Literature DB >> 18641028

Long-term responses and outcomes following immunosuppressive therapy in large granular lymphocyte leukemia-associated pure red cell aplasia: a Nationwide Cohort Study in Japan for the PRCA Collaborative Study Group.

Naohito Fujishima1, Ken-ichi Sawada, Makoto Hirokawa, Kazuo Oshimi, Koichi Sugimoto, Akira Matsuda, Masanao Teramura, Masamitsu Karasawa, Ayako Arai, Yuji Yonemura, Shinji Nakao, Akio Urabe, Mitsuhiro Omine, Keiya Ozawa.   

Abstract

Large granular lymphocyte leukemia-associated pure red cell aplasia accounts for a significant portion of secondary pure red cell aplasia cases. However, because of its rarity, long-term responses and relapse rates after immunosuppressive therapy are largely unknown. We conducted a nationwide survey in Japan and collected 185 evaluable patients. Fourteen patients with large granular lymphocyte leukemia-associated pure red cell aplasia were evaluated. Cyclophosphamide, cyclosporine A and prednisolone produced remissions in 6/8, 1/4 and 0/2 patients respectively. Seven and 5 patients were maintained on cyclophosphamide or cyclosporine A respectively. Two patients relapsed after stopping cyclophosphamide, and 2 patients relapsed during maintenance therapy with cyclosporine A. The median relapse-free survival in the cyclophosphamide - and the cyclosporine A groups was 53 and 123 months respectively. Large granular lymphocyte leukemia-associated pure red cell aplasia showed a good response to either cyclophosphamide or cyclosporine A. Most patients continued to receive maintenance therapy and it remains uncertain whether cyclophosphamide or cyclosporine A can induce a maintenance-free hematologic response in large granular lymphocyte leukemia-associated pure red cell aplasia.

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Year:  2008        PMID: 18641028     DOI: 10.3324/haematol.12871

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  28 in total

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2.  Large granular lymphocyte disorders: new etiopathogenetic clues as a rationale for innovative therapeutic approaches.

Authors:  Renato Zambello; Gianpietro Semenzato
Journal:  Haematologica       Date:  2009-10       Impact factor: 9.941

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Authors:  Yoshihiro Michishita; Makoto Hirokawa; Yong-Mei Guo; Yukiko Abe; Jiajia Liu; Kumi Ubukawa; Naohito Fujishima; Masumi Fujishima; Tomoko Yoshioka; Yoshihiro Kameoka; Hirobumi Saito; Hiroyuki Tagawa; Naoto Takahashi; Kenichi Sawada
Journal:  Int J Hematol       Date:  2011-08-20       Impact factor: 2.490

4.  Guest editorial: the seven wonders of erythropoiesis.

Authors:  Kenichi Sawada
Journal:  Int J Hematol       Date:  2011-01-12       Impact factor: 2.490

Review 5.  The pathogenesis and treatment of large granular lymphocyte leukemia.

Authors:  Steven Nathaniel Steinway; Francis LeBlanc; Thomas P Loughran
Journal:  Blood Rev       Date:  2014-03-07       Impact factor: 8.250

6.  Response to cyclosporine A and corticosteroids in adult patients with acquired pure red cell aplasia: serial experience at a single center.

Authors:  Xuemei Wu; Suli Wang; Xingyu Lu; Wenyi Shen; Chun Qiao; Yujie Wu; Ruinan Lu; Shuai Wang; Jianfu Zhang; Ming Hong; Yu Zhu; Jianyong Li; Guangsheng He
Journal:  Int J Hematol       Date:  2018-03-27       Impact factor: 2.490

7.  Long-term follow-up of patients with moderate aplastic anemia and pure red cell aplasia treated with daclizumab.

Authors:  Elaine M Sloand; Matthew J Olnes; Barbara Weinstein; Colin Wu; Jaroslaw Maciejewski; Phillip Scheinberg; Neal S Young
Journal:  Haematologica       Date:  2010-03       Impact factor: 9.941

8.  How I treat LGL leukemia.

Authors:  Thierry Lamy; Thomas P Loughran
Journal:  Blood       Date:  2010-12-29       Impact factor: 22.113

Review 9.  Pure red cell aplasia.

Authors:  Robert T Means
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

10.  Frequent STAT3 mutations in CD8+ T cells from patients with pure red cell aplasia.

Authors:  Toru Kawakami; Nodoka Sekiguchi; Jun Kobayashi; Tatsuya Imi; Kazuyuki Matsuda; Taku Yamane; Sayaka Nishina; Yasushi Senoo; Hitoshi Sakai; Toshiro Ito; Tomonobu Koizumi; Makoto Hirokawa; Shinji Nakao; Hideyuki Nakazawa; Fumihiro Ishida
Journal:  Blood Adv       Date:  2018-10-23
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