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微血管密度在预测病理分期为T3期前列腺腺癌复发中的作用。

Role of microvessel density in predicting recurrence in pathologic Stage T3 prostatic adenocarcinoma.

作者信息

Gettman M T, Pacelli A, Slezak J, Bergstralh E J, Blute M, Zincke H, Bostwick D G

机构信息

Department of Urology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Urology. 1999 Sep;54(3):479-85. doi: 10.1016/s0090-4295(99)00202-2.

Abstract

OBJECTIVES

Extraprostatic extension of prostatic adenocarcinoma (pathologic Stage T3) increases the risk of recurrence after radical prostatectomy compared with organ-confined prostate cancer. Use of microvessel density in predicting cancer recurrence in Stage pT3 cancer is poorly understood. We evaluated known predictors of recurrence, including Gleason grade, preoperative serum prostate-specific antigen (PSA), DNA ploidy, seminal vesicle involvement, and surgical margin status in comparison with optimized microvessel density (OMVD) and area-weighted microvessel density (AWMVD) in patients with Stage pT3 prostate cancer.

METHODS

Between 1987 and 1989, 290 previously untreated patients underwent radical prostatectomy and were found to have pathologic Stage T3 adenocarcinoma. No patient received adjuvant therapy. Embedded prostatectomy specimens from 211 patients with sufficient tissue for immunohistochemical staining with factor VIII-related antigen were studied by computer-assisted digital image analysis for OMVD and AWMVD. The correlation of Gleason grade, preoperative PSA, DNA ploidy, seminal vesicle involvement, surgical margin positivity, OMVD, and AWMVD with clinical or biochemical failure was assessed using the Cox proportional hazards model. Biochemical failure was defined as a postoperative increase in PSA greater than 0.2 ng/mL, and clinical failure was defined as a positive biopsy or metastasis on bone scan.

RESULTS

The mean follow-up +/- SD for all patients was 7.1 +/- 1.8 years, with 43 deaths (9 due to prostate cancer) and 124 cases of clinical and/or biochemical recurrence. The mean OMVD was 65.0 +/- 17.3, and the mean AWMVD was 8.2 +/- 5.3. OMVD and AWMVD were not predictors of cancer recurrence or significantly associated with DNA ploidy or preoperative PSA. AWMVD was associated with Gleason grade (P = 0.003). The estimated relative risk (adjusted for other cancer variables) of clinical and biochemical recurrence associated with a change in OMVD from the 25th percentile (53.5) to the 75th percentile (75.4) was 1.14 (95% confidence interval 0.92 to 1.42). The estimated relative risk (adjusted) of clinical and biochemical recurrence associated with a change in AWMVD from the 25th percentile (4.8) to the 75th percentile (10.4) was 1.17 (95% confidence interval 0.97 to 1.42). Gleason grade, preoperative PSA, DNA ploidy, and seminal vesicle involvement were predictors of clinical and/or biochemical recurrence in univariate and multivariate analyses.

CONCLUSIONS

Microvessel density, assessed by OMVD and AWMVD, did not predict recurrence in patients with pathologic Stage T3 adenocarcinoma of the prostate (TNM Stage T3N0M0). DNA ploidy, Gleason grade, preoperative PSA, and seminal vesicle involvement remained the best predictors of clinical and/or biochemical recurrence in this group of patients.

摘要

目的

与局限性前列腺癌相比,前列腺腺癌的前列腺外侵犯(病理分期T3)会增加根治性前列腺切除术后复发的风险。微血管密度在预测pT3期癌症复发方面的作用尚不清楚。我们评估了已知的复发预测因素,包括 Gleason 分级、术前血清前列腺特异性抗原(PSA)、DNA倍体、精囊受累情况和手术切缘状态,并与pT3期前列腺癌患者的优化微血管密度(OMVD)和面积加权微血管密度(AWMVD)进行比较。

方法

1987年至1989年间,290例未经治疗的患者接受了根治性前列腺切除术,病理检查发现为T3期腺癌。所有患者均未接受辅助治疗。对211例有足够组织用于因子VIII相关抗原免疫组化染色的前列腺切除标本进行计算机辅助数字图像分析,以测定OMVD和AWMVD。使用Cox比例风险模型评估Gleason分级、术前PSA、DNA倍体、精囊受累情况、手术切缘阳性、OMVD和AWMVD与临床或生化失败的相关性。生化失败定义为术后PSA升高超过0.2 ng/mL,临床失败定义为活检阳性或骨扫描发现转移。

结果

所有患者的平均随访时间±标准差为7.1±1.8年,43例死亡(9例死于前列腺癌),124例发生临床和/或生化复发。平均OMVD为65.0±17.3,平均AWMVD为8.2±5.3。OMVD和AWMVD不是癌症复发的预测因素,与DNA倍体或术前PSA无显著相关性。AWMVD与Gleason分级相关(P = 0.003)。与OMVD从第25百分位数(53.5)变化到第75百分位数(75.4)相关的临床和生化复发的估计相对风险(校正其他癌症变量后)为1.14(95%置信区间0.92至1.42)。与AWMVD从第25百分位数(4.8)变化到第75百分位数(10.4)相关的临床和生化复发的估计相对风险(校正后)为1.17(95%置信区间0.97至1.42)。在单因素和多因素分析中,Gleason分级、术前PSA、DNA倍体和精囊受累情况是临床和/或生化复发的预测因素。

结论

通过OMVD和AWMVD评估的微血管密度不能预测前列腺病理分期为T3腺癌(TNM分期T3N0M0)患者的复发。DNA倍体、Gleason分级、术前PSA和精囊受累情况仍然是该组患者临床和/或生化复发的最佳预测因素。

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