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Use of programmed cell death protein 1 (PD-1) inhibitor therapy in HIV-infected patients with advanced cancer: a single-center study from China.

Authors :
Wu, Luling
Su, Jie
Yang, Junyang
Gu, Ling
Zhang, Renfang
Liu, Li
Lu, Hongzhou
Chen, Jun
Source :
Infectious Agents & Cancer; 5/30/2023, Vol. 18 Issue 1, p1-10, 10p
Publication Year :
2023

Abstract

Background: Anti-PD-1 antibodies have been approved for treating several cancer. However, data regarding the safety and efficacy of these agents in HIV-infected patients with cancer is lacking, because these patients are frequently omitted from clinical trials. Objectives: The primary aim of our research is to assess the safety, activity, and long-term outcomes of PD-1 inhibitors in the treatment of HIV-infected patients with advanced cancer. Method: We retrospectively analyzed data from HIV-infected patients with advanced cancers who were treated with PD-1 inhibitors at Shanghai Public Health Clinical Center, Shanghai, China. Results: Fifteen HIV-infected patients (all are men; asian; median age, 44) with cancer who were treated with chemotherapy and/or combined the other oncology treatments [along with combined antiretroviral therapy (cART)] prior to Sintilimab (12 out of 15) or Nivolumab (1 out of 11) or Camrelizumab (2 out of 11) injection were identified. Eight patients responded to treatment (disease control rate 53.3%), with 1 got partial response (PR) and 7 were stable. Most treatment-emergent adverse events (TEAEs) were grade 1 or 2 including anemia, leukopenia, hyperglycemia, granulocytopenia, and thrombocytopenia. Eight patients (53.3%) experienced treatment-related AEs (TRAEs) with grades 3/4including myelosuppression, infection, and neurological disorders. CD4<superscript>+</superscript> T cell count and plasma HIV RNA remained stable throughout the treatment. Conclusions: When used in HIV-infected patients with advanced malignancies, PD-1 inhibitors tend to have favorable efficacy, manageable side effects, and no deteriorated impacts on plasma HIV-RNA and CD4<superscript>+</superscript> T cell count. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17509378
Volume :
18
Issue :
1
Database :
Complementary Index
Journal :
Infectious Agents & Cancer
Publication Type :
Academic Journal
Accession number :
163987709
Full Text :
https://doi.org/10.1186/s13027-023-00512-z