Upper tract urothelial carcinoma: a clinicopathologic study including microsatellite instability analysis

Blaszyk, Hagen and Wang, Linan and Dietmaier, Wolfgang and Hofstädter, Ferdinand and Burgart, Lawrence J. and Cheville, John C. and Hartmann, Arndt (2002) Upper tract urothelial carcinoma: a clinicopathologic study including microsatellite instability analysis. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 15 (8), pp. 790-797.

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Abstract

Urothelial carcinoma of the renal pelvis and ureter may develop as a manifestation of the hereditary nonpolyposis colorectal cancer syndrome that is characterized by mutations in a number of DNA mismatch repair genes and detectable as microsatellite instability. In this study, we examined microsatellite instability and the clinicopathologic features of urothelial carcinoma of the renal pelvis (n = 61) and ureter (n = 53) from 114 consecutive patients surgically treated from 1985-1992. Clinical data were obtained through chart review. Matched normal and tumor DNA was extracted from paraffin-embedded tissue, and a panel of six microsatellite loci was analyzed. The male-female ratio was 2.8:1 with a median age of 70 years (range, 28 to 92 y). Microsatellite analysis was successful in 67 tumors, and 21 (31.3%) patients had tumors that exhibited microsatellite instability. Patients with microsatellite-unstable tumors were significantly more likely to have additional nonurologic cancers (P =.015) including colorectal carcinoma (P =.001) compared with patients with tumors that did not exhibit microsatellite instability. In addition, patients with microsatellite-unstable tumors showed more colorectal cancers in their family (P =.026) and were more likely to have higher grade urothelial carcinoma of the upper tract (P =.028). Grade and stage, but not microsatellite status, were the strongest predictors of cancer-specific survival. This study found the highest frequency of microsatellite instability in upper urothelial tract carcinomas reported to date and highlights upper tract urothelial carcinoma as a marker of the hereditary nonpolyposis colorectal cancer syndrome in some patients. These findings reinforce the importance of obtaining cancer histories in patients with upper tract urothelial carcinoma to subsequently identify individuals with the hereditary nonpolyposis colorectal cancer syndrome and at-risk relatives for surveillance and management programs.

Item Type:Article
Institutions: Medicine > Lehrstuhl für Pathologie
Identification Number:
ValueType
12181263PubMed ID
10.1097/01.MP.0000024263.25043.0CDOI
Classification:
NotationType
AdultMESH
AgedMESH
Aged, 80 and overMESH
Colorectal Neoplasms, Hereditary Nonpolyposis/pathologyMESH
DNA, Neoplasm/analysisMESH
FemaleMESH
HumansMESH
Kidney Pelvis/pathologyMESH
MaleMESH
Microsatellite Repeats/geneticsMESH
Middle AgedMESH
Polymerase Chain ReactionMESH
Risk FactorsMESH
SmokingMESH
Ureteral Neoplasms/pathologyMESH
Urologic Neoplasms/pathologyMESH
Subjects:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Unknown
Created at the University of Regensburg:Unknown
Owner:Gertraud Kellers
Deposited On:18 Jun 2010 10:43
Last Modified:18 Jun 2010 10:43
Item ID:15403
Owner Only: item control page