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病理分期不改变经计算机断层扫描确定为T1期的肾脏病变的预后。

Pathological stage does not alter the prognosis for renal lesions determined to be stage T1 by computerized tomography.

作者信息

Roberts William W, Bhayani Sam B, Allaf Mohamad E, Chan Theresa Y, Kavoussi Louis R, Jarrett Thomas W

机构信息

Department of Urology, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

J Urol. 2005 Mar;173(3):713-5. doi: 10.1097/01.ju.0000153638.15018.58.

Abstract

PURPOSE

Pathological stage has been the most widely used prognosticator for evaluating surgically managed cases of renal cell carcinoma. Minimally invasive surgical approaches are being increasingly used to treat small masses for which traditionally pathological information is lacking (morcellation) or absent (radio frequency ablation or cryoablation). Preoperative cross-sectional imaging by computerized tomography (CT) or magnetic resonance imaging has been used to stage renal tumors clinically but it can lead to variances with traditional pathological staging systems, particularly with respect to microscopic invasion beyond the renal capsule. In this study we assessed whether radiographically staged clinical T1 lesions that were pathological T1 behave differently than those that were clinical stage T1 and up staged to pT3a.

MATERIALS AND METHODS

The records of 296 patients who underwent surgical treatment for renal cell carcinoma at The Johns Hopkins Hospital between 1990 and 1999 were retrospectively reviewed. All patients had undergone preoperative CT or magnetic resonance imaging, which was used to assign a clinical stage and size (largest diameter) to each tumor in accordance with the 1997 TNM staging system. Following surgical resection pathological stage, size and tumor grade were determined. Only the 186 patients with clinical T1 tumors were included in this analysis.

RESULTS

Of the 186 patients who were clinically found to have T1 lesions 125 (67%) had pathological T1 and 57 (31%) had pathological T3a lesions. All surgical margins and lymph nodes were negative at surgical resection. Mean tumor size +/- SD was 3.9 +/- 1.5 cm for pT1 lesions and 3.8 +/- 1.5 cm for pT3a lesions. When comparing these pathological groups using Kaplan-Meier analysis, 5-year recurrence-free survival was not statistically different in patients with pT1 and pT3a lesions (90.6 and 97.5%, respectively).

CONCLUSIONS

Patients in whom the initial classification of T1 renal cell carcinoma by CT was up graded to T3a on pathological analysis (invasion of fat within Gerota's fascia) showed the same recurrence-free survival rate as patients with pathologically confirmed T1 lesions. Thus, smaller tumors (less than 7 cm) that are up graded to T3a based on capsule invasion behave much like T1 tumors and exact pathological T staging does not appear to impact overall survival.

摘要

目的

病理分期一直是评估接受手术治疗的肾细胞癌病例最广泛使用的预后指标。微创外科手术方法越来越多地用于治疗传统上缺乏病理信息(碎块化)或不存在病理信息(射频消融或冷冻消融)的小肿块。术前通过计算机断层扫描(CT)或磁共振成像进行的横断面成像已用于对肾肿瘤进行临床分期,但它可能导致与传统病理分期系统存在差异,特别是在超出肾包膜的微观浸润方面。在本研究中,我们评估了影像学分期为临床T1且病理为T1的病变与临床分期为T1且病理分期上调至pT3a的病变在行为上是否不同。

材料与方法

回顾性分析了1990年至1999年间在约翰霍普金斯医院接受肾细胞癌手术治疗的296例患者的记录。所有患者均接受了术前CT或磁共振成像,根据1997年TNM分期系统为每个肿瘤确定临床分期和大小(最大直径)。手术切除后确定病理分期、大小和肿瘤分级。本分析仅纳入了186例临床T1肿瘤患者。

结果

在临床发现有T1病变的186例患者中,125例(67%)病理为T1,57例(31%)病理为T3a病变。手术切除时所有手术切缘和淋巴结均为阴性。pT1病变的平均肿瘤大小±标准差为3.9±1.5 cm,pT3a病变为3.8±1.5 cm。使用Kaplan-Meier分析比较这些病理组时,pT1和pT3a病变患者的5年无复发生存率无统计学差异(分别为90.6%和97.5%)。

结论

通过CT最初分类为T1的肾细胞癌患者,经病理分析上调至T3a(肾周筋膜内脂肪浸润),其无复发生存率与病理证实为T1病变的患者相同。因此,基于包膜侵犯上调至T3a的较小肿瘤(小于7 cm)的行为与T1肿瘤非常相似,确切的病理T分期似乎不影响总体生存。

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