Moussa Mohammad Jad, Tabet Georges C, Siefker-Radtke Arlene O, Xiao Lianchun, Wilson Nathaniel R, Gao Jianjun, Logothetis Christopher J, Grivas Petros, Lee Byron, Shah Amishi Y, Msaouel Pavlos, Li Roger, Clemente Leticia Campos, Zhao Jianping, Tannir Nizar M, Kamat Ashish M, Hansel Donna E, Guo Charles C, Campbell Matthew T, Alhalabi Omar
Division of Cancer Medicine, Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Division of Pathology and Laboratory Medicine, Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Cancer Med. 2025 Jan;14(2):e70594. doi: 10.1002/cam4.70594.
Small cell neuroendocrine carcinoma of the urinary tract (SCNEC-URO) has an inferior prognosis compared to conventional urothelial carcinoma (UC). Here, we evaluate the predictors and patterns of relapse after surgery.
We identified a definitive-surgery cohort (n = 224) from an institutional database of patients with cT1-T4NxM0 SCNEC-URO treated in 1985-2021. Histopathologic review was conducted by independent pathologists. Relapse event was the time-to-event outcome, and relapse probabilities were estimated using a competing risk method with cumulative incidence functions (CIFs). Fine-Gray distribution models assessed covariate associations.
Most patients (161, 71.9%) received neoadjuvant chemotherapy (neoCTX). Ninety two (41%) patients had relapse with 77 (83.7%) having distant organs as first metastatic sites, including 10 (10.9%) with exclusive central nervous system (CNS) metastases, mostly (9/10) within 1 year of surgery. Patients with pathologic complete response (pCR) after neoCTx had the lowest 5-year CIF (16.5% [95% CI 9.3%-25.6%]). Patients with remaining exclusively small cell (SC) histology had the highest CIF (85.7% [95% CI 46.6-96.9]). Patients with eradicated SCNEC but remaining UC components had an intermediate-risk CIF (32.5% [95% CI 18.6-47.2]). Multivariable analysis adjusting for neoCTx, clinical stage at diagnosis (T3/4, N0/N+ vs. T1/T2, N0), and pathologic stage (pN+ vs. pN0) demonstrated that any SCNEC histology at resection (vs. pCR) was associated with relapse risk (hazard ratio = 3.69 [95% CI 1.91-7.13], p = 0.0001).
SCNEC-URO is a systemic disease with high risk of distant relapse including CNS. Our findings highlight unmet needs for neoadjuvant/adjuvant approaches targeting the rare SCNEC subtype and suggest adding CNS surveillance within the first year after definitive surgery to high-risk patients. PRÉCIS (CONDENSED ABSTRACT): Alongside neoadjuvant chemotherapy and cancer stage, histology at resection strongly impacts relapse risk in small cell neuroendocrine carcinomas of the urinary tract. The incidence of brain metastasis is notably higher than in "traditional" urothelial cancer within the first year after surgery, especially if small cell cancer persists, thus necessitating close neurological monitoring during this period.
与传统尿路上皮癌(UC)相比,尿路小细胞神经内分泌癌(SCNEC-URO)的预后较差。在此,我们评估手术治疗后的复发预测因素和复发模式。
我们从一个机构数据库中确定了一个接受根治性手术的队列(n = 224),该数据库收录了1985 - 2021年接受治疗的cT1-T4NxM0期SCNEC-URO患者。由独立病理学家进行组织病理学复查。复发事件为事件发生时间结局,使用具有累积发病率函数(CIF)的竞争风险方法估计复发概率。Fine-Gray分布模型评估协变量关联。
大多数患者(161例,71.9%)接受了新辅助化疗(neoCTX)。92例(41%)患者出现复发,其中77例(83.7%)以远处器官作为首个转移部位,包括10例(10.9%)仅发生中枢神经系统(CNS)转移,大多数(9/10)发生在术后1年内。新辅助化疗后达到病理完全缓解(pCR)的患者5年CIF最低(16.5% [95% CI 9.3% - 25.6%])。仅残留小细胞(SC)组织学的患者CIF最高(85.7% [95% CI 46.6 - 96.9])。SCNEC已根除但仍残留UC成分的患者具有中等复发风险CIF(32.5% [95% CI 18.6 - 47.2])。对新辅助化疗、诊断时的临床分期(T3/4、N0/N + 与T1/T2、N0)和病理分期(pN + 与pN0)进行多变量分析表明,切除时存在任何SCNEC组织学(与pCR相比)与复发风险相关(风险比 = 3.69 [95% CI 1.91 - 7.13],p = 0.0001)。
SCNEC-URO是一种具有远处复发高风险的全身性疾病,包括中枢神经系统复发。我们的研究结果突出了针对罕见SCNEC亚型的新辅助/辅助治疗方法的未满足需求,并建议对高危患者在根治性手术后的第一年内增加中枢神经系统监测。摘要(精简摘要):除了新辅助化疗和癌症分期外,切除时的组织学对尿路小细胞神经内分泌癌的复发风险有强烈影响。术后第一年内脑转移的发生率明显高于“传统”尿路上皮癌,特别是如果小细胞癌持续存在,因此在此期间需要密切的神经学监测。