Table 1.
Drug | Target(s) | Trial | Patient population | Trial design | Primary outcome |
---|---|---|---|---|---|
RAIR-DTC | |||||
Sorafenib | VEGFR1–3, RET, RAF, PDGFRβ | DECISION (22) | 417 Patients with progressive RAIR-DTC | Placebo-controlled phase III | Median PFS = 10.8 months (sorafenib) vs. 5.8 months (placebo) |
Lenvatinib | VEGFR1–3, FGFR1–4, PDGFRα, RET, KIT | SELECT (23) | 392 Patients with progressive RAIR-DTC | Placebo-controlled phase III | Median PFS = 18.3 months (lenvatinib) vs. 3.6 months (placebo) |
MTC | |||||
Vandetanib | VEGFR1–3, RET, EGFR, BRK, TIE2, EPHR, SRC | ZETA (63) | 331 Patients with RECIST measurable MTC | Placebo-controlled phase III | Median PFS = 30.5 months (est.) (vandetanib) vs. 19.3 months (placebo) |
Cabozantinib | VEGFR1–3, RET, MET, KIT, TRKB, FLT-3 | EXAM (65) | 330 Patients with progressive MTC | Placebo-controlled phase III | Median PFS = 11.2 months (cabozantinib) vs. 4.0 months (placebo) |
MTC, medullary thyroid carcinoma; PFS, progression-free survival; RAIR-DTC, radioiodine-resistant differentiated thyroid cancer; RECIST, Response Evaluation Criteria in Solid Tumors.