2022
DOI: 10.1038/s41591-021-01600-6
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Atezolizumab with enzalutamide versus enzalutamide alone in metastatic castration-resistant prostate cancer: a randomized phase 3 trial

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Cited by 148 publications
(114 citation statements)
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“…The phase III IMbassador 250 trial was the first study to investigate an immunotherapy combination with atezolizumab plus enzalutamide vs. enzalutamide alone in 759 mCRPC patients who progressed on abiraterone and were ineligible for or refused a taxane regimen [ 37 ]. This study did not meet the primary endpoint of improved overall survival in unselected patients (stratified HR 1.12, 95% CI 0.91–1.37, p = 0.28).…”
Section: Immune Checkpoint Inhibitors In Castration-resistant Prostat...mentioning
confidence: 99%
“…The phase III IMbassador 250 trial was the first study to investigate an immunotherapy combination with atezolizumab plus enzalutamide vs. enzalutamide alone in 759 mCRPC patients who progressed on abiraterone and were ineligible for or refused a taxane regimen [ 37 ]. This study did not meet the primary endpoint of improved overall survival in unselected patients (stratified HR 1.12, 95% CI 0.91–1.37, p = 0.28).…”
Section: Immune Checkpoint Inhibitors In Castration-resistant Prostat...mentioning
confidence: 99%
“…In turn, these activate a cGAS/STING-mediated interferon response [ 36 ]. However, the inconsistency surrounding clinical outcomes in patients bearing cancers with DDR alterations and treated with immune checkpoint inhibitors questions its relevance as a biomarker [ 37 , 38 ].…”
Section: Immune Response and The Role Of The Microenvironment In Pros...mentioning
confidence: 99%
“…In the IMbassador250 phase 3 clinical trial, a combination of PD-L1 inhibitor atezolizumab and enzalutamide was compared to enzalutamide alone in patients with mCRPC who had progressed on abiraterone and docetaxel or were not candidates for a taxane regimen (NCT03016312). The combination of atezolizumab and enzalutamid did not show an OS improvement (15.2 months (95% CI: 14.0, 17.0) vs. enzalutamide alone (16.6 months (95% CI: 14.7, 18.4), requiring early termination of the study [ 38 , 141 ]. In line with previous findings, low effector T cell and macrophage signatures, as well as reduced MHC class I and immune checkpoint signatures were observed in the majority of patients.…”
Section: Immunotherapeutic Treatment Approachesmentioning
confidence: 99%
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