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 inMolecular and clinical oncology Vol. 16; no. 5; p. 104
Main Authors Nose, Taku, Funakoshi, Yohei, Suto, Hirotaka, Nagatani, Yoshiaki, Imamura, Yoshinori, Toyoda, Masanori, Kiyota, Naomi, Minami, Hironobu
Format Journal Article
LanguageEnglish
Published England Spandidos Publications 01.05.2022
Spandidos Publications UK Ltd
D.A. Spandidos
Subjects
Online AccessGet full text
ISSN2049-9450
2049-9469
DOI10.3892/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.
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
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Issue 5
Keywords occupancy
nivolumab re-challenge
programmed cell death-1
Language English
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Snippet 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...
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SourceType Open Access Repository
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StartPage 104
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
URI https://www.ncbi.nlm.nih.gov/pubmed/35463212
https://www.proquest.com/docview/2656075266
https://pubmed.ncbi.nlm.nih.gov/PMC9022082
Volume 16
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