Your browser doesn't support javascript.
loading
Clinical and Immunologic Responses to a B-Cell Epitope Vaccine in Patients with HER2/neu-Overexpressing Advanced Gastric Cancer-Results from Phase Ib Trial IMU.ACS.001.
Wiedermann, Ursula; Garner-Spitzer, Erika; Chao, Yee; Maglakelidze, Marina; Bulat, Iurie; Dechaphunkul, Arunee; Arpornwirat, Wichit; Charoentum, Chaiyut; Yen, Chia-Jui; Yau, Thomas Cheung; Tanasanvimon, Suebpong; Maneechavakajorn, Jedzada; Sookprasert, Aumkhae; Bai, Li-Yuan; Chou, Wen-Chi; Ungtrakul, Teerapat; Drinic, Mirjana; Tobias, Joshua; Zielinski, Christoph C; Chong, Leslie; Ede, Nicholas J; Marino, Mark T; Good, Anthony J.
Afiliação
  • Wiedermann U; Institute of Specific Prophylaxis and Tropical Medicine, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria. ursula.wiedermann@meduniwien.ac.at.
  • Garner-Spitzer E; Institute of Specific Prophylaxis and Tropical Medicine, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
  • Chao Y; Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Maglakelidze M; ARENSIA Exploratory Medicine LLC, Tbilisi, Georgia.
  • Bulat I; ARENSIA Exploratory Medicine Research Unit, Institute of Oncology, Chisinau, Republic of Moldova.
  • Dechaphunkul A; Department of Medicine, Songklanagarind Hospital, Prince of Songkla University, Hat Yai, Thailand.
  • Arpornwirat W; NCI, Bangkok, Thailand.
  • Charoentum C; Maharaj Nakorn Chiang Mai Hospital, Mueang Chiang Mai District, Thailand.
  • Yen CJ; National Cheng Kung University, Tainan, Taiwan.
  • Yau TC; Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong.
  • Tanasanvimon S; King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
  • Maneechavakajorn J; Rajavithi Hospital, Bangkok, Thailand.
  • Sookprasert A; Srinagarind Hospital, Khon Kaen, Thailand.
  • Bai LY; China Medical University Hospital, Taichung City, Taiwan.
  • Chou WC; Linkou Chang Gung Memorial Hospital, Taoyuan City, Taiwan.
  • Ungtrakul T; Faculty of Medicine and Public Health, HRH Princess Chulabhorn College of Medical Science, Bangkok, Thailand.
  • Drinic M; Institute of Specific Prophylaxis and Tropical Medicine, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
  • Tobias J; Institute of Specific Prophylaxis and Tropical Medicine, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
  • Zielinski CC; Central European Cooperative Oncology Group, Vienna, Austria.
  • Chong L; Imugene Limited, Sydney, Australia.
  • Ede NJ; Imugene Limited, Sydney, Australia.
  • Marino MT; Imugene Limited, Sydney, Australia.
  • Good AJ; Imugene Limited, Sydney, Australia.
Clin Cancer Res ; 27(13): 3649-3660, 2021 07 01.
Article em En | MEDLINE | ID: mdl-33879458
PURPOSE: HER2/neu is overexpressed in up to 30% of gastroesophageal adenocarcinomas (GEA) and linked to poor prognosis. Recombinant mAbs to treat HER2/neu-overexpressing cancers are effective with limitations, including resistance and toxicity. Therefore, we developed a therapeutic B-cell epitope vaccine (IMU-131/HER-Vaxx) consisting of three fused B-cell epitopes from the HER2/neu extracellular domain coupled to CRM197 and adjuvanted with Montanide. This phase Ib study aimed to evaluate the optimal/safe dose leading to immunogenicity and clinical responses (https//clinicaltrials.gov/ct2/show/NCT02795988). PATIENTS AND METHODS: A total of 14 patients with HER2/neu-overexpressing GEA were enrolled, and dose escalation (10, 30, 50 µg) was performed in three cohorts (C). Immunogenicity was evaluated by HER2-specific Abs and cellular responses, clinical responses by CT scans according to RECIST version 1.1. RESULTS: IMU-131 was safe without vaccine-related significant local/systemic reactions or serious adverse events. A total of 11 of 14 patients were evaluable for changes in tumor size and vaccine-specific immune responses. One patient showed complete, 5 partial responses, and 4 stable diseases as their best response. HER2-specific IgG levels were dose dependent. In contrast to patients in C1 and C2, all patients in C3 mounted substantial HER2-specific Ab levels. In addition, cellular vaccine responses, such as Th1-biased cytokine ratios and reduced regulatory T cell numbers, were generated. Progression-free survival was prolonged in C3, correlating with the vaccine-specific humoral and cellular responses. CONCLUSIONS: IMU-131 was well tolerated and safe. The induced HER2-specific Abs and cellular responses were dose dependent and correlated with clinical responses. The highest dose (50 µg) was recommended for further evaluation in a phase II trial, with chemotherapy + IMU-131 or chemotherapy alone, which is currently ongoing.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Epitopos de Linfócito B / Vacinas Anticâncer / Imunogenicidade da Vacina Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Epitopos de Linfócito B / Vacinas Anticâncer / Imunogenicidade da Vacina Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Áustria