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0% versus 1.3%, p=0.0068, 59k versus 12k*10 /l, p=0.0081) and at the moment of toxicity (5.2% versus 1.2%, p=0.0106 and 47k versus 16k*10 /l, p=0.0466). Baseline percentage NKT cells predicted pulmonary toxicity with 0.78 sensitivity and 1.0 specificity. Our results suggest that baseline CD4+ effector cells may be predictive of antitumor responses and baseline NKT cells may be predictive of pulmonary toxicity. These results warrant further validation. Our results suggest that baseline CD4+ effector cells may be predictive of antitumor r