Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence.
Adult
Biomarkers, Tumor
/ metabolism
Breast Neoplasms
/ drug therapy
Carcinoma, Ductal, Breast
/ drug therapy
Carcinoma, Lobular
/ drug therapy
Female
Follow-Up Studies
Gene Expression Regulation, Neoplastic
Humans
Middle Aged
Neoplasm Invasiveness
Neoplasm Recurrence, Local
/ immunology
Peptide Fragments
Prognosis
Prospective Studies
Receptor, ErbB-2
/ immunology
Receptors, Estrogen
/ metabolism
Receptors, Progesterone
/ metabolism
Single-Blind Method
Survival Rate
Vaccines, Subunit
/ administration & dosage
AE37
Breast cancer
GP2
HER2
Immunotherapy
Vaccine
Journal
Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
27
10
2019
accepted:
08
04
2020
pubmed:
24
4
2020
medline:
2
12
2020
entrez:
24
4
2020
Statut:
ppublish
Résumé
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. 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. 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. 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.
Identifiants
pubmed: 32323103
doi: 10.1007/s10549-020-05638-x
pii: 10.1007/s10549-020-05638-x
pmc: PMC7188712
doi:
Substances chimiques
Biomarkers, Tumor
0
Peptide Fragments
0
Receptors, Estrogen
0
Receptors, Progesterone
0
Vaccines, Subunit
0
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
391-401Subventions
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NIH HHS
ID : CA016672
Pays : United States
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