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. 2018 Sep 6;5(3):100. doi: 10.3390/medicines5030100

Table 2.

Characterization of targeted therapy.

Target Therapy Class Target Total Cohort Control Group Combinational Group Significance
n = 310 n = 126 n = 184
Monoclonal antibodies
  bevacizumab, n (%) VEGFR 76 (24.5) 11 (8.7) 65 (35.3) *** a)
  cetuximab, n (%) EGFR 23 (7.4) 5 (4.0) 18 (9.8)
  panitumumab, n (%) EGFR 12 (3.9) 2 (1.6) 10 (5.4)
  rituximab, n (%) CD20 33 (10.6) 27 (21.4) 6 (3.3) *** a)
trastuzumab, n (%) HER2 107 (34.5) 61 (48.4) 46 (25.0) *** a)
Immunotherapy
  ipilimumab, n (%) CTLA-4 1 (0.3) 1 (0.5)
  nivolumab, n (%) PD-1 3 (1.0) 3 (1.6)
  pembrolizumab, n (%) PD-1 5 (1.6) 2 (1.6) 1 (0.5)
Tyrosine kinase inhibitors
  erlotinib, n (%) EGFR 38 (12.3) 3 (2.4) 35 (19.0) *** a)
  gefitinib, n (%) EGFR 9 (2.9) 3 (2.4) 6 (3.3)
  sorafenib, n (%) Dual Raf-kinase/VEGFR 7 (2.3) 7 (3.8)
  sunitinib, n (%) Receptor tyrosine kinases 7 (2.3) 1 (0.8) 6 (3.3)

Most frequent applied targeted therapies in the control (targeted therapy) and combinational group (targeted + VA) with their respective molecular targets. n, number of patients; %, as percent from total patient number n from each group; Significance code: a) p ≤ 0.001, “—” not statistically significant; CTLA-4, cytotoxic T lymphocyte-associated antigen 4; CD20, B-lymphocyte antigen CD20; EGFR, endothelial growth factor receptor; HER2, human epidermal growth factor receptor 2; PD1, programmed cell death protein 1; Raf, rapidly accelerated fibrosarcoma; VEGFR, vascular endothelial growth factor receptor.