Amb motiu del tancament d'estiu, la validació de documents es reprendrà a partir del 28 d'agost de 2026. Disculpeu les molèsties.
Con motivo del cierre de verano, la validación de documentos se reanudará a partir del 28 de agosto de 2026. Disculpad las molestias
Due to the summer closure, document validation will resume starting August 28, 2026. We apologize for any inconvenience.

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/227677

A Novel Heterologous Prime-boost Strategy Using RUTI Vaccine to Improve the Bacillus Calmette-Guérin Response in Non–muscle-invasive Bladder Cancer Patients: Phase 1 RUTIVAC-1 Trial

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

Intravesical bacillus Calmette-Gu & eacute;rin (BCG) is the standard treatment for high-risk non- muscle-invasive bladder cancer (NMIBC); however, recurrence and progression remain major challenges. To explore a heterologous prime-boost strategy, we conducted the RUTIVAC-1 trial (NCT03191578) to evaluate RUTI, a nonlive vaccine, derived from Mycobacterium tuberculosis, as a systemic primer prior to intravesical BCG in high-risk NMIBC patients. The immunogenicity, safety, and preliminary efficacy of RUTI was evaluated. In this phase 1, randomized, double-blind, placebo-controlled trial, 40 NMIBC patients were randomized 1:1 to receive two subcutaneous doses of RUTI (25 lg) or placebo before BCG treatment. Immunogenicity was assessed by flow cytometry, and clinical follow-up was extended to 5 yr. RUTI induced a systemic vaccine-specific response, increasing activation markers on CD4+ and CD8+ T cells, supporting effective immune priming. Regulatory T-cell expansion was observed in the placebo group but not in RUTI-vaccinated patients, who also exhibited amore heterogeneous and polyfunctional specific immune response. RUTI was safe and well tolerated, with only mild injectionsite reactions. Exploratory analyses showed a trend toward reduced recurrence, progression, and death, with improved 5-yr progression-free survival. The small sample size and baseline imbalances were the limitations. This phase 1 study supports the safety and immunogenicity of RUTI and provides encouraging data that warrant confirmation in larger t rials to establish its potential clinical benefit as a novel therapeutic strategy.

Matèries

Matèries (anglès)

Citació

Citació

BUISAN, Oscar, et al. A Novel Heterologous Prime-boost Strategy Using RUTI Vaccine to Improve the Bacillus Calmette-Guérin Response in Non–muscle-invasive Bladder Cancer Patients: Phase 1 RUTIVAC-1 Trial. European Urology. 2025. Vol. 89, num. 2, pags. 114-120. [consulted: 18 of August of 2026]. Available at: https://hdl.handle.net/2445/227677

Exportar metadades

JSON - METS

Compartir registre