 0.3 ng/mL; p < 0.001), and 64 patients (91.1%) had a median 66.6% decrease in primary tumor SUV after ADT (13.2 vs. 4.8, p < 0.001). The primary tumor SUV response rate was significantly higher in patients with Gleason score (GS) of 7 than in patients with GS > 7 (59.5% vs. 40.5%; p = 0.04), and it was significantly lower in patients with inadequate treatment response than in those with complete (CR) or partial response (PR) (1.1% vs. 66.1%; p < 0.001). There was a strong and significant correlation (Spearman = 0.41, p < 0.001) and a high concordance (91.5%) between PSA response and SUV response after ADT. With a median follow-up time of 76.1 months, the 5-year bDFS and PCSS rates were 77.2% and 92.2%, respectively. Nineteen patients (26.7%) patients had recurrence at a median of 44.6 months after the completion of RT. In multivariate analysis, lymph node metastasis, GS greater than 7, and SD/PD after nADT were independent predictors of worse bDFS. However, no significant factor for PCSS was identified. In the multivariable logistic regression analysis, advanced age, GS of > 7 disease, lymph node metastasis, and SD or PD after nADT were independent predictors of BF.
These results imply that the metabolic response measured with [Ga]Ga-PSMA-11-PET/CT after nADT could be used to predict progression in high-risk PCa patients treated with definitive RT.
我们研究了在接受根治性放疗(RT)的高危前列腺癌(PCa)患者中,新辅助雄激素剥夺治疗(nADT)后,用镓-68标记的前列腺特异性膜抗原正电子发射断层扫描([Ga]Ga-PSMA-11-PET/CT)测量的原发肿瘤SUV早期变化及血清PSA值的预后意义。
回顾性分析71例PCa患者的临床资料和SUV参数。计算ADT开始前后的血清PSA和原发肿瘤SUV值。采用单变量和多变量分析,研究预测生化无病生存(bDFS)和前列腺癌特异性生存(PCSS)的预后因素。此外,采用逻辑回归分析确定生化失败(BF)的预测因素。
除1例患者外,所有患者血清PSA下降98.8%(21.8 ng/mL对0.3 ng/mL;p<0.001),64例患者(91.1%)ADT后原发肿瘤SUV中位数下降66.6%(13.2对4.8,p<0.001)。Gleason评分(GS)为7的患者原发肿瘤SUV反应率显著高于GS>7的患者(59.5%对40.5%;p = 0.04),治疗反应不足的患者显著低于完全缓解(CR)或部分缓解(PR)的患者(1.1%对66.1%;p<0.001)。ADT后PSA反应与SUV反应之间存在强且显著的相关性(Spearman = 0.41,p<0.001)和高度一致性(91.5%)。中位随访时间为76.1个月,5年bDFS和PCSS率分别为77.2%和92.2%。19例患者(26.7%)在RT完成后中位44.6个月复发。多变量分析中,淋巴结转移、GS大于7以及nADT后的疾病稳定/进展(SD/PD)是bDFS较差的独立预测因素。然而,未发现PCSS的显著因素。多变量逻辑回归分析中,高龄、GS>7的疾病、淋巴结转移以及nADT后的疾病稳定或进展是BF的独立预测因素。
这些结果表明,nADT后用[Ga]Ga-PSMA-11-PET/CT测量的代谢反应可用于预测接受根治性RT的高危PCa患者的病情进展。