18F-PSMA-1007 PET/CT在预测国际泌尿病理协会前列腺癌病理分级中的应用价值

Application value of 18F-PSMA-1007 PET/CT in predicting the International Society of Urological Pathology grading in prostate cancer

  • 摘要:
    目的 探讨18F-前列腺特异性膜抗原(PSMA)-1007 PET/CT在预测国际泌尿病理协会(ISUP)前列腺癌病理分级中的价值。
    方法 回顾性分析2021年1月至2023年8月于山西医科大学第一医院行18F-PSMA-1007 PET/CT检查且经组织病理学检查确诊的70例前列腺癌患者的临床和病理资料,患者年龄(70.7±8.4)岁。按照ISUP分级标准分为低级别前列腺癌(ISUP 1~3级)和高级别前列腺癌(ISUP 4~5级)2组。对2组患者的临床病理资料和最大标准化摄取值(SUVmax)、平均标准化摄取值(SUVmean)、标准化摄取值峰值(SUVpeak)的差异进行分析比较。计量资料的2组间比较采用独立样本t检验或Mann-Whitney U检验;计数资料的2组间比较采用卡方检验。将差异有统计学意义的指标纳入二元Logistic回归分析,建立Logistic预测模型;采用受试者工作特征(ROC)曲线评价模型的诊断效能,采用Delong检验比较不同指标或模型的曲线下面积(AUC)的差异。
    结果 70例前列腺癌患者中,低级别前列腺癌组26例、高级别前列腺癌组44例。2组的总前列腺特异性抗原水平28.13(9.35,88.86) ng/ml 对97.97(46.72,312.47) ng/ml)、SUVmax7.81(5.13,19.06)对30.93(18.01,50.12)、SUVmean3.66(2.50,6.74)对13.43(7.75,21.81)、SUVpeak6.43(3.33,11.20)对16.20(11.14,31.07)的差异均有统计学意义(Z=3.13~4.70,均P<0.05)。二元Logistic回归分析结果显示,SUVmaxOR=1.08,95%CI:1.01~1.11,P=0.012)、SUVmeanOR=1.06,95%CI:1.02~1.14,P=0.013)均为ISUP前列腺癌病理分级的独立预测因子。ROC曲线分析结果显示,SUVmax、SUVmean和Logistic预测模型诊断高级别前列腺癌的AUC分别为0.71、0.69和0.86,灵敏度分别为74.0%、86.0%和83.0%,特异度分别为68.9%、56.2%和79.3%。Logistic预测模型与SUVmax、SUVmean的AUC的两两比较的差异均有统计学意义(Z=1.98、2.23,均P<0.05)。SUVmax与SUVmean的AUC之间的差异无统计学意义(Z=0.58,P=0.560)。
    结论 基于18F-PSMA-1007 PET/CT的SUVmax和SUVmean的Logistic预测模型对诊断高级别前列腺癌具有较高的价值,与单个参数相比,Logistic预测模型在预测ISUP前列腺癌病理分级中具有较高的价值。

     

    Abstract:
    Objective  To investigate the value of 18F-prostate specific membrane antigen (PSMA)-1007 PET/CT in predicting the International Society of Urological Pathology (ISUP) grading in prostate cancer.
    Methods  A retrospective analysis was conducted on the clinical and pathological data of 70 patients with prostate cancer who underwent 18F-PSMA-1007 PET/CT examination and were histopathologically confirmed in the First Hospital of Shanxi Medical University from January 2021 to August 2023. The mean age of the cohort was 70.7±8.4 years. In accordance with the ISUP grading system, the patients were classified into two groups: low-grade prostate cancer (ISUP 1–3) and high-grade prostate cancer (ISUP 4–5). The differences in clinicopathological data, maximum standardized uptake value (SUVmax), mean standardized uptake value (SUVmean), and peak standardized uptake value (SUVpeak) between the two groups were analyzed and compared. The comparison between two groups of quantitative data was conducted using independent sample t-test or Mann-Whitney U test; The comparison between two groups of counting data was conducted using chi square test. The statistically significant indicators were incorporated into a binary Logistic regression analysis to develop a Logistic prediction model. The diagnostic efficacy of the model was assessed using the receiver operating characteristic (ROC) curve, and the differences in the area under the curve (AUC) between the various indicators and models were evaluated through the Delong test.
    Results  Among the 70 prostate cancer patients, 26 cases belonged to the low-grade prostate cancer group and 44 cases to the high-grade prostate cancer group. The two groups exhibited statistically significant differences (Z=3.13–4.70, all P<0.05) in total prostate-specific antigen (28.13 (9.35, 88.86) ng/ml vs. 97.97 (46.72, 312.47) ng/ml), SUVmax (7.81 (5.13, 19.06) vs. 30.93 (18.01, 50.12)), SUVmean (3.66 (2.50, 6.74) vs. 13.43 (7.75, 21.81)), and SUVpeak (6.43 (3.33, 11.20) vs. 16.20 (11.14, 31.07)). The results of the binary Logistic regression analysis indicated that SUVmax (OR=1.08, 95%CI: 1.01–1.11, P=0.012) and SUVmean (OR=1.06, 95%CI: 1.02–1.14, P=0.013) were independent predictors of ISUP grading in prostate cancer. The results of the ROC curve analysis demonstrated that the AUCs for diagnosing high-grade prostate cancer using SUVmax, SUVmean, and the Logistic prediction model alone were 0.71, 0.69, and 0.86, respectively. The sensitivity values were 74.0%, 86.0%, and 83.0%, respectively, while the specificity values were 68.9%, 56.2%, and 79.3%, respectively. Pairwise comparisons of AUCs between the Logistic prediction model and SUVmax and between the Logistic prediction model and SUVmean revealed statistically significant differences (Z=1.98, 2.23; both P<0.05). By contrast, no statistically significant difference in AUCs was observed between SUVmax and SUVmean (Z=0.58, P=0.560).
    Conclusions  The Logistic prediction model based on SUVmax and SUVmean from 18F-PSMA-1007 PET/CT has high diagnostic value for high-grade prostate cancer. Compared with individual parameters, this model provides more favorable value for predicting ISUP grading in prostate cancer.

     

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