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Reassessment of p53 immunohistochemistry thresholds in invasive high grade bladder cancer shows a better correlation with TP53 and FGFR3 mutations
被引:14
|作者:
Hodgson, Anjelica
[1
,2
]
Rhijn, Bas W. G. van
[3
,4
]
Kim, Sung Sun
[2
,5
,6
]
Ding, Colleen
[5
]
Saleeb, Rola
[2
,5
]
Vesprini, Danny
[7
,8
]
Liu, Stanley K.
[7
,8
]
Yousef, George M.
[2
,5
,9
]
Kwast, Theodorus H. van der
[2
,10
]
Xu, Bin
[11
]
Downes, Michelle R.
[1
,2
]
机构:
[1] Sunnybrook Hlth Sci Ctr, Div Anat Pathol, Dept Lab Med & Mol Diagnost, Room E400,2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[3] Antoni van Leeuwenhoek Hosp, Dept Surg Oncol Urol, Netherlands Canc Inst, Amsterdam, Netherlands
[4] Univ Regensburg, Dept Urol, Caritas St Josef Med Ctr, Regensburg, Germany
[5] St Michaels Hosp, Li Ka Shing Knowledge Inst, Anat Pathol, Toronto, ON, Canada
[6] Chonnam Natl Univ, Dept Pathol, Sch Med, Gwangju, South Korea
[7] Sunnybrook Hlth Sci Ctr, Odette Canc Ctr, Radiat Oncol, 2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
[8] Univ Toronto, 2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
[9] Hosp Sick Children, Dept Pediat Lab Med, Toronto, ON, Canada
[10] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
[11] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
关键词:
Bladder cancer;
Urothelial carcinoma;
p53;
immunohistochemistry;
TP53;
mutation;
FGFR3;
TRANSITIONAL-CELL CARCINOMA;
GROWTH-FACTOR RECEPTOR-3;
GENE-MUTATIONS;
PROGNOSTIC-FACTOR;
ACTIVATING MUTATIONS;
EXPRESSION;
PATHWAYS;
MARKER;
TRANSFORMATION;
HETEROGENEITY;
D O I:
10.1016/j.prp.2020.153186
中图分类号:
R36 [病理学];
学科分类号:
100104 ;
摘要:
FGFR3 mutations are frequently mutually exclusive of TP53 mutations in invasive high grade urothelial carcinoma (HGUC) and p53 immunohistochemistry is often used as a surrogate for TP53 mutations. A 10 % staining cut off has been used in HGUC for designation as p53 positive or negative however, a novel contemporary method we have previously proposed (0% or 50 % abnormal vs. 1-49 % wild type) has shown significant correlation with oncologic outcome as well. We aimed to compare how a >= 10 % vs. 0 % and >= 50 % cut off p53 assessment method correlates with TP53 and FGFR3 mutation status. Tissue microarrays created from three retrospective cohorts (two cystectomy cohorts (cohort A, n = 206 and cohort B, n = 91; one T1 transurethral resection cohort (cohort C, n = 47)) were stained with p53 and scored by two blinded reviewers using both p53 scoring schemes. 50 cases from cohort A were assessed for TP53 and FGFR3 mutation status using next generation sequencing and FGFR3 mutation status was separately assessed in cohorts B and C using SNaPshot methodology. 202 (58.7 %) and 142 (41.3 %) cases showed abnormal and wild type p53 staining, respectively. Using the 10 % cut off, 254 cases were positive (73.8 %) and 90 cases were negative (26.2 %). 27 (14.4 %) and 15 (30 %) assessed cases demonstrated FGFR3 and TP53 mutations, respectively; 19/27 FGFR3 mutated showed a wild type pattern of p53 expression while 15/15 TP53 mutated tumours showed an abnormal pattern of p53 expression. There was a significant correlation between the contemporary p53 scoring scheme and TP53 and FGFR3 mutations (p < 0.0001 and p = 0.002, respectively). Improved sensitivity, specificity, positive predictive value, and negative predictive value for TP53 mutation was also seen compared to the 10 % cut off; specifically, the sensitivity and negative predictive value were 100 %. These findings might be of clinical relevance in the era of precision medicine.
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