de Jong Joep J, Proudfoot James A, Daneshmand Siamak, Svatek Robert S, Narayan Vikram, Davicioni Elai, Joshi Shreyas, Dahmen Aaron, Li Roger, Inman Brant A, Shah Paras, Chaplin Iftach, Wright Jonathan, Gibb Ewan A, Lotan Yair
Erasmus University Medical Center, Rotterdam, The Netherlands.
Veracyte Inc., San Diego, CA, USA.
Eur Urol Open Sci. 2025 Jan 27;73:24-30. doi: 10.1016/j.euros.2024.12.009. eCollection 2025 Mar.
Many patients with bladder cancer are understaged. Previous work revealed that molecular subtyping using Decipher Bladder improves clinical staging. This multicenter validation study evaluated Decipher Bladder for upstaging in patients who underwent radical cystectomy (RC) without neoadjuvant therapy.
The Decipher Bladder genomic subtyping classifier (GSC; Veracyte, San Diego, CA, USA) was performed on bladder tumor specimens from patients with high-grade, clinically organ-confined (cTa-T2N0M0) urothelial carcinoma who subsequently underwent RC without neoadjuvant chemotherapy. The primary endpoint was pathological upstaging to non-organ-confined (NOC) disease (pT3+ and/or N+) at RC. The secondary endpoints included overall survival (OS) and pathological upstaging to MIBC+ disease (pT2+ and/or N+) at RC within clinically non-muscle-invasive bladder cancer (cNMIBC) cases.
A total of 226 patients (134 cNMIBC [cTa/Tis/T1] and 92 cT2) were analyzed from eight participating institutions. Upstaging to NOC disease was observed in 33% of patients (19% for cNMIBC and 53% for cT2). Molecular subtyping identified 138 luminal and 88 nonluminal tumors. Rates of upstaging to NOC were 41% in nonluminal and 28% in luminal tumors (univariable = 0.04), which was not independently significant after adjusting for clinical variables. Upstaging to MIBC+ in cNMIBC patients was lower in luminal versus nonluminal tumors (32% vs 51%, multivariable = 0.03). Patients with nonluminal tumors had worse OS on multivariable analyses ( < 0.05). Limitations include retrospective design and sample size.
Luminal tumors represent less aggressive disease, reflected by lower rates of pathological upstaging and favorable OS with RC compared with nonluminal tumors.
Molecular subtyping suggests that in clinically non-muscle-invasive bladder cancer, luminal tumors harbor less aggressive disease, as reflected by lower rates of pathological upstaging to muscle-invasive disease and favorable outcomes with radical cystectomy, in comparison with nonluminal bladder cancer.
许多膀胱癌患者分期不足。既往研究表明,使用Decipher Bladder进行分子亚型分析可改善临床分期。这项多中心验证研究评估了Decipher Bladder在未接受新辅助治疗而行根治性膀胱切除术(RC)的患者中上调分期的情况。
对高级别、临床局限于器官(cTa-T2N0M0)的尿路上皮癌患者的膀胱肿瘤标本进行Decipher Bladder基因组亚型分类器(GSC;美国加利福尼亚州圣地亚哥市Veracyte公司)检测,这些患者随后接受了RC且未接受新辅助化疗。主要终点是RC时病理分期上调至非局限于器官(NOC)疾病(pT3+和/或N+)。次要终点包括总生存期(OS)以及临床非肌层浸润性膀胱癌(cNMIBC)病例中RC时病理分期上调至肌层浸润性膀胱癌+疾病(pT2+和/或N+)。
来自8个参与机构的226例患者(134例cNMIBC [cTa/Tis/T1]和92例cT2)接受了分析。33%的患者出现分期上调至NOC疾病(cNMIBC为19%,cT2为53%)。分子亚型分析鉴定出138例腔面型和88例非腔面型肿瘤。非腔面型肿瘤分期上调至NOC的比例为41%,腔面型肿瘤为28%(单变量P = 0.04),在调整临床变量后无独立显著性。cNMIBC患者中,腔面型肿瘤上调至MIBC+的比例低于非腔面型肿瘤(32%对51%,多变量P = 0.03)。多变量分析显示,非腔面型肿瘤患者的OS较差(P<0.05)。局限性包括回顾性设计和样本量。
腔面型肿瘤代表侵袭性较低的疾病,与非腔面型肿瘤相比,其病理分期上调率较低且RC后的OS较好。
分子亚型分析表明,在临床非肌层浸润性膀胱癌中,与非腔面型膀胱癌相比,腔面型肿瘤侵袭性较低,表现为病理分期上调至肌层浸润性疾病的比例较低以及根治性膀胱切除术后预后良好。