Oncotarget

Clinical Research Papers:

Primary analysis of a prospective, randomized, single-blinded phase II trial evaluating the HER2 peptide GP2 vaccine in breast cancer patients to prevent recurrence

Elizabeth A. Mittendorf, Alexandros Ardavanis, Jennifer K. Litton, Nathan M. Shumway, Diane F. Hale, James L. Murray, Sonia A. Perez, Sathibalan Ponniah, Constantin N. Baxevanis, Michael Papamichail and George E. Peoples _

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Oncotarget. 2016; 7:66192-66201. https://doi.org/10.18632/oncotarget.11751

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Abstract

Elizabeth A. Mittendorf1,*, Alexandros Ardavanis2, Jennifer K. Litton3, Nathan M. Shumway4, Diane F. Hale5, James L. Murray3, Sonia A. Perez2, Sathibalan Ponniah6, Constantin N. Baxevanis2, Michael Papamichail2 and George E. Peoples7,*

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

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

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

4 Department of Hematology/Oncology, Brooke Army Medical Center, Ft. Sam Houston, TX, USA

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

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

7 Cancer Vaccine Development Program, San Antonio, TX, USA

* These authors have contributed equally to this work

Correspondence to:

Elizabeth A. Mittendorf, email:

George E. Peoples, email:

Keywords: vaccine, cytotoxic T lymphocytes, breast cancer, HER2, trastuzumab

Received: February 07, 2016 Accepted: July 09, 2016 Published: August 31, 2016

Abstract

GP2 is a HER2-derived, HLA-A2+ restricted peptide. Phase I studies showed GP2 administered with GM-CSF to be safe and immunogenic. Here we report the primary analysis of a prospective, randomized, multicenter phase II adjuvant trial conducted to determine the vaccine’s efficacy. The trial enrolled HLA-A2+, clinically disease-free, node-positive and high-risk node-negative breast cancer patients with tumors expressing HER2 (immunohistochemistry[IHC] 1+-3+). Patients were randomized to GP2+GM-CSF versus GM-CSF alone. Disease-free survival (DFS) was analyzed in intention-to-treat (ITT) and per-treatment cohorts; pre-specified subgroup analyses were performed for patients with IHC 3+ or FISH+ disease. The trial enrolled 180 patients; 89 received GP2+GM-CSF and 91 received GM-CSF alone. The groups were well-matched for clinicopathologic characteristics. Toxicities have been minimal. The Kaplan-Meier estimated 5-year DFS rate in the ITT analyses was 88% (95% CI:78-94%) in vaccinated vs. 81% (95% CI:69-89%) (P = 0.43) in control patients after a 34 month median follow-up. In the per-treatment analysis, the estimated 5-year DFS rates were 94% (95% CI:83-98%) and 85% (73-92%) (P = 0.17). In IHC 3+/FISH+ patients, the estimated 5-year DFS rate was 94% (82-98%) in vaccinated patients (n = 51) vs. 89% (71-96%) in control patients (n = 50), (P = 0.86) in the ITT analyses and 100% vs. 89% (71-96%) in vaccinated vs. control patients in the per-treatment analyses (P = 0.08). While the overall ITT analysis did not demonstrate benefit to vaccination, this trial confirmed that the GP2 vaccine is safe and suggests that vaccination may have clinical activity, particularly in patients with HER2 overexpression who received the full vaccine series (ie per-treatment group).


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