Ahmanson Translational Imaging Division, Department of Molecular and Medical Pharmacology, UCLA, Los Angeles, California.
Department of Radiation Oncology, UCLA, Los Angeles, California; and.
J Nucl Med. 2018 Apr;59(4):557-567. doi: 10.2967/jnumed.117.196444. Epub 2018 Jan 4.
Radiotherapy and radical prostatectomy are the definitive treatment options for patients with localized prostate cancer. A rising level of prostate-specific antigen after radical prostatectomy indicates prostate cancer recurrence, and these patients may still be cured with salvage radiotherapy. To maximize chance for cure, the irradiated volumes should completely encompass the extent of disease. Therefore, accurate estimation of the location of disease is critical for radiotherapy planning in both the definitive and the salvage settings. Current first-line imaging for prostate cancer has limited sensitivity for detection of disease both at initial staging and at biochemical recurrence. Integration of PET into routine evaluation of prostate cancer patients may improve both staging accuracy and radiotherapy planning. F-FDG PET/CT is now routinely used in radiation planning for several cancer types. However, F-FDG PET/CT has low sensitivity for prostate cancer. Additional PET probes evaluated in prostate cancer include F-sodium fluoride, C-acetate, C- or F-choline, F-fluciclovine, and Ga- or F-labeled ligands that bind prostate-specific membrane antigen (PSMA). PSMA ligands appear to be the most sensitive and specific but have not yet received Food and Drug Administration New Drug Application approval for use in the United States. Retrospective and prospective investigations suggest a potential major impact of PET/CT on prostate radiation treatment planning. Prospective trials randomizing patients to routine radiotherapy planning versus PET/CT-aided planning may show meaningful clinical outcomes. Prospective clinical trials evaluating the addition of F-fluciclovine PET/CT for planning of salvage radiotherapy with clinical endpoints are under way. Prospective trials evaluating the clinical impact of PSMA PET/CT on prostate radiation planning are indicated.
放射治疗和根治性前列腺切除术是局部前列腺癌患者的明确治疗选择。根治性前列腺切除术后前列腺特异性抗原水平升高表明前列腺癌复发,这些患者仍可通过挽救性放疗治愈。为了最大限度地提高治愈机会,受照射的体积应完全包含疾病的范围。因此,准确估计疾病的位置对于明确治疗和挽救性治疗的放疗计划都至关重要。目前,用于前列腺癌的一线影像学检查在初始分期和生化复发时对疾病的检测均具有有限的敏感性。将 PET 整合到前列腺癌患者的常规评估中可能会提高分期准确性和放疗计划。18F-氟代脱氧葡萄糖(F-FDG)PET/CT 现在已常规用于几种癌症类型的放射治疗计划。然而,F-FDG PET/CT 对前列腺癌的敏感性较低。在前列腺癌中评估的其他 PET 探针包括 18F-氟化钠、11C-乙酸盐、11C-或 18F-胆碱、18F-氟代鸟氨酸(fluciclovine)以及与前列腺特异性膜抗原(PSMA)结合的 Ga-或 18F-标记配体。PSMA 配体似乎最敏感和特异,但尚未获得美国食品和药物管理局(FDA)批准用于美国的新药申请。回顾性和前瞻性研究表明,PET/CT 对前列腺放射治疗计划可能具有重大影响。将患者随机分配至常规放疗计划与 PET/CT 辅助计划的前瞻性试验可能会显示出有意义的临床结果。正在进行前瞻性临床试验,评估氟代鸟氨酸 PET/CT 用于挽救性放疗计划的临床终点。需要前瞻性临床试验来评估 PSMA PET/CT 对前列腺放射治疗计划的临床影响。