Transition of the PD‑1 occupancy of nivolumab on T cells after discontinuation and response of nivolumab re‑challenge
Although nivolumab is administered every two or four weeks, high programmed cell death-1 (PD-1) binding of nivolumab on T cells lasting for several months has been reported. A relationship between the PD-1 occupancy rate on T-cells and the efficacy of nivolumab is not yet fully understood. The prese...
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Published in | Molecular and clinical oncology Vol. 16; no. 5; p. 104 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Spandidos Publications
01.05.2022
Spandidos Publications UK Ltd D.A. Spandidos |
Subjects | |
Online Access | Get full text |
ISSN | 2049-9450 2049-9469 |
DOI | 10.3892/mco.2022.2537 |
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Abstract | Although nivolumab is administered every two or four weeks, high programmed cell death-1 (PD-1) binding of nivolumab on T cells lasting for several months has been reported. A relationship between the PD-1 occupancy rate on T-cells and the efficacy of nivolumab is not yet fully understood. The present study used flow cytometric analyses to determine the time-dependence of PD-1 occupancy in five patients who discontinued nivolumab. The relationship between PD-1 occupancy at relapse and the efficacy of re-challenge was also studied. Occupancies after discontinuation were measured at a total of 32 points. The data indicated that it took 32.4 and 48.9 weeks to decrease occupancy by 50 and 70%, respectively. Subsequently, two patients had recurrence and were re-challenged with nivolumab. At that time, one patient had 70.8% occupancy while the other had 6.6%. Treatment was effective only for the patient with lower occupancy. Overall, the present study suggests that re-challenge with nivolumab may be efficacious in patients with low occupancy at recurrence. |
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AbstractList | Although nivolumab is administered every two or four weeks, high programmed cell death-1 (PD-1) binding of nivolumab on T cells lasting for several months has been reported. A relationship between the PD-1 occupancy rate on T-cells and the efficacy of nivolumab is not yet fully understood. The present study used flow cytometric analyses to determine the time-dependence of PD-1 occupancy in five patients who discontinued nivolumab. The relationship between PD-1 occupancy at relapse and the efficacy of re-challenge was also studied. Occupancies after discontinuation were measured at a total of 32 points. The data indicated that it took 32.4 and 48.9 weeks to decrease occupancy by 50 and 70%, respectively. Subsequently, two patients had recurrence and were re-challenged with nivolumab. At that time, one patient had 70.8% occupancy while the other had 6.6%. Treatment was effective only for the patient with lower occupancy. Overall, the present study suggests that re-challenge with nivolumab may be efficacious in patients with low occupancy at recurrence. Although nivolumab is administered every two or four weeks, high programmed cell death-1 (PD-1) binding of nivolumab on T cells lasting for several months has been reported. A relationship between the PD-1 occupancy rate on T-cells and the efficacy of nivolumab is not yet fully understood. The present study used flow cytometric analyses to determine the time-dependence of PD-1 occupancy in five patients who discontinued nivolumab. The relationship between PD-1 occupancy at relapse and the efficacy of re-challenge was also studied. Occupancies after discontinuation were measured at a total of 32 points. The data indicated that it took 32.4 and 48.9 weeks to decrease occupancy by 50 and 70%, respectively. Subsequently, two patients had recurrence and were re-challenged with nivolumab. At that time, one patient had 70.8% occupancy while the other had 6.6%. Treatment was effective only for the patient with lower occupancy. Overall, the present study suggests that re-challenge with nivolumab may be efficacious in patients with low occupancy at recurrence. Key words: occupancy, nivolumab re-challenge, programmed cell death-1 |
ArticleNumber | 104 |
Audience | Academic |
Author | Toyoda, Masanori Imamura, Yoshinori Nose, Taku Nagatani, Yoshiaki Funakoshi, Yohei Minami, Hironobu Kiyota, Naomi Suto, Hirotaka |
AuthorAffiliation | 1 Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650-0017, Japan 2 Cancer Center, Kobe University Hospital, Kobe, Hyōgo 650-0017, Japan |
AuthorAffiliation_xml | – name: 2 Cancer Center, Kobe University Hospital, Kobe, Hyōgo 650-0017, Japan – name: 1 Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650-0017, Japan |
Author_xml | – sequence: 1 givenname: Taku surname: Nose fullname: Nose, Taku organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 2 givenname: Yohei surname: Funakoshi fullname: Funakoshi, Yohei organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 3 givenname: Hirotaka surname: Suto fullname: Suto, Hirotaka organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 4 givenname: Yoshiaki surname: Nagatani fullname: Nagatani, Yoshiaki organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 5 givenname: Yoshinori surname: Imamura fullname: Imamura, Yoshinori organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 6 givenname: Masanori surname: Toyoda fullname: Toyoda, Masanori organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 7 givenname: Naomi surname: Kiyota fullname: Kiyota, Naomi organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan – sequence: 8 givenname: Hironobu surname: Minami fullname: Minami, Hironobu organization: Department of Medicine, Division of Medical Oncology/Hematology, Kobe University, Hospital and Graduate School of Medicine, Kobe, Hyōgo 650‑0017, Japan |
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Keywords | occupancy nivolumab re-challenge programmed cell death-1 |
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SubjectTerms | Analysis Antibodies Apoptosis Binding sites Cancer therapies Cell death Clinical trials Flow cytometry Immunotherapy Lung cancer Lymphocytes Metastasis Monoclonal antibodies Oncology Patients T cells Targeted cancer therapy Trends |
Title | Transition of the PD‑1 occupancy of nivolumab on T cells after discontinuation and response of nivolumab re‑challenge |
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