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The interplay of cell cycle and DNA repair gene alterations in upper tract urothelial carcinoma: predictive and prognostic implications

机译:细胞周期和DNA修复基因改变在上部尿路上皮癌中的相互作用:预测和预后意义

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Upper tract urothelial carcinoma (UTUC) is rare but can occur sporadically outside the context of Lynch syndrome. In these cases, knowing whether non-mismatch repair (MMR), DNA damage response and repair (DDR), and cell cycle gene alterations may predict responses to chemotherapy or immunotherapy and survival is of clinical importance. This study examined the germline and somatic mutational landscape of two UTUC patients with differential responses to programmed death 1 (PD-1)/PD-ligand 1 (PD-L1) immune checkpoint inhibitors and queried three independent UTUC cohort studies for co-occurrence of key cell cycle and DDR genes, as well as for their associations with overall survival (OS). TP53 and RB1 emerged as potential determinants of shorter OS in UTUC cohort patients, regardless of concurrent DDR alterations, and if prospectively assessed in larger studies they might also explain resistance to PD-1/PD-L1 blockade despite PD-L1 expression.
机译:上部传染尿路上皮癌(UTUC)是罕见的,但可以在林奇综合征的背景下散发出来。在这些情况下,知道是否无匹配修复(MMR),DNA损伤反应和修复(DDR)和细胞周期基因改变可能预测对化疗或免疫疗法的反应,生存是临床重要性。本研究检测了两种utuc患者的种系和体细胞突变景观,差异反应对编程死亡1(pd-1)/ pd-ligand 1(pd-l1)免疫检查点抑制剂,并查询三个独立的utuc队列研究,用于共同发生关键细胞周期和DDR基因,以及它们与整体存活(OS)的关联(OS)。 TP53和RB1作为utuc队队​​患者中较短OS的潜在决定因素,无论同时的DDR改变如何,如果在较大的研究中进行预期评估,则尽管PD-L1表达,它们也可能解释对PD-1 / PD-L1封闭的抵抗力。

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