Table 1.
The objective response rates of “immune active” tumors and “immune quiescent” tumors to immune checkpoint inhibitors.
Classification | Tumor type | Objective Response Rates | References |
---|---|---|---|
Immune active tumors | Melanomas (with a combinational treatment of nivolumab and ipilimumab) | 53% | Wolchok et al., 2013 |
Non-small cell lung cancer (Squamous cell type) | 20% | Brahmer et al., 2015 | |
Non-small cell lung cancer (Adenocarcinoma) | 19.2% | Paz-Ares et al., 2015 | |
Gastroesophageal adenocarcinoma (PD-L1+ tumor) | 22% | Muro et al., 2015 | |
Colorectal carcinoma (MSI tumors) | 40% | Le et al., 2015a | |
Renal cell cancer | 20–30% | Motzer et al., 2015; McDermott et al., 2015 | |
Squamous cell carcinoma of the head and neck | 18.2% | Seiwert et al., 2015 | |
Hepatocellular carcinoma | 23% | El-Khoueiry et al., 2015 | |
Hodgkin’s Lymphoma | 87% | Ansell et al., 2015 | |
Immune quiescent tumors | Pancreatic adenocarcinoma | ~0% | Brahmer et al., 2012 |
Colorectal carcinoma (MSS tumors) | 0% | Le et al., 2015a | |
Non-responsive melanoma, NSCLC, GA, RCC, SCCHN, HCC, etc. | 0% | See above |
NSCLC, non-small cell lung cancer; SCCHN, squamous cell carcinoma of the head and neck; HCC, hepatocellular carcinoma; GA, gastroesophageal adenocarcinoma; RCC, renal cell carcinoma; MSI, microsatellite instable; MSS, microsatellite stable.