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Phase II Trial of Nelipepimut-S Peptide Vaccine in Women with Ductal Carcinoma In Situ.
O'Shea, Anne E; Clifton, Guy T; Qiao, Na; Heckman-Stoddard, Brandy M; Wojtowicz, Malgorzata; Dimond, Eileen; Bedrosian, Isabelle; Weber, Diane; Garber, Judy E; Husband, Alexander; Pastorello, Ricardo; Lee, J Jack; Hernandez, Mike; Liu, Diane D; Vornik, Lana A; Brown, Powel H; Alatrash, Gheath; Peoples, George E; Mittendorf, Elizabeth A.
Afiliação
  • O'Shea AE; Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, Texas.
  • Clifton GT; Department of Surgery, Brooke Army Medical Center, Ft. Sam Houston, Texas.
  • Qiao N; Department of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Heckman-Stoddard BM; Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland.
  • Wojtowicz M; Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland.
  • Dimond E; Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland.
  • Bedrosian I; Department of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Weber D; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Garber JE; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Husband A; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, Massachusetts.
  • Pastorello R; Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Lee JJ; Harvard Medical School, Boston, Massachusetts.
  • Hernandez M; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Liu DD; Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Vornik LA; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, Massachusetts.
  • Brown PH; Division of Breast Surgery, Department of Surgery, Brigham and Women's Hospital, Boston, Massachusetts.
  • Alatrash G; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Peoples GE; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Mittendorf EA; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Prev Res (Phila) ; 16(6): 333-341, 2023 06 01.
Article em En | MEDLINE | ID: mdl-37259799
ABSTRACT
NeuVax is a vaccine comprised of the HER2-derived MHC class I peptide E75 (nelipepimut-S, NPS) combined with GM-CSF. We completed a randomized trial of preoperative vaccination with NeuVax versus GM-CSF alone in patients with ductal carcinoma in situ (DCIS). The primary objective was to evaluate for NPS-specific cytotoxic T lymphocyte (CTL) responses. Patients with human leukocyte antigen (HLA)-A2-positive DCIS were enrolled and randomized 21 to NeuVax versus GM-CSF alone and received two inoculations prior to surgery. The number of NPS-specific CTL was measured pre-vaccination, at surgery, and 1 and 3 to 6 months post-operation by dextramer assay. Differences in CTL responses between groups and between pre-vaccination and 1-month post-operation were analyzed using a two-sample t test or Wilcoxon rank sum test. The incidence and severity of adverse events were compared between groups. Overall, 45 patients were registered; 20 patients were HLA-A2 negative, 7 declined participation, 1 withdrew, and 4 failed screening for other reasons. The remaining 13 were randomized to NeuVax (n = 9) or GM-CSF alone (n = 4). Vaccination was well-tolerated with similar treatment-related toxicity between groups with the majority (>89%) of adverse events being grade 1. The percentage of NPS-specific CTLs increased in both arms between baseline (pre-vaccination) and 1-month post-operation. The increase was numerically greater in the NPS+GM-CSF arm, but the difference was not statistically significant. NPS+GM-CSF is safe and well-tolerated when given preoperatively to patients with DCIS. In patients with HLA-A2-positive DCIS, two inoculations with NPS+GM-CSF can induce in vivo immunity and a continued antigen-specific T-cell response 1-month postsurgery. PREVENTION RELEVANCE This trial showed that vaccination of patients with HLA-A2-positive DCIS with NeuVax in the preoperative setting can induce a sustained antigen-specific T-cell response. This provides proof of principle that vaccination in the preoperative or adjuvant setting may stimulate an adaptive immune response that could potentially prevent disease recurrence.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Intraductal não Infiltrante / Vacinas Anticâncer Tipo de estudo: Clinical_trials Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Intraductal não Infiltrante / Vacinas Anticâncer Tipo de estudo: Clinical_trials Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article