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Clinically approved combination immunotherapy: Current status, limitations, and future perspective.

Publication ,  Journal Article
Lu, L; Zhan, M; Li, X-Y; Zhang, H; Dauphars, DJ; Jiang, J; Yin, H; Li, S-Y; Luo, S; Li, Y; He, Y-W
Published in: Curr Res Immunol
2022

Immune-checkpoint inhibitor-based combination immunotherapy has become a first-line treatment for several major types of cancer including hepatocellular carcinoma (HCC), renal cell carcinoma, lung cancer, cervical cancer, and gastric cancer. Combination immunotherapy counters several immunosuppressive elements in the tumor microenvironment and activates multiple steps of the cancer-immunity cycle. The anti-PD-L1 antibody, atezolizumab, plus the anti-vascular endothelial growth factor antibody, bevacizumab, represents a promising class of combination immunotherapy. This combination has produced unprecedented clinical efficacy in unresectable HCC and become a landmark in HCC therapy. Advanced HCC patients treated with atezolizumab plus bevacizumab demonstrated impressive improvements in multiple clinical endpoints including overall survival, progress-free survival, objective response rate, and patient-reported quality of life when compared to current first-line treatment with sorafenib. However, atezolizumab plus bevacizumab first-line therapy has limitations. First, cancer patients falling into the criteria for the combination therapy may need to be further selected to reap benefits while avoiding some potential pitfalls. Second, the treatment regimen of atezolizumab plus bevacizumab at a fixed dose may require adjustment for optimal normalization of the tumor microenvironment to obtain maximum efficacy and reduce adverse events. Third, utilization of predictive biomarkers is urgently needed to guide the entire treatment process. Here we review the current status of clinically approved combination immunotherapies and the underlying immune mechanisms. We further provide a perspective analysis of the limitations for combination immunotherapies and potential approaches to overcome the limitations.

Duke Scholars

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Published In

Curr Res Immunol

DOI

EISSN

2590-2555

Publication Date

2022

Volume

3

Start / End Page

118 / 127

Location

Netherlands

Related Subject Headings

  • 3204 Immunology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Lu, L., Zhan, M., Li, X.-Y., Zhang, H., Dauphars, D. J., Jiang, J., … He, Y.-W. (2022). Clinically approved combination immunotherapy: Current status, limitations, and future perspective. Curr Res Immunol, 3, 118–127. https://doi.org/10.1016/j.crimmu.2022.05.003
Lu, Ligong, Meixiao Zhan, Xian-Yang Li, Hui Zhang, Danielle J. Dauphars, Jun Jiang, Hua Yin, et al. “Clinically approved combination immunotherapy: Current status, limitations, and future perspective.Curr Res Immunol 3 (2022): 118–27. https://doi.org/10.1016/j.crimmu.2022.05.003.
Lu L, Zhan M, Li X-Y, Zhang H, Dauphars DJ, Jiang J, et al. Clinically approved combination immunotherapy: Current status, limitations, and future perspective. Curr Res Immunol. 2022;3:118–27.
Lu, Ligong, et al. “Clinically approved combination immunotherapy: Current status, limitations, and future perspective.Curr Res Immunol, vol. 3, 2022, pp. 118–27. Pubmed, doi:10.1016/j.crimmu.2022.05.003.
Lu L, Zhan M, Li X-Y, Zhang H, Dauphars DJ, Jiang J, Yin H, Li S-Y, Luo S, Li Y, He Y-W. Clinically approved combination immunotherapy: Current status, limitations, and future perspective. Curr Res Immunol. 2022;3:118–127.
Journal cover image

Published In

Curr Res Immunol

DOI

EISSN

2590-2555

Publication Date

2022

Volume

3

Start / End Page

118 / 127

Location

Netherlands

Related Subject Headings

  • 3204 Immunology