Department of Urology, UT Southwestern Medical Center, Dallas, TX, USA.
Department of Surgery, Urology Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Eur Urol Focus. 2019 May;5(3):365-368. doi: 10.1016/j.euf.2018.01.005. Epub 2018 Feb 1.
Urothelial carcinoma of the upper tract (UTUC) presents specific challenges regarding accurate staging and tumor sampling. We aimed to assess the feasibility of applying next-generation sequencing to biopsy specimens and gauged the concordance of their genetic profiles with matched radical nephroureterectomy (RNU) specimens. Of the 39 biopsy specimens collected, 36 (92%) had adequate material for sequencing using a hybridization-based exon capture assay (MSK-IMPACT). The most frequently altered genes across the patient cohort were consistent with the urothelial carcinoma-associated alterations identified in a cohort of 130 RNU specimens previously sequenced at our center, including mutations in the TERT promoter (64%), hotspot activating mutations in FGFR3 (64%), and frequent mutations in chromatin remodeling genes. For 12 patients, a matching tumor sample from a subsequent RNU was sequenced. We found a high level of concordance between matched biopsy and RNU specimens, up to 92% for the likely pathogenic alterations. PATIENT SUMMARY: We evaluated the feasibility of genomic characterization of tumor tissue collected at the time of ureteroscopic biopsy and found high concordance with subsequent radical nephroureterectomy specimens. Molecular characterization of urothelial carcinoma of the upper tract biopsies could guide treatment decision-making and identify high-risk patients who could benefit from neoadjuvant chemotherapy and low-risk patients who could benefit from conservative or organ-sparing strategies.
上尿路上皮癌(UTUC)在准确分期和肿瘤取样方面存在特殊挑战。我们旨在评估将下一代测序应用于活检标本的可行性,并评估其遗传谱与匹配的根治性肾输尿管切除术(RNU)标本的一致性。在收集的 39 个活检标本中,36 个(92%)有足够的材料用于基于杂交的外显子捕获分析(MSK-IMPACT)进行测序。在整个患者队列中最常改变的基因与我们中心先前对 130 个 RNU 标本进行测序的队列中确定的尿路上皮癌相关改变一致,包括 TERT 启动子突变(64%)、FGFR3 热点激活突变(64%)和染色质重塑基因的频繁突变。对于 12 名患者,对随后的 RNU 中的匹配肿瘤样本进行了测序。我们发现匹配的活检和 RNU 标本之间具有高度一致性,高达 92%的可能致病性改变是一致的。患者总结:我们评估了在输尿管镜活检时收集的肿瘤组织进行基因组特征分析的可行性,发现与随后的根治性肾输尿管切除术标本高度一致。上尿路上皮癌活检的分子特征可以指导治疗决策,并确定可以从新辅助化疗中受益的高危患者以及可以从保守或器官保留策略中受益的低危患者。