Retifanlimab in Advanced Penile Squamous Cell Carcinoma: The Phase 2 ORPHEUS Study

The phase 2 ORPHEUS trial is one of the first prospective studies evaluating the efficacy and safety of retifanlimab (an anti-PD-1 agent) in patients with metastatic penile squamous cell carcinoma. Retifanlimab exhibited signals of clinical activity, with a manageable safety profile. Patients with a...

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Hauptverfasser: García Del Muro, Xavier, Páez López-Bravo, David, Cuéllar-Rivas, Miler Andrés, Maroto, Pablo, Giannatempo, Patrizia, Castellano, Daniel, Climent, Miguel A., Valderrama, Begoña P., Gómez de Liaño, Alfonso, López-Montero, Laura, Mina, Leonardo, Alcalá-López, Daniel, Sampayo-Cordero, Miguel, Necchi, Andrea
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container_title European urology oncology
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creator García Del Muro, Xavier
Páez López-Bravo, David
Cuéllar-Rivas, Miler Andrés
Maroto, Pablo
Giannatempo, Patrizia
Castellano, Daniel
Climent, Miguel A.
Valderrama, Begoña P.
Gómez de Liaño, Alfonso
López-Montero, Laura
Mina, Leonardo
Alcalá-López, Daniel
Sampayo-Cordero, Miguel
Necchi, Andrea
description The phase 2 ORPHEUS trial is one of the first prospective studies evaluating the efficacy and safety of retifanlimab (an anti-PD-1 agent) in patients with metastatic penile squamous cell carcinoma. Retifanlimab exhibited signals of clinical activity, with a manageable safety profile. Patients with advanced penile squamous cell carcinoma (PSCC) have poor outcomes and very limited therapeutic options are available. Most PSCC cases have high PD-L1 expression, which is associated with worse prognosis. Immunotherapy targeting PD-L1 could benefit patients with PSCC. Our aim was to evaluate the efficacy and safety of the anti-PD-1 antibody retifanlimab in patients with advanced/metastatic PSCC. ORPHEUS was a single-arm, multicenter, phase 2 trial in 18 patients with advanced/metastatic PSCC, previously untreated with anti-PD-1/anti-PD-L1 agents. Patients received retifanlimab 500 mg intravenously every 4 wk for up to 2 yr. The primary endpoint was the objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumors v1.1. Secondary endpoints included the clinical benefit rate (CBR), disease control rate, duration of response (DoR), time to response, progression-free survival (PFS), overall survival (OS), maximum tumor shrinkage, and safety. The Wilson method was used for the primary endpoint, and the Clopper-Pearson and Kaplan-Meier methods for secondary endpoints. Median follow-up was 7.2 mo. The ORR was 16.7% (95% confidence interval [CI] 5.8–39.2); three patients had a partial response. Median DoR was 3.3 mo (range 1.8–8.5). The CBR was 22.2% (95% CI 6.4–47.6%). Median PFS was 2.0 mo (95% CI 1.6–3.3) and median OS was 7.2 mo (95% CI 3.0–9.8). One patient (5.6%) experienced grade 3 treatment-related adverse events (TRAEs). There were no grade ≥4 TRAEs. The small sample size is the main limitation. Single-agent retifanlimab exhibited signals of clinical activity in advanced/metastatic PSCC, with no new safety signals. Further investigation of retifanlimab in this setting is warranted. Advanced penile cancer of the squamous cell type is a rare tumor with poor prognosis. The aggressiveness of this cancer is usually associated with high levels of a protein called PD-L1. We investigated whether retifanlimab, an immunotherapy drug against PD-1, has activity against this type of penile cancer. Tumor regression or stabilization occurred in one-third of the patients and the side effects were manageable.
doi_str_mv 10.1016/j.euo.2024.04.021
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Retifanlimab exhibited signals of clinical activity, with a manageable safety profile. Patients with advanced penile squamous cell carcinoma (PSCC) have poor outcomes and very limited therapeutic options are available. Most PSCC cases have high PD-L1 expression, which is associated with worse prognosis. Immunotherapy targeting PD-L1 could benefit patients with PSCC. Our aim was to evaluate the efficacy and safety of the anti-PD-1 antibody retifanlimab in patients with advanced/metastatic PSCC. ORPHEUS was a single-arm, multicenter, phase 2 trial in 18 patients with advanced/metastatic PSCC, previously untreated with anti-PD-1/anti-PD-L1 agents. Patients received retifanlimab 500 mg intravenously every 4 wk for up to 2 yr. The primary endpoint was the objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumors v1.1. Secondary endpoints included the clinical benefit rate (CBR), disease control rate, duration of response (DoR), time to response, progression-free survival (PFS), overall survival (OS), maximum tumor shrinkage, and safety. The Wilson method was used for the primary endpoint, and the Clopper-Pearson and Kaplan-Meier methods for secondary endpoints. Median follow-up was 7.2 mo. The ORR was 16.7% (95% confidence interval [CI] 5.8–39.2); three patients had a partial response. Median DoR was 3.3 mo (range 1.8–8.5). The CBR was 22.2% (95% CI 6.4–47.6%). Median PFS was 2.0 mo (95% CI 1.6–3.3) and median OS was 7.2 mo (95% CI 3.0–9.8). One patient (5.6%) experienced grade 3 treatment-related adverse events (TRAEs). There were no grade ≥4 TRAEs. The small sample size is the main limitation. Single-agent retifanlimab exhibited signals of clinical activity in advanced/metastatic PSCC, with no new safety signals. Further investigation of retifanlimab in this setting is warranted. Advanced penile cancer of the squamous cell type is a rare tumor with poor prognosis. The aggressiveness of this cancer is usually associated with high levels of a protein called PD-L1. We investigated whether retifanlimab, an immunotherapy drug against PD-1, has activity against this type of penile cancer. Tumor regression or stabilization occurred in one-third of the patients and the side effects were manageable.</description><identifier>ISSN: 2588-9311</identifier><identifier>EISSN: 2588-9311</identifier><identifier>DOI: 10.1016/j.euo.2024.04.021</identifier><identifier>PMID: 38749903</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Clinical trial ; Immune checkpoint inhibitor ; Immunotherapy ; Metastatic ; PD-L1 ; Penile cancer ; Penile squamous cell carcinoma ; Retifanlimab</subject><ispartof>European urology oncology, 2024-05</ispartof><rights>2024</rights><rights>Copyright © 2024 European Association of Urology. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1503-8aa2705fe24c69c96be37b53022a0ca8d1336a1bc4cfc00751b4131cb4c95ed13</cites><orcidid>0009-0007-9108-341X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38749903$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García Del Muro, Xavier</creatorcontrib><creatorcontrib>Páez López-Bravo, David</creatorcontrib><creatorcontrib>Cuéllar-Rivas, Miler Andrés</creatorcontrib><creatorcontrib>Maroto, Pablo</creatorcontrib><creatorcontrib>Giannatempo, Patrizia</creatorcontrib><creatorcontrib>Castellano, Daniel</creatorcontrib><creatorcontrib>Climent, Miguel A.</creatorcontrib><creatorcontrib>Valderrama, Begoña P.</creatorcontrib><creatorcontrib>Gómez de Liaño, Alfonso</creatorcontrib><creatorcontrib>López-Montero, Laura</creatorcontrib><creatorcontrib>Mina, Leonardo</creatorcontrib><creatorcontrib>Alcalá-López, Daniel</creatorcontrib><creatorcontrib>Sampayo-Cordero, Miguel</creatorcontrib><creatorcontrib>Necchi, Andrea</creatorcontrib><title>Retifanlimab in Advanced Penile Squamous Cell Carcinoma: The Phase 2 ORPHEUS Study</title><title>European urology oncology</title><addtitle>Eur Urol Oncol</addtitle><description>The phase 2 ORPHEUS trial is one of the first prospective studies evaluating the efficacy and safety of retifanlimab (an anti-PD-1 agent) in patients with metastatic penile squamous cell carcinoma. 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Secondary endpoints included the clinical benefit rate (CBR), disease control rate, duration of response (DoR), time to response, progression-free survival (PFS), overall survival (OS), maximum tumor shrinkage, and safety. The Wilson method was used for the primary endpoint, and the Clopper-Pearson and Kaplan-Meier methods for secondary endpoints. Median follow-up was 7.2 mo. The ORR was 16.7% (95% confidence interval [CI] 5.8–39.2); three patients had a partial response. Median DoR was 3.3 mo (range 1.8–8.5). The CBR was 22.2% (95% CI 6.4–47.6%). Median PFS was 2.0 mo (95% CI 1.6–3.3) and median OS was 7.2 mo (95% CI 3.0–9.8). One patient (5.6%) experienced grade 3 treatment-related adverse events (TRAEs). There were no grade ≥4 TRAEs. The small sample size is the main limitation. Single-agent retifanlimab exhibited signals of clinical activity in advanced/metastatic PSCC, with no new safety signals. Further investigation of retifanlimab in this setting is warranted. 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Retifanlimab exhibited signals of clinical activity, with a manageable safety profile. Patients with advanced penile squamous cell carcinoma (PSCC) have poor outcomes and very limited therapeutic options are available. Most PSCC cases have high PD-L1 expression, which is associated with worse prognosis. Immunotherapy targeting PD-L1 could benefit patients with PSCC. Our aim was to evaluate the efficacy and safety of the anti-PD-1 antibody retifanlimab in patients with advanced/metastatic PSCC. ORPHEUS was a single-arm, multicenter, phase 2 trial in 18 patients with advanced/metastatic PSCC, previously untreated with anti-PD-1/anti-PD-L1 agents. Patients received retifanlimab 500 mg intravenously every 4 wk for up to 2 yr. The primary endpoint was the objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumors v1.1. Secondary endpoints included the clinical benefit rate (CBR), disease control rate, duration of response (DoR), time to response, progression-free survival (PFS), overall survival (OS), maximum tumor shrinkage, and safety. The Wilson method was used for the primary endpoint, and the Clopper-Pearson and Kaplan-Meier methods for secondary endpoints. Median follow-up was 7.2 mo. The ORR was 16.7% (95% confidence interval [CI] 5.8–39.2); three patients had a partial response. Median DoR was 3.3 mo (range 1.8–8.5). The CBR was 22.2% (95% CI 6.4–47.6%). Median PFS was 2.0 mo (95% CI 1.6–3.3) and median OS was 7.2 mo (95% CI 3.0–9.8). One patient (5.6%) experienced grade 3 treatment-related adverse events (TRAEs). There were no grade ≥4 TRAEs. The small sample size is the main limitation. Single-agent retifanlimab exhibited signals of clinical activity in advanced/metastatic PSCC, with no new safety signals. Further investigation of retifanlimab in this setting is warranted. 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subjects Clinical trial
Immune checkpoint inhibitor
Immunotherapy
Metastatic
PD-L1
Penile cancer
Penile squamous cell carcinoma
Retifanlimab
title Retifanlimab in Advanced Penile Squamous Cell Carcinoma: The Phase 2 ORPHEUS Study
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