Chronic myelomonocytic leukemia (CMML) is a rare type of blood cancer. Some people live a long time with CMML, but others go on to develop acute myeloid leukemia (AML).

Chronic myelomonocytic leukemia (CMML) is a chronic type of blood cancer. This means it develops more slowly than acute leukemias. There is currently no cure, but drug treatment, chemotherapy, and stem cell treatment can help manage it and may lead to remission.

Here, we look at what CMML is, why it happens, the treatment options, and the outlook for a person with this type of leukemia.

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CMML is a rare type of blood cancer. In the United States, 1 to 2 people in every 100,000 receive a CMML diagnosis each year.

CMML usually affects older adults and is rare in young people. In children, it is called juvenile myelomonocytic leukemia (JMML).

In CMML, two changes occur.

One is that alterations in the DNA of blood cells affect blood cell production.

The other is that the body starts producing too many immature white blood cells, known as blasts. These cells enter the bloodstream and crowd out other blood cells. These white blood cells never reach maturity and are unable to keep the body healthy.

People with CMML may have low levels of certain blood cells or too many blood cells overall.

Around 15% to 30% of people with CMML go on to develop acute myeloid leukemia (AML).

Various subtypes can help people understand how CMML affects an individual.

Subtype 0, 1, or 2

One classification is by the number of blasts, or immature blood cells, in the bone marrow.

Most people have under 5% blast cells among the developing blood cells in their bone marrow and none in their blood.

In CMML, blast counts fall into one of three categories, or subtypes:

SubtypeBlasts in bone marrowBlasts in blood
CMML-05%2%
CMML-15% to 9%2% to 4%
CMML-210% to 19%5% to 19%

The higher the level of blasts, the more likely CMML is to cause severe illness. Levels can also increase over time.

MD-CMML vs. MP-CMML

Doctors may also refer to myelodysplastic CMML (MD-CMML) or myeloproliferative CMML (MP-CMML).

The difference depends on whether CMML is associated with faulty blood cell production or the overproduction of white blood cells. The types are based on white blood cell levels.

In MD-CMML, the white blood cell count is below 13,000 per microliter. Overall, the blood cell count tends to be low.

MP-CMML is when the white blood cell count is equal to or above 13,000 per microliter. The person will likely have a high blood cell count.

CMML vs. JMML

Doctors refer to CMML when it affects adults. In people under 18 years old, it is called juvenile myelomonocytic leukemia (JMML).

JMML usually appears before the age of 4 years old. It affects males two to three times more often than females.

CMML vs. AMML

In people with CMML, symptoms appear over time. It is also possible to have acute myelomonocytic leukemia (AMML), in which symptoms appear suddenly.

The symptoms of CMML vary between individuals and depend on their blood count.

People with MD-CMML may experience:

Symptoms of MP-CMML include:

People with minor changes may have no symptoms.

Experts do not know precisely why CMML happens, but risk factors seem to include:

  • being 60 years of age or older
  • being male
  • previous treatment with chemotherapy
  • genetic changes that happen during a person’s lifetime

CMML does not appear to be an inherited disease.

Risk factors for JMML

JMML, which affects children, also appears to stem from genetic changes after birth. These changes are not inherited, and the person will not pass them on to their children.

However, children with other genetic features present from birth, such as Noonan’s syndrome, may be more likely to develop JMML.

To test for CMML, a doctor may recommend:

They will likely consider blood readings over at least 3 months to see if the changes are consistent. They will then assess the results using standard criteria to decide if a person has CMML and, if so, which type.

Treatment can help manage CMML and may cure it in some cases. However, not everyone with CMML will need treatment, and for some, it may not be the best option.

Factors affecting the decision include:

  • existing symptoms
  • the risk of CMML worsening or developing into AML
  • the person’s age
  • overall health status
  • the type of treatment available
  • how treatment will affect the person’s quality of life

The doctor may discuss the following therapies:

  • drug treatment
  • chemotherapy
  • bone marrow transplant
  • iron chelation therapy, in some cases
  • supportive care, such as counseling
  • treatment for symptoms such as anemia

For children with JMML, a stem cell transplant is the main treatment option.

The outlook for CMML will depend on the type and how it affects the individual. Factors that increase the risk include blood counts, age, and overall health.

In some cases, the risk is low, and the person can live with CMML without needing treatment.

However, some people have a high risk type. In around 15% of cases, CMML can develop into a more serious form of leukemia over the next 3 to 5 years.

Some researchers suggest a person with high risk CMML may live on average another 16 months after diagnosis and those with low risk factors another 8 years. However, these are averages, and some people see complete remission.

For children with JMML, around 50% of those who undergo hematopoietic stem cell transplant experience long-term remission. However, around 35% to 40% have a relapse, often within a year.

A person with low risk CMML may not need any treatment or lifestyle changes, although a doctor may recommend regular blood tests to monitor the condition.

A person with high risk CMML may need intensive treatment that will affect their daily life. However, some people who undergo treatment experience long-term remission.

Counseling can help anyone with CMML to manage the concerns and anxiety that can arise from living with a long-term condition.

CMML is a rare type of blood cancer. It usually affects older people. One form, JMML, can appear in young children.

The outlook varies widely, depending on the type of CMML and how it affects the individual. For some, it can become life threatening. Others, however, develop no symptoms or experience long-term remission.