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Comparisons of Underlying Mechanisms, Clinical Efficacy and Safety Between Anti-PD-1 and Anti-PD-L1 Immunotherapy: The State-of-the-Art Review and Future Perspectives
- Source :
- Frontiers in Pharmacology, Frontiers in Pharmacology, Vol 12 (2021)
- Publication Year :
- 2021
- Publisher :
- Frontiers Media S.A., 2021.
-
Abstract
- Over the past decade, diverse PD-1/PD-L1 blockades have demonstrated significant clinical benefit in across a wide range of tumor and cancer types. With the increasing number of PD-1/PD-L1 blockades available in the market, differences between the clinical performance of each of them started to be reported. Here, we provide a comprehensive historical and biological perspective regarding the underlying mechanism and clinical performance of PD-1/PD-L1 blockades, with an emphasis on the comparisons of their clinical efficacy and safety. The real-world evidence indicated that PD-1 blockade may be more effective than the PD-L1, though no significant differences were found as regards to their safety profiles. Future head-to-head studies are warranted for direct comparison between them. Finally, we summarize the yet to be elucidated questions and future promise of anti-PD-1/PD-L1 immunotherapy, including a need to explore novel biomarkers, novel combinatorial strategies, and their clinical use on chronic infection.
- Subjects :
- 0301 basic medicine
atezolizumab
safety
medicine.medical_specialty
medicine.medical_treatment
efficacy
RM1-950
Pembrolizumab
Review
PD-1/PD-L1
03 medical and health sciences
0302 clinical medicine
Atezolizumab
medicine
Pharmacology (medical)
Clinical efficacy
Intensive care medicine
Pharmacology
nivolumab
Mechanism (biology)
business.industry
tislelizumab
Immunotherapy
Blockade
Chronic infection
030104 developmental biology
030220 oncology & carcinogenesis
Therapeutics. Pharmacology
immunotherapy
pembrolizumab
Nivolumab
business
Subjects
Details
- Language :
- English
- ISSN :
- 16639812
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Frontiers in Pharmacology
- Accession number :
- edsair.doi.dedup.....46e9433fd77490e6f2fe5407e16c0c6b