Objective: To gain a deeper understanding of the hot topics and future prospects of programmed cell death 1 (PD-1)/programmed cell death ligand 1 (PD-L1) inhibitors treatment of cancer through scientometric analysis of the top-100 most cited clinical trials. Materials and methods: We searched the Web of Science Core Collection database from 1980 to June 2019. Two reviewers independently screened the top-100 most cited clinical trials that defined by the National Institutes of Health starting from the most cited article. Title, year of publication, citations, type of cancer, and focused aspects of outcomes were extracted from included clinical trials. VOSviewer software (version 1.6.9) and Excel 2016 were used to do statistical analysis. The...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
Monoclonal antibodies that inhibit “immune checkpoint” through programmed cell death-1 and its ligan...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
Monoclonal antibodies that inhibit “immune checkpoint” through programmed cell death-1 and its ligan...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
The programmed death receptor 1 (PD1) and its ligand programmed death receptor ligand 1 (PDL1) are t...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
BackgroundImmunotherapy for lung cancer has been a hot research area for years. This bibliometric an...
Monoclonal antibodies that inhibit “immune checkpoint” through programmed cell death-1 and its ligan...