Barbato Francesco, Fendler Wolfgang Peter, Rauscher Isabel, Herrmann Ken, Wetter Axel, Ferdinandus Justin, Seifert Robert, Nader Michael, Rahbar Kambiz, Hadaschik Boris, Eiber Matthias, Gafita Andrei, Weber Manuel
University of Duisburg-Essen and German Cancer Consortium (DKTK)-University Hospital Essen, Germany.
Klinikum Rechts der Isar, Department of Nuclear Medicine, Technical University of Munich.
J Nucl Med. 2021 May 14;62(12):1747-50. doi: 10.2967/jnumed.121.262120.
Conventional imaging low-(LVD) versus high-volume disease (HVD) are associated with survival in metastatic hormone-sensitive prostate cancer (mHSPC) according to CHAARTED and STAMPEDE trials. We propose a compatible quantitative PSMA-PET framework for disease volume assessment in mHSPC. Three PET centers screened their PSMA-PET database for mHSPC patients. CT versus PSMA-PET stage, lesion number, and classification of LVD vs. HVD were determined by one blinded reader; PSMA-positive tumor volume (PSMA-TV) was quantified semi-automatically. 85 CT-based CHAARTED-LVD and 20 CT-based CHAARTED-HVD patients were included. A PSMA-TV of 40 ml was the optimal cutoff between CT-based CHAARTED-LVD (non-unifocal) and HVD (non-M1c) (AUC 0.86). Stratification into PET-LVD (unifocal or oligometastatic/disseminated <40 mL) and PET-HVD (oligometastatic/disseminated ≥~40 mL or M1c) had 13% misalignment with CHAARTED criteria. PSMA-PET criteria with volume quantification deliver comparable LVD/HVD discrimination with additional subgroups for unifocal, oligometastatic and disseminated disease, critical for guidance of targeted or multimodal therapy.
根据CHAARTED和STAMPEDE试验,传统成像中低体积疾病(LVD)与高体积疾病(HVD)与转移性激素敏感性前列腺癌(mHSPC)的生存率相关。我们提出了一种适用于mHSPC疾病体积评估的PSMA-PET定量框架。三个PET中心在其PSMA-PET数据库中筛选mHSPC患者。由一名盲法阅片者确定CT与PSMA-PET分期、病灶数量以及LVD与HVD的分类;半自动定量PSMA阳性肿瘤体积(PSMA-TV)。纳入了85例基于CT的CHAARTED-LVD患者和20例基于CT的CHAARTED-HVD患者。40 ml的PSMA-TV是基于CT的CHAARTED-LVD(非单灶性)和HVD(非M1c)之间的最佳截断值(AUC 0.86)。分层为PET-LVD(单灶性或寡转移/播散性<40 mL)和PET-HVD(寡转移/播散性≥~40 mL或M1c)与CHAARTED标准有13%的偏差。具有体积定量的PSMA-PET标准在区分LVD/HVD方面具有可比性,还为单灶性、寡转移和播散性疾病提供了额外的亚组,这对于靶向或多模式治疗的指导至关重要。