TABLE 3.
Authors | Agent | Study design | Target | n |
Response Rate (DCR) |
PFS (mo) |
OS (mo) |
---|---|---|---|---|---|---|---|
Cytotoxic agents | |||||||
Loehrer et al 29 | Pemetrexed | Ph II | — | 11 | 9.1% | 2.9 | 9.8 |
Wakelee et al 30 | Amrubicin | Ph II | — | 19 | 10.5% | 8.5 | 18.1 |
Palmieri et al 18 | Capecitabine + gemcitabine | Ph II | — | 8 | 37.5% | 6 | N/A |
Tsukita et al 25 | S‐1 | Ph II | — | 20 | 25% | 5.4 | 22.7 |
Present study | S‐1 | Ph II | — | 26 | 30.8% (80.8%) | 4.3 | 27.4 |
Molecular‐targeted agents | |||||||
Thomas et al 12 | Sunitinib | Ph II | c‐KIT, PDGFR | 23 | 26% (65%) | 7.2 | Not reached |
Zucali et al 13 | Everolimus | Ph II | mTOR | 12 | 25% (41%) | 12.1 a | 24.0 a |
Rajan et al 22 | Cixutumumab | Ph II | IGF‐1R | 12 | 0% | 1.7 | 8.4 |
Giaccone et al 31 | Belinostat | Ph II | HDAC | 16 | 0% (50%) | 5.8 | 12.4 |
Besse et al 32 |
Milciclib (PHA‐848125AC) |
Ph II | CDK, src family | 26 | 4.2% | 9.76 | Not reached |
Bedano et al 33 | Erlotinib + bevacizumab | Ph II | EGFR, VEGF | 7 | 0 | N/A | N/A |
Kurup et al 34 | Gefitinib | Ph II | EGFR | 7 | 0 | N/A | N/A |
Giaccone et al 35 | Imatinib | Ph II | c‐KIT mutation | 5 | 0 | N/A | N/A |
Loehrer et al 36 | Octreotide + prednisone | Ph II | somatostatin receptor | 6 | 0 | 4.5 | 23.4 |
Gubens et al 37 | Saracatinib (AZD0530) | Ph II | src family | 9 | 0 | 3.6 | 6.7 |
Itoh et al 26 | Lenvatinib | Ph II | VEGFR, FGFR, RET, c‐Kit etc | 42 | 38.1% | 9.3 | Not reached |
Immune check point inhibitors | |||||||
Cho et al 14 | Pembrolizumab | Ph II | PD‐1 | 26 | 19.2% (73%) | 6.1 | N/A |
Giaccone et al 15 | Pembrolizumab | Ph II | PD‐1 | 40 | 22.5% (75%) | 4.2 | 24.9 |
Katsuya et al 38 | Nivolumab | Ph II | PD‐1 | 15 | 0% (73.3%) | 3.8 | N/A |
Abbreviations: CDK, cyclin‐dependent kinase; DCR, disease control rate; epidermal growth factor; HDAC, histone deacetylase; IGF‐1R, insulin‐like growth factor 1 receptor; mTOR, mammalian target of rapamycin; n, number; OS, overall survival; PDGFR, platelet‐derived growth factor; PD‐L1, programmed death‐1; PFS, progression‐free survival; Ph II, phase II; Retrosp, retrospective; VEGF, vascular endothelial growth factor.
Survival data include thymoma and thymic carcinoma.