Expression of MAGE-A3/6 in Primary Breast Cancer is Associated With Hormone Receptor Negative Status, High Histologic Grade, and Poor Survival

被引:41
作者
Ayyoub, Maha [1 ]
Scarlata, Clara-Maria [1 ]
Hamai, Ahmed [1 ]
Pignon, Pascale [1 ]
Valmori, Danila [2 ]
机构
[1] Inst Cancerol Ouest, INSERM, U1102, Equipe Labellisee Ligue Canc, F-44800 Nantes, France
[2] Univ Nantes, Fac Med, Nantes, France
关键词
breast cancer; cancer-testis antigens; MAGE-A3/6; immunotherapy; CELL LUNG-CANCER; TCR GENE-THERAPY; CANCER/TESTIS ANTIGENS; PHASE-II; T-CELLS; MELANOMA; PROTEIN; FAMILY; IMMUNOTHERAPY; REGRESSION;
D O I
10.1097/CJI.0000000000000013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cancer testis antigen (CTA), melanoma-associated antigen A3/6 (MAGE-A3/6), is expressed in human cancers of different histologic types, to variable extents, and is an important target for immunotherapy. In this study, to address the potential of MAGE-A3/6 as an immunotherapeutic target in breast cancer (BC), we assessed MAGE-A3/6 expression by PCR in a cohort of 362 primary BC tumors and analyzed the correlation between MAGE-A3/6 expression, tumors hormone receptor (HR) status, and other clinicopathologic features. We found expression of MAGE-A3/6 in 10% of primary BC tumors. MAGE-A3/6 expression was significantly correlated with estrogen receptor (ER) and progesterone receptor (PR) negative status and was frequent in ER- (29%) and in PR- (24%) tumors. MAGE-A3/6 expression was also significantly associated with high histologic grade but not with patients age, tumor size, tumor type, lymph-node invasion, and human epidermal growth factor receptor 2 (HER2) overexpression. Consistent with the associated poor clinicopathologic features, patients with MAGE-A3/6-expressing tumors had a worse disease-specific survival as compared with patients with MAGE-A3/6(-) tumors. The frequent expression of MAGE-A3/6 in tumors of patients with primary HR- BC, who have, for a large part, limited therapeutic options, encourages the selection of BC patients bearing MAGE-A3/6-expressing tumors for targeted immunotherapy.
引用
收藏
页码:73 / 76
页数:4
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