Abdel-Aty Hoda, Hujairi Nabil, Murray Iain, Yogeswaran Yathushan, van As Nicholas, James Nicholas
Division of Radiotherapy and Imaging, Institute of Cancer Research, London, SW3 6JB, United Kingdom.
Department of Radiotherapy, Royal Marsden NHS Foundation Trust, London, SW3 6JJ, United Kingdom.
BJR Open. 2024 Nov 8;6(1):tzae040. doi: 10.1093/bjro/tzae040. eCollection 2024 Jan.
To quantify the stage-shift with prostate-specific membrane antigen (PSMA) PET/CT imaging in metastatic prostate cancer and explore treatment implications.
Single-centre, retrospective analysis of patients with newly diagnosed [F]PSMA-1007 or [Ga]Ga-PSMA-11 PET/CT-detected metastatic prostate cancer who had baseline bone scintigraphy between January 2015 and May 2021. Patients were subclassified into oligometastatic and polymetastatic disease utilizing the STAMPEDE2 trial (ISRCTN66357938/NCT06320067) definition. Patient, tumour, and treatment characteristics were collected. PSMA PET/CT concordance with conventional imaging (bone scintigraphy and low-dose CT of PET) was identified by number and site of metastases, and subgroup assigned. Spearman's rank correlation and linear regression modelling determined the association between the imaging modalities.
We analysed 62 patients with a median age was 72 years (range 48-86). On PSMA PET/CT, 31/62 (50%) patients had oligometastatic disease, and 31/62 (50%) had polymetastatic disease. Prostate radiotherapy was delivered in 20/31 (65%) patients with oligometastatic disease and 17/31 (55%) with polymetastatic disease. 23/62 (37%) patients were reclassified as M0 on conventional imaging. PSMA PET/CT had a 2.9-fold increase in detecting bone metastases. Bone metastases concordance was found in 10/50 (20%) by number and 30/33 (91%) by site. PSMA PET/CT had a 2.2-fold increase in detecting nodal metastases. Nodal metastases concordance was found in 5/46 (11%) by number and 25/26 (96%) by site. There was significant positive correlation between PSMA PET/CT and conventional imaging for detecting bone [ = 0.25 (<0.001)] and nodal metastases [ = 0.19 (<0.001)]. 16/31 (52%) had oligometastatic disease concordance.
The magnitude of PSMA PET/CT-driven stage-shift is highly variable and unpredictable with implications on treatment decisions, future trial design, and potentially clinical outcomes.
The magnitude of "frame-shift" with PSMA PET/CT imaging is highly variable and unpredictable which may unreliably change treatment decisions dependent on image-defined disease extent. Prospective randomized trials are required to determine the relationship between PSMA PET/CT-guided treatment choices and outcomes.
量化转移性前列腺癌患者经前列腺特异性膜抗原(PSMA)PET/CT成像后的分期变化,并探讨其对治疗的影响。
对2015年1月至2021年5月期间因[F]PSMA-1007或[Ga]Ga-PSMA-11 PET/CT检测出转移性前列腺癌且进行了基线骨闪烁显像的患者进行单中心回顾性分析。利用STAMPEDE2试验(ISRCTN66357938/NCT06320067)的定义将患者分为寡转移和多转移疾病亚组。收集患者、肿瘤和治疗特征。通过转移灶的数量和部位确定PSMA PET/CT与传统成像(骨闪烁显像和PET低剂量CT)的一致性,并进行亚组划分。采用Spearman等级相关和线性回归模型确定成像方式之间的关联。
我们分析了62例患者,中位年龄为72岁(范围48 - 86岁)。在PSMA PET/CT上,31/62(50%)的患者为寡转移疾病,31/62(50%)为多转移疾病。20/31(65%)的寡转移疾病患者和17/31(55%)的多转移疾病患者接受了前列腺放疗。23/62(37%)的患者在传统成像上被重新分类为M0。PSMA PET/CT检测骨转移的能力提高了2.9倍。按转移灶数量计算,10/50(20%)的骨转移情况一致,按部位计算,30/33(91%)一致。PSMA PET/CT检测淋巴结转移的能力提高了2.2倍。按转移灶数量计算,5/46(11%)的淋巴结转移情况一致,按部位计算,25/26(96%)一致。PSMA PET/CT与传统成像在检测骨转移[ρ = 0.25(<0.001)]和淋巴结转移[ρ = 0.19(<0.001)]方面存在显著正相关。16/31(52%)的患者寡转移疾病情况一致。
PSMA PET/CT驱动的分期变化程度高度可变且不可预测,对治疗决策、未来试验设计以及潜在的临床结果均有影响。
PSMA PET/CT成像的“分期变化”程度高度可变且不可预测,这可能会不可靠地改变依赖于图像定义的疾病范围的治疗决策。需要进行前瞻性随机试验来确定PSMA PET/CT引导的治疗选择与结果之间的关系。