Shengli Clinical Medical College, Fujian Medical University, Fuzhou, 350001, China.
Department of Urology, Fujian Provincial Hospital, Fuzhou, 350001, China.
Sci Rep. 2020 Dec 3;10(1):21073. doi: 10.1038/s41598-020-78174-9.
The study aimed to compare the clinicopathological features and prognosis between type I and type II papillary renal cell carcinoma (PRCC) and to investigate whether the subtypes of PRCC would affect oncological outcomes. A total of 102 patients with PRCC were recruited, of which 42 were type I PRCC and 60 type II. The clinicopathological features and oncologic outcomes of the patients were evaluated. The type II cases had a higher WHO/ISUP grading (P < 0.001), T (P = 0.003), N (P = 0.010) stage and stage grouping (P = 0.011) than the type I. During a median follow-up period of 61.4 months, 1-year cancer specific survival (CSS) of the type I was 100%, 5-year CSS was 95.2%, the 1-year CSS of the type II was 96.2%, and 5-year CSS was 75.7%. The univariate analysis showed that subtype, symptoms, TNM, stage grouping, WHO/ISUP grading and surgical methods appeared to affect prognosis of the patients with PRCC. However, multivariate analysis revealed that only stage grouping was the independent risk factor. After the stage grouping factor was adjusted for the analysis, there were no statistically significant differences in CSS (P = 0.214) and PFS (P = 0.190) between the localized type I and type II PRCC groups. Compared with type I PRCC, type II had higher pathological T, N stage and WHO/ISUP grading. However, it was the Stage grouping that made a great difference to oncological outcomes, rather than the subtype of PRCC.
本研究旨在比较Ⅰ型和Ⅱ型乳头状肾细胞癌(PRCC)的临床病理特征和预后,并探讨 PRCC 的亚型是否会影响肿瘤学结局。共纳入 102 例 PRCC 患者,其中Ⅰ型 42 例,Ⅱ型 60 例。评估了患者的临床病理特征和肿瘤学结局。Ⅱ型病例的 WHO/ISUP 分级更高(P<0.001)、T 期(P=0.003)、N 期(P=0.010)和分期分组(P=0.011)更高。在中位随访 61.4 个月期间,Ⅰ型的 1 年癌症特异性生存率(CSS)为 100%,5 年 CSS 为 95.2%,Ⅱ型的 1 年 CSS 为 96.2%,5 年 CSS 为 75.7%。单因素分析显示,亚型、症状、TNM、分期分组、WHO/ISUP 分级和手术方式似乎影响 PRCC 患者的预后。然而,多因素分析显示,只有分期分组是独立的危险因素。在对分析进行分期分组因素调整后,局限性Ⅰ型和Ⅱ型 PRCC 组之间 CSS(P=0.214)和 PFS(P=0.190)无统计学差异。与Ⅰ型 PRCC 相比,Ⅱ型 PRCC 的病理 T、N 分期和 WHO/ISUP 分级更高。然而,对肿瘤学结局影响最大的是分期分组,而不是 PRCC 的亚型。