PD‐L1 expression and CD8‐positive T cells are associated with favorable survival in HER2‐positive invasive breast cancer. Issue 6 (19th September 2018)
- Record Type:
- Journal Article
- Title:
- PD‐L1 expression and CD8‐positive T cells are associated with favorable survival in HER2‐positive invasive breast cancer. Issue 6 (19th September 2018)
- Main Title:
- PD‐L1 expression and CD8‐positive T cells are associated with favorable survival in HER2‐positive invasive breast cancer
- Authors:
- Hou, Yanjun
Nitta, Hiroaki
Wei, Lai
Banks, Peter M
Lustberg, Maryam
Wesolowski, Robert
Ramaswamy, Bhuvaneswari
Parwani, Anil V.
Li, Zaibo - Abstract:
- Abstract: Programmed cell death 1 (PD‐1) and its ligand (PD‐L1) are key physiologic suppressors of the cytotoxic immune reaction. However, to date, the combination of PD1/PD‐L1 expression and tumor‐infiltrating lymphocytes (TILs) and antigen‐presenting cells has been only minimally reported in breast carcinoma, in particular in relation to HER2‐positive cases. The goal of this study was to evaluate both cellular tumoral immune reaction and PD‐L1/PD1 distribution in HER2‐positive cases, as well as any associations with clinical outcome using conventional chemotherapy combined with HER2 blocking. Multicolor immunohistochemical multiplex assays simultaneously demonstrating PD1, PD‐L1, and CD8 or PD‐L1, CD3, and CD163 were performed on tissue microarrays (TMA) representing 216 pretreatment cases of HER2‐positive invasive breast carcinoma. PD‐L1 expression was identified in 38 cases (18%), including 12 cases (6%) with PD‐L1 labeling of tumor cells and 26 cases (12%) with PD‐L1 labeling of immune cells only. Ten of 12 cases with PD‐L1 staining of tumor cells showed staining of associated immune cells as well. With this assay method, PD1 was detectable in many fewer cases (6 cases or 3%). PD‐L1 expression was positively associated with high Nottingham grade, negative ER and PR, the absence of lymph node metastasis, and high levels of CD8 + cells. The overall survival by univariate analysis was positively associated with lower tumor stage, the absence of lymph node metastasis, PD‐L1Abstract: Programmed cell death 1 (PD‐1) and its ligand (PD‐L1) are key physiologic suppressors of the cytotoxic immune reaction. However, to date, the combination of PD1/PD‐L1 expression and tumor‐infiltrating lymphocytes (TILs) and antigen‐presenting cells has been only minimally reported in breast carcinoma, in particular in relation to HER2‐positive cases. The goal of this study was to evaluate both cellular tumoral immune reaction and PD‐L1/PD1 distribution in HER2‐positive cases, as well as any associations with clinical outcome using conventional chemotherapy combined with HER2 blocking. Multicolor immunohistochemical multiplex assays simultaneously demonstrating PD1, PD‐L1, and CD8 or PD‐L1, CD3, and CD163 were performed on tissue microarrays (TMA) representing 216 pretreatment cases of HER2‐positive invasive breast carcinoma. PD‐L1 expression was identified in 38 cases (18%), including 12 cases (6%) with PD‐L1 labeling of tumor cells and 26 cases (12%) with PD‐L1 labeling of immune cells only. Ten of 12 cases with PD‐L1 staining of tumor cells showed staining of associated immune cells as well. With this assay method, PD1 was detectable in many fewer cases (6 cases or 3%). PD‐L1 expression was positively associated with high Nottingham grade, negative ER and PR, the absence of lymph node metastasis, and high levels of CD8 + cells. The overall survival by univariate analysis was positively associated with lower tumor stage, the absence of lymph node metastasis, PD‐L1 expression, and high levels of CD8 + cells. Therefore, our data suggest cytotoxic immune reaction mediated by CD8‐positive T cells and PD‐L1 expression may predict a better outcome in patients with HER2‐positive breast carcinoma managed with conventional chemotherapy and HER2‐blocking therapy. These findings recommend clinical trials utilizing checkpoint blocking immunotherapy in some form for HER2‐positive breast cancer. … (more)
- Is Part Of:
- Breast journal. Volume 24:Issue 6(2018)
- Journal:
- Breast journal
- Issue:
- Volume 24:Issue 6(2018)
- Issue Display:
- Volume 24, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 24
- Issue:
- 6
- Issue Sort Value:
- 2018-0024-0006-0000
- Page Start:
- 911
- Page End:
- 919
- Publication Date:
- 2018-09-19
- Subjects:
- breast carcinoma -- cytotoxic T cells -- HER2 -- PD1 -- PD‐L1
Breast -- Diseases -- Periodicals
Breast -- Cancer -- Periodicals
618.19 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1075-122x;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1524-4741 ↗
http://www.blackwellpublishing.com/journal.asp?ref=1075-122X ↗
https://www.hindawi.com/journals/tbj/ ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=tbj ↗ - DOI:
- 10.1111/tbj.13112 ↗
- Languages:
- English
- ISSNs:
- 1075-122X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2277.494100
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8618.xml