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Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial
BACKGROUND: Angiogenic factors promote the growth of tumor vasculature, modulate lymphocyte trafficking into tumors, and inhibit maturation of dendritic cells. We hypothesized that MEDI3617, a human IgG1 kappa monoclonal antibody directed against human angiopoietin-2, in combination with tremelimuma...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593712/ https://www.ncbi.nlm.nih.gov/pubmed/34772758 http://dx.doi.org/10.1136/jitc-2021-003318 |
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author | Ott, Patrick A Nazzaro, Matthew Pfaff, Kathleen L Gjini, Evisa Felt, Kristen D Wolff, Jacquelyn O Buchbinder, Elizabeth I Haq, Rizwan Sullivan, Ryan J Lawrence, Donald P McDermott, David F Severgnini, Mariano Giobbie-Hurder, Anita Rodig, Scott J Stephen Hodi, F |
author_facet | Ott, Patrick A Nazzaro, Matthew Pfaff, Kathleen L Gjini, Evisa Felt, Kristen D Wolff, Jacquelyn O Buchbinder, Elizabeth I Haq, Rizwan Sullivan, Ryan J Lawrence, Donald P McDermott, David F Severgnini, Mariano Giobbie-Hurder, Anita Rodig, Scott J Stephen Hodi, F |
author_sort | Ott, Patrick A |
collection | PubMed |
description | BACKGROUND: Angiogenic factors promote the growth of tumor vasculature, modulate lymphocyte trafficking into tumors, and inhibit maturation of dendritic cells. We hypothesized that MEDI3617, a human IgG1 kappa monoclonal antibody directed against human angiopoietin-2, in combination with tremelimumab (treme), an IgG2 monoclonal antibody blocking cytotoxic T-lymphocyte-associated protein- (CTLA-4), is safe in patients with advanced melanoma. METHODS: In a phase I, 3+3 dose escalation trial, patients with metastatic or unresectable melanoma received treme in combination with MEDI3617. The primary objectives of the study were safety and determination of recommended phase II dose (RP2D). The secondary objectives included determination of 6-month and 1-year overall survival and best overall response rate. Immune cell populations and soluble factors were assessed in peripheral blood and metastatic tumors using Fluorescence activated cell sorting (FACS), Luminex, and multiplexed immunofluorescence. RESULTS: Fifteen patients (median age: 62) were enrolled in the study (3 patients in cohort 1: treme at 10 mg/kg and MEDI3617 at 200 mg; and 12 patients in cohort 2: treme at 10 mg/kg and MEDI3617 at 600 mg). The most common all-grade treatment-related adverse events were rash, pruritus, fatigue, and extremity edema. No dose-limiting toxicities were observed. Cohort 2 was determined to be the RP2D. There were no patients with confirmed immune-related complete response or immune-related partial response. Six of 15 patients had immune-related stable disease, resulting in a disease control rate of 0.40 (95% CI 0.16 to 0.68). An increase in frequencies of circulating inducible T-cell costimulator (ICOS)(+) and human leukocyte antigen (HLA)-DR(+) CD4(+) and CD8(+) T cells and production of Interleukin-2 and Interleukin-10 was observed post therapy. CONCLUSIONS: Tremelimumab in combination with MEDI3617 is safe in patients with advanced melanoma. Angiopoietin-2 inhibition in combination with immune checkpoint inhibition warrants further exploration. TRIAL REGISTRATION NUMBER: NCT02141542. |
format | Online Article Text |
id | pubmed-8593712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-85937122021-11-24 Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial Ott, Patrick A Nazzaro, Matthew Pfaff, Kathleen L Gjini, Evisa Felt, Kristen D Wolff, Jacquelyn O Buchbinder, Elizabeth I Haq, Rizwan Sullivan, Ryan J Lawrence, Donald P McDermott, David F Severgnini, Mariano Giobbie-Hurder, Anita Rodig, Scott J Stephen Hodi, F J Immunother Cancer Clinical/Translational Cancer Immunotherapy BACKGROUND: Angiogenic factors promote the growth of tumor vasculature, modulate lymphocyte trafficking into tumors, and inhibit maturation of dendritic cells. We hypothesized that MEDI3617, a human IgG1 kappa monoclonal antibody directed against human angiopoietin-2, in combination with tremelimumab (treme), an IgG2 monoclonal antibody blocking cytotoxic T-lymphocyte-associated protein- (CTLA-4), is safe in patients with advanced melanoma. METHODS: In a phase I, 3+3 dose escalation trial, patients with metastatic or unresectable melanoma received treme in combination with MEDI3617. The primary objectives of the study were safety and determination of recommended phase II dose (RP2D). The secondary objectives included determination of 6-month and 1-year overall survival and best overall response rate. Immune cell populations and soluble factors were assessed in peripheral blood and metastatic tumors using Fluorescence activated cell sorting (FACS), Luminex, and multiplexed immunofluorescence. RESULTS: Fifteen patients (median age: 62) were enrolled in the study (3 patients in cohort 1: treme at 10 mg/kg and MEDI3617 at 200 mg; and 12 patients in cohort 2: treme at 10 mg/kg and MEDI3617 at 600 mg). The most common all-grade treatment-related adverse events were rash, pruritus, fatigue, and extremity edema. No dose-limiting toxicities were observed. Cohort 2 was determined to be the RP2D. There were no patients with confirmed immune-related complete response or immune-related partial response. Six of 15 patients had immune-related stable disease, resulting in a disease control rate of 0.40 (95% CI 0.16 to 0.68). An increase in frequencies of circulating inducible T-cell costimulator (ICOS)(+) and human leukocyte antigen (HLA)-DR(+) CD4(+) and CD8(+) T cells and production of Interleukin-2 and Interleukin-10 was observed post therapy. CONCLUSIONS: Tremelimumab in combination with MEDI3617 is safe in patients with advanced melanoma. Angiopoietin-2 inhibition in combination with immune checkpoint inhibition warrants further exploration. TRIAL REGISTRATION NUMBER: NCT02141542. BMJ Publishing Group 2021-11-12 /pmc/articles/PMC8593712/ /pubmed/34772758 http://dx.doi.org/10.1136/jitc-2021-003318 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Clinical/Translational Cancer Immunotherapy Ott, Patrick A Nazzaro, Matthew Pfaff, Kathleen L Gjini, Evisa Felt, Kristen D Wolff, Jacquelyn O Buchbinder, Elizabeth I Haq, Rizwan Sullivan, Ryan J Lawrence, Donald P McDermott, David F Severgnini, Mariano Giobbie-Hurder, Anita Rodig, Scott J Stephen Hodi, F Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial |
title | Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial |
title_full | Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial |
title_fullStr | Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial |
title_full_unstemmed | Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial |
title_short | Combining CTLA-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase I trial |
title_sort | combining ctla-4 and angiopoietin-2 blockade in patients with advanced melanoma: a phase i trial |
topic | Clinical/Translational Cancer Immunotherapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593712/ https://www.ncbi.nlm.nih.gov/pubmed/34772758 http://dx.doi.org/10.1136/jitc-2021-003318 |
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