Treatment characteristics, efficacy and safety of thrombopoietin analogues in routine management of primary immune thrombocytopenia

被引:12
作者
Mingot-Castellano, Maria E. [1 ]
Caparros, Isabel S. [2 ]
Fernandez, Fernando [3 ]
del Mar Perera-Alvarez, Maria [4 ]
Jimenez-Barcenas, Reyes [5 ]
Casaus Garcia, Alberto [6 ]
Gonzalez-Silva, Manuel [7 ]
Yera-Cobo, Maria [8 ]
Nieto-Hernandez, Maria M. [9 ]
Rodriguez-Fernandez, Maria J. [10 ]
Diaz-Canales, Dana [1 ]
机构
[1] Reg Univ Hosp Malaga, Dept Hematol, Malaga, Spain
[2] Virgen de la Victoria Univ Hosp, Dept Hematol, Malaga, Spain
[3] Insular Gran Canaria Univ Hosp, Dept Hematol, Las Palmas Gran Canaria, Spain
[4] Dr Negrin Univ Hosp Gran Canaria, Dept Hematol, Las Palmas Gran Canaria, Spain
[5] Virgen del Rocio Reg Univ Hosp, Dept Hematol, Seville, Spain
[6] Punta Europa Hosp, Dept Hematol, Algeciras, Spain
[7] La Linea de la Concepcion Hosp, Dept Hematol, La Linea Concepcion, Spain
[8] Puerta del Mar Univ Hosp, Dept Hematol, Cadiz, Spain
[9] Med & Surg Hosp Jaen, Dept Hematol, Jaen, Spain
[10] Motril Hosp, Dept Hematol, Motril, Spain
关键词
anticoagulants; antiplatelet agents; immune thrombocytopenia; switching; thrombopoietin analogues; RECEPTOR-AGONISTS; LONG-TERM; PLATELET PRODUCTION; ADULT PATIENTS; ELTROMBOPAG; ROMIPLOSTIM; PURPURA; REMISSION; ITP;
D O I
10.1097/MBC.0000000000000726
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thrombopoietin receptor agonist (TPO-RAs) have demonstrated good efficacy and tolerance in clinical trials in refractory chronic primary immune thrombocytopenia (ITP) or chronic ITP with contraindication for splenectomy. No head-to-head study is available, and differences in trials design do not allow comparisons. Information on the use of TPO-RAs in nonchronic ITP is scant. We described our experience with TPO-RAs in ITP (chronic, persistent and newly diagnosed ITP) in routine clinical practice. Retrospective series of 100 adult ITP patients was analysed; 41 treated with eltrombopag, 37 with romiplostim and 22 with both. Response-related and safety variables were evaluated. With a median follow-up of 86.5 weeks (interquartile range, 34.3-128 weeks), no differences were found in response rate, time to response, stability of response or response duration based on the type of TPO-RA used. Of all, 25% of patients with newly diagnosed or persistent ITP and 7.2% with chronic responded and maintained their response when TPO-RAs were stopped. Regarding safety, two developed bone marrow fibrosis grade 3, with loss of response to both drugs. Incidence of vascular events was 7%. Both TPO-RAs may be useful in all types of ITP, not only chronic but also persistent and newly diagnosed. Similar results were noted in efficacy and safety variables for both drugs.
引用
收藏
页码:374 / 380
页数:7
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