Abstract |
Myelodysplastic syndrome (MDS) comprises a spectrum of heterogeneous diseases. Most patients present with ineffective hematopoiesis. The pathophysiology involves immune-mediated effects, cytokine dysregulation, and apoptosis, among others. We treated 14 transfusion-requiring patients with MDS, 10 with refractory anemia (RA) and four with RA with excess blasts ( RAEB) with a 4-day course of antithymocyte globulin (ATG) followed by intermittent etanercept for 4 months. Among 13 evaluable patients, five are red blood cell and platelet transfusion independent for intervals extending beyond 2 years, and two have normalized their peripheral blood parameters. One additional patient showed a transient rise of platelet and neutrophil counts, for an overall response rate of 46%. Responding patients showed striking improvements in marrow cell abnormalities as characterized by flow cytometry. These data show that a combination of ATG plus etanercept offers effective palliative therapy for unselected patients with MDS. Further trials incorporating these two agents are warranted.
|
Authors | H Joachim Deeg, Peter Y Z Jiang, Leona A Holmberg, Bart Scott, Effie W Petersdorf, Frederick R Appelbaum |
Journal | Leukemia research
(Leuk Res)
Vol. 28
Issue 11
Pg. 1177-80
(Nov 2004)
ISSN: 0145-2126 [Print] England |
PMID | 15380342
(Publication Type: Clinical Trial, Journal Article, Research Support, U.S. Gov't, P.H.S.)
|
Chemical References |
- Antilymphocyte Serum
- Immunoglobulin G
- Receptors, Tumor Necrosis Factor
- Etanercept
|
Topics |
- Antilymphocyte Serum
(therapeutic use)
- Etanercept
- Humans
- Immunoglobulin G
(therapeutic use)
- Myelodysplastic Syndromes
(drug therapy, pathology, therapy)
- Pilot Projects
- Receptors, Tumor Necrosis Factor
(therapeutic use)
|