Thalidomide in agnogenic and secondary myelofibrosis
- 1 November 2001
- journal article
- clinical trial
- Published by Wiley in British Journal of Haematology
- Vol. 115 (2), 313-315
- https://doi.org/10.1046/j.1365-2141.2001.03072.x
Abstract
Myelofibrosis with myeloid metaplasia (MMM) is a clonal disorder involving disregulation of angiogenesis and immunomodulatory mechanisms. Thalidomide (Thal) retains antiangiogenic, immunomodulatory and cytokine regulatory properties and recently it has been used successfully in multiple myeloma. Here, we report our experience in 10 MMM patients treated with Thal. Patients with agnogenic MMM treated in an early phase of the disease obtained significant benefits from the therapy and remain transfusion‐free. In contrast, all secondary MMM failed to respond. These preliminary findings confirm that Thal plays a role in MMM therapy, although the efficacy in the different phases of the disease must be further evaluated.Keywords
This publication has 8 references indexed in Scilit:
- Evaluation and clinical correlations of bone marrow angiogenesis in myelofibrosis with myeloid metaplasiaBlood, 2000
- Myelofibrosis with Myeloid MetaplasiaNew England Journal of Medicine, 2000
- Antitumor Activity of Thalidomide in Refractory Multiple MyelomaNew England Journal of Medicine, 1999
- The Italian Consensus Conference on Diagnostic Criteria for Myelofibrosis with Myeloid MetaplasiaBritish Journal of Haematology, 1999
- Prognostic factors in agnogenic myeloid metaplasia: a report on 195 cases with a new scoring system [see comments]Blood, 1996
- Thalidomide is an inhibitor of angiogenesis.Proceedings of the National Academy of Sciences, 1994
- Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: demonstration of heterogeneity in lineage involvementBritish Journal of Haematology, 1994
- Myelofibrosis with myeloid metaplasia: clinical and haematological parameters predicting survival in a series of 133 patientsBritish Journal of Haematology, 1990