Phase I study of chidamide (CS055/HBI-8000), a new histone deacetylase inhibitor, in patients with advanced solid tumors and lymphomas
M Dong, ZQ Ning, PY Xing, JL Xu, HX Cao… - Cancer chemotherapy …, 2012 - Springer
M Dong, ZQ Ning, PY Xing, JL Xu, HX Cao, GF Dou, ZY Meng, YK Shi, XP Lu, FY Feng
Cancer chemotherapy and pharmacology, 2012•SpringerAbstract Purpose Chidamide (CS055/HBI-8000) is a new benzamide class of histone
deacetylase inhibitor with marked anti-tumor activity. This study reports the phase I results.
Methods Patients with advanced solid tumors or lymphomas received oral doses of 5, 10,
17.5, 25, 32.5, or 50 mg chidamide either twice (BIW) or three times (TIW) per week for 4
consecutive weeks every 6 weeks. Safety, characteristics of pharmacokinetics (PK) and
pharmacodynamics (PD), and preliminary efficacy were evaluated. Results A total of 31 …
deacetylase inhibitor with marked anti-tumor activity. This study reports the phase I results.
Methods Patients with advanced solid tumors or lymphomas received oral doses of 5, 10,
17.5, 25, 32.5, or 50 mg chidamide either twice (BIW) or three times (TIW) per week for 4
consecutive weeks every 6 weeks. Safety, characteristics of pharmacokinetics (PK) and
pharmacodynamics (PD), and preliminary efficacy were evaluated. Results A total of 31 …
Purpose
Chidamide (CS055/HBI-8000) is a new benzamide class of histone deacetylase inhibitor with marked anti-tumor activity. This study reports the phase I results.
Methods
Patients with advanced solid tumors or lymphomas received oral doses of 5, 10, 17.5, 25, 32.5, or 50 mg chidamide either twice (BIW) or three times (TIW) per week for 4 consecutive weeks every 6 weeks. Safety, characteristics of pharmacokinetics (PK) and pharmacodynamics (PD), and preliminary efficacy were evaluated.
Results
A total of 31 patients were enrolled. No DLTs were identified in the BIW cohorts up to 50 mg. DLTs were grade 3 diarrhea and vomiting in two patients in the TIW cohort at 50 mg, respectively. PK analysis revealed t1/2 of 16.8–18.3 h, T max of 1–2 h in most cases, and a dose-related increase in C max and AUC. Significant induction of histone H3 acetylation in peripheral white blood cells was observed after a single dose of chidamide. Four patients with T-cell lymphomas and 1 patient with submandibular adenoid cystic carcinoma achieved a partial response.
Conclusions
Chidamide was generally well tolerated in patients with advanced solid tumors or lymphomas in the tested regimens. Favorable PK and PD profiles, as well as encouraging preliminary anti-tumor activity, were demonstrated.
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