Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Mayo Clinic, Rochester, MN, USA.
Eur Urol. 2019 Aug;76(2):200-206. doi: 10.1016/j.eururo.2019.04.036. Epub 2019 May 12.
Upstaging of clinical T1-T2 urothelial carcinoma (UC) to non-organ-confined (NOC) pathological stage ≥T3 or N+ at radical cystectomy (RC) is common. Tools for stratifying patients who may have NOC disease are limited.
To determine an association of a genomic subtyping classifier (GSC) with pathological upstaging in multi-institutional cohort of patients with cT1-T2 UC treated with RC.
DESIGN, SETTING, AND PARTICIPANTS: Precystectomy transurethral specimens from 206 patients with high-grade, cT1-T2, N0M0 UC, who underwent RC without neoadjuvant chemotherapy, underwent GSC testing.
Uni- and multivariable logistic regression analyses evaluated GSC for upstaging, defined as pT3/T4 and/or pTanyN1-3 disease at RC.
Pathological upstaging occurred in 23% of cT1 and 57% of cT2 cases. Lower rates of upstaging to NOC was seen for luminal versus nonluminal tumors (34% vs 51%, p=0.02). The differences in upstaging were confined to T stage, with no difference in node positivity for luminal versus nonluminal patients (cT1: 13% for both [p>0.9], cT2: 15% and 23% [p=0.6], respectively). Fewer patients with luminal tumors were upstaged to ≥pT3Nany compared with nonluminal tumors (Mantel-Haenszel p=0.002; cT1: 13% vs 30%, cT2: 34% vs 58%). On multivariable logistic regression analysis, nonluminal patients were more likely to be upstaged to ≥pT3 at RC (p<0.001). Limitations include retrospective design and sample size.
Molecular subtyping of clinically localized UC demonstrated that luminal tumors have lower rates of upstaging to non-organ-confined disease compared with nonluminal tumors. If validated, these data can help inform which patients may need multimodal therapy.
Determining whether bladder cancer has spread beyond the bladder is challenging at diagnosis. In this paper, genomics helped identify patients who were more likely to have aggressive disease that has spread outside the bladder. These patients may benefit from chemotherapy prior to surgery.
在接受根治性膀胱切除术 (RC) 的临床 T1-T2 尿路上皮癌 (UC) 患者中,将临床 T1-T2 升级为非器官受限 (NOC) 病理分期≥T3 或 N+的情况很常见。用于分层可能患有 NOC 疾病的患者的工具有限。
确定基因组亚分型分类器 (GSC) 是否与接受 RC 治疗的多机构队列中临床 T1-T2 UC 患者的病理升级相关。
设计、设置和参与者:对 206 名患有高级别、cT1-T2、N0M0 UC 的患者进行了经尿道膀胱镜检查,这些患者在未接受新辅助化疗的情况下接受了 RC,并进行了 GSC 检测。
单变量和多变量逻辑回归分析评估了 GSC 用于升级,定义为 RC 时 pT3/T4 和/或 pTanyN1-3 疾病。
cT1 的升级率为 23%,cT2 的升级率为 57%。与非腔型肿瘤相比,腔型肿瘤的 NOC 升级率较低 (34% vs 51%,p=0.02)。升级差异仅限于 T 期,腔型和非腔型患者的淋巴结阳性率没有差异 (cT1:两者均为 13%[p>0.9],cT2:分别为 15%和 23%[p=0.6])。与非腔型肿瘤相比,腔型肿瘤患者升级为≥pT3Nany 的比例较低 (Mantel-Haenszel p=0.002;cT1:13%比 30%,cT2:34%比 58%)。多变量逻辑回归分析显示,非腔型患者更有可能在 RC 时升级为≥pT3(p<0.001)。局限性包括回顾性设计和样本量。
临床局限性 UC 的分子分型表明,与非腔型肿瘤相比,腔型肿瘤升级为非器官受限疾病的比例较低。如果得到验证,这些数据可以帮助确定哪些患者可能需要多模式治疗。
在诊断时确定膀胱癌是否已扩散到膀胱以外是具有挑战性的。在本文中,基因组学有助于确定更有可能患有侵袭性疾病的患者,这些疾病已扩散到膀胱以外。这些患者可能受益于手术前的化疗。