Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study

被引:22
作者
Pezzuto, Federica [1 ]
Serio, Gabriella [2 ]
Fortarezza, Francesco [1 ]
Scattone, Anna [3 ]
Caporusso, Concetta [2 ]
Punzi, Alessandra [2 ]
Cavone, Domenica [4 ]
Pennella, Antonio [5 ]
Marzullo, Andrea [2 ]
Vimercati, Luigi [4 ]
机构
[1] Univ Padua, Dept Cardiac Thorac Vasc Sci & Publ Hlth, I-35128 Padua, Italy
[2] Univ Bari, Dept Emergency & Organ Transplantat, Pathol Div, I-70124 Bari, Italy
[3] IRCCS, Pathol Div, Natl Canc Inst Giovanni Paolo II, I-70124 Bari, Italy
[4] Univ Bari, Dept Interdisciplinary Med, Occupat Hlth Div, I-70124 Bari, Italy
[5] Univ Foggia, Dept Surg, Pathol Div, I-71122 Foggia, Italy
关键词
diffuse malignant peritoneal mesothelioma; prognostic factors; Ki67; WT-1; p16; CDKN2A; TUMOR GENE WT1; HOMOZYGOUS DELETION; SURVIVAL; CHEMOTHERAPY; CDKN2A;
D O I
10.3390/diagnostics10060386
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diffuse malignant peritoneal mesothelioma (DMPM) is a rare malignant neoplasm with a poor survival. Although some advances in knowledge have been obtained for the pleural form, much less is known about DMPM. Advantages in terms of prognosis are still limited and strong efforts need to be made. The aim of our study was to correlate several histological and molecular factors with survival in a large cohort of 45 DMPMs. We evaluated histotype, nuclear grade, mitotic count, necrosis, inflammation, desmoplastic reaction, Ki67 percentage, WT-1 expression, p16 protein by immunohistochemistry and CDKN2A deletion by FISH. Our results showed that epithelioid histotype, nuclear grade 2, mitotic count <= 5 x mm(2), absence of desmoplasia and p16/CDKN2A deletion, low Ki67 value, and high WT-1 expression were correlated with the most prolonged survival (p= 0.0001). Moreover, p16 loss in immunohistochemistry reflected CDKN2A deletion detected with FISH, and both were correlated with the worst survival (p= 0.0001). At multivariate analysis, Ki67 value, WT-1 expression and p16/CDKN2A deletion emerged as independent prognostic factors (p= 0.01,p= 0.0001 andp= 0.01, respectively). These parameters are easy to analyse at the time of DMPM diagnosis and may support better patient stratification, prediction of treatment effectiveness and therapeutic optimization.
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