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Camrelizumab for cancers in patients living with HIV: one-single center experience

OBJECTIVES: The primary objective was to evaluate the safety of the anti-PD-1 antibody camrelizumab in people living with HIV (PLWH); the secondary objective was to evaluate tumor response. METHODS: From May 8, 2018, to December 10, 2021, twenty-four patients with HIV and advanced cancer as well as...

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Autores principales: Wu, Menghua, Zheng, Xin, Zhang, Yu, Song, Jian, Zhao, Jimao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108516/
https://www.ncbi.nlm.nih.gov/pubmed/37062823
http://dx.doi.org/10.1186/s12981-023-00518-y
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author Wu, Menghua
Zheng, Xin
Zhang, Yu
Song, Jian
Zhao, Jimao
author_facet Wu, Menghua
Zheng, Xin
Zhang, Yu
Song, Jian
Zhao, Jimao
author_sort Wu, Menghua
collection PubMed
description OBJECTIVES: The primary objective was to evaluate the safety of the anti-PD-1 antibody camrelizumab in people living with HIV (PLWH); the secondary objective was to evaluate tumor response. METHODS: From May 8, 2018, to December 10, 2021, twenty-four patients with HIV and advanced cancer as well as a CD4(+) T-cell count greater than or equal to 100 cells/µL were treated with camrelizumab in daily practice. We describe the demographic characteristics, safety, and clinical course of these 24 PLWH with cancer treated with camrelizumab. Safety was assessed using the current Common Terminology Criteria for Adverse Events (CTCAE). The tumor response was assessed according to the Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1). RESULTS: The median number of cycles was 8 (4–26). Only two grade 3 adverse reactions were reported (no toxic deaths or immune-related deaths). Among the 24 patients, 2 (8%) complete responses and 6 (25%) partial responses were observed. 7 patients (29%) were at stable tumor status and others progressed. CONCLUSIONS: Data from the present study strongly support the use of camrelizumab (monoclonal antibodies targeting the PD-1 pathway) in this population, as it appears to be a feasible approach with no deleterious effects on PLWH and tolerability and acceptable efficacy. In addition, these findings further support the inclusion of PLWH with cancer in clinical trials evaluating the safety and efficacy of ICIs on cancer.
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spelling pubmed-101085162023-04-18 Camrelizumab for cancers in patients living with HIV: one-single center experience Wu, Menghua Zheng, Xin Zhang, Yu Song, Jian Zhao, Jimao AIDS Res Ther Research OBJECTIVES: The primary objective was to evaluate the safety of the anti-PD-1 antibody camrelizumab in people living with HIV (PLWH); the secondary objective was to evaluate tumor response. METHODS: From May 8, 2018, to December 10, 2021, twenty-four patients with HIV and advanced cancer as well as a CD4(+) T-cell count greater than or equal to 100 cells/µL were treated with camrelizumab in daily practice. We describe the demographic characteristics, safety, and clinical course of these 24 PLWH with cancer treated with camrelizumab. Safety was assessed using the current Common Terminology Criteria for Adverse Events (CTCAE). The tumor response was assessed according to the Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1). RESULTS: The median number of cycles was 8 (4–26). Only two grade 3 adverse reactions were reported (no toxic deaths or immune-related deaths). Among the 24 patients, 2 (8%) complete responses and 6 (25%) partial responses were observed. 7 patients (29%) were at stable tumor status and others progressed. CONCLUSIONS: Data from the present study strongly support the use of camrelizumab (monoclonal antibodies targeting the PD-1 pathway) in this population, as it appears to be a feasible approach with no deleterious effects on PLWH and tolerability and acceptable efficacy. In addition, these findings further support the inclusion of PLWH with cancer in clinical trials evaluating the safety and efficacy of ICIs on cancer. BioMed Central 2023-04-16 /pmc/articles/PMC10108516/ /pubmed/37062823 http://dx.doi.org/10.1186/s12981-023-00518-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wu, Menghua
Zheng, Xin
Zhang, Yu
Song, Jian
Zhao, Jimao
Camrelizumab for cancers in patients living with HIV: one-single center experience
title Camrelizumab for cancers in patients living with HIV: one-single center experience
title_full Camrelizumab for cancers in patients living with HIV: one-single center experience
title_fullStr Camrelizumab for cancers in patients living with HIV: one-single center experience
title_full_unstemmed Camrelizumab for cancers in patients living with HIV: one-single center experience
title_short Camrelizumab for cancers in patients living with HIV: one-single center experience
title_sort camrelizumab for cancers in patients living with hiv: one-single center experience
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108516/
https://www.ncbi.nlm.nih.gov/pubmed/37062823
http://dx.doi.org/10.1186/s12981-023-00518-y
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