Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
Division of Cancer Biology and Genetics, Queen's Cancer Research Institute, Queen's University, Kingston, ON, Canada.
J Pathol Clin Res. 2022 Mar;8(2):143-154. doi: 10.1002/cjp2.245. Epub 2021 Oct 26.
Intrinsic molecular subtypes may explain marked variation between bladder cancer patients in prognosis and response to therapy. Complex testing algorithms and little attention to more prevalent, early-stage (non-muscle invasive) bladder cancers (NMIBCs) have hindered implementation of subtyping in clinical practice. Here, using a three-antibody immunohistochemistry (IHC) algorithm, we identify the diagnostic and prognostic associations of well-validated proteomic features of basal and luminal subtypes in NMIBC. By IHC, we divided 481 NMIBCs into basal (GATA3 /KRT5 ) and luminal (GATA3 /KRT5 variable) subtypes. We further divided the luminal subtype into URO (p16 low), URO-KRT5 (KRT5 ), and genomically unstable (GU) (p16 high) subtypes. Expression thresholds were confirmed using unsupervised hierarchical clustering. Subtypes were correlated with pathology and outcomes. All NMIBC cases clustered into the basal/squamous (basal) or one of the three luminal (URO, URO-KRT5 , and GU) subtypes. Although uncommon in this NMIBC cohort, basal tumors (3%, n = 16) had dramatically higher grade (100%, n = 16, odds ratio [OR] = 13, relative risk = 3.25) and stage, and rapid progression to muscle invasion (median progression-free survival = 35.4 months, p = 0.0001). URO, the most common subtype (46%, n = 220), showed rapid recurrence (median recurrence-free survival [RFS] = 11.5 months, p = 0.039) compared to its GU counterpart (29%, n = 137, median RFS = 16.9 months), even in patients who received intravesical immunotherapy (p = 0.049). URO-KRT5 tumors (22%, n = 108) were typically low grade (66%, n = 71, OR = 3.7) and recurred slowly (median RFS = 38.7 months). Therefore, a simple immunohistochemical algorithm can identify clinically relevant molecular subtypes of NMIBC. In routine clinical practice, this three-antibody algorithm may help clarify diagnostic dilemmas and optimize surveillance and treatment strategies for patients.
内在分子亚型可能解释了膀胱癌患者在预后和对治疗反应方面的显著差异。复杂的测试算法和对更为常见的早期(非肌肉浸润性)膀胱癌(NMIBC)的关注不足,阻碍了亚型在临床实践中的应用。在这里,我们使用三抗体免疫组化(IHC)算法,确定了 NMIBC 中基底和腔型亚型的经过充分验证的蛋白质组特征的诊断和预后相关性。通过 IHC,我们将 481 例 NMIBC 分为基底(GATA3/KRT5)和腔型(GATA3/KRT5 可变)亚型。我们进一步将腔型亚型分为 URO(p16 低)、URO-KRT5(KRT5)和基因组不稳定(GU)(p16 高)亚型。使用无监督层次聚类法确认表达阈值。对亚型与病理学和结局进行相关性分析。所有 NMIBC 病例均聚类为基底/鳞状(基底)或三种腔型(URO、URO-KRT5 和 GU)中的一种。尽管在这个 NMIBC 队列中并不常见,但基底肿瘤(3%,n=16)的分级明显更高(100%,n=16,优势比[OR] = 13,相对风险= 3.25),分期更早,并且更迅速进展为肌肉浸润(无进展生存期[PFS]中位数= 35.4 个月,p= 0.0001)。URO 是最常见的亚型(46%,n=220),与 GU 亚型相比,复发更快(无复发生存期[RFS]中位数= 11.5 个月,p= 0.039),即使在接受膀胱内免疫治疗的患者中也是如此(p= 0.049)。URO-KRT5 肿瘤(22%,n=108)通常为低级别(66%,n=71,OR= 3.7),复发缓慢(RFS 中位数= 38.7 个月)。因此,简单的免疫组化算法可以识别 NMIBC 的临床相关分子亚型。在常规临床实践中,这种三抗体算法可能有助于阐明诊断难题,并优化患者的监测和治疗策略。