Cargando…
Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma
BACKGROUND & AIMS: Nivolumab, a programmed death (PD)-1 (PD-1) inhibitor, led to durable responses, manageable safety, and increased survival in patients with advanced hepatocellular carcinoma (HCC). In our retrospective analysis, we studied the immunobiology and potential associations between b...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751218/ https://www.ncbi.nlm.nih.gov/pubmed/32710922 http://dx.doi.org/10.1016/j.jhep.2020.07.026 |
_version_ | 1783625623546101760 |
---|---|
author | Sangro, Bruno Melero, Ignacio Wadhawan, Samir Finn, Richard S. Abou-Alfa, Ghassan K. Cheng, Ann-Lii Yau, Thomas Furuse, Junji Park, Joong-Won Boyd, Zachary Tang, Hao (Tracy) Shen, Yun Tschaika, Marina Neely, Jaclyn El-Khoueiry, Anthony |
author_facet | Sangro, Bruno Melero, Ignacio Wadhawan, Samir Finn, Richard S. Abou-Alfa, Ghassan K. Cheng, Ann-Lii Yau, Thomas Furuse, Junji Park, Joong-Won Boyd, Zachary Tang, Hao (Tracy) Shen, Yun Tschaika, Marina Neely, Jaclyn El-Khoueiry, Anthony |
author_sort | Sangro, Bruno |
collection | PubMed |
description | BACKGROUND & AIMS: Nivolumab, a programmed death (PD)-1 (PD-1) inhibitor, led to durable responses, manageable safety, and increased survival in patients with advanced hepatocellular carcinoma (HCC). In our retrospective analysis, we studied the immunobiology and potential associations between biomarkers and outcomes with nivolumab in HCC. METHODS: Fresh and archival tumour samples from dose-escalation and dose-expansion phases of the CheckMate 040 trial were analysed by immunohistochemistry and RNA sequencing to assess several inflammatory gene expression signatures, including CD274 (PD-ligand 1 [PD-L1]), CD8A, LAG3, and STAT1. Biomarkers were assessed for association with clinical outcomes (best overall response by blinded independent central review per RECIST v1.1 and overall survival [OS]). RESULTS: Complete or partial tumour responses were observed in PD-L1–positive and PD-L1–negative patients treated with nivolumab monotherapy. Median OS was 28.1 (95% CI 18.2–n.a.) vs. 16.6 months (95% CI 14.2–20.2) for patients with tumour PD-L1 ≥1% vs. <1% (p = 0.03). Increased CD3 and CD8 showed a non-significant trend towards improved OS (both p = 0.08), and macrophage markers were not associated with OS. Tumour PD-1 and PD-L1 expression were associated with improved OS (p = 0.05 and p = 0.03, respectively). An inflammatory gene signature consisting of 4 genes was associated with improved objective response rate (p = 0.05) and OS (p = 0.01). CONCLUSIONS: PD-1 and PD-L1 expression, biomarkers of inflammation, and inflammatory gene signatures trended with improved survival and response. While further confirmation within a larger phase III trial is needed to evaluate predictive value of these biomarkers, these exploratory analyses suggest that anti-tumour immune response may play a role in the treatment benefit of nivolumab in HCC. LAY SUMMARY: Certain tests may be used to provide a picture of how a tumour is escaping the immune system, allowing it to continue to grow and create more tumours. Therapies such as nivolumab are designed to help the immune system fight the tumour. These tests may be used to determine how effective such therapies will be in the treatment of advanced liver cancer. NCT NUMBER: NCT01658878. |
format | Online Article Text |
id | pubmed-7751218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-77512182020-12-21 Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma Sangro, Bruno Melero, Ignacio Wadhawan, Samir Finn, Richard S. Abou-Alfa, Ghassan K. Cheng, Ann-Lii Yau, Thomas Furuse, Junji Park, Joong-Won Boyd, Zachary Tang, Hao (Tracy) Shen, Yun Tschaika, Marina Neely, Jaclyn El-Khoueiry, Anthony J Hepatol Article BACKGROUND & AIMS: Nivolumab, a programmed death (PD)-1 (PD-1) inhibitor, led to durable responses, manageable safety, and increased survival in patients with advanced hepatocellular carcinoma (HCC). In our retrospective analysis, we studied the immunobiology and potential associations between biomarkers and outcomes with nivolumab in HCC. METHODS: Fresh and archival tumour samples from dose-escalation and dose-expansion phases of the CheckMate 040 trial were analysed by immunohistochemistry and RNA sequencing to assess several inflammatory gene expression signatures, including CD274 (PD-ligand 1 [PD-L1]), CD8A, LAG3, and STAT1. Biomarkers were assessed for association with clinical outcomes (best overall response by blinded independent central review per RECIST v1.1 and overall survival [OS]). RESULTS: Complete or partial tumour responses were observed in PD-L1–positive and PD-L1–negative patients treated with nivolumab monotherapy. Median OS was 28.1 (95% CI 18.2–n.a.) vs. 16.6 months (95% CI 14.2–20.2) for patients with tumour PD-L1 ≥1% vs. <1% (p = 0.03). Increased CD3 and CD8 showed a non-significant trend towards improved OS (both p = 0.08), and macrophage markers were not associated with OS. Tumour PD-1 and PD-L1 expression were associated with improved OS (p = 0.05 and p = 0.03, respectively). An inflammatory gene signature consisting of 4 genes was associated with improved objective response rate (p = 0.05) and OS (p = 0.01). CONCLUSIONS: PD-1 and PD-L1 expression, biomarkers of inflammation, and inflammatory gene signatures trended with improved survival and response. While further confirmation within a larger phase III trial is needed to evaluate predictive value of these biomarkers, these exploratory analyses suggest that anti-tumour immune response may play a role in the treatment benefit of nivolumab in HCC. LAY SUMMARY: Certain tests may be used to provide a picture of how a tumour is escaping the immune system, allowing it to continue to grow and create more tumours. Therapies such as nivolumab are designed to help the immune system fight the tumour. These tests may be used to determine how effective such therapies will be in the treatment of advanced liver cancer. NCT NUMBER: NCT01658878. 2020-07-22 2020-12 /pmc/articles/PMC7751218/ /pubmed/32710922 http://dx.doi.org/10.1016/j.jhep.2020.07.026 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Sangro, Bruno Melero, Ignacio Wadhawan, Samir Finn, Richard S. Abou-Alfa, Ghassan K. Cheng, Ann-Lii Yau, Thomas Furuse, Junji Park, Joong-Won Boyd, Zachary Tang, Hao (Tracy) Shen, Yun Tschaika, Marina Neely, Jaclyn El-Khoueiry, Anthony Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
title | Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
title_full | Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
title_fullStr | Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
title_full_unstemmed | Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
title_short | Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
title_sort | association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751218/ https://www.ncbi.nlm.nih.gov/pubmed/32710922 http://dx.doi.org/10.1016/j.jhep.2020.07.026 |
work_keys_str_mv | AT sangrobruno associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT meleroignacio associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT wadhawansamir associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT finnrichards associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT aboualfaghassank associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT chengannlii associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT yauthomas associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT furusejunji associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT parkjoongwon associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT boydzachary associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT tanghaotracy associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT shenyun associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT tschaikamarina associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT neelyjaclyn associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma AT elkhoueiryanthony associationofinflammatorybiomarkerswithclinicaloutcomesinnivolumabtreatedpatientswithadvancedhepatocellularcarcinoma |