Literature DB >> 12047970

Treatment of hypereosinophilic syndrome with imatinib mesilate.

Gerald J Gleich1, Kristin M Leiferman, Animesh Pardanani, Ayalew Tefferi, Joseph H Butterfield.   

Abstract

Patients with hypereosinophilic syndrome show persistent eosinophilia without recognised cause. We treated five such patients with 100 mg imatinib mesilate (formerly STI-571) daily; four male patients with normal serum interleukin 5 showed complete haematological responses; a female patient who did not respond had raised serum interleukin-5 concentrations. One patient developed leucopenia after 4 days of treatment; counts returned to normal when treatment was stopped. After 1 month, eosinophilia recurred; with further treatment for 2 days, eosinophil counts again became normal. All patients who responded stopped other treatments and reduced imatinib mesilate to 200 mg per week. This drug effectively controls eosinophilia in patients with hypereosinophilic syndrome and normal interleukin-5 concentrations.

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Year:  2002        PMID: 12047970     DOI: 10.1016/S0140-6736(02)08505-7

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  56 in total

1.  A young man with persistent eosinophilia.

Authors:  E Messa; D Cilloni; G Saglio
Journal:  Intern Emerg Med       Date:  2007-06       Impact factor: 3.397

2.  The FIP1L1-PDGFRA fusion gene cooperates with IL-5 to induce murine hypereosinophilic syndrome (HES)/chronic eosinophilic leukemia (CEL)-like disease.

Authors:  Yoshiyuki Yamada; Marc E Rothenberg; Andrew W Lee; Hiroko Saito Akei; Eric B Brandt; David A Williams; Jose A Cancelas
Journal:  Blood       Date:  2006-01-17       Impact factor: 22.113

Review 3.  Hypereosinophilic syndrome variants: diagnostic and therapeutic considerations.

Authors:  Florence Roufosse
Journal:  Haematologica       Date:  2009-09       Impact factor: 9.941

4.  Attacking cancer at its foundation.

Authors:  Nicholas Lydon
Journal:  Nat Med       Date:  2009-10       Impact factor: 53.440

5.  [Hypereosinophilic syndrome].

Authors:  F Moosig; G Richardt; C Merten; W L Gross
Journal:  Internist (Berl)       Date:  2013-04       Impact factor: 0.743

Review 6.  Biological Modulators in Eosinophilic Diseases.

Authors:  Panida Sriaroon; Mark Ballow
Journal:  Clin Rev Allergy Immunol       Date:  2016-04       Impact factor: 8.667

Review 7.  Idiopathic hypereosinophilic syndrome in children: 3 cases with review of literature.

Authors:  Jayashree Kanthila; Nalini Bhaskaranand
Journal:  Indian J Pediatr       Date:  2012-06-28       Impact factor: 1.967

Review 8.  Biology of the eosinophil.

Authors:  Carine Blanchard; Marc E Rothenberg
Journal:  Adv Immunol       Date:  2009       Impact factor: 3.543

9.  Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and the proliferation of primary erythroid cells from patients with myeloproliferative disorders.

Authors:  Elizabeth O Hexner; Cynthia Serdikoff; Mahfuza Jan; Cezary R Swider; Candy Robinson; Shi Yang; Thelma Angeles; Stephen G Emerson; Martin Carroll; Bruce Ruggeri; Pawel Dobrzanski
Journal:  Blood       Date:  2007-11-05       Impact factor: 22.113

10.  Eosinophil ribonucleases and their cutaneous lesion-forming activity.

Authors:  Douglas A Plager; Mark D P Davis; Amy G Andrews; Michael J Coenen; Terry J George; Gerald J Gleich; Kristin M Leiferman
Journal:  J Immunol       Date:  2009-08-28       Impact factor: 5.422

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