The role of programmed death ligand-1 and tumor-infiltrating lymphocytes in breast cancer overexpressing HER2 gene.
The role of programmed death ligand-1 and tumor-infiltrating lymphocytes in breast cancer overexpressing HER2 gene.
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DOI:
10.1007/s10549-018-4745-7
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发表时间:
2018-07
影响因子:
3.8
通讯作者:
Khoury T
中科院分区:
文献类型:
--
作者:
Li Y;Opyrchal M;Yao S;Peng X;Yan L;Jabbour H;Khoury T
The purpose of the study is to investigate the prognostic significance of PD-L1 expression and tumor infiltrating lymphocytes (TILs) in HER2+ breast cancer (BC). HER2+ BC cases (n=191) were collected between 1996 and 2013. Tissue microarray (TMA) slides were stained with two clones of PD-L1 antibodies (28-8 and 22C3) and the percentage of positive membranous staining was scored. TILs of the full sections were also scored using percentage scale. Clone 28-8 had expression in ≥1% of the tumor cells in 25.7% of the cases, while clone 22C3 in ≥1% of the tumor cells was expressed in 11.5% of the cases. In the multivariate analysis, higher expression of PD-L1 (clone 28-8) in tumor correlated with lower risk of tumor recurrence, with HR of 0.4 (p=0.033). Higher level of TILs (>15%) predicts better overall survival (OS) in all patients with HR of 0.35 (p=0.0046). In the group of patients who were treated with trastuzumab-based adjuvant chemotherapy, lower PD-L1 (clone 28-8) expression in TILs correlated with tumor recurrence (p=0.034). In the group of patients who were treated with non-trastuzumab-based adjuvant chemotherapy, lower TILs and lower PD-L1 (clone 28-8) expression in tumor had borderline statistical significance in association with tumor recurrence, p=0.064 and 0.083, respectively. In the group of patients who were treated with trastuzumab-based adjuvant chemotherapy, PD-L1 or TILs was not statistically significant to predict 5-year survival. In the group of patients who were treated with non-trastuzumab-based adjuvant chemotherapy, low TILs (p=0.009) correlated with 5-year death due to disease. We conclude that PD-L1 may have prognostic significance in HER2+ BCs.
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DOI:
10.1016/s1470-2045(16)30631-3
发表时间:
2017-01
期刊:
The Lancet. Oncology
影响因子:
--
作者:
Luen SJ;Salgado R;Fox S;Savas P;Eng-Wong J;Clark E;Kiermaier A;Swain SM;Baselga J;Michiels S;Loi S
通讯作者:
Loi S
影响因子:
45.3
作者:
Adams, Sylvia;Gray, Robert J.;Badve, Sunil S.
通讯作者:
Badve, Sunil S.
影响因子:
3.3
作者:
Baptista, Mauricio Z.;Sarian, Luis Otavio;Vassal, Jose
通讯作者:
Vassal, Jose
影响因子:
7
作者:
Mittal, Deepak;Gubin, Matthew M.;Schreiber, Robert D.;Smyth, Mark J.
通讯作者:
Smyth, Mark J.
DOI:
10.1056/nejmoa1200694
发表时间:
2012-06-28
期刊:
The New England journal of medicine
影响因子:
--
作者:
Brahmer JR;Tykodi SS;Chow LQ;Hwu WJ;Topalian SL;Hwu P;Drake CG;Camacho LH;Kauh J;Odunsi K;Pitot HC;Hamid O;Bhatia S;Martins R;Eaton K;Chen S;Salay TM;Alaparthy S;Grosso JF;Korman AJ;Parker SM;Agrawal S;Goldberg SM;Pardoll DM;Gupta A;Wigginton JM
通讯作者:
Wigginton JM