High cyclin A expression, but not Ki67, is associated with early recurrence in desmoid tumors

被引:5
作者
Santti, Kirsi [1 ,2 ]
Ihalainen, Hanna [1 ,2 ,3 ]
Ronty, Mikko [2 ,4 ]
Boehling, Tom [2 ,4 ]
Karlsson, Christina [5 ]
Haglund, Caj [2 ,6 ,7 ]
Tarkkanen, Maija [1 ,2 ]
Blomqvist, Carl [1 ,2 ,8 ]
机构
[1] Helsinki Univ Hosp, Comprehens Canc Ctr, POB 180, Helsinki 00029, Finland
[2] Univ Helsinki, Helsinki, Finland
[3] Helsinki Univ Hosp, Dept Plast Surg, Helsinki, Finland
[4] HUSLAB, Dept Pathol, Helsinki, Finland
[5] Orebro Univ, Sch Hlth Sci, Dept Med Diagnost, Orebro, Sweden
[6] Helsinki Univ Hosp, Dept Surg, Helsinki, Finland
[7] Univ Helsinki, Res Program Unit, Translat Canc Biol, Helsinki, Finland
[8] Orebro Univ Hosp, Dept Oncol, Orebro, Sweden
关键词
aggressive fibromatosis; biomarkers; cyclins; immunohistochemistry; prognostic factors; SOFT-TISSUE SARCOMAS; FAMILIAL ADENOMATOUS POLYPOSIS; AGGRESSIVE FIBROMATOSIS; BREAST-CANCER; PROGNOSTIC-FACTORS; KI-67; EXPRESSION; FREE SURVIVAL; BETA-CATENIN; RADIOTHERAPY; METAANALYSIS;
D O I
10.1002/jso.25121
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives: Desmoid tumors are soft-tissue tumors originating from myofibroblasts with a tendency to recur after surgery. High expression of proliferation markers is associated with shortened progression-free and/or overall survival in many neoplasms, including soft-tissue sarcomas. We investigated the prognostic role of cyclin A and Ki67 in desmoid tumors by immunohistochemistry. Methods: The study included 76 patients with desmoid tumor operated at Helsinki University Hospital between 1987 and 2011. A tissue micro array (TMA) was constructed and the TMA sections were immunostained with cyclin A and Ki67 antibodies. A computer-assisted image analysis was performed. Results: Cyclin A expression was evaluable in 74 and Ki67 in 70 patients. Cyclin A immunopositivity varied from 0% to 9.9%, with a mean of 1.9%. Cyclin A expression correlated significantly with Ki67. Cyclin A expression was associated with recurrence-free survival (HR 1.9, 95% CI = 1.1-3.2, P = .02), as were positive margin (HR 6.0, 95% CI = 1.6-22.5, P = .008) and extremity location (HR 5.3, 95% CI = 1.7-16.8, P = 0.005). Ki67 immunopositivity varied from 0.33% to 13.8%, with a mean of 4.6%, but had no significant prognostic impact (HR 1.1, P = .2). Conclusions: Our study indicates that cyclin A may be a new prognostic biomarker in surgically treated desmoid tumors.
引用
收藏
页码:192 / 198
页数:7
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