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abstract
Purpose
Upper
tract urothelial carcinoma (UTUC) is rare and less well studied than
bladder cancer (BC). It remains questionable if findings in BC can
safely be extrapolated to UTUC. We prospectively evaluate molecular
profiles of UTUC and BC using a cell cycle biomarker panel.
Materials and Methods
Immunohistochemical
staining for p21, p27, p53, cyclin E and Ki-67 was prospectively
performed on 96 UTUC and 159 BC patients with non-metastatic high-grade
UC treated with extirpative surgery. Data was compared between two
groups according to the pathological stage. Primary outcome was
assessment of differences in marker expression. Secondary outcome was
difference in survival according to marker status.
Results
Over
a median follow up of 22.0 months, 31.2% of patients with UTUC and
28.3% of patients with BC recurred and 20.8% and 27.7% died of UTUC and
BC, respectively. Number of altered markers was not significantly
different between the study groups. 34 patients (35.4%) with UTUC and 62
patients (39.0%) with BC had an unfavorable marker score (MS) (>2
markers altered). There were no significant differences between UTUC and
BC in alteration status of markers, number of altered markers and MS
when sub-stratified by pathologic stage. There were no significant
differences in survival outcomes between UTUC and BC patients, according
to number of altered markers and MS.
Conclusions
Our
results demonstrate molecular similarity of UTUC and BC regarding cell
cycle and proliferative tissue markers. These findings have important
implications and support further extrapolation of treatment paradigms
established in BC to UTUC.
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