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膀胱癌和上尿路肿瘤作为首发和继发的原发性肿瘤。

Bladder and upper urinary tract cancers as first and second primary cancers.

机构信息

Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Cancer Rep (Hoboken). 2021 Dec;4(6):e1406. doi: 10.1002/cnr2.1406. Epub 2021 Jun 11.

Abstract

BACKGROUND

Previous population-based studies on second primary cancers (SPCs) in urothelial cancers have focused on known risk factors in bladder cancer patients without data on other urothelial sites of the renal pelvis or ureter.

AIMS

To estimate sex-specific risks for any SPCs after urothelial cancers, and in reverse order, for urothelial cancers as SPCs after any cancer. Such two-way analysis may help interpret the results.

METHODS

We employed standardized incidence ratios (SIRs) to estimate bidirectional relative risks of subsequent cancer associated with urothelial cancers. Patient data were obtained from the Swedish Cancer Registry from years 1990 through 2015.

RESULTS

We identified 46 234 urinary bladder cancers (75% male), 940 ureteral cancers (60% male), and 2410 renal pelvic cancers (57% male). After male bladder cancer, SIRs significantly increased for 9 SPCs, most for ureteral (SIR 41.9) and renal pelvic (17.2) cancers. In the reversed order (bladder cancer as SPC), 10 individual FPCs were associated with an increased risk; highest associations were noted after renal pelvic (21.0) and ureteral (20.9) cancers. After female bladder cancer, SIRs of four SPCs were significantly increased, most for ureteral (87.8) and pelvic (35.7) cancers. Female bladder, ureteral, and pelvic cancers associated are with endometrial cancer.

CONCLUSIONS

The risks of recurrent urothelial cancers were very high, and, at most sites, female risks were twice over the male risks. Risks persisted often to follow-up periods of >5 years, motivating an extended patient follow-up. Lynch syndrome-related cancers were associated with particularly female urothelial cancers, calling for clinical vigilance.

摘要

背景

先前基于人群的尿路上皮癌(UC)第二原发癌(SPC)研究主要集中在膀胱癌患者的已知风险因素上,而没有肾盂或输尿管其他部位尿路上皮的相关数据。

目的

评估尿路上皮癌患者发生任何 SPC 的性别特异性风险,并按相反顺序评估其他任何癌症发生尿路上皮癌的 SPC 风险。这种双向分析可能有助于解释结果。

方法

我们采用标准化发病比(SIR)来评估与尿路上皮癌相关的后续癌症的双向相对风险。患者数据来自 1990 年至 2015 年的瑞典癌症登记处。

结果

我们共确定了 46234 例膀胱癌(75%为男性)、940 例输尿管癌(60%为男性)和 2410 例肾盂癌(57%为男性)。在男性膀胱癌之后,9 种 SPC 的 SIR 显著增加,其中输尿管癌(SIR 41.9)和肾盂癌(17.2)的 SIR 增加最多。在相反的顺序(膀胱癌作为 SPC)中,10 种个体的 FPC 与风险增加相关;肾盂癌(21.0)和输尿管癌(20.9)的关联最高。在女性膀胱癌之后,4 种 SPC 的 SIR 显著增加,其中输尿管癌(87.8)和骨盆癌(35.7)的 SIR 增加最多。女性膀胱癌、输尿管癌和骨盆癌与子宫内膜癌相关。

结论

复发性尿路上皮癌的风险非常高,在大多数部位,女性风险是男性的两倍。风险持续存在,往往超过 5 年的随访期,需要对患者进行长期随访。林奇综合征相关癌症与女性尿路上皮癌尤其相关,需要临床警惕。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f770/8714543/0b7d2cb556d4/CNR2-4-e1406-g001.jpg

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