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Phase I Trial of a Modified Vaccinia Ankara Priming Vaccine Followed by a Fowlpox Virus Boosting Vaccine Modified to Express Brachyury and Costimulatory Molecules in Advanced Solid Tumors.

Authors :
Collins JM
Donahue RN
Tsai YT
Manu M
Palena C
Gatti-Mays ME
Marté JL
Madan RA
Karzai F
Heery CR
Strauss J
Abdul-Sater H
Cordes L
Schlom J
Gulley JL
Bilusic M
Source :
The oncologist [Oncologist] 2020 Jul; Vol. 25 (7), pp. 560-e1006. Date of Electronic Publication: 2019 Dec 26.
Publication Year :
2020

Abstract

Lessons Learned: Modified vaccinia Ankara-Bavarian Nordic (MVA-BN)-Brachyury followed by fowlpox virus-BN-Brachyury was well tolerated upon administration to patients with advanced cancer. Sixty-three percent of patients developed CD4+ and/or CD8+ T-cell responses to brachyury after vaccination. BN-Brachyury vaccine also induced T-cell responses against CEA and MUC1, which are cascade antigens, that is, antigens not encoded in the vaccines.<br />Background: Brachyury, a transcription factor, plays an integral role in the epithelial-mesenchymal transition, metastasis, and tumor resistance to chemotherapy. It is expressed in many tumor types, and rarely in normal tissues, making it an ideal immunologic target. Bavarian Nordic (BN)-Brachyury consists of vaccination with modified vaccinia Ankara (MVA) priming followed by fowlpox virus (FPV) boosting, each encoding transgenes for brachyury and costimulatory molecules.<br />Methods: Patients with metastatic solid tumors were treated with two monthly doses of MVA-brachyury s.c., 8 × 10 <superscript>8</superscript> infectious units (IU), followed by FPV-brachyury s.c., 1 × 10 <superscript>9</superscript> IU, for six monthly doses and then every 3 months for up to 2 years. The primary objective was to determine safety and tolerability.<br />Results: Eleven patients were enrolled from March 2018 to July 2018 (one patient was nonevaluable). No dose-limiting toxicities were observed. The most common treatment-related adverse event was grade 1/2 injection-site reaction observed in all patients. Best overall response was stable disease in six patients, and the 6-month progression-free survival rate was 50%. T cells against brachyury and cascade antigens CEA and MUC1 were detected in the majority of patients.<br />Conclusion: BN-Brachyury vaccine is well tolerated and induces immune responses to brachyury and cascade antigens and demonstrates some evidence of clinical benefit.<br /> (© AlphaMed Press; the data published online to support this summary are the property of the authors.)

Details

Language :
English
ISSN :
1549-490X
Volume :
25
Issue :
7
Database :
MEDLINE
Journal :
The oncologist
Publication Type :
Academic Journal
Accession number :
31876334
Full Text :
https://doi.org/10.1634/theoncologist.2019-0932