First-in-human study of FAZ053, an anti-programmed death-ligand 1 (anti-PD-L1) monoclonal antibody, alone and in combination with spartalizumab (anti-PD-1), in patients with advanced malignancies

FAZ053 monotherapy was well tolerated and effective in maintaining disease control in various tumors including ASPS and chordoma. The anticipated synergistic effect of combined programmed cell death protein 1 (PD-1) and PD-L1 inhibition was not observed. These findings contribute to the growing evidence that rare, phenotypically 'immune cold' sarcomas, such as ASPS and chordoma, can become responsive to immune checkpoint inhibitors.

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Publication Details

Journal
ESMO Open
Published
2025-05-16
DOI
https://doi.org/10.1016/j.esmoop.2025.105051
Citations
2
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
2.09

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article

First-in-human study of FAZ053, an anti-programmed death-ligand 1 (anti-PD-L1) monoclonal antibody, alone and in combination with spartalizumab (anti-PD-1), in patients with advanced malignancies

Filip Janku, Jennifer Mataraza, A. Gucalp, Sebastian Szpakowski et al.
2 citations
ESMO Open
Cancer Immunotherapy and Biomarkers
2.09
article

First-in-human study of FAZ053, an anti-programmed death-ligand 1 (anti-PD-L1) monoclonal antibody, alone and in combination with spartalizumab (anti-PD-1), in patients with advanced malignancies

Filip Janku, Jennifer Mataraza, A. Gucalp, Sebastian Szpakowski, Ralf D. Reiners, S. Takahashi, Philippe Lucien Bedard, Ravit Geva, Kartik Subramanian, Xiaoling Chen, Juan Martín-Liberal, David S.P. Tan, Ching‐Lung Lai, R. Kan, Albiruni Abdul Razak
article en
2 citations

Abstract

FAZ053 monotherapy was well tolerated and effective in maintaining disease control in various tumors including ASPS and chordoma. The anticipated synergistic effect of combined programmed cell death protein 1 (PD-1) and PD-L1 inhibition was not observed. These findings contribute to the growing evidence that rare, phenotypically 'immune cold' sarcomas, such as ASPS and chordoma, can become responsive to immune checkpoint inhibitors.

ESMO OpenVol. 10(6)
Memorial Sloan Kettering Cancer Center (US), Tel Aviv Sourasky Medical Center (IL), Princess Margaret Cancer Centre (CA), Novartis (China) (CN), Novartis (United States) (US), The Cancer Institute Hospital (JP)
Amgen, Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, GlaxoSmithKline, Sanofi, Gilead Sciences, Karyopharm Therapeutics, Novartis Pharmaceuticals Corporation, Les Laboratories Pierre Fabre, Iterion Therapeutics, Daiichi-Sankyo, Eisai, Astellas Pharma, Servier, Ipsen, Symphogen, Genentech, Chugai Pharmaceutical, Daiichi Sankyo Europe
Good health and well-being
Openalex Percentile: Top 12%
Cancer Immunotherapy and Biomarkers
2.09
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