The association between variant histology and prognostic, histomorphological and clinical aspects of bladder urothelial carcinoma

IF 1.5 4区 医学 Q3 PATHOLOGY Annals of Diagnostic Pathology Pub Date : 2024-08-22 DOI:10.1016/j.anndiagpath.2024.152373
Pelin Akbas , Sibel Bektas , Gokhan Yazici
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Abstract

This study underscores the imperative consideration of histological subtypes and divergent differentiation in accurately estimating bladder urothelial carcinoma prognosis and guiding treatment decisions. A comparative analysis was conducted, examining clinical, histological, and prognostic factors between conventional urothelial carcinoma and urothelial carcinoma with variant histology in a clinical sample. A retrospective analysis of slides and other clinicopathologic data was conducted these cases, with an emphasis on key diagnostic elements. We examined 829 cases of urothelial carcinoma of the bladder, comprising of 744 transurethral resection (TUR) and 85 radical cystectomy (RS) specimens, an analysis that showed that 80.5 % (667 cases) were conventional urothelial carcinoma (CUC) and that 19.5 % (162 cases) exhibited variant histology (hereafter “urothelial carcinoma with subtype histology” [UCSH]). TNM classifications for the RS cases were as follows: 2 cases were stage group 0a, 11 stage group 1, 16 stage group 2, 45 stage group 3a, 2 stage group 3b, 1 stage group 4a, and 8 stage group 4b. Only 2 of the RS cases were found to be non-invasive. Among 744 TUR specimens, 387 were found to have a non-invasive tumor whereas 357 had invasive tumors. The most prevalent subtype in the UCSH group was urothelial carcinoma with squamous differentiation, accounting for 54.3 % (88 cases). Notably, 8.02 % (13 cases) exhibited more than one histological subtype. Papillary configuration, histological grade, lamina propria, muscularis mucosa and serosa invasion, lymphovascular invasion, presence of urothelial carcinoma in situ, and overall survival significantly differed between the UCSH and CUC groups (p < 0.05). However, mean age, gender, tumor size, lymphocytic response, disease-free survival, and survival status did not differ significantly (p > 0.05). Among the UCSH group, lower levels of papillary configuration, higher histological grade, higher degree of lamina propria, muscularis mucosa and serosa invasion, and the presence of carcinoma in situ corresponded to higher percentage of histological subtype morphology (p < 0.05). No significant difference in survival status was observed between the groups with and without subtype histology (p = 0.083). This study found that clinical and histopathological prognostic factors associated with a more aggressive disease were linked to the presence and percentage of histological subtypes. Recognizing histological subtype is crucial for treatment decisions and prognosis prediction in urothelial carcinoma cases with these subtypes.

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膀胱尿路上皮癌变异组织学与预后、组织形态学和临床方面的关系
这项研究强调,在准确估计膀胱尿路上皮癌预后和指导治疗决策时,必须考虑组织学亚型和分化差异。本研究进行了一项比较分析,研究了临床样本中传统尿路上皮癌和组织学变异尿路上皮癌的临床、组织学和预后因素。我们对这些病例的切片和其他临床病理数据进行了回顾性分析,重点关注关键诊断要素。我们检查了 829 例膀胱尿路上皮癌病例,其中包括 744 例经尿道切除术(TUR)和 85 例根治性膀胱切除术(RS)标本,分析结果显示,80.5%(667 例)为传统尿路上皮癌(CUC),19.5%(162 例)呈现变异组织学(以下简称 "亚型组织学尿路上皮癌"[UCSH])。RS病例的TNM分类如下:2 例为 0a 期,11 例为 1 期,16 例为 2 期,45 例为 3a 期,2 例为 3b 期,1 例为 4a 期,8 例为 4b 期。在 RS 病例中,只有 2 例为非侵入性病例。在 744 例 TUR 标本中,387 例为非浸润性肿瘤,357 例为浸润性肿瘤。在 UCSH 组中,最常见的亚型是鳞状分化的尿路上皮癌,占 54.3%(88 例)。值得注意的是,8.02%(13 例)的患者表现出一种以上的组织学亚型。UCSH 组和 CUC 组在乳头构造、组织学分级、固有层、粘膜肌层和浆膜浸润、淋巴管浸润、是否存在尿路原位癌以及总生存率方面存在显著差异(p <0.05)。但是,平均年龄、性别、肿瘤大小、淋巴细胞反应、无病生存期和生存状态没有明显差异(p >0.05)。在 UCSH 组中,较低的乳头状构型,较高的组织学分级,较高的固有层、粘膜肌层和浆膜浸润程度,以及原位癌的存在与较高的组织学亚型形态百分比相对应(p <0.05)。有亚型组织学形态和无亚型组织学形态组的生存状况无明显差异(P = 0.083)。这项研究发现,与侵袭性更强的疾病相关的临床和组织病理学预后因素与组织学亚型的存在和比例有关。识别组织学亚型对于具有这些亚型的尿路上皮癌病例的治疗决策和预后预测至关重要。
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来源期刊
CiteScore
3.90
自引率
5.00%
发文量
149
审稿时长
26 days
期刊介绍: A peer-reviewed journal devoted to the publication of articles dealing with traditional morphologic studies using standard diagnostic techniques and stressing clinicopathological correlations and scientific observation of relevance to the daily practice of pathology. Special features include pathologic-radiologic correlations and pathologic-cytologic correlations.
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