Department of Urology, Peking University First Hospital, Institute of Urology, Peking University, National Urological Cancer Center, Beijing, China.
Department of Urology, Peking University First Hospital, Institute of Urology, Peking University, National Urological Cancer Center, Beijing, China.
Clin Genitourin Cancer. 2024 Dec;22(6):102192. doi: 10.1016/j.clgc.2024.102192. Epub 2024 Aug 12.
To provide a comprehensive understanding of the clinical features of patients with synchronous and metachronous upper tract urothelial carcinoma (UTUC) and bladder urothelial carcinoma (BUC) and inform surgical and postoperative adjuvant treatment planning.
A total of 292 consecutive patients with synchronous and metachronous UTUC-BUC were retrospectively enrolled and were categorized into three groups: (1) UTUC metachronous BUC (N = 185, UTUC-mBUC), (2) BUC-metachronous UTUC (N = 43, BUC-mUTUC), (3) synchronous UTUC-BUC (N = 64, sUTUC-BUC). We compared pathological characteristics and survival data among groups with Wilcoxon's rank sum tests, Pearson's chi-squared, and the Kaplan-Meier method.
In the sUTUC-BUC group, a higher proportion of patients exhibited UTUC tumors with grade G3 (56%, P = .001) and stage T4 (6%, P < .001) than group UTUC-mBUC (G3 = 16%, T4 = 0%). The proportion of patients with variant histology subtype in group sUTUC-BUC was higher than that of metachronous UTUC-BUC, involving squamous (P = .003), adenoid (P = .012), and sarcomatoid (P < .001) differentiation. It was also observed that the maximum diameter of the UTUC tumor of group sUTUC-BUC (median = 3.5) was significantly larger than group UTUC-mBUC (median = 2.5, P = .002) and group BUC-mUTUC (median = 2.2, P < .001). Notably, sUTUC-BUC has an increased risk of cancer-specific death compared with UTUC-mBUC (P < .001) and BUC-mUTUC (P < .001). On multivariable Cox regression, synchronous UTUC-BUC was an independent predictor of both RFS (P < .001; vs. UTUC-mBUC: HR 0.555, P = .004; vs. BUC-mUTUC: HR 0.279, P < .001) and CSS (P < .001, HR 29.737). Moreover, sUTUC-BUC showed a better response to intravesical therapy and chemotherapy with higher cancer-specific survival (P < .001) and recurrence-free survival (P = .034).
The prognosis and pathological characteristics among different metachronous and synchronous UTUC and BUC were diverse. The synchronous UTUC-BUC group showed variant histology subtype, high-grade tumors, advanced tumors, multifocal UTUC, worse cancer-specific survival, but better response to intravesical therapy and chemotherapy.
全面了解同时性和异时性上尿路上皮癌(UTUC)和膀胱尿路上皮癌(BUC)患者的临床特征,并为手术和术后辅助治疗方案提供信息。
回顾性纳入 292 例同时性和异时性 UTUC-BUC 连续患者,并分为三组:(1)UTUC 异时性 BUC(N=185,UTUC-mBUC);(2)BUC 异时性 UTUC(N=43,BUC-mUTUC);(3)同时性 UTUC-BUC(N=64,sUTUC-BUC)。我们使用 Wilcoxon 秩和检验、Pearson χ2 检验和 Kaplan-Meier 方法比较组间的病理特征和生存数据。
在 sUTUC-BUC 组中,与 UTUC-mBUC 组相比(G3=16%,T4=0%),更多的患者表现出 G3 级(56%,P=0.001)和 T4 期(6%,P<.001)的 UTUC 肿瘤。sUTUC-BUC 组变异组织学亚型的比例高于异时性 UTUC-BUC,涉及鳞癌(P=0.003)、腺样(P=0.012)和肉瘤样分化(P<.001)。还观察到 sUTUC-BUC 的 UTUC 肿瘤最大直径(中位数=3.5)明显大于 UTUC-mBUC(中位数=2.5,P=0.002)和 BUC-mUTUC(中位数=2.2,P<.001)。值得注意的是,sUTUC-BUC 的癌症特异性死亡风险高于 UTUC-mBUC(P<.001)和 BUC-mUTUC(P<.001)。多变量 Cox 回归分析显示,同时性 UTUC-BUC 是 RFS(P<.001;与 UTUC-mBUC 相比:HR 0.555,P=0.004;与 BUC-mUTUC 相比:HR 0.279,P<.001)和 CSS(P<.001,HR 29.737)的独立预测因素。此外,sUTUC-BUC 对膀胱内治疗和化疗的反应更好,具有更高的癌症特异性生存率(P<.001)和无复发生存率(P=0.034)。
不同的同时性和异时性 UTUC 和 BUC 之间的预后和病理特征存在差异。sUTUC-BUC 组表现为变异组织学亚型、高级别肿瘤、晚期肿瘤、多灶性 UTUC、癌症特异性生存率较差,但对膀胱内治疗和化疗反应更好。