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前列腺活检时,对于癌的微小病灶是否应给予Gleason评分?

Should a Gleason score be assigned to a minute focus of carcinoma on prostate biopsy?

作者信息

Rubin M A, Dunn R, Kambham N, Misick C P, O'Toole K M

机构信息

Department of Pathology of the University of Michigan, Ann Arbor 48109-0054, USA.

出版信息

Am J Surg Pathol. 2000 Dec;24(12):1634-40. doi: 10.1097/00000478-200012000-00007.

Abstract

The grading system for prostate carcinoma devised by Gleason is a strong prognostic indicator. The primary and secondary patterns are combined to give a tumor score, referred to as Gleason score or sum. Gleason scores on biopsy correlate with the prostatectomy Gleason scores, and in combination with pretreatment serum prostate-specific antigen and digital rectal examination results, predict tumor stage and lymph node status. However, when only a minute focus of tumor is present on biopsy, the Gleason score is assigned by doubling the Gleason pattern. The goal of this study was to determine if a Gleason score assigned to a minimal focus of adenocarcinoma had predictive value. Paired biopsies and prostatectomy specimens from 963 cases of men with clinically localized prostate cancer were examined. Minimal tumor on biopsy was defined as less than 1 mm or 5% involvement of one biopsy core; excluded from this definition were biopsies where two Gleason patterns could be identified and/or tumor was seen on more than one biopsy core. Terms often used to describe these lesions include "single minute focus of carcinoma" or "adenocarcinoma, too small to give a Gleason grade." One hundred five cases (10.9%) met the above criteria for minimal carcinoma. The correlation of Gleason scores between biopsies and prostatectomy specimens overall was good with exact agreement for 57% of cases and a difference of +/-1 unit in 92% of cases. The correlation for the minimal tumors on biopsy and prostatectomy was slightly worse with exact agreement in 52.4% (55 of 105) and a difference of +/-1 unit in 87.6% (92 of 105). The majority of minimal tumors (83.8% or 88 of 105) were assigned a Gleason score of 6. A total of 31.8% of these 88 cases were upgraded and 5.7% were downgraded. Multivariate analysis on all cases looking for predictors of tumor stage found biopsy Gleason score, perineural invasion, pretreatment prostatic-specific antigen, and digital rectal examination all predicted higher tumor stage with odds ratios of 1.86 (95% confidence interval [CI], 1.53-2.27; p = 0.0001), 2.06 (95% CI, 1.43-2.95; p = 0.0001), 1.08 (95% CI, 1.05-1.11; p = 0.0001), and 1.41 (95% CI, 1.04-1.91; p = 0.0289), respectively. In a model restricted to the 105 cases with minimal carcinoma, pretreatment prostatic-specific antigen was the only independent predictor of higher tumor stage with an odds ratio of 1.15 (95% CI, 1.01-1.31; p = 0.0380); Gleason score was not found to significantly predict higher tumor stage (odds ratio, 1.156; p = 0.6680). The results of this study confirm that biopsy Gleason score in most cases predicts prostatectomy Gleason score and tumor stage. However, for cases with minimal tumor on biopsy, the assigned Gleason score did not predict tumor stage. To properly convey this uncertainty to clinicians, a cautionary note should accompany Gleason scores derived from a minimal focus of carcinoma.

摘要

由格里森设计的前列腺癌分级系统是一个强有力的预后指标。主要和次要模式相结合得出一个肿瘤评分,称为格里森评分或总分。活检时的格里森评分与前列腺切除术后的格里森评分相关,并且与治疗前血清前列腺特异性抗原和直肠指检结果相结合,可预测肿瘤分期和淋巴结状态。然而,当活检时仅存在微小肿瘤灶时,格里森评分通过将格里森模式加倍来确定。本研究的目的是确定赋予腺癌微小病灶的格里森评分是否具有预测价值。对963例临床局限性前列腺癌男性患者的配对活检和前列腺切除标本进行了检查。活检时的微小肿瘤定义为小于1毫米或一个活检核心的累及率小于5%;不符合此定义的活检包括可识别两种格里森模式和/或在多个活检核心上可见肿瘤的活检。常用于描述这些病变的术语包括“癌的单个微小病灶”或“腺癌,太小以至于无法给出格里森分级”。105例(10.9%)符合上述微小癌的标准。活检和前列腺切除标本之间的格里森评分总体相关性良好,57%的病例完全一致,92%的病例相差±1个单位。活检和前列腺切除时微小肿瘤的相关性稍差,52.4%(105例中的55例)完全一致,87.6%(105例中的92例)相差±1个单位。大多数微小肿瘤(105例中的88例,83.8%)被赋予格里森评分为6分。这88例病例中共有31.8%的病例升级,5.7%的病例降级。对所有病例进行多因素分析以寻找肿瘤分期的预测因素,发现活检格里森评分、神经周围侵犯、治疗前前列腺特异性抗原和直肠指检均预测更高的肿瘤分期,优势比分别为1.86(95%置信区间[CI],1.53 - 2.27;p = 0.0001)、2.06(95%CI,1.43 - 2.95;p = 0.0001)、1.08(95%CI,1.05 - 1.11;p = 0.0001)和1.41(95%CI,1.04 - 1.91;p = 0.0289)。在一个仅限于105例微小癌病例的模型中,治疗前前列腺特异性抗原是更高肿瘤分期的唯一独立预测因素,优势比为1.15(95%CI,1.01 - 1.31;p = 0.0380);未发现格里森评分能显著预测更高的肿瘤分期(优势比,1.156;p = 0.6680)。本研究结果证实,在大多数情况下,活检格里森评分可预测前列腺切除术后的格里森评分和肿瘤分期。然而,对于活检时肿瘤微小的病例,所赋予的格里森评分并不能预测肿瘤分期。为了向临床医生正确传达这种不确定性,对于源自癌微小病灶的格里森评分应附带警示说明。

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