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膀胱癌病理分期面临的挑战:鉴于近期有关膀胱组织解剖学差异的研究和观察结果,对评估病理分期新方法的建议

Challenges in Pathologic Staging of Bladder Cancer: Proposals for Fresh Approaches of Assessing Pathologic Stage in Light of Recent Studies and Observations Pertaining to Bladder Histoanatomic Variances.

作者信息

Paner Gladell P, Montironi Rodolfo, Amin Mahul B

机构信息

*Department of Pathology and Surgery, Section of Urology, University of Chicago, Chicago, IL ‡Department of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, Memphis, TN †Section of Pathological Anatomy, School of Medicine, Polytechnic University of the Marche Region, Ancona, Italy.

出版信息

Adv Anat Pathol. 2017 May;24(3):113-127. doi: 10.1097/PAP.0000000000000152.

DOI:10.1097/PAP.0000000000000152
PMID:28398951
Abstract

The paradigm of pathologic stage (pT) categorization in bladder cancer remains the depth of invasion into the different histologic layers of the bladder wall. However, the approaches to assigning pT stage category toward an enhanced outcome stratification have been marked by challenges and innovations, due in part to our growing appreciation of the surprisingly perplexing bladder histoanatomy. Upstaging of pT1 tumors after radical cystectomy is substantial and underscores the potential value of pT1 substaging in transurethral resection (TUR) specimens. The 2017 American Joint Committee on Cancer tumor-node-metastasis system recommends pT1 substaging but recognizes the need to optimize the approach. Over the years, the cut-off for microinvasion has been significantly lowered to 0.5 mm and is now a promising scheme for pT1 (micrometric) substaging. Unlike the micrometric approach, histoanatomic substaging using muscularis mucosae (MM) and vascular plexus as landmarks is less feasible in TUR specimens and inconsistent in stratifying the outcome of pT1 tumors. The lamina propria possesses inherent variations in depth, MM, and vascular plexus dispositions that should be factored in future pT1 substaging proposals. Histoanatomic variations among the bladder regions also occur, and studies suggest that trigone and bladder neck cancers may have more adverse outcomes. The muscularis propria (MP), besides being the essential histologic landmark for assigning pT2 stage category, is also considered a surrogate for the adequacy of TUR, furthering the importance of identifying its presence in TUR specimens. MP, however, may be mimicked by hyperplastic or isolated MP-like MM muscle bundles in the lamina propria with overstaging implications, and caution should be exercised in distinguishing these 2 muscle types morphologically and immunohistochemically. Presence of additional superficial MP unique from the detrusor muscle proper may also complicate staging at the trigone and ureter insertion sites. With regard to the depth of MP invasion, large and multicenter studies have reaffirmed the prognostic significance of pT2a/b subcategories. It is revealed that there are at least 3 ways used to demarcate the irregular MP to perivesical soft tissue junction, and use of a common criterion indicates improvement in pT2b/pT3a staging reproducibility. Although studies have shown significantly poorer outcome in pT3b compared with pT3a tumors, this designation has a substantial reliance on the prosector's gross assessment of perivesical soft tissue invasion which if performed incorrectly may lead to staging inaccuracy of pT3 tumors. The 8th edition of the American Joint Committee on Cancer has updated the staging schema for bladder cancers with concomitant prostatic stromal invasion and cancers within bladder diverticula. Because of 2 possible pT designations, prostatic stromal invasion in TUR specimens should not be automatically staged as either pT4a or pT2 (urethral). Recent data support that bladder cancer invading into the seminal vesicle has comparable outcome to pT4b tumors. Interestingly, several studies in pT4a tumors, which are staged based on sex-specific organs, have shown poorer outcome in females than males after radical cystectomy, and while there are possibly several reasons, they may also include anatomic factors. Despite the progress has been made, work remains to be done to inform future bladder cancer pT category definitions and their reproducibility in application and prognostication.

摘要

膀胱癌病理分期(pT)分类的范式仍然是肿瘤浸润膀胱壁不同组织学层次的深度。然而,由于我们越来越认识到膀胱组织解剖结构令人惊讶地复杂,在确定pT分期类别以实现更好的预后分层方面,方法既面临挑战,也有创新。根治性膀胱切除术后pT1肿瘤的分期上调情况很显著,这凸显了pT1亚分期在经尿道切除术(TUR)标本中的潜在价值。2017年美国癌症联合委员会肿瘤-淋巴结-转移系统推荐进行pT1亚分期,但也认识到需要优化该方法。多年来,微浸润的临界值已大幅降至0.5毫米,目前这是一种很有前景的pT1(微尺寸)亚分期方案。与微尺寸方法不同,以黏膜肌层(MM)和血管丛为标志的组织解剖亚分期在TUR标本中不太可行,且在对pT1肿瘤的预后进行分层时也不一致。固有层在深度、MM和血管丛分布方面存在内在差异,在未来的pT1亚分期方案中应予以考虑。膀胱各区域之间也存在组织解剖学差异,研究表明三角区和膀胱颈部癌可能有更差的预后。固有肌层(MP)除了是确定pT2分期类别的重要组织学标志外,还被视为TUR充分性的替代指标,这进一步凸显了在TUR标本中识别其存在的重要性。然而,固有层中增生性或孤立的MP样MM肌束可能会模仿MP,导致分期过高,在通过形态学和免疫组织化学区分这两种肌肉类型时应谨慎。三角区和输尿管插入部位存在与逼尿肌本身不同的额外浅表MP,这也可能使分期复杂化。关于MP浸润深度,大型多中心研究再次证实了pT2a/b亚类别的预后意义。研究表明,至少有3种方法用于划分不规则MP与膀胱周围软组织的交界处,采用共同标准可提高pT2b/pT3a分期的可重复性。尽管研究表明pT3b肿瘤的预后明显比pT3a肿瘤差,但该分类很大程度上依赖于病理学家对膀胱周围软组织浸润的大体评估,如果评估错误可能导致pT3肿瘤分期不准确。美国癌症联合委员会第8版更新了伴有前列腺基质浸润的膀胱癌以及膀胱憩室内癌的分期方案。由于可能有两种pT分类,TUR标本中的前列腺基质浸润不应自动分期为pT4a或pT2(尿道)。最近的数据支持,侵犯精囊的膀胱癌与pT4b肿瘤的预后相当。有趣的是,几项针对基于性别特异性器官进行分期的pT4a肿瘤的研究表明,根治性膀胱切除术后女性的预后比男性差,虽然可能有多种原因,但也可能包括解剖学因素。尽管已经取得了进展,但仍有工作要做,以完善未来膀胱癌pT分类的定义及其在应用和预后判断中的可重复性。

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