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Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study

PURPOSE: We assessed the safety and antitumor activity of avelumab, a fully human anti–programmed death-ligand 1 (PD-L1) IgG1 antibody, in patients with refractory metastatic urothelial carcinoma. METHODS: In this phase Ib, multicenter, expansion cohort, patients with urothelial carcinoma progressin...

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Autores principales: Apolo, Andrea B., Infante, Jeffrey R., Balmanoukian, Ani, Patel, Manish R., Wang, Ding, Kelly, Karen, Mega, Anthony E., Britten, Carolyn D., Ravaud, Alain, Mita, Alain C., Safran, Howard, Stinchcombe, Thomas E., Srdanov, Marko, Gelb, Arnold B., Schlichting, Michael, Chin, Kevin, Gulley, James L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493051/
https://www.ncbi.nlm.nih.gov/pubmed/28375787
http://dx.doi.org/10.1200/JCO.2016.71.6795
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author Apolo, Andrea B.
Infante, Jeffrey R.
Balmanoukian, Ani
Patel, Manish R.
Wang, Ding
Kelly, Karen
Mega, Anthony E.
Britten, Carolyn D.
Ravaud, Alain
Mita, Alain C.
Safran, Howard
Stinchcombe, Thomas E.
Srdanov, Marko
Gelb, Arnold B.
Schlichting, Michael
Chin, Kevin
Gulley, James L.
author_facet Apolo, Andrea B.
Infante, Jeffrey R.
Balmanoukian, Ani
Patel, Manish R.
Wang, Ding
Kelly, Karen
Mega, Anthony E.
Britten, Carolyn D.
Ravaud, Alain
Mita, Alain C.
Safran, Howard
Stinchcombe, Thomas E.
Srdanov, Marko
Gelb, Arnold B.
Schlichting, Michael
Chin, Kevin
Gulley, James L.
author_sort Apolo, Andrea B.
collection PubMed
description PURPOSE: We assessed the safety and antitumor activity of avelumab, a fully human anti–programmed death-ligand 1 (PD-L1) IgG1 antibody, in patients with refractory metastatic urothelial carcinoma. METHODS: In this phase Ib, multicenter, expansion cohort, patients with urothelial carcinoma progressing after platinum-based chemotherapy and unselected for PD-L1 expression received avelumab 10 mg/kg intravenously every 2 weeks. The primary objectives were safety and tolerability. Secondary objectives included confirmed objective response rate (Response Evaluation Criteria in Solid Tumors [RECIST] version 1.1), progression-free survival, overall survival (OS), and PD-L1–associated clinical activity. PD-L1 positivity was defined as expression by immunohistochemistry on ≥ 5% of tumor cells. RESULTS: Forty-four patients were treated with avelumab and followed for a median of 16.5 months (interquartile range, 15.8 to 16.7 months). The data cutoff was March 19, 2016. The most frequent treatment-related adverse events of any grade were fatigue/asthenia (31.8%), infusion-related reaction (20.5%), and nausea (11.4%). Grades 3 to 4 treatment-related adverse events occurred in three patients (6.8%) and included asthenia, AST elevation, creatine phosphokinase elevation, and decreased appetite. The confirmed objective response rate by independent central review was 18.2% (95% CI, 8.2% to 32.7%; five complete responses and three partial responses). The median duration of response was not reached (95% CI, 12.1 weeks to not estimable), and responses were ongoing in six patients (75.0%), including four of five complete responses. Seven of eight responding patients had PD-L1–positive tumors. The median progression-free survival was 11.6 weeks (95% CI, 6.1 to 17.4 weeks); the median OS was 13.7 months (95% CI, 8.5 months to not estimable), with a 12-month OS rate of 54.3% (95% CI, 37.9% to 68.1%). CONCLUSION: Avelumab was well tolerated and associated with durable responses and prolonged survival in patients with refractory metastatic UC.
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spelling pubmed-54930512018-03-16 Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study Apolo, Andrea B. Infante, Jeffrey R. Balmanoukian, Ani Patel, Manish R. Wang, Ding Kelly, Karen Mega, Anthony E. Britten, Carolyn D. Ravaud, Alain Mita, Alain C. Safran, Howard Stinchcombe, Thomas E. Srdanov, Marko Gelb, Arnold B. Schlichting, Michael Chin, Kevin Gulley, James L. J Clin Oncol ORIGINAL REPORTS PURPOSE: We assessed the safety and antitumor activity of avelumab, a fully human anti–programmed death-ligand 1 (PD-L1) IgG1 antibody, in patients with refractory metastatic urothelial carcinoma. METHODS: In this phase Ib, multicenter, expansion cohort, patients with urothelial carcinoma progressing after platinum-based chemotherapy and unselected for PD-L1 expression received avelumab 10 mg/kg intravenously every 2 weeks. The primary objectives were safety and tolerability. Secondary objectives included confirmed objective response rate (Response Evaluation Criteria in Solid Tumors [RECIST] version 1.1), progression-free survival, overall survival (OS), and PD-L1–associated clinical activity. PD-L1 positivity was defined as expression by immunohistochemistry on ≥ 5% of tumor cells. RESULTS: Forty-four patients were treated with avelumab and followed for a median of 16.5 months (interquartile range, 15.8 to 16.7 months). The data cutoff was March 19, 2016. The most frequent treatment-related adverse events of any grade were fatigue/asthenia (31.8%), infusion-related reaction (20.5%), and nausea (11.4%). Grades 3 to 4 treatment-related adverse events occurred in three patients (6.8%) and included asthenia, AST elevation, creatine phosphokinase elevation, and decreased appetite. The confirmed objective response rate by independent central review was 18.2% (95% CI, 8.2% to 32.7%; five complete responses and three partial responses). The median duration of response was not reached (95% CI, 12.1 weeks to not estimable), and responses were ongoing in six patients (75.0%), including four of five complete responses. Seven of eight responding patients had PD-L1–positive tumors. The median progression-free survival was 11.6 weeks (95% CI, 6.1 to 17.4 weeks); the median OS was 13.7 months (95% CI, 8.5 months to not estimable), with a 12-month OS rate of 54.3% (95% CI, 37.9% to 68.1%). CONCLUSION: Avelumab was well tolerated and associated with durable responses and prolonged survival in patients with refractory metastatic UC. American Society of Clinical Oncology 2017-07-01 2017-04-04 /pmc/articles/PMC5493051/ /pubmed/28375787 http://dx.doi.org/10.1200/JCO.2016.71.6795 Text en © 2017 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle ORIGINAL REPORTS
Apolo, Andrea B.
Infante, Jeffrey R.
Balmanoukian, Ani
Patel, Manish R.
Wang, Ding
Kelly, Karen
Mega, Anthony E.
Britten, Carolyn D.
Ravaud, Alain
Mita, Alain C.
Safran, Howard
Stinchcombe, Thomas E.
Srdanov, Marko
Gelb, Arnold B.
Schlichting, Michael
Chin, Kevin
Gulley, James L.
Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study
title Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study
title_full Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study
title_fullStr Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study
title_full_unstemmed Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study
title_short Avelumab, an Anti–Programmed Death-Ligand 1 Antibody, In Patients With Refractory Metastatic Urothelial Carcinoma: Results From a Multicenter, Phase Ib Study
title_sort avelumab, an anti–programmed death-ligand 1 antibody, in patients with refractory metastatic urothelial carcinoma: results from a multicenter, phase ib study
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493051/
https://www.ncbi.nlm.nih.gov/pubmed/28375787
http://dx.doi.org/10.1200/JCO.2016.71.6795
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