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Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence
PURPOSE: AE37 and GP2 are HER2 derived peptide vaccines. AE37 primarily elicits a CD4+ response while GP2 elicits a CD8+ response against the HER2 antigen. These peptides were tested in a large randomized trial to assess their ability to prevent recurrence in HER2 expressing breast cancer patients....
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188712/ https://www.ncbi.nlm.nih.gov/pubmed/32323103 http://dx.doi.org/10.1007/s10549-020-05638-x |
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author | Brown, Tommy A. Mittendorf, Elizabeth A. Hale, Diane F. Myers, John W. Peace, Kaitlin M. Jackson, Doreen O. Greene, Julia M. Vreeland, Timothy J. Clifton, G. Travis Ardavanis, Alexandros Litton, Jennifer K. Shumway, Nathan M. Symanowski, J. Murray, James L. Ponniah, Sathibalan Anastasopoulou, E. A. Pistamaltzian, N. F. Baxevanis, Constantin N. Perez, Sonia A. Papamichail, Michael Peoples, George E. |
author_facet | Brown, Tommy A. Mittendorf, Elizabeth A. Hale, Diane F. Myers, John W. Peace, Kaitlin M. Jackson, Doreen O. Greene, Julia M. Vreeland, Timothy J. Clifton, G. Travis Ardavanis, Alexandros Litton, Jennifer K. Shumway, Nathan M. Symanowski, J. Murray, James L. Ponniah, Sathibalan Anastasopoulou, E. A. Pistamaltzian, N. F. Baxevanis, Constantin N. Perez, Sonia A. Papamichail, Michael Peoples, George E. |
author_sort | Brown, Tommy A. |
collection | PubMed |
description | PURPOSE: AE37 and GP2 are HER2 derived peptide vaccines. AE37 primarily elicits a CD4+ response while GP2 elicits a CD8+ response against the HER2 antigen. These peptides were tested in a large randomized trial to assess their ability to prevent recurrence in HER2 expressing breast cancer patients. The primary analyses found no difference in 5-year overall disease-free survival (DFS) but possible benefit in subgroups. Here, we present the final landmark analysis. METHODS: In this 4-arm, prospective, randomized, single-blinded, multi-center phase II trial, disease-free node positive and high-risk node negative breast cancer patients enrolled after standard of care therapy. Six monthly inoculations of vaccine (VG) vs. control (CG) were given as the primary vaccine series with 4 boosters at 6-month intervals. Demographic, safety, immunologic, and DFS data were evaluated. RESULTS: 456 patients were enrolled; 154 patients in the VG and 147 in CG for AE37, 89 patients in the VG and 91 in CG for GP2. The AE37 arm had no difference in DFS as compared to CG, but pre-specified exploratory subgroup analyses showed a trend towards benefit in advanced stage (p = 0.132, HR 0.573 CI 0.275–1.193), HER2 under-expression (p = 0.181, HR 0.756 CI 0.499–1.145), and triple-negative breast cancer (p = 0.266, HR 0.443 CI 0.114–1.717). In patients with both HER2 under-expression and advanced stage, there was significant benefit in the VG (p = 0.039, HR 0.375 CI 0.142–0.988) as compared to CG. The GP2 arm had no significant difference in DFS as compared to CG, but on subgroup analysis, HER2 positive patients had no recurrences with a trend toward improved DFS (p = 0.052) in VG as compared to CG. CONCLUSIONS: This phase II trial reveals that AE37 and GP2 are safe and possibly associated with improved clinical outcomes of DFS in certain subgroups of breast cancer patients. With these findings, further evaluations are warranted of AE37 and GP2 vaccines given in combination and/or separately for specific subsets of breast cancer patients based on their disease biology. |
format | Online Article Text |
id | pubmed-7188712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-71887122020-05-04 Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence Brown, Tommy A. Mittendorf, Elizabeth A. Hale, Diane F. Myers, John W. Peace, Kaitlin M. Jackson, Doreen O. Greene, Julia M. Vreeland, Timothy J. Clifton, G. Travis Ardavanis, Alexandros Litton, Jennifer K. Shumway, Nathan M. Symanowski, J. Murray, James L. Ponniah, Sathibalan Anastasopoulou, E. A. Pistamaltzian, N. F. Baxevanis, Constantin N. Perez, Sonia A. Papamichail, Michael Peoples, George E. Breast Cancer Res Treat Clinical Trial PURPOSE: AE37 and GP2 are HER2 derived peptide vaccines. AE37 primarily elicits a CD4+ response while GP2 elicits a CD8+ response against the HER2 antigen. These peptides were tested in a large randomized trial to assess their ability to prevent recurrence in HER2 expressing breast cancer patients. The primary analyses found no difference in 5-year overall disease-free survival (DFS) but possible benefit in subgroups. Here, we present the final landmark analysis. METHODS: In this 4-arm, prospective, randomized, single-blinded, multi-center phase II trial, disease-free node positive and high-risk node negative breast cancer patients enrolled after standard of care therapy. Six monthly inoculations of vaccine (VG) vs. control (CG) were given as the primary vaccine series with 4 boosters at 6-month intervals. Demographic, safety, immunologic, and DFS data were evaluated. RESULTS: 456 patients were enrolled; 154 patients in the VG and 147 in CG for AE37, 89 patients in the VG and 91 in CG for GP2. The AE37 arm had no difference in DFS as compared to CG, but pre-specified exploratory subgroup analyses showed a trend towards benefit in advanced stage (p = 0.132, HR 0.573 CI 0.275–1.193), HER2 under-expression (p = 0.181, HR 0.756 CI 0.499–1.145), and triple-negative breast cancer (p = 0.266, HR 0.443 CI 0.114–1.717). In patients with both HER2 under-expression and advanced stage, there was significant benefit in the VG (p = 0.039, HR 0.375 CI 0.142–0.988) as compared to CG. The GP2 arm had no significant difference in DFS as compared to CG, but on subgroup analysis, HER2 positive patients had no recurrences with a trend toward improved DFS (p = 0.052) in VG as compared to CG. CONCLUSIONS: This phase II trial reveals that AE37 and GP2 are safe and possibly associated with improved clinical outcomes of DFS in certain subgroups of breast cancer patients. With these findings, further evaluations are warranted of AE37 and GP2 vaccines given in combination and/or separately for specific subsets of breast cancer patients based on their disease biology. Springer US 2020-04-22 2020 /pmc/articles/PMC7188712/ /pubmed/32323103 http://dx.doi.org/10.1007/s10549-020-05638-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Trial Brown, Tommy A. Mittendorf, Elizabeth A. Hale, Diane F. Myers, John W. Peace, Kaitlin M. Jackson, Doreen O. Greene, Julia M. Vreeland, Timothy J. Clifton, G. Travis Ardavanis, Alexandros Litton, Jennifer K. Shumway, Nathan M. Symanowski, J. Murray, James L. Ponniah, Sathibalan Anastasopoulou, E. A. Pistamaltzian, N. F. Baxevanis, Constantin N. Perez, Sonia A. Papamichail, Michael Peoples, George E. Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence |
title | Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence |
title_full | Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence |
title_fullStr | Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence |
title_full_unstemmed | Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence |
title_short | Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence |
title_sort | prospective, randomized, single-blinded, multi-center phase ii trial of two her2 peptide vaccines, gp2 and ae37, in breast cancer patients to prevent recurrence |
topic | Clinical Trial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188712/ https://www.ncbi.nlm.nih.gov/pubmed/32323103 http://dx.doi.org/10.1007/s10549-020-05638-x |
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