Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence.


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
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

391-401

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NIH HHS
ID : CA016672
Pays : United States

Références

Nat Med. 2000 Apr;6(4):443-6
pubmed: 10742152
Cancer. 2006 Jun 1;106(11):2309-17
pubmed: 16596621
Curr Drug Targets Immune Endocr Metabol Disord. 2005 Dec;5(4):365-71
pubmed: 16375690
Clin Cancer Res. 2019 Jul 15;25(14):4248-4254
pubmed: 31036542
Cancer Immunol Immunother. 2005 Aug;54(8):721-8
pubmed: 16010587
Annu Rev Immunol. 2003;21:305-34
pubmed: 12471050
Science. 1989 May 12;244(4905):707-12
pubmed: 2470152
Vaccine. 2010 Nov 3;28(47):7476-82
pubmed: 20858449
Cancer Immunol Immunother. 2007 May;56(5):601-13
pubmed: 16960693
J Pathol. 2006 Nov;210(3):358-62
pubmed: 16981252
Clin Cancer Res. 1999 Jun;5(6):1289-97
pubmed: 10389911
Clin Cancer Res. 2008 Feb 1;14(3):797-803
pubmed: 18245541
Ann Oncol. 2014 Sep;25(9):1735-42
pubmed: 24907636
Int J Cancer. 2007 Nov 1;121(9):2031-41
pubmed: 17634957
Oncotarget. 2016 Oct 4;7(40):66192-66201
pubmed: 27589688
Eur J Cancer. 1992;28A(4-5):859-64
pubmed: 1524909
Ann Oncol. 2016 Jul;27(7):1241-8
pubmed: 27029708
Clin Adv Hematol Oncol. 2016 Nov;14(11):922-933
pubmed: 27930644
Ann Surg Oncol. 2006 Aug;13(8):1085-98
pubmed: 16865596
J Immunol. 2015 Mar 1;194(5):2049-56
pubmed: 25710958
Clin Cancer Res. 2010 Jul 1;16(13):3495-506
pubmed: 20466887
J Clin Oncol. 2008 Jul 10;26(20):3426-33
pubmed: 18612158
J Immunother Cancer. 2017 Apr 18;5:39
pubmed: 28428887
Br J Cancer. 2014 Jul 29;111(3):532-8
pubmed: 24937677
Clin Immunol. 2018 Oct;195:28-35
pubmed: 30025819
Clin Cancer Res. 2016 May 1;22(9):2105-10
pubmed: 26867935
Cancer Immunol Immunother. 2004 Jun;53(6):490-6
pubmed: 14740174
Front Immunol. 2019 Aug 14;10:1939
pubmed: 31475002

Auteurs

Tommy A Brown (TA)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

Elizabeth A Mittendorf (EA)

Department of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Division of Breast Surgery, Department of Surgery, Breast Oncology Program, Brigham and Women's Hospital, Dana-Farber/Brigham and Women's Hospital, Boston, MA, USA.

Diane F Hale (DF)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

John W Myers (JW)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

Kaitlin M Peace (KM)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

Doreen O Jackson (DO)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

Julia M Greene (JM)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

Timothy J Vreeland (TJ)

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

G Travis Clifton (GT)

Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, San Antonio, TX, USA.

Alexandros Ardavanis (A)

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

Jennifer K Litton (JK)

Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Nathan M Shumway (NM)

Texas Oncology PA, San Antonio, TX, USA.

J Symanowski (J)

Department of Cancer Biostatistics, Levine Cancer Institute, Charlotte, NC, USA.

James L Murray (JL)

Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Sathibalan Ponniah (S)

Cancer Vaccine Development Laboratory, Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.

E A Anastasopoulou (EA)

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

N F Pistamaltzian (NF)

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

Constantin N Baxevanis (CN)

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

Sonia A Perez (SA)

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

Michael Papamichail (M)

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

George E Peoples (GE)

Department of Surgery, Uniformed Services Health University, Bethesda, MD, USA. gpeoples@cancerinsight.com.
Cancer Vaccine Development Program, 1305 East Houston Street, San Antonio, TX, 78205, USA. gpeoples@cancerinsight.com.

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Classifications MeSH