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Table 1 Classification of ICIs

From: A comprehensive review on immune checkpoint inhibitors induced cardiotoxicity characteristics and associated factors

Generic name and date of FDA approbation

Subclass

Mechanism of action

indications

Ipilumab

CTLA-4 ICI

Ipilumab enables the patient’s T cells to attack a broader range of antigens rather than inducing an increase in T cells. Ipilimumab binding to CTLA-4 blocks the inhibitory signal, thus, allowing CTLs to kill cancer cells [31,32,33]

Melanomas

Colorectal carcinoma

Oesophageal cancer

Hepatocellular carcinoma

Non-small cell lung cancers

Renal cell cancers [38]

nivolumab

PD1 ICI

relieves immune cells from pathological immune suppression and allows them to recognize and combat tumor cells by inhibiting PD-1 activity [43]

Esophageal squamous cell carcinoma (ESCC)

Classical Hodgkin Lymphoma

Hepatocellular carcinoma

Colorectal cancer

Urothelial carcinoma

Small cell lung carcinoma, metastasis

Pleural mesothelial

Renal cell carcinoma [40,41,42]

Pembrolizumab [44]

PD1 ICI

Like Nivolumab

Melanoma, non-small cell lung cancer, head and neck squamous cell cancer, classical Hodgkin lymphoma, urothelial carcinoma, GIT cancers cervical cancer hepatocellular carcinoma and Merkel cell carcinoma

Atezolizumab

PDL1 ICI

increase the number of proliferating CD8 + T cells by inducing increases in IL-18, IFN, and CXCL11 and a temporary decrease in IL-6 [45, 46]. by inhibiting PD-L1, thus increasing T-cell-mediated immunity against tumors

Safe and efficacious in a wide range of solid tumors and hematologic malignancies metastatic NSCLC unresponsive to platinum-containing chemotherapy extensive-stage small-cell lung cancer [20, 47]