- There are abnormal blood-forming cells that develop in the bone marrow.
- At first, these cells interfere with the production of the normal blood cells and eat up the nutrition meant for them.
- These cancers occur when certain stem cells in the bone marrow fail to mature into healthy blood cells. The blasts (immature cells) don't work properly, and they take up space in the bone marrow or blood.
- This leaves less room for the growth of healthy red blood cells, white blood cells, and platelets.
- MDS hinders stem cell growth into blood cells and platelets. People with MDS don’t have enough healthy blood cells.
- MDS affects people older than 60 years. It's more common in men than in women. Symptoms rarely appear in the early stages.
What are the signs and symptoms of MDS?
The early stages of myelodysplastic syndrome (MDS) are typically symptom-less, and the condition is often detected when a routine blood test reveals a low blood cell count. When MDS symptoms eventually develop, their nature often depends on which type of blood cells are involved.
- Skin infections such as boils and abscesses.
- Sinus infections (characterized by nasal congestion).
- Lung infections (characterized by coughing and shortness of breath).
- Urinary tract infections (characterized by painful and frequent urination).
Other common symptoms may include:
What are the causes of and risk factors for MDS?
- When MDS develops without any known cause, it is called de novo MDS.
- MDS is the commonest disease that develops as a side effect of chemotherapy or radiotherapy. It is called therapy-related MDS or t-MDS.
- Some people with MDS have a change, or mutation, in the JAK2 (Janus kinase 2) gene. People with MDS often have changes in certain chromosomes.
- MDS can sometimes be inherited (passed from parent to child).
Risk factors may include:
What are the treatment options for MDS?
Myelodysplastic syndrome (MDS) is usually not curable. The only way to cure the condition is with bone marrow stem-cell transplantation. The treatment for MDS typically focuses on symptom management, slowing down disease progression, and heading off potential complications. Several medications that can help to manage the symptoms some of which include:
- Lenalidomide: This is prescribed for a patient with chromosomal abnormality.
- Immunosuppressive therapy: This suppresses the immune system and may also reduce the need for red blood cell transfusions.
- Azacytidine and Decitabine: These medications are used to stimulate the red blood cells to mature. This can reduce a patient’s further anemic symptoms.
- Epogen, Procrit, and Aranesp: These medications can increase the red blood cell count, reducing the need for transfusions and lessening symptoms.
- Neupogen and Zarxio: These medications can increase the white blood cell count, helping to protect the body from infections.
- Chemotherapy: Chemotherapy is the use of anticancer, or cytotoxic, drugs to destroy cancer cells. It may also be used to treat people with MDS. The most common chemotherapy drugs used to treat MDS are Cytosar and Ara-C (cytarabine). Cytarabine may be combined with Idamycin (idarubicin).
- Blood transfusion: A blood transfusion may be used to increase the cell count, reduce symptoms, slow disease progression, and prevent complications (such as bleeding and infections).
- Bone marrow transplant: During a bone marrow transplant, the patient will first undergo a course of intensive chemotherapy to remove all abnormal or defective blood cells from the bone marrow. Next, the abnormal bone marrow stem cells (which are failing to produce healthy blood cells) are replaced with functional bone marrow stem cells (supplied by a healthy donor). Bone marrow transplants are the only way to cure MDS. However, the procedure may have significant side effects, which makes it unsuitable for the majority of patients with MDS.