TY - JOUR
T1 - Electrocardiographic characterization of ramucirumab on the corrected qt interval in a phase ii study of patients with advanced solid tumors
AU - Olszanski, Anthony J.
AU - Smith, David C.
AU - Camacho, Luis H.
AU - Thompson, John
AU - Ramalingam, Suresh S.
AU - Donald Harvey, R.
AU - Campos, Luis
AU - Ferry, David
AU - Tang, Shande
AU - Gao, Ling
AU - Safran, Howard
N1 - Publisher Copyright:
© AlphaMed Press 2016.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Background. Ramucirumab is a human immunoglobulin G1 monoclonal antibody that specifically blocks vascular endothelial growth factor receptor-2 and is approved for the treatment of advanced gastric, non-small cell lung, and colorectal cancers. This phase II study was conducted to determine if treatment with ramucirumab causes prolongation of the corrected QT interval usingFridericia’s formula(QTcF) inpatientswithadvancedcancer. Methods. Patients received intravenous ramucirumab (10 mg/kg) every 21days for3 cycles.The first 16 patients received moxifloxacin (400 mg orally), an antibiotic associated with mild QT prolongation as a positive control. During cycle 3, determination of QTcF prolongation was made with triplicate electrocardiograms at multiple time points to compare with baseline. Results. Sixty-six patients received therapy; 51 patients completed 9 or more weeks of therapy for the complete QTcF evaluation period. The upper limit of the 90% two-sided confidence intervals for the least square means of change in QTcF from baseline at each time point was less than 10milliseconds. Concentration-QTcF analysisshowedavisible, but not significant, negative association between ramucirumab concentration and QTcF change from baseline. Conclusion. Ramucirumab at a dose of 10 mg/kg administered every 21 days for 3 cycles did not produce a statistically or clinically significant prolongation of QTcF.
AB - Background. Ramucirumab is a human immunoglobulin G1 monoclonal antibody that specifically blocks vascular endothelial growth factor receptor-2 and is approved for the treatment of advanced gastric, non-small cell lung, and colorectal cancers. This phase II study was conducted to determine if treatment with ramucirumab causes prolongation of the corrected QT interval usingFridericia’s formula(QTcF) inpatientswithadvancedcancer. Methods. Patients received intravenous ramucirumab (10 mg/kg) every 21days for3 cycles.The first 16 patients received moxifloxacin (400 mg orally), an antibiotic associated with mild QT prolongation as a positive control. During cycle 3, determination of QTcF prolongation was made with triplicate electrocardiograms at multiple time points to compare with baseline. Results. Sixty-six patients received therapy; 51 patients completed 9 or more weeks of therapy for the complete QTcF evaluation period. The upper limit of the 90% two-sided confidence intervals for the least square means of change in QTcF from baseline at each time point was less than 10milliseconds. Concentration-QTcF analysisshowedavisible, but not significant, negative association between ramucirumab concentration and QTcF change from baseline. Conclusion. Ramucirumab at a dose of 10 mg/kg administered every 21 days for 3 cycles did not produce a statistically or clinically significant prolongation of QTcF.
KW - Adult
KW - Aged
KW - Aged, 80 and over
KW - Antibodies, Monoclonal, Humanized
KW - Antibodies, Monoclonal/administration & dosage
KW - Carcinoma, Non-Small-Cell Lung/complications
KW - Cardiotoxicity/drug therapy
KW - Colorectal Neoplasms/complications
KW - Dose-Response Relationship, Drug
KW - Drug-Related Side Effects and Adverse Reactions/pathology
KW - Electrocardiography
KW - Female
KW - Heart Rate/drug effects
KW - Humans
KW - Male
KW - Middle Aged
KW - Ramucirumab
KW - Stomach Neoplasms/complications
UR - http://www.scopus.com/inward/record.url?scp=84963813192&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000374131000003&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1634/theoncologist.2015-0467
DO - 10.1634/theoncologist.2015-0467
M3 - Article
C2 - 26984445
SN - 1083-7159
VL - 21
SP - 402
EP - 403
JO - Oncologist
JF - Oncologist
IS - 4
ER -