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Programmed death ligand 1-positive immune cells in primary tumor or metastatic axillary lymph nodes can predict prognosis of triple-negative breast cancer even when present at < 1% in the tumor region

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Title: Programmed death ligand 1-positive immune cells in primary tumor or metastatic axillary lymph nodes can predict prognosis of triple-negative breast cancer even when present at < 1% in the tumor region
Authors: Tomioka, Nobumoto Browse this author
Hatanaka, Kanako C. Browse this author
Okuyama, Dai Browse this author
Watanabe, Ken-ichi Browse this author
Yamamoto, Mitsugu Browse this author
Maeda, Hideki Browse this author
Tachikawa, Hanae Browse this author
Kuwahara, Sayuri Browse this author
Shimizu, Ai Browse this author
Suzuki, Hiroaki Browse this author
Hatanaka, Yutaka Browse this author
Takahashi, Masato Browse this author
Keywords: PD-L1
TILs
TNBC
TME
ICI
Issue Date: 1-May-2023
Publisher: Springer
Journal Title: Breast cancer
Volume: 30
Issue: 3
Start Page: 497
End Page: 505
Publisher DOI: 10.1007/s12282-023-01442-9
Abstract: BackgroundThe efficacy of pre-operative systemic treatment (PST) combined with immune checkpoint inhibition (ICI) for triple-negative breast cancer (TNBC) has been recognized recently as being independent of the degree of programmed death ligand-1 (PD-L1) positivity of infiltrating immune cells, especially for patients with axillary lymph node metastasis (ALNM).MethodsTNBC patients with ALNM were treated surgically between 2002 and 2016 in our facility (n = 109), of whom 38 received PST before resection. The presence of tumor-infiltrating lymphocytes (TILs) expressing CD3, CD8, CD68, PD-L1 (detected by antibody SP142) and FOXP3 at primary and metastatic LN sites was quantified.ResultsThe size of invasive tumor and the number of metastatic axillary LN were confirmed as prognostic markers. The numbers of both CD8+ and FOXP3+ TILs at primary sites were also recognized as prognostic markers, especially for overall survival (OS) (CD8, p = 0.026; FOXP3, p < 0.001). The presence of CD8+, FOXP3+ and PD-L1+ cells was better maintained in LN after PST and may contribute to improved antitumor immunity. Provided they were present as clusters of >= 70 positive cells, even < 1% of immune cells expressing PD-L1 at primary sites predicted a more favorable prognosis for both disease-free survival (DFS) (p = 0.004) and OS (p = 0.020). This was the case not only for 30 matched surgical patients, but also in all 71 surgical only patients (DFS: p < 0.001 and OS: p = 0.002).ConclusionsPD-L1+ , CD8+ or FOXP3+ immune cells in the tumor microenvironment (TME) at both primary and metastatic sites are significant on prognosis, which could be a clue to expect the potential for better responses to the combination of chemotherapy and ICI, especially for patients with ALNM.
Type: article
URI: http://hdl.handle.net/2115/89178
Appears in Collections:北海道大学病院 (Hokkaido University Hospital) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

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