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. 2013 Jul 25;5(3):919–942. doi: 10.3390/cancers5030919

Table 4.

Belinostat in published phase II clinical trials in solid tumors.

 Disease  Regimen No. pts.  PFS Efficacy Ref.
Recurrent or refractory malignant pleural mesothelioma Belinostat: 1 g/m2 IV on days 1 to 5 of a 21-day cycle 13 Median: 1 m. SD 2 pts. [81]
Recurrent or refractory advanced thymic epithelial tumors Belinostat: 1 g/m2 IV on days 1 to 5 of a 21-day cycle 41 6-m.- PFS: 46% RR 8%
CB 68%
[82]
Unresectable hepatocellular carcinoma Belinostat: 1,400 mg/m2 per day, on days 1–5 every 3 weeks 54 Median: 2.64 m. PR 2.4%
SD 45.2%
[83]
Platinum resistant EOC and LMP ovarian tumors Belinostat: 1 g/m2 IV on days 1 to 5 of a 21-day cycle 32 EOC:
Median: 2.3 m. LMP:
Median: 13.4 m.
EOC: SD 9/15 pts LMP: PR 2/12 pts [84]
Previously treated ovarian, fallopian tube, or primary peritoneal carcinoma Belinostat: 1g/m² IV daily for
5 days of a 21-day cycle +Carboplatin: AUC 5 on day three of 21-day cycles
29 Median: 3.3 m. RR 7.4% CR 3.7% PR 3.7% SD 44.4% [85]
Previously treated ovarian cancer Belinostat: 1g/m² IV daily for
5 days of a 21-day cycle +Carboplatin: AUC 5 +Paclitaxel: 175 mg/m² both on day 3 of each 21-day cycle
35 6-m. PFS: 48% RR 43% [86]

Abbreviations: 6-m.-PFS, progression free survival at 6 months; AUC, area under the curve; CB, clinical benefit; CR, complete response; EOC, epithelial ovarian cancer; LMP, micropapillary; m., months; No., number; PFS, progression free survival; pts, patients; Ref., references; RR, objective response rate.