PLATON: use of romiplostim to treat chronic primary immune thrombocytopenia

memo - Magazine of European Medical Oncology - Tập 13 - Trang 227-234 - 2020
Georgi Mihaylov1, Barbara Skopec2, Zuzana Sninska3, Nikolai Tzvetkov4, Olga Cerna5, Vladlen Ivanushkin6, Daniela Niepel7, Katja Björklöf8, Peter Černelč2,9
1Clinic of Clinical Hematology, Specialized Hospital for Active Treatment of Hematology Diseases EAD, Sofia, Bulgaria
2Department of Hematology, University Medical Center Ljubljana, Ljubljana, Slovenia
3Department of Hematology and Blood Transfusion, University Hospital St. Cyril and Metod, Bratislava, Slovakia
4Clinic of Hematology, University Multiprofile Hospital for Active Treatment “Dr. Georgi Stranski” EAD, Pleven, Bulgaria
5Department Of Clinical Hematology,, University Hospital Kralovske Vinohrady, Prague, Czech Republic
6Department of Biostatistics, Quartesian, Kharkov, Ukraine
7Global Medical Affairs, Amgen (Global) GmbH, Rotkreuz, Switzerland
8Medical Affairs, Amgen (Europe North East), Rotkreuz, Switzerland
9Department of Biostatistics, Quartesian, Princeton, USA

Tóm tắt

Chronic primary immune thrombocytopenia (ITP) is an autoimmune disease involving the formation of antibodies to thrombocytes, leading to increased platelet destruction and chronic thrombocytopenia. Additionally, impaired platelet production is due to relative thrombopoietin deficiency. Romiplostim, a thrombopoietin receptor agonist, normalized platelet counts in affected patients in randomized controlled trials and real-world observational studies. The present study collected real-world practice data from Central and Eastern Europe, i.e. Slovakia, Slovenia, Bulgaria, Russia, and Czech Republic, between December 2010 and July 2017. This was an ambidirectional observational, noninterventional cohort study within the approved romiplostim indication. One-hundred patients were analyzed. Prior to romiplostim start, 98% had received other ITP medications and, in the prior 6 months, 40% had experienced bleeding events. Romiplostim was started 1.92 years (median) after ITP diagnosis. The median mean on-study dose was 2.62 µg/kg/week. During romiplostim treatment, platelet counts rapidly normalized to >50 × 109/L, 20% of patients experienced bleeding events (none grade 3/4), and 13% required splenectomy. At the end of study, 25% of patients were in remission. One patient experienced serious adverse drug reactions (thrombosis, dysphagia), none were fatal. In conclusion, romiplostim dosing, effectiveness and safety in these unselected ITP patients seemed comparable with observations in clinical trials and similarly designed observational studies.

Tài liệu tham khảo

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