Phase I safety, pharmacokinetics, and inhibition of src activity study of saracatinib in patients with solid tumors
Purpose: This dose-escalation study evaluated the safety, tolerability, and pharmacokinetics (PK) of the oral Src inhibitor saracatinib (AZD0530) in patients with advanced solid malignancies. Tumor biopsy samples were taken to investigate the effect of saracatinib on Src activity in tumors. Experimental Design: Part A of the study followed a multiple-ascending dose design to establish the maximum tolerated dose (MTD) of saracatinib. Part B was a randomized, parallel-group, cohort-expansion phase to further assess tolerated doses. Safety, tolerability, and Src activity (immunohistochemistry and lysate-based methodologies) were assessed after 21 days of once-daily oral dosing. PK was assessed after single and multiple dosing. Results: In part A, 30 patients received once-daily saracatinib at doses of 60 to 250 mg; the MTD was established as 175 mg. In part B, 51 patients were randomized to receive 50 mg (n = 16), 125 mg (n = 16), or 175 mg (n = 19) of saracatinib. The most common grade ≥3 events considered to be treatment related were anemia, diarrhea, and asthenia. Tumor Src activity was reduced following saracatinib treatment. The area under the concentration-time curve and Cmax of saracatinib increased with increasing dose. Saracatinib accumulated 4- to 5-fold on once-daily dosing to reach steady-state exposure after 10 to 17 days of dosing. The half-life was ∼40 hours. Conclusions: Saracatinib was well tolerated in patients with advanced solid malignancies. A reduction in tumor Src activity was observed. PK data show that saracatinib is suitable for once-daily oral dosing. Based on this study, the recommended dose for the phase II studies was chosen to be 175 mg/d.
|Keywords||activity, adult, aged, anemia, anorexia, antineoplastic activity, area under the curve, article, asthenia, breast tumor, cancer fatigue, cancer hormone therapy, cancer immunotherapy, cancer radiotherapy, chemotherapy induced emesis, clinical assessment, clinical trial, colorectal tumor, competitive inhibition, controlled clinical trial, controlled study, coughing, diarrhea, drug accumulation, drug clearance, drug dose, drug dose increase, drug fatality, drug half life, drug metabolite, drug safety, drug screening, drug tolerability, enzyme, escalation, febrile neutropenia, female, human, immunohistochemistry, kidney failure, kidney tumor, leukopenia, m 594347, major clinical study, male, maximum plasma concentration, maximum tolerated dose, multicenter study, myalgia, n (5 chloro 1,3 benzodioxol 4 yl) 7 [2 (4 methyl 1 iperazinyl)ethoxy] 5 (tetrahydro 2h pyran 4 yloxy) 4 quinazolinamine, nausea, neutropenia, open study, ovary tumor, pancreas tumor, phase 1 clinical trial, pneumonia, priority journal, protein tyrosine kinase, randomized controlled trial, recommended drug dose, respiratory failure, saracatinib, septic shock, single drug dose, solid tumor, steady state, therapy effect, thrombocytopenia, tumor biopsy, unclassified drug|
|Persistent URL||dx.doi.org/10.1158/1078-0432.CCR-10-0748, hdl.handle.net/1765/21297|
Baselga, J., Cervantes, A., Martinelli, E., Chirivella, I., Hoekman, K., Hurwitz, H.I., … Tabernero, J.. (2010). Phase I safety, pharmacokinetics, and inhibition of src activity study of saracatinib in patients with solid tumors. Clinical Cancer Research, 16(19), 4876–4883. doi:10.1158/1078-0432.CCR-10-0748