Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)

Abstract Background Small cell lung cancer (SCLC) accounts for 10–15% of all lung malignancies and its prognosis is dismal. Although early studies have shown promising clinical activity of immune checkpoint blockers, the immune composition and expression of potentially actionable immunostimulatory t...

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Main Authors: Daniel Carvajal-Hausdorf, Mehmet Altan, Vamsidhar Velcheti, Scott N. Gettinger, Roy S. Herbst, David L. Rimm, Kurt A. Schalper
Format: Article
Language:English
Published: BMJ Publishing Group 2019-03-01
Series:Journal for ImmunoTherapy of Cancer
Online Access:http://link.springer.com/article/10.1186/s40425-019-0540-1
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author Daniel Carvajal-Hausdorf
Mehmet Altan
Vamsidhar Velcheti
Scott N. Gettinger
Roy S. Herbst
David L. Rimm
Kurt A. Schalper
author_facet Daniel Carvajal-Hausdorf
Mehmet Altan
Vamsidhar Velcheti
Scott N. Gettinger
Roy S. Herbst
David L. Rimm
Kurt A. Schalper
author_sort Daniel Carvajal-Hausdorf
collection DOAJ
description Abstract Background Small cell lung cancer (SCLC) accounts for 10–15% of all lung malignancies and its prognosis is dismal. Although early studies have shown promising clinical activity of immune checkpoint blockers, the immune composition and expression of potentially actionable immunostimulatory targets in this malignancy are poorly understood. Methods Using multiplexed quantitative immunofluorescence (QIF), we measured the levels of 3 different B7 family ligands PD-L1, B7-H3, B7-H4 and major tumor infiltrating lymphocyte (TIL) subsets in 90 SCLC samples represented in tissue microarray format. Associations between the marker levels, clinicopathological variables and survival were studied. Results PD-L1 protein was detected in 7.3%, B7-H3 in 64.9% and B7-H4 in 2.6% of SCLC cases. The markers showed limited co-expression and were not associated with the level of TILs, age, gender and stage. Elevated B7-H4 was associated with shorter 5-year overall survival. The levels of CD3+, CD8+ and CD20+ TILs and the ratio of total/effector T-cells were significantly lower in SCLC than in non-small cell lung cancer. High levels of CD3+, but not CD8+ or CD20+ TILs were significantly associated with longer survival. Conclusions Taken together, our study indicate variable expression and clinical role of B7-family ligands in SCLC with predominant expression of the candidate target B7-H3 and the presence of a limited cytotoxic anti-tumor immune response. These results support the evaluation of B7-H3 blockers and/or pro-inflammatory therapies in SCLC.
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spelling doaj.art-95ad26b6988545f3b24fc5c049322f042022-12-22T02:09:28ZengBMJ Publishing GroupJournal for ImmunoTherapy of Cancer2051-14262019-03-01711910.1186/s40425-019-0540-1Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)Daniel Carvajal-Hausdorf0Mehmet Altan1Vamsidhar Velcheti2Scott N. Gettinger3Roy S. Herbst4David L. Rimm5Kurt A. Schalper6Department of Pathology, Yale School of MedicineMedical Oncology, Yale School of Medicine and Yale Cancer CenterThoracic Oncology, New York UniversityMedical Oncology, Yale School of Medicine and Yale Cancer CenterMedical Oncology, Yale School of Medicine and Yale Cancer CenterDepartment of Pathology, Yale School of MedicineDepartment of Pathology, Yale School of MedicineAbstract Background Small cell lung cancer (SCLC) accounts for 10–15% of all lung malignancies and its prognosis is dismal. Although early studies have shown promising clinical activity of immune checkpoint blockers, the immune composition and expression of potentially actionable immunostimulatory targets in this malignancy are poorly understood. Methods Using multiplexed quantitative immunofluorescence (QIF), we measured the levels of 3 different B7 family ligands PD-L1, B7-H3, B7-H4 and major tumor infiltrating lymphocyte (TIL) subsets in 90 SCLC samples represented in tissue microarray format. Associations between the marker levels, clinicopathological variables and survival were studied. Results PD-L1 protein was detected in 7.3%, B7-H3 in 64.9% and B7-H4 in 2.6% of SCLC cases. The markers showed limited co-expression and were not associated with the level of TILs, age, gender and stage. Elevated B7-H4 was associated with shorter 5-year overall survival. The levels of CD3+, CD8+ and CD20+ TILs and the ratio of total/effector T-cells were significantly lower in SCLC than in non-small cell lung cancer. High levels of CD3+, but not CD8+ or CD20+ TILs were significantly associated with longer survival. Conclusions Taken together, our study indicate variable expression and clinical role of B7-family ligands in SCLC with predominant expression of the candidate target B7-H3 and the presence of a limited cytotoxic anti-tumor immune response. These results support the evaluation of B7-H3 blockers and/or pro-inflammatory therapies in SCLC.http://link.springer.com/article/10.1186/s40425-019-0540-1
spellingShingle Daniel Carvajal-Hausdorf
Mehmet Altan
Vamsidhar Velcheti
Scott N. Gettinger
Roy S. Herbst
David L. Rimm
Kurt A. Schalper
Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)
Journal for ImmunoTherapy of Cancer
title Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)
title_full Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)
title_fullStr Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)
title_full_unstemmed Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)
title_short Expression and clinical significance of PD-L1, B7-H3, B7-H4 and TILs in human small cell lung Cancer (SCLC)
title_sort expression and clinical significance of pd l1 b7 h3 b7 h4 and tils in human small cell lung cancer sclc
url http://link.springer.com/article/10.1186/s40425-019-0540-1
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