| Literature DB >> 26791378 |
Akira Kitanaka1, Katsuto Takenaka2, Kotaro Shide1, Toshihiro Miyamoto2, Tadakazu Kondo3, Keiya Ozawa4, Mineo Kurokawa5, Koichi Akashi2, Kazuya Shimoda6.
Abstract
We retrospectively analyzed the outcomes of 14 patients with primary myelofibrosis who were treated with splenic irradiation (SI) for symptomatic splenomegaly between January 2000 and December 2012 at 12 hospitals. Median age at the time of SI was 67 years (range 47-76). The median dose of radiation per course was 5 Gy, administered in a median of eight fractions. Spleen size was reduced in 93 % of patients, and persisted for a median of 2.2 months (range 0.1-13.8). Symptom relief occurred in 86 % of patients, and lasted for a median of 2.5 months (range 0.1-16.5). Although SI provided a high rate of palliation for patients with symptomatic splenomegaly, the responses were transient. Significant thrombopenia (<25 × 10(9)/L) occurred in eight patients (57 %), and neutropenia (<0.5 × 10(9)/L) was observed in seven (50 %). Nine patients (64 %) required an increased number of red blood cell transfusions after SI. Five patients (36 %) developed serious infections, with two deaths (14 %), as a result of SI-induced cytopenia. The median survival for all patients after SI was 18.5 months (range 0.1-71.9). The Dynamic International Prognostic Scoring System model effectively distinguished the prognosis after SI between patients in the intermediate-2 and high-risk groups.Entities:
Keywords: Myelofibrosis; Palliation; Splenic irradiation; Splenomegaly
Mesh:
Year: 2016 PMID: 26791378 DOI: 10.1007/s12185-016-1940-3
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490