Apolo Andrea B, Pandit-Taskar Neeta, Morris Michael J
Genitourinary Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
J Nucl Med. 2008 Dec;49(12):2031-41. doi: 10.2967/jnumed.108.050658. Epub 2008 Nov 7.
There are presently no accurate methods of imaging prostate cancer metastases to bone. An unprecedented number of novel imaging agents, based on the biology of the disease, are now available for testing. We reviewed contemporary molecular imaging modalities that have been tested in humans with metastatic prostate cancer, with consideration of the studies' adherence to current prostate cancer clinical trial designs. Articles from the years 2002 to 2008 on PET using (18)F-FDG, (11)C-choline, (18)F-choline, (18)F-flouride, (11)C-acetate, (11)C-methionine, and (18)F-fluoro-5alpha-dihydrotestosterone in patients with metastatic prostate cancer were reviewed. Although these studies are encouraging, most focus on the rising population with prostate-specific antigen, and many involve small numbers of patients and do not adhere to consensus criteria for clinical trial designs in prostate cancer. Hence, although many promising agents are available for testing, such studies would benefit from closer collaboration between those in the fields of medical oncology and nuclear medicine.
目前尚无准确的成像方法用于检测前列腺癌骨转移。基于该疾病生物学特性的新型成像剂数量空前,现已可供测试。我们回顾了已在转移性前列腺癌患者中进行测试的当代分子成像模式,并考量了这些研究对当前前列腺癌临床试验设计的遵循情况。对2002年至2008年间有关使用(18)F-FDG、(11)C-胆碱、(18)F-胆碱、(18)F-氟化物、(11)C-醋酸盐、(11)C-蛋氨酸以及(18)F-氟-5α-二氢睾酮进行PET检查的转移性前列腺癌患者的文章进行了回顾。尽管这些研究令人鼓舞,但大多数关注的是前列腺特异性抗原水平升高的人群,且许多研究纳入的患者数量较少,未遵循前列腺癌临床试验设计的共识标准。因此,尽管有许多有前景的成像剂可供测试,但此类研究若能在医学肿瘤学和核医学领域之间加强合作将更有益处。