UGC Approved Journal no 63975(19)

ISSN: 2349-5162 | ESTD Year : 2014
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Published in:

Volume 9 Issue 2
February-2022
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

7.95 impact factor calculated by Google scholar

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Published Paper ID:
JETIR2202470


Registration ID:
320690

Page Number

e548-e561

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Title

REVIEW ON: IMMUNO-ONCOLOGY AGENTS FOR CANCER THERAPY

Abstract

Until lately, cancer treatment involved four primary kinds of treatment: surgery, radiotherapy, chemotherapy and targeted therapy. Over the earlier decade, immuno-oncology (IO) has emerged as a novel and critical method for managing cancer therapy through the stimulation of the body’s own immune system to kill cancer cells. This recently recognised technique of treating cancer is quickly developing, with many accelerated endorsement by the US Food and Drug Administration and European Medicines Agency in 2019. Immune checkpoint inhibitors, in particular, have had exceptional effectiveness across a wide range of cancers and are the most well-established therapeutic class of IO drugs to date. Biomarker testing for the programmed death-ligand 1 (PD-L1) checkpoint target has been created and is currently mandatory before therapy with pembrolizumab (Keytruda, Merck) when used for non-small-cell lung carcinoma, gastric cancer, head and neck squamous cell carcinoma and cervical cancer, just as before treatment with atezolizumab (Tecentriq, Roche) when used for urothelial carcinoma. However, the significance of PD-L1 expression for checkpoint inhibition therapy in other tumour types remains unclear. Combining IO drugs with conventional therapy has recently been studied, and patient outcomes have shown to be significantly improved. While IO agents are fast transforming the standard of treatment for cancer patients, there are still numerous obstacles to overcome in terms of managing their side effects and ensuring that healthcare systems, such as the NHS, can finance these expensive therapies. In addition to cancer vaccines and chimeric antigen receptor T-cell treatments, the IO pipeline contains chimeric antigen receptor T-cell therapies, both of which have their own set of toxicity and cost-effectiveness concerns.

Key Words

cancer, tumours, immuno-oncology, immunotherapy, antitumour, immunosuppression, immunosurveillance

Cite This Article

"REVIEW ON: IMMUNO-ONCOLOGY AGENTS FOR CANCER THERAPY ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.9, Issue 2, page no.e548-e561, February-2022, Available :http://www.jetir.org/papers/JETIR2202470.pdf

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2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"REVIEW ON: IMMUNO-ONCOLOGY AGENTS FOR CANCER THERAPY ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.9, Issue 2, page no. ppe548-e561, February-2022, Available at : http://www.jetir.org/papers/JETIR2202470.pdf

Publication Details

Published Paper ID: JETIR2202470
Registration ID: 320690
Published In: Volume 9 | Issue 2 | Year February-2022
DOI (Digital Object Identifier):
Page No: e548-e561
Country: nashik, maharastra, India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


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