Safety and Antitumor Activity of a Novel aCD25 Treg Depleter RG6292 as a Single Agent and in Combination with Atezolizumab in Patients with Solid Tumors

RG6292 (vopikitug) targets CD25 (IL-2Rα) and mediates regulatory T-cell depletion while not interfering with IL-2 signaling. Peripheral and intratumoral Treg depletion was shown in two phase I studies. However, RG6292 alone or in combination with atezolizumab was insufficient to reverse and rescue from established resistance mechanisms in solid tumors.

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Publication Details

Journal
Cancer Research Communications
Published
2025-02-21
DOI
https://doi.org/10.1158/2767-9764.crc-24-0638
Citations
11
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
11.50

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article

Safety and Antitumor Activity of a Novel aCD25 Treg Depleter RG6292 as a Single Agent and in Combination with Atezolizumab in Patients with Solid Tumors

Gabriel Schnetzler, Daniel J. Renouf, Enrique Gómez Alcaide, Aung Naing et al.
11 citations
Cancer Research Communications
Cancer Immunotherapy and Biomarkers
11.50
article

Safety and Antitumor Activity of a Novel aCD25 Treg Depleter RG6292 as a Single Agent and in Combination with Atezolizumab in Patients with Solid Tumors

Gabriel Schnetzler, Daniel J. Renouf, Enrique Gómez Alcaide, Aung Naing, Vaios Karanikas, Tamara Tanos, Miguel F. Sanmamed, Linxinyu Xu, Bernard Doger de Spéville, Nicole Justies, Vladimir Galvao, Michael Ong, Kristoffer Staal Rohrberg, Valentina Gambardella, Stephen J. Luen, Samira Curdt, Emiliano Calvo, Maria Amann, Nicolas Städler, Christophe Boetsch, María E. Rodríguez-Ruiz, Jean‐Pascal Machiels, Rachel Galot, Eva Rossmann, Anna Spreafico, T Kolben, Yuying Xie, Kevin Smart
article en
11 citations

Abstract

RG6292 (vopikitug) targets CD25 (IL-2Rα) and mediates regulatory T-cell depletion while not interfering with IL-2 signaling. Peripheral and intratumoral Treg depletion was shown in two phase I studies. However, RG6292 alone or in combination with atezolizumab was insufficient to reverse and rescue from established resistance mechanisms in solid tumors.

Cancer Research CommunicationsVol. 5(3)
Roche (Switzerland) (CH), University of Copenhagen (DK), BC Cancer Agency (CA), Cliniques Universitaires Saint-Luc (BE), University Health Network (CA), The University of Texas MD Anderson Cancer Center (US), Peter MacCallum Cancer Centre (AU), Ottawa Hospital (CA), Copenhagen University Hospital (DK), Princess Margaret Cancer Centre (CA), Rigshospitalet (DK), Roche (Canada) (CA), Roche Pharma AG (Germany) (DE), Hospital Clínico Universitario de Valencia (ES), Centro Oncológico de Galicia (ES), Vall d'Hebron Institut de Recerca (ES), Navarre Institute of Health Research (ES), Roche (United Kingdom) (GB), Hospital Universitario Fundación Jiménez Díaz (ES), Clinica Universidad de Navarra (ES), Vall d'Hebron Institute of Oncology (ES), IT University of Copenhagen (DK), Universidad de Navarra (ES), UCLouvain (BE)
Pfizer, AstraZeneca, BeiGene, Symphogen, Genentech
Good health and well-being
Openalex Percentile: Top 1%
Cancer Immunotherapy and Biomarkers
11.50
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