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Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients
BACKGROUND: Long-term survival of stage IV melanoma patients has improved significantly with the development of immune checkpoint inhibitors (CIs). Reliable biomarkers to predict response and clinical outcome are needed. METHODS: We investigated the role of melanoma-associated antibodies as predicti...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383238/ https://www.ncbi.nlm.nih.gov/pubmed/30786924 http://dx.doi.org/10.1186/s40425-019-0523-2 |
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author | Fässler, Mirjam Diem, Stefan Mangana, Joanna Hasan Ali, Omar Berner, Fiamma Bomze, David Ring, Sandra Niederer, Rebekka del Carmen Gil Cruz, Cristina Pérez Shibayama, Christian Ivan Krolik, Michal Siano, Marco Joerger, Markus Recher, Mike Risch, Lorenz Güsewell, Sabine Risch, Martin Speiser, Daniel E. Ludewig, Burkhard Levesque, Mitchell P. Dummer, Reinhard Flatz, Lukas |
author_facet | Fässler, Mirjam Diem, Stefan Mangana, Joanna Hasan Ali, Omar Berner, Fiamma Bomze, David Ring, Sandra Niederer, Rebekka del Carmen Gil Cruz, Cristina Pérez Shibayama, Christian Ivan Krolik, Michal Siano, Marco Joerger, Markus Recher, Mike Risch, Lorenz Güsewell, Sabine Risch, Martin Speiser, Daniel E. Ludewig, Burkhard Levesque, Mitchell P. Dummer, Reinhard Flatz, Lukas |
author_sort | Fässler, Mirjam |
collection | PubMed |
description | BACKGROUND: Long-term survival of stage IV melanoma patients has improved significantly with the development of immune checkpoint inhibitors (CIs). Reliable biomarkers to predict response and clinical outcome are needed. METHODS: We investigated the role of melanoma-associated antibodies as predictive markers for CI therapy in two independent cohorts. In cohort 1, a prospective study, we measured specific antibodies before treatment, after one week and after six to nine weeks of treatment. Cohort 2 consisted of serum samples prior to CI therapy initiation. ELISA assays were performed to quantify specific IgG directed against melanocyte differentiation antigens tyrosinase-related proteins 1 and 2 (TRP1/TYRP1 and TRP2/TYRP2), glycoprotein 100 (gp100), MelanA/MART1, and the cancer-testis antigen NY-ESO-1. Response was defined as either complete or partial remission on CT scan according to RECIST 1.1. RESULTS: In cohort 1, baseline levels of these antibodies were higher in the responder group, although statistical significance was only reached for NY-ESO-1 (p = 0.007). In cohort 2, significantly higher antibody baseline levels for MelanA/MART1 (p = 0.003) and gp100 (p = 0.029) were found. After pooling the results from both cohorts, higher levels of MelanA/MART1 (p = 0.013), TRP1/TYRP1 (p = 0.048), TRP2/TYRP2 (p = 0.047) and NY-ESO-1 (p = 0.005) specific antibodies at baseline were independently associated with response. CONCLUSIONS: Melanoma-associated antibodies may be candidate biomarkers for response and survival in metastatic melanoma patients being treated with CIs. These markers may be used to complement patient assessment, in combination with PD-L1 status, tumor-infiltrating lymphocytes and tumor mutational burden, with the aim to predict outcome of CI treatment in patients with metastatic melanoma. TRIAL REGISTRATION: Ethikkommission Ostschweiz, EKOS 16/079 https://ongoingprojects.swissethics.ch/runningProjects_list.php?q=%28BASECID~contains~2016-00998%29&orderby=dBASECID. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40425-019-0523-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6383238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63832382019-03-01 Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients Fässler, Mirjam Diem, Stefan Mangana, Joanna Hasan Ali, Omar Berner, Fiamma Bomze, David Ring, Sandra Niederer, Rebekka del Carmen Gil Cruz, Cristina Pérez Shibayama, Christian Ivan Krolik, Michal Siano, Marco Joerger, Markus Recher, Mike Risch, Lorenz Güsewell, Sabine Risch, Martin Speiser, Daniel E. Ludewig, Burkhard Levesque, Mitchell P. Dummer, Reinhard Flatz, Lukas J Immunother Cancer Research Article BACKGROUND: Long-term survival of stage IV melanoma patients has improved significantly with the development of immune checkpoint inhibitors (CIs). Reliable biomarkers to predict response and clinical outcome are needed. METHODS: We investigated the role of melanoma-associated antibodies as predictive markers for CI therapy in two independent cohorts. In cohort 1, a prospective study, we measured specific antibodies before treatment, after one week and after six to nine weeks of treatment. Cohort 2 consisted of serum samples prior to CI therapy initiation. ELISA assays were performed to quantify specific IgG directed against melanocyte differentiation antigens tyrosinase-related proteins 1 and 2 (TRP1/TYRP1 and TRP2/TYRP2), glycoprotein 100 (gp100), MelanA/MART1, and the cancer-testis antigen NY-ESO-1. Response was defined as either complete or partial remission on CT scan according to RECIST 1.1. RESULTS: In cohort 1, baseline levels of these antibodies were higher in the responder group, although statistical significance was only reached for NY-ESO-1 (p = 0.007). In cohort 2, significantly higher antibody baseline levels for MelanA/MART1 (p = 0.003) and gp100 (p = 0.029) were found. After pooling the results from both cohorts, higher levels of MelanA/MART1 (p = 0.013), TRP1/TYRP1 (p = 0.048), TRP2/TYRP2 (p = 0.047) and NY-ESO-1 (p = 0.005) specific antibodies at baseline were independently associated with response. CONCLUSIONS: Melanoma-associated antibodies may be candidate biomarkers for response and survival in metastatic melanoma patients being treated with CIs. These markers may be used to complement patient assessment, in combination with PD-L1 status, tumor-infiltrating lymphocytes and tumor mutational burden, with the aim to predict outcome of CI treatment in patients with metastatic melanoma. TRIAL REGISTRATION: Ethikkommission Ostschweiz, EKOS 16/079 https://ongoingprojects.swissethics.ch/runningProjects_list.php?q=%28BASECID~contains~2016-00998%29&orderby=dBASECID. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40425-019-0523-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-20 /pmc/articles/PMC6383238/ /pubmed/30786924 http://dx.doi.org/10.1186/s40425-019-0523-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Fässler, Mirjam Diem, Stefan Mangana, Joanna Hasan Ali, Omar Berner, Fiamma Bomze, David Ring, Sandra Niederer, Rebekka del Carmen Gil Cruz, Cristina Pérez Shibayama, Christian Ivan Krolik, Michal Siano, Marco Joerger, Markus Recher, Mike Risch, Lorenz Güsewell, Sabine Risch, Martin Speiser, Daniel E. Ludewig, Burkhard Levesque, Mitchell P. Dummer, Reinhard Flatz, Lukas Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
title | Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
title_full | Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
title_fullStr | Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
title_full_unstemmed | Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
title_short | Antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
title_sort | antibodies as biomarker candidates for response and survival to checkpoint inhibitors in melanoma patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383238/ https://www.ncbi.nlm.nih.gov/pubmed/30786924 http://dx.doi.org/10.1186/s40425-019-0523-2 |
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