Insulin-like growth factor-1 receptor is associated with better prognosis in classical Hodgkin's lymphoma: Correlation with MET expression

被引:3
作者
Koh, Young Wha [1 ]
Yoon, Dok Hyun [2 ]
Suh, Cheolwon [2 ]
Cha, Hee Jeong [3 ]
Huh, Jooryung [4 ]
机构
[1] Ajou Univ, Sch Med, Dept Pathol, Suwon 441749, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Pathol, Ulsan 680749, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pathol, Seoul 138736, South Korea
关键词
Hodgkin's lymphoma; IGF-1R; MET; prognosis; MACROPHAGE-STIMULATING PROTEIN; REED-STERNBERG CELLS; TYROSINE KINASE; C-MET; PLASMINOGEN-ACTIVATOR; BREAST-CANCER; PHASE-I; MULTIPLE-MYELOMA; TUMOR-GROWTH; IGF-I;
D O I
10.1111/iep.12128
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The purpose of this study was to examine the prognostic significance of insulin-like growth factor-1 receptor (IGF-1R) expression alone and in relation to the expression of the MET- receptor and the MET-homologous receptor RON, in classical Hodgkin's lymphoma (cHL). Tumour samples from patients with cHL (n=202; median age 37.5years) were analysed retrospectively for IGF-R1, MET or RON expression by immunohistochemistry using tissue microarrays. The median follow-up time was 3.7years (range, 0.1-20years). Twenty-nine patients (14.3%) expressed IGF-1R protein in Hodgkin/Reed-Sternberg (HRS) cells, which was associated with a better overall survival (OS) (P=0.036). IGF-1R expression was closely associated with MET receptor expression and low level of lactate dehydrogenase. In patients with cHL receiving doxorubicin, bleomycin, vinblastine and dacarbazine, those expressing IGF-1R showed a trend towards better OS and event-free survival than IGF-1R-negative patients (P=0.129 and P=0.115 respectively), but statistical significance was not reached. This study suggests that IGF-1R expression could be associated with better clinical outcome in cHL but is significantly associated with the expression of MET receptor.
引用
收藏
页码:232 / 239
页数:8
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