Duan Heying, Ghanouni Pejman, Daniel Bruce, Rosenberg Jarrett, Davidzon Guido A, Aparici Carina Mari, Kunder Christian, Sonn Geoffrey A, Iagaru Andrei
Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Stanford University, Stanford, California.
Division of Body MRI, Department of Radiology, Stanford University, Stanford, California.
J Nucl Med. 2023 Apr;64(4):592-597. doi: 10.2967/jnumed.122.264783. Epub 2022 Nov 3.
Focal therapy for localized prostate cancer (PC) using high-intensity focused ultrasound (HIFU) is gaining in popularity as it is noninvasive and associated with fewer side effects than standard whole-gland treatments. However, better methods to evaluate response to HIFU ablation are an unmet need. Prostate-specific membrane antigen (PSMA) and gastrin-releasing peptide receptors are both overexpressed in PC. In this study, we evaluated a novel approach of using both Ga-RM2 and Ga-PSMA11 PET/MRI in each patient before and after HIFU to assess the accuracy of target tumor localization and response to treatment. Fourteen men, 64.5 ± 8.0 y old (range, 48-78 y), with newly diagnosed PC were prospectively enrolled. Before HIFU, the patients underwent prostate biopsy, multiparametric MRI, Ga-PSMA11, and Ga-RM2 PET/MRI. Response to treatment was assessed at a minimum of 6 mo after HIFU with prostate biopsy ( = 13), as well as Ga-PSMA11 and Ga-RM2 PET/MRI ( = 14). The SUV and SUV of known or suspected PC lesions were collected. Pre-HIFU biopsy revealed 18 cancers, of which 14 were clinically significant (Gleason score ≥ 3 + 4). Multiparametric MRI identified 18 lesions; 14 of them were at least score 4 in the Prostate Imaging-Reporting and Data System. Ga-PSMA11 and Ga-RM2 PET/MRI each showed 23 positive intraprostatic lesions; 21 were congruent in 13 patients, and 5 were incongruent in 5 patients. Before HIFU, Ga-PSMA11 identified all target tumors, whereas Ga-RM2 PET/MRI missed 2 tumors. After HIFU, Ga-RM2 and Ga-PSMA11 PET/MRI both identified clinically significant residual disease in 1 patient. Three significant ipsilateral recurrent lesions were identified, whereas 1 was missed by Ga-PSMA11. The pretreatment level of prostate-specific antigen decreased significantly after HIFU, by 66%. Concordantly, the pretreatment SUV decreased significantly after HIFU for Ga-PSMA11 ( = 0.001) and Ga-RM2 ( = 0.005). This pilot study showed that Ga-PSMA11 and Ga-RM2 PET/MRI identified the target tumor for HIFU in 100% and 86% of cases, respectively, and accurately verified response to treatment. PET may be a useful tool in the guidance and monitoring of treatment success in patients receiving focal therapy for PC. These preliminary findings warrant larger studies for validation.
使用高强度聚焦超声(HIFU)对局限性前列腺癌(PC)进行聚焦治疗正日益受到欢迎,因为它是非侵入性的,且与标准的全腺治疗相比副作用更少。然而,目前仍需要更好的方法来评估对HIFU消融的反应。前列腺特异性膜抗原(PSMA)和胃泌素释放肽受体在PC中均有过表达。在本研究中,我们评估了一种新方法,即在每位患者接受HIFU治疗前后使用Ga-RM2和Ga-PSMA11 PET/MRI,以评估靶肿瘤定位的准确性和对治疗的反应。前瞻性纳入了14名新诊断为PC的男性,年龄64.5±8.0岁(范围48 - 78岁)。在HIFU治疗前,患者接受了前列腺活检、多参数MRI、Ga-PSMA11和Ga-RM2 PET/MRI检查。在HIFU治疗后至少6个月,通过前列腺活检(n = 13)以及Ga-PSMA11和Ga-RM2 PET/MRI(n = 14)评估治疗反应。收集已知或疑似PC病变的SUV和SUV。HIFU治疗前的活检发现18处癌症,其中14处具有临床意义(Gleason评分≥3 + 4)。多参数MRI识别出18个病变;其中14个在前列腺影像报告和数据系统中至少为4分。Ga-PSMA11和Ga-RM2 PET/MRI各自显示23处前列腺内阳性病变;13例患者中有21处病变一致,5例患者中有5处病变不一致。在HIFU治疗前,Ga-PSMA11识别出所有靶肿瘤,而Ga-RM2 PET/MRI漏诊了2个肿瘤。HIFU治疗后,Ga-RM2和Ga-PSMA11 PET/MRI均在1例患者中识别出具有临床意义的残留疾病。识别出3处同侧显著复发病变,而Ga-PSMA11漏诊了1处。HIFU治疗后前列腺特异性抗原的预处理水平显著下降,下降了66%。同样,HIFU治疗后Ga-PSMA11(P = 0.001)和Ga-RM2(P = 0.005)的预处理SUV也显著下降。这项初步研究表明,Ga-PSMA11和Ga-RM2 PET/MRI分别在100%和86%的病例中识别出HIFU的靶肿瘤,并准确验证了对治疗的反应。PET可能是指导和监测接受PC聚焦治疗患者治疗成功的有用工具。这些初步发现值得进行更大规模的研究以进行验证。