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. 2016 Apr 28;16(2):99–108. doi: 10.4110/in.2016.16.2.99

Table I. Summary of clinical studies of dendritic cell-based immunotherapy for CRC (a search of the PubMed from 2004 to 2015).

Author Cell types Number of patients Clinical outcome Adverse events
Hunyadi et al. (44) DC+autologous tumor cell lysates 6 patients Survival for 6-years (5 of 6) No adverse effects
DC+CEA peptide 6 patients Survival for 6-years (3 of 3)
Morse et al. (65) DC+Poxvectors encoding CEA and MUC1 (PANVAC) 37 patients 2 of 37 death No grade 3/4 toxicity except grade 3 urticaria on the DC+PANVAC
PANVAC+GM-CSF 37 patients 5 of 37 death
Sakakibara et al. (41) DC+CEA peptide 10 patients PD (7), SD (1), withdrawal (2) No adverse effects except grade I fever
Toh et al. (42) DC+MAGE 20 patients PD (11), PR (1), SD (7), withdrawal (1) Mild grade 1 or 2 toxicity
Burgdorf et al. (43) DC+MAGE 20 patients 24% of SD (4) No adverse effects
Kavanagh et al. (46) DC+CEA peptide 21 patients 11 of all patients evaluated, PD (11) No significant toxicity
Morse et al. (66) DC+Fowlpox vector encoding CEA and costimulatory molecules 11 patients, 3 patients (NSCLC) PD (8), SD/MR (6) No grade 3/4 toxicity
Liu et al. (40) DC+CEA peptide 10 patients PD (8), SD (2) No grade 2/3 toxicity
Matsuda et al. (67) DC+CEA peptide 7 patients PD (5), SD (2) No adverse effects

DC, dendritic cell; CEA, carcinoembryonic antigen; GM-CSF, granulocyte-macrophage colony-stimulating factor; PD, progressive disease; SD, stable disease; PR, partial response; MR, minor response; MAGE, melanoma-associated antigen; CRC, colorectal cancer; NSCLC, non-small cell lung cancer.