Department of Radiology, Emory University Hospital, 1364 Clifton Rd, Atlanta, GA 30322, USA.
Radiology. 2011 Jun;259(3):852-61. doi: 10.1148/radiol.11102023. Epub 2011 Apr 14.
To compare the diagnostic performance of the synthetic amino acid analog radiotracer anti-1-amino-3-fluorine 18-fluorocyclobutane-1-carboxylic acid (anti-3-(18)F-FACBC) with that of indium 111 ((111)In)-capromab pendetide in the detection of recurrent prostate carcinoma.
This prospective study was approved by the institutional review board and complied with HIPAA guidelines. Written informed consent was obtained. Fifty patients (mean age, 68.3 years ± 8.1 [standard deviation]; age range, 50-90 years) were included in the study on the basis of the following criteria: (a) Recurrence of prostate carcinoma was suspected after definitive therapy for localized disease, (b) bone scans were negative, and (c) anti-3-(18)F-FACBC positron emission tomography (PET)/computed tomography (CT) and (111)In-capromab pendetide single photon emission computed tomography (SPECT)/CT were performed within 6 weeks of each other. Studies were evaluated by two experienced interpreters for abnormal uptake suspicious for recurrent disease in the prostate bed and extraprostatic locations. The reference standard was a combination of tissue correlation, imaging, laboratory, and clinical data. Diagnostic performance measures were calculated and tests of the statistical significance of differences determined by using the McNemar χ(2) test as well as approximate tests based on the difference between two proportions.
For disease detection in the prostate bed, anti-3-(18)F-FACBC had a sensitivity of 89% (32 of 36 patients; 95% confidence interval [CI]: 74%, 97%), specificity of 67% (eight of 12 patients; 95% CI: 35%, 90%), and accuracy of 83% (40 of 48 patients; 95% CI: 70%, 93%). (111)In-capromab pendetide had a sensitivity of 69% (25 of 36 patients; 95% CI: 52%, 84%), specificity of 58% (seven of 12 patients; 95% CI: 28%, 85%), and accuracy of 67% (32 of 48 patients; 95% CI: 52%, 80%). In the detection of extraprostatic recurrence, anti-3-(18)F-FACBC had a sensitivity of 100% (10 of 10 patients; 95% CI: 69%, 100%), specificity of 100% (seven of seven patients; 95% CI: 59%, 100%), and accuracy of 100% (17 of 17 patients; 95% CI: 80%, 100%). (111)In-capromab pendetide had a sensitivity of 10% (one of 10 patients; 95% CI: 0%, 45%), specificity of 100% (seven of seven patients; 95% CI: 59%, 100%), and accuracy of 47% (eight of 17 patients; 95% CI: 23%, 72%).
anti-3-(18)F-FACBC PET/CT was more sensitive than (111)In-capromab pendetide SPECT/CT in the detection of recurrent prostate carcinoma and is highly accurate in the differentiation of prostatic from extraprostatic disease.
http://radiology.rsna.org/lookup/suppl/doi:10.1148/radiol.11102023/-/DC1.
比较合成氨基酸类似物放射性示踪剂抗-1-氨基-3-氟-18-氟环丁烷-1-羧酸(抗-3-(18)F-FACBC)与铟 111(111)In)-卡普罗单抗肽在检测复发性前列腺癌中的诊断性能。
本前瞻性研究获得机构审查委员会批准,并符合 HIPAA 指南。获得书面知情同意。根据以下标准纳入 50 例患者(平均年龄,68.3 岁±8.1[标准差];年龄范围,50-90 岁):(a)局限性疾病根治性治疗后怀疑前列腺癌复发,(b)骨扫描阴性,(c)抗-3-(18)F-FACBC 正电子发射断层扫描(PET)/计算机断层扫描(CT)和(111)In-卡普罗单抗肽单光子发射计算机断层扫描(SPECT)/CT 在 6 周内进行。两名有经验的解释者对前列腺床和前列腺外部位可疑复发性疾病的摄取异常进行了评估。参考标准是组织相关性、影像学、实验室和临床数据的综合。通过使用 McNemar χ(2)检验以及基于两个比例差异的近似检验来计算诊断性能指标,并确定差异的统计学显著性检验。
对于前列腺床疾病的检测,抗-3-(18)F-FACBC 的敏感性为 89%(36 例患者中的 32 例;95%置信区间[CI]:74%,97%),特异性为 67%(12 例患者中的 8 例;95%CI:35%,90%),准确性为 83%(48 例患者中的 40 例;95%CI:70%,93%)。(111)In-卡普罗单抗肽的敏感性为 69%(36 例患者中的 25 例;95%CI:52%,84%),特异性为 58%(12 例患者中的 7 例;95%CI:28%,85%),准确性为 67%(48 例患者中的 32 例;95%CI:52%,80%)。在检测前列腺外复发方面,抗-3-(18)F-FACBC 的敏感性为 100%(10 例患者中的 10 例;95%CI:69%,100%),特异性为 100%(7 例患者中的 7 例;95%CI:59%,100%),准确性为 100%(17 例患者中的 17 例;95%CI:80%,100%)。(111)In-卡普罗单抗肽的敏感性为 10%(10 例患者中的 1 例;95%CI:0%,45%),特异性为 100%(7 例患者中的 7 例;95%CI:59%,100%),准确性为 47%(17 例患者中的 8 例;95%CI:23%,72%)。
抗-3-(18)F-FACBC PET/CT 比(111)In-卡普罗单抗肽 SPECT/CT 更敏感,可检测复发性前列腺癌,并且在区分前列腺内和前列腺外疾病方面具有高度准确性。
http://radiology.rsna.org/lookup/suppl/doi:10.1148/radiol.11102023/-/DC1.