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Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial

Purpose: Determine the prognostic and predictive significance of tumor associated antigen (TAA)-specific serum antibodies in melanoma patients of a large adjuvant vaccination phase III trial. Patients and methods: Serum IgG antibodies were measured against a panel of 43 antigens by a bead-based mult...

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Autores principales: Michels, Judith, Becker, Natalia, Suciu, Stefan, Kaiser, Iris, Benner, Axel, Kosaloglu-Yalcin, Zeynep, Agoussi, Sandrine, Halama, Niels, Pawlita, Michael, Waterboer, Tim, Eichmüller, Stefan B., Jäger, Dirk, Eggermont, Alexander M. M., Zörnig, Inka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980408/
https://www.ncbi.nlm.nih.gov/pubmed/29872552
http://dx.doi.org/10.1080/2162402X.2018.1428157
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author Michels, Judith
Becker, Natalia
Suciu, Stefan
Kaiser, Iris
Benner, Axel
Kosaloglu-Yalcin, Zeynep
Agoussi, Sandrine
Halama, Niels
Pawlita, Michael
Waterboer, Tim
Eichmüller, Stefan B.
Jäger, Dirk
Eggermont, Alexander M. M.
Zörnig, Inka
author_facet Michels, Judith
Becker, Natalia
Suciu, Stefan
Kaiser, Iris
Benner, Axel
Kosaloglu-Yalcin, Zeynep
Agoussi, Sandrine
Halama, Niels
Pawlita, Michael
Waterboer, Tim
Eichmüller, Stefan B.
Jäger, Dirk
Eggermont, Alexander M. M.
Zörnig, Inka
author_sort Michels, Judith
collection PubMed
description Purpose: Determine the prognostic and predictive significance of tumor associated antigen (TAA)-specific serum antibodies in melanoma patients of a large adjuvant vaccination phase III trial. Patients and methods: Serum IgG antibodies were measured against a panel of 43 antigens by a bead-based multiplex assay in 970 stage II melanoma patients of the EORTC18961 trial, evaluating adjuvant ganglioside GM2-KLH/QS-21 vaccination versus observation. Primary end point was relapse-free survival (RFS). Patients' sera at baseline, after 12 and 48 weeks of study treatment and at the last available time point (at recurrence/remission) were evaluated. Results: Prognostic clinical variables are gender, surgical confirmation of lymph node-negative status, Breslow thickness and ulceration of the primary. Prognostic spontaneous antibody responses were associated with a significant dismal (GM2, Rhod_E2, SSX2) or good prognosis (CyclinB1, SCYE1v1) for RFS, distant metastasis-free (DMFS) or overall survival (OS). Predictive spontaneous antibody responses based on significant interaction with treatment were RhodN p = 0.02, Rab38 p = 0.04 for RFS, RhodE2 p = 0.006, Recoverin p = 0.04 for DMFS and RhodE2 p = 0.003; Recoverin p = 0.04, NA17.A p = 0.04, for OS respectively. The subgroups of patients according to antibody responses for RFS were determined for RhodN sero-negative (n = 849, HR = 1.07, p = 0.6); RhodN sero-positive (n = 121,HR = 0.42, p = 0.01) and Rab38 sero-negative (n = 682, HR = 1.12, p = 0.42), Rab38 sero-positive (n = 288, HR = 0.65, p = 0.04) patients respectively. Conclusion: We identified prognostic serum antibody responses against TAA in stage II melanoma patients. A set of antibody responses correlated with a beneficial outcome for GM2 vaccination.
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spelling pubmed-59804082018-06-05 Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial Michels, Judith Becker, Natalia Suciu, Stefan Kaiser, Iris Benner, Axel Kosaloglu-Yalcin, Zeynep Agoussi, Sandrine Halama, Niels Pawlita, Michael Waterboer, Tim Eichmüller, Stefan B. Jäger, Dirk Eggermont, Alexander M. M. Zörnig, Inka Oncoimmunology Original Research Purpose: Determine the prognostic and predictive significance of tumor associated antigen (TAA)-specific serum antibodies in melanoma patients of a large adjuvant vaccination phase III trial. Patients and methods: Serum IgG antibodies were measured against a panel of 43 antigens by a bead-based multiplex assay in 970 stage II melanoma patients of the EORTC18961 trial, evaluating adjuvant ganglioside GM2-KLH/QS-21 vaccination versus observation. Primary end point was relapse-free survival (RFS). Patients' sera at baseline, after 12 and 48 weeks of study treatment and at the last available time point (at recurrence/remission) were evaluated. Results: Prognostic clinical variables are gender, surgical confirmation of lymph node-negative status, Breslow thickness and ulceration of the primary. Prognostic spontaneous antibody responses were associated with a significant dismal (GM2, Rhod_E2, SSX2) or good prognosis (CyclinB1, SCYE1v1) for RFS, distant metastasis-free (DMFS) or overall survival (OS). Predictive spontaneous antibody responses based on significant interaction with treatment were RhodN p = 0.02, Rab38 p = 0.04 for RFS, RhodE2 p = 0.006, Recoverin p = 0.04 for DMFS and RhodE2 p = 0.003; Recoverin p = 0.04, NA17.A p = 0.04, for OS respectively. The subgroups of patients according to antibody responses for RFS were determined for RhodN sero-negative (n = 849, HR = 1.07, p = 0.6); RhodN sero-positive (n = 121,HR = 0.42, p = 0.01) and Rab38 sero-negative (n = 682, HR = 1.12, p = 0.42), Rab38 sero-positive (n = 288, HR = 0.65, p = 0.04) patients respectively. Conclusion: We identified prognostic serum antibody responses against TAA in stage II melanoma patients. A set of antibody responses correlated with a beneficial outcome for GM2 vaccination. Taylor & Francis 2018-02-12 /pmc/articles/PMC5980408/ /pubmed/29872552 http://dx.doi.org/10.1080/2162402X.2018.1428157 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Original Research
Michels, Judith
Becker, Natalia
Suciu, Stefan
Kaiser, Iris
Benner, Axel
Kosaloglu-Yalcin, Zeynep
Agoussi, Sandrine
Halama, Niels
Pawlita, Michael
Waterboer, Tim
Eichmüller, Stefan B.
Jäger, Dirk
Eggermont, Alexander M. M.
Zörnig, Inka
Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial
title Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial
title_full Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial
title_fullStr Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial
title_full_unstemmed Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial
title_short Multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage II melanoma patients of the EORTC18961 trial
title_sort multiplex bead-based measurement of humoral immune responses against tumor-associated antigens in stage ii melanoma patients of the eortc18961 trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980408/
https://www.ncbi.nlm.nih.gov/pubmed/29872552
http://dx.doi.org/10.1080/2162402X.2018.1428157
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