» Articles » PMID: 18245541

Combined Clinical Trial Results of a HER2/neu (E75) Vaccine for the Prevention of Recurrence in High-risk Breast Cancer Patients: U.S. Military Cancer Institute Clinical Trials Group Study I-01 and I-02

Abstract

Purpose: E75 is an immunogenic peptide from the HER2/neu protein, which is overexpressed in many breast cancer patients. We have conducted two overlapping E75 vaccine trials to prevent recurrence in node-positive (NP) and node-negative (NN) breast cancer patients.

Experimental Design: E75 (HER2/neu 369-377) + granulocyte macrophage colony-stimulating factor was given intradermally to previously treated, disease-free NP breast cancer patients in a dose escalation safety trial and to NN breast cancer patients in a dose optimization study. Local and systemic toxicity was monitored. Immunologic responses were assessed using in vitro assays and in vivo delayed-type hypersensitivity responses. Clinical recurrences were documented.

Results: One hundred and eighty-six patients were enrolled in the two studies (NP, 95; NN, 91). Human leucocyte antigen A2 (HLA-A2) and HLA-A3 patients were vaccinated (n = 101), whereas all others (n = 85) were followed prospectively as controls. Toxicities were minimal, and a dose-dependent immunologic response to the vaccine was shown. Planned primary analysis revealed a recurrence rate of 5.6% in vaccinated patients compared with 14.2% in the controls (P = 0.04) at a median of 20 months follow-up. As vaccine-specific immunity waned over time, the difference in recurrence lost significance at 26 months median follow-up (8.3% versus 14.8%); however, a significant difference in the pattern of recurrence persisted.

Conclusions: E75 is safe and effective in raising a dose-dependent HER2/neu immunity in HLA-A2 and HLA-A3 NP and NN breast cancer patients. More importantly, E75 may reduce recurrences in disease-free, conventionally treated, high-risk breast cancer patients. These findings warrant a prospective, randomized phase III trial of the E75 vaccine with periodic booster to prevent breast cancer recurrences.

Citing Articles

Short Peptides as Powerful Arsenal for Smart Fighting Cancer.

Bojarska J, Wolf W Cancers (Basel). 2024; 16(19).

PMID: 39409876 PMC: 11476321. DOI: 10.3390/cancers16193254.


Emerging treatments in HER2-positive advanced breast cancer: Keep raising the bar.

Agostinetto E, Curigliano G, Piccart M Cell Rep Med. 2024; 5(6):101575.

PMID: 38759648 PMC: 11228398. DOI: 10.1016/j.xcrm.2024.101575.


Antigen-Clustered Nanovaccine Achieves Long-Term Tumor Remission by Promoting B/CD 4 T Cell Crosstalk.

Li C, Clauson R, Bugada L, Ke F, He B, Yu Z ACS Nano. 2024; 18(13):9584-9604.

PMID: 38513119 PMC: 11130742. DOI: 10.1021/acsnano.3c13038.


Update on current and new potential immunotherapies in breast cancer, from bench to bedside.

Alaluf E, Shalamov M, Sonnenblick A Front Immunol. 2024; 15:1287824.

PMID: 38433837 PMC: 10905744. DOI: 10.3389/fimmu.2024.1287824.


Phase II Trial of Nelipepimut-S Peptide Vaccine in Women with Ductal Carcinoma In Situ.

OShea A, Clifton G, Qiao N, Heckman-Stoddard B, Wojtowicz M, Dimond E Cancer Prev Res (Phila). 2023; 16(6):333-341.

PMID: 37259799 PMC: 10903526. DOI: 10.1158/1940-6207.CAPR-22-0388.