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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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.
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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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