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Myelodysplastic Syndromes

Myelodysplastic syndromes (MDS) are a group of diseases characterized by ineffective hematopoiesis. For unknown reasons, the bone marrow begins producing dysplastic myeloid stem cells. As the cells progress toward differentiation, they stall in the maturation process. These cells have chromosomal abnormalities, typically an addition or deletion, which they pass on to their progeny.13

The cells also produce toxins that cause extensive apoptosis of healthy cells, helping the dysplastic cell lines achieve an advantage over healthy cells in subsequent generations. The result is very active hematopoiesis that produces many immature myeloblasts and ineffective blood cells. Since the blasts do not mature, the population of healthy blood cells declines, as do the functions associated with the cells.13,14

DACOGEN® (decitabine) for Injection is a hypomethylating agent indicated to treat patients with MDS, including

  • Previously treated and untreated MDS
  • De novo and secondary MDS
  • All French-American-British (FAB) subtypes (RA, RARS, RAEB, RAEB-t, CMML)
  • Intermediate-1, Intermediate-2, and High-risk International Prognostic Scoring System (IPSS) groups.1

For more about MDS, visit the following sections of this Web site:

And be sure to visit the Treatment with DACOGEN section of this Web site to learn how DACOGEN is believed to target DNA methylation to help treat MDS.

Abbrevations: RA = refractory anemia; RARS = refractory anemia with ringed sideroblasts; RAEB = refractory anemia with excess blasts; RAEB-t = refractory anemia with excess blasts in transformation; CMML = chronic myelomonocytic leukemia.

References

IMPORTANT SAFETY INFORMATION

DACOGEN may cause fetal harm when administered to a pregnant woman. Women of childbearing potential should be advised to avoid becoming pregnant while using DACOGEN. Men should be advised not to father a child while receiving treatment with DACOGEN, and for 2 months afterwards. The most commonly occurring adverse reactions include neutropenia, thrombocytopenia, anemia, pyrexia, fatigue, nausea, cough, petechiae, constipation, diarrhea, and hyperglycemia.

DACOGEN is available by prescription only. Please see the important product information for DACOGEN for more information. This site does not contain everything that is known about DACOGEN. If you would like to know more, talk to your healthcare professional.

This web site contains information relating to various medical conditions and their treatment. Such information is provided for educational purposes only and is not meant to be a substitute for the advice of a physician or other health care professional. You should not use this information for diagnosing a health problem or disease. Individual responses to DACOGEN treatment may vary.

This site is intended for health care professionals in the United States only. The products discussed herein may have different product labeling in different countries.

All information collected in this Web site is held in strictest confidence and will only be used for purposes as specified and will not be sold or distributed to other parties.

 
Dacogen® is a registered trademark of SuperGen, Inc., Dublin, CA, U.S.A. used under license.
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All rights reserved. DAC135-B 5/08