| Literature DB >> 29332223 |
Emi Togasaki1,2,3, Naomi Shimizu4,5, Yuhei Nagao1, Chika Kawajiri-Manako1, Ryoh Shimizu1, Nagisa Oshima-Hasegawa1, Tomoya Muto1, Shokichi Tsukamoto1, Shio Mitsukawa1,4, Yusuke Takeda1, Naoya Mimura1,4, Chikako Ohwada1, Masahiro Takeuchi1, Emiko Sakaida1, Tohru Iseki1,4, Hideyuki Yoshitomi6, Masayuki Ohtsuka6, Masaru Miyazaki3,6, Chiaki Nakaseko7,8,9.
Abstract
Thrombopoietin-receptor agonists have been recently introduced for a second-line treatment of immune thrombocytopenia (ITP). Splenectomy has tended to be avoided because of its complications, but the response rate of splenectomy is 60-80% and it has still been considered for steroid-refractory ITP. We performed partial splenic embolization (PSE) as an alternative to splenectomy. Between 1988 and 2013, 91 patients with steroid-resistant ITP underwent PSE at our hospital, and we retrospectively analyzed the efficacy and long-term outcomes of PSE. The complete response rate (CR, platelets > 100 × 109/L) was 51% (n = 46), and the overall response rate (CR plus response (R), > 30 × 109/L) was 84% (n = 76). One year after PSE, 70% of patients remained CR and R. The group with peak platelet count after PSE ≥ 300 × 109/L (n = 29) exhibited a significantly higher platelet count than the group with platelet count < 300 × 109/L (n = 40) at any time point after PSE. The failure-free survival (FFS) rates at 1, 5, and 10 years were 78, 56, and 52%, respectively. Second PSE was performed in 20 patients who relapsed (n = 14) or had no response to the initial PSE (n = 6), and the overall response was achieved in 63% patients. There were no PSE-related deaths. These results indicate that PSE is a safe and effective alternative therapy to splenectomy for patients with steroid-resistant ITP as it generates long-term, durable responses.Entities:
Keywords: Immune thrombocytopenia (ITP); Partial splenic embolization; Splenectomy; Steroids; Thrombopoietin-receptor agonists
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Year: 2018 PMID: 29332223 DOI: 10.1007/s00277-018-3232-x
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673