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首页> 外文期刊>Urology >Impact of multiple biopsy cores on predicting final tumor volume in prostate cancer detected by a single microscopic focus of cancer on biopsy.
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Impact of multiple biopsy cores on predicting final tumor volume in prostate cancer detected by a single microscopic focus of cancer on biopsy.

机译:多个活检核心对预测前列腺癌最终肿瘤体积的影响,该结果由对活检的癌症的单个微观焦点检测到。

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OBJECTIVES: To compare the impact that the number of biopsy cores have on final pathologic findings when minimal disease is detected at biopsy. Discordance has been noted between transrectal ultrasound-guided biopsy results and tumor volume even when minimal amounts of tumor are found on biopsy. METHODS: We identified patients who had undergone radical retropubic prostatectomy for a single microscopic focus of adenocarcinoma from a prospectively maintained surgical database. Patients were stratified into two groups: those with six biopsies or less and those with seven or more. The Gleason score, margin status, presence of extracapsular extension, and percentage of tumor volume were compared. RESULTS: A total of 102 patients in our database had a single microscopic focus of adenocarcinoma detected by needle biopsy. Of these patients, 65 underwent six or fewer biopsies and 37 underwent seven or more at transrectal ultrasonography. Of the 37 patients in group 2, 27 (73%) had a final tumor volume of less than 5% compared with 24 (37%) of 65 patients in group 1 (P 0.002). Of the group 2 patients, 15 (75%) with Stage T1c had an estimated tumor volume of less than 5% compared with only 11 (34%) in group 1 (P = 0.01). No statistically significant difference was noted between the two groups for margin status, presence of extracapsular extension, or Gleason score. CONCLUSIONS: A single microscopic focus of cancer obtained after multiple cores predicts for a significantly lower tumor volume on final pathologic examination across clinical stages. In the context of greater tissue sampling, the minimal disease designation may carry more predictive value and be a useful parameter in stratifying patients with Stage T1c and other good-risk factors with regard to surgical outcome.
机译:目的:比较在活检中发现最小的疾病时,活检核心数目对最终病理发现的影响。经直肠超声引导的活检结果与肿瘤体积之间存在不一致,即使在活检中发现少量肿瘤时也是如此。方法:我们从前瞻性维持的手术数据库中鉴定出进行了根治性耻骨后前列腺切除术的单个微观腺癌患者。患者分为两组:活检次数少于或等于6次的患者和活检次数大于或等于7人的患者。比较了格里森评分,边缘状态,囊外延伸的存在以及肿瘤体积的百分比。结果:在我们的数据库中,共有102例患者通过针刺活检发现了单个显微镜下的腺癌。在这些患者中,经直肠超声检查的65例进行了6次或更少的活检,37例进行了7次或更多的活检。第2组的37位患者中,有27位(73%)的最终肿瘤体积小于5%,而第1组的65位患者中有24位(37%)(P = 0.002)。在第2组患者中,有15名(75%)的T1c期肿瘤估计小于5%,而第1组中只有11名(34%)(P = 0.01)。两组之间的边缘状态,囊外延伸的存在或格里森评分没有统计学上的显着差异。结论:多个核心后获得的癌症的单个微观焦点预测,在整个临床阶段的最终病理检查中,肿瘤体积将显着降低。在进行更多组织采样的情况下,最小化的疾病标识可能具有更大的预测价值,并且对于将T1c期和其他具有高风险因素的患者进行手术结局进行分层是有用的参数。

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