TY - JOUR
T1 - Oral eltrombopag for up to three years is safe and well-tolerated in Japanese patients with previously treated chronic immune thrombocytopenia
T2 - An open-label, extension study
AU - Katsutani, Shinya
AU - Tomiyama, Yoshiaki
AU - Kimura, Akiro
AU - Miyakawa, Yoshitaka
AU - Okamoto, Shinichiro
AU - Okoshi, Yasushi
AU - Ninomiya, Haruhiko
AU - Kosugi, Hiroshi
AU - Ishii, Kazuyoshi
AU - Ikeda, Yasuo
AU - Hattori, Toshihiro
AU - Katsura, Koichi
AU - Kanakura, Yuzuru
N1 - Funding Information:
Acknowledgments Funding for this study (NCT00828750) was provided by GlaxoSmithKline (GSK). All listed authors meet the criteria for authorship set forth by the International Committee for Medical Journal Editors. The authors wish to acknowledge the following individuals for their contributions and critical review during the development of this manuscript on behalf of GSK: Ted Everson, PhD, and Meher Dustoor, PhD, of AOI Communications, L.P., for medical writing and editorial assistance, and Kimberly Marino and Michael Arning of GSK for critical review.
Funding Information:
Conflict of interest S. Katsutani has no conflict relevant to the subject matter or materials included in this manuscript. Y. Tomiyama has received honoraria from GlaxoSmithKline (GSK) and Kyowa Hakko Kirin Co., Ltd. A. Kimura has received honoraria from GSK. Y. Miyakawa has received honoraria from GSK, Kyowa Hakko Kirin Co., Ltd., and Eisai Co., Ltd., and royalty from Ono Pharmaceuticals Co., Ltd. Y. Ikeda has acted as a consultant to Sanofi-Aventis and AstraZeneca, has received research funding from Sanofi-Aventis, and has received honoraria from Sanofi-Aventis, GSK, and Kyowa Hakko Kirin Co., Ltd. T. Hattori and K. Katsura are employees of GSK. S. Okamoto, Y. Okoshi, H. Ninomiya, H. Kosugi, and K. Ishii have no conflicts of interest relevant to the subject matter or materials included in this manuscript. Y. Kanakura has received grants from GSK and Kyowa Hakko Kirin Co., Ltd., through the Osaka University.
PY - 2013/9
Y1 - 2013/9
N2 - Eltrombopag is an oral, nonpeptide, thrombopoietin receptor agonist approved for treatment of chronic immune thrombocytopenia (ITP). The safety, tolerability, and efficacy of eltrombopag for up to 3 years were evaluated in 19 Japanese patients with chronic ITP who had completed a prior 6-month study. Patients received eltrombopag once daily at the last dosage received in the prior study (12.5, 25, or 50 mg). Dose adjustments and treatment interruptions were permitted to maintain platelet counts of 50,000-200,000/μL. Primary evaluations were safety and tolerability of long-term eltrombopag treatment. The median duration of exposure was 27.5 months (range, 9.9-32.3). Adverse events were similar to those reported with short-term use of eltrombopag, and none led to treatment discontinuation. Nine serious adverse events were reported. Median platelet counts began to increase after 1 week of treatment and remained above 50,000/μL for most assessments. Bleeding episodes decreased from 63 % at baseline to 21 % after 2 weeks of treatment and remained below baseline for all assessments. Of 15 patients receiving concomitant baseline ITP medications, 10 permanently discontinued or achieved a sustained reduction of at least one treatment without requiring rescue treatment. Long-term treatment with eltrombopag was safe, well tolerated, and effective in Japanese patients with chronic ITP.
AB - Eltrombopag is an oral, nonpeptide, thrombopoietin receptor agonist approved for treatment of chronic immune thrombocytopenia (ITP). The safety, tolerability, and efficacy of eltrombopag for up to 3 years were evaluated in 19 Japanese patients with chronic ITP who had completed a prior 6-month study. Patients received eltrombopag once daily at the last dosage received in the prior study (12.5, 25, or 50 mg). Dose adjustments and treatment interruptions were permitted to maintain platelet counts of 50,000-200,000/μL. Primary evaluations were safety and tolerability of long-term eltrombopag treatment. The median duration of exposure was 27.5 months (range, 9.9-32.3). Adverse events were similar to those reported with short-term use of eltrombopag, and none led to treatment discontinuation. Nine serious adverse events were reported. Median platelet counts began to increase after 1 week of treatment and remained above 50,000/μL for most assessments. Bleeding episodes decreased from 63 % at baseline to 21 % after 2 weeks of treatment and remained below baseline for all assessments. Of 15 patients receiving concomitant baseline ITP medications, 10 permanently discontinued or achieved a sustained reduction of at least one treatment without requiring rescue treatment. Long-term treatment with eltrombopag was safe, well tolerated, and effective in Japanese patients with chronic ITP.
KW - Bleeding
KW - Platelets
KW - Thrombopoietin receptor agonist
UR - http://www.scopus.com/inward/record.url?scp=84884669269&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84884669269&partnerID=8YFLogxK
U2 - 10.1007/s12185-013-1401-1
DO - 10.1007/s12185-013-1401-1
M3 - Article
C2 - 23896965
AN - SCOPUS:84884669269
SN - 0925-5710
VL - 98
SP - 323
EP - 330
JO - International journal of hematology
JF - International journal of hematology
IS - 3
ER -