ON THIS PAGE: You will learn about the different ways doctors use to treat people with CML. To see other pages in this guide, use the colored boxes on the right side of your screen, or click “Next” at the bottom.
This section outlines treatments that are the standard of care (the best proven treatments available) for this specific type of cancer. When making treatment plan decisions, patients are also encouraged to consider clinical trials as an option. A clinical trial is a research study to test a new treatment to prove it is safe, effective, and possibly better than the standard treatment. Your doctor can help you review all treatment options. For more information, see the Clinical Trials  and Latest Research  sections.
In cancer care, different types of doctors often work together to create a patient’s overall treatment plan that combines different types of treatments. This is called a multidisciplinary team .
Descriptions of the most common treatment options for CML are listed below, followed by information on measuring treatment effectiveness and the common treatment recommendations outlined by the disease phase . Treatments for CML have improved greatly in the last 12 years, completely changing how treatment is given and helped many patients live longer.
Treatment options and recommendations depend on several factors, including the phase of the disease, possible side effects, and the patient’s preferences and overall health. Take time to learn about your treatment options and be sure to ask questions about things that are unclear. Also, talk about the goals of each treatment with your doctor and what you can expect while receiving the treatment. Learn more about making treatment decisions .
Targeted therapy is a treatment that attacks the cancer’s specific genes, proteins, or the tissue environment that contributes to cancer growth and survival. This type of treatment blocks the growth and spread of cancer cells while limiting damage to normal cells. For CML, targeted therapy is given by a medical oncologist, a doctor who specializes in treating cancer with medication, or a hematologist, a doctor who specializes in treating blood disorders.
Recent studies show that not all cancers have the same targets. To find the most effective treatment, your doctor may run tests to identify the genes, proteins, and other factors involved in your leukemia. As a result, doctors can better match each patient with the most effective treatment whenever possible. In addition, many research studies are taking place now to find out more about specific molecular targets and new treatments directed at them. Learn more about targeted treatments .
For CML, the target is the unique protein called the BCR-ABL tyrosine kinase enzyme. There are five drugs currently used to target tyrosine kinase enzymes for CML, called tyrosine kinase inhibitors or TKIs: imatinib (Gleevec), dasatinib (Sprycel), and nilotinib (Tasigna), bosutinib (Bosulif), and ponatinib (Iclusig). All five drugs can stop the BCR-ABL enzyme from working, which causes the CML cells to die quickly. These drugs are described in more detail below.
It is important to note that men and women taking TKIs should avoid fathering children or becoming pregnant while taking the drugs because of risk to the developing child. To find the best treatment, patients should talk with their doctors about the risks and benefits of these drugs, including the possible side effects and how they can be managed. If a patient experiences too many side effects, another TKI can be used instead.
Imatinib. Imatinib was the first targeted therapy approved (in 2001) by the U.S Food and Drug Administration (FDA) for CML. It is given in pill form once or twice a day and causes fewer side effects than the chemotherapy (see below) used to treat CML in the past. Nearly all patients with chronic phase CML have their blood counts return to normal and their spleen shrink after receiving this drug. Most importantly, 80% to 90% of patients newly diagnosed with chronic phase CML who receive imatinib no longer have detectable levels of cells with the Philadelphia chromosome. Imatinib may also be used to treat some adults with other types of cancer, such as acute lymphoblastic leukemia (ALL)  with the presence of the Philadelphia chromosome.
The recurrence rate for patients whose CML completely responds to imatinib is very low, and patients with few numbers of cells with the Philadelphia chromosome remaining will stay in chronic phase longer by taking imatinib than they might have with previous treatments. Although it is too soon to know how long these responses will last or if patients will be cured with this medication alone, there are many patients who have been treated with imatinib since the first clinical trials in 1999 who still have no detectable cells with the Philadelphia chromosome.
The side effects of imatinib are mild but can include slight nausea (very uncommon when imatinib is taken with food), changes in blood counts, fluid retention, swelling around the eyes, fatigue, and muscle cramps.
Dasatinib. In 2010, dasatinib was approved by the FDA as an initial treatment for patients with newly diagnosed chronic phase CML. It is a pill that may be taken once or twice a day depending on the dose. The side effects include anemia, neutropenia (low levels of white blood cells), thrombocytopenia (low platelet counts), and the build-up of fluid around the lungs or heart. The doctor will monitor a patient’s blood counts frequently after starting dasatinib and may adjust the dose or stop giving the drug temporarily if the patient’s blood counts drop too low. Dasatinib may also cause bleeding, fluid retention, diarrhea, rash, headache, fatigue, and nausea. Dasatinib requires stomach acid in order to be absorbed so patients should not take anti-acid medications.
Nilotinib. Nilotinib was also approved by the FDA in 2010 as an initial treatment for patients with newly diagnosed chronic phase CML. It is a capsule that patients take by mouth twice a day on an empty stomach. Common side effects include low blood counts, rash, headache, nausea, and itching. Other possible but uncommon serious side effects include high blood sugar levels, fluid build up, and swelling of the pancreas or liver. The most serious side effect of nilotinib includes possible life-threatening heart problems that can lead to an irregular heartbeat and possible sudden death. However, this side effect is very rare. There can be interactions with other medications that may increase the risks.
Bosutinib. In 2012, bosutinib was approved by the FDA to treat CML when one of the other tyrosine kinase inhibitor drugs was not effective or if a patient experienced too many side effects. The most common side effects include diarrhea, nausea and vomiting, low levels of blood cells, abdominal pain, fatigue, fever, allergic reactions, and liver problems.
Ponatinib. Ponatinib was also approved by the FDA in 2012 for patients when one of the other tyrosine kinase inhibitor drugs was not effective or if a patient experienced too many side effects. However, in October 2013 they recommended that the safety of the drug be re-evaluated because of the risk of life-threatening blood clots and narrowing of blood vessels. Patients taking this drug should talk with their doctors about the risks and benefits of continuing to take the drug, as other treatment options may be available.
Measuring treatment effectiveness. Patients receiving a TKI should receive regular check-ups with the health care team to see how well the treatment is working. The response of CML includes:
A complete hematologic response: the white blood cell and platelet counts have returned to normal, the spleen is of normal size and cannot be felt on physical examination, and there are no CML symptoms.A partial response: the blood counts are still abnormal, there may still be some immature blasts in the blood, and the spleen may still be enlarged, but the symptoms and blood test results are improved compared with those before treatment. These responses are not stable, and there is a risk that the CML will worsen without more effective treatment.
Other specific tests are used to find the number of cells that have the Philadelphia chromosome or contain the BCR-ABL fusion gene. When CML is diagnosed, the Philadelphia chromosome is found in almost all of a person’s bone marrow and blood cells. Once a person’s CML shows a complete hematologic response, the doctor then looks for a cytogenetic response.
- A complete cytogenetic response means that there are no cells with the Philadelphia chromosome found on the routine cytogenetic tests.
- A partial cytogenetic response means that between 1% and 34% of the cells still have the Philadelphia chromosome.
- A minor cytogenetic response means that more than 35% of the cells still have the Philadelphia chromosome.
An important goal of treatment is to achieve a complete cytogenetic response. This requires performing a bone marrow biopsy and is generally done three to six months after starting treatment when blood tests suggest that there are fewer leukemia cells. It is not clear whether any of these drugs can cure CML, and the disease may come back if treatment is stopped. If treatment with one of these drugs has worked, a patient no longer has evidence of cells with the Philadelphia chromosome and has normal levels of blood cells. This is called a complete cytogenetic remission. It is currently recommended that these drugs should be continued throughout the person’s life to prevent the CML from recurring.
Monitoring. More sensitive blood tests, such as FISH and PCR (see Diagnosis ), are usually done every three months on a blood sample after a person has a cytogenetic response in the bone marrow cells. Patients who have no cells with the Philadelphia chromosome on regular cytogenetic tests often need to have PCR testing to find a molecular response, which means that amount of cells with the BCR-ABL gene have been greatly reduced and further bone marrow tests are not necessary. Patients who have a rapid decrease in the number of cells with the Philadelphia chromosome by three months after starting treatment appear to have the best long-term outcomes.
The most sensitive test to look for remaining CML is called a quantitative reverse transcriptase PCR (Q-RT-PCR) test. This test is recommended every three months on a blood sample. Generally, this test can find one CML cell remaining among 10,000 or more normal blood cells, so, when this test is negative, it is very likely that the CML is nearly gone. On the other hand, if the results of this test begin to rise, then the current treatment is no longer working, and it may be time to switch medications before the disease recurs.
Sometimes, a tyrosine kinase drug stops working and the CML develops resistance to it. Resistance can occur if patients do not take their medication regularly, as prescribed . Even if patients do take the medication correctly, CML may become resistant to tyrosine kinase inhibitors, which is why it is important to receive regular monitoring with cytogenetic testing, FISH, or PCR to monitor how well the drug is continuing to work.
Both dasatinib and nilotinib have been shown to produce a complete cytogenetic response in newly diagnosed patients sooner and in more patients when compared with imatinib; however, imatinib has been used for longer. There is no difference in overall survival when using either imatinib or these other drugs as initial treatment. Bosutinib and ponatinib are newer drugs but both have also produced complete cytogenetic responses in patients with CML. If the medication you start with stops working, the dose may be increased or a different tyrosine kinase drug may still be effective.
Chemotherapy is the use of drugs to kill cancer cells, usually by stopping the cancer cells’ ability to grow and divide. In systemic chemotherapy, the drugs travel through the bloodstream to reach cancer cells throughout the body. A chemotherapy regimen (schedule) usually consists of a specific number of cycles given over a set period of time. A patient may receive one drug at a time or combinations of different drugs at the same time.
A drug called hydroxyurea (Hydrea, Droxia) is often given to lower the number of white blood cells until the definite diagnosis of CML is made with the tests described in the Diagnosis  section. Given in capsule form, this drug works well to return blood cells to normal levels within a few days or weeks and reduce the size of the spleen, but it does not reduce the percentage of cells with the Philadelphia chromosome and does not prevent blast crisis alone. Although hydroxyurea has few side effects, most patients newly diagnosed with chronic phase CML receive imatinib or other tyrosine kinase inhibitors (see above) as soon as possible. Side effects of chemotherapy depend on the specific drug and the dosage and usually go away when treatment is complete.
In 2012, the drug omacetaxine mepesuccinate (Synribo) was approved by the FDA for patients with chronic or accelerated phase CML that is not responding to one of the TKIs described above. Omacetaxine is given by subcutaneous (under the skin) injection daily for seven to 14 days. The most common side effects include thrombocytopenia, anemia, neutropenia, diarrhea, nausea, fatigue, weakness, skin irritation where the drug was given, fever, and infection.
Learn more about chemotherapy  and preparing for treatment . The medications used to treat cancer are continually being evaluated. Talking with your doctor is often the best way to learn about the medications prescribed for you, their purpose, and their potential side effects or interactions with other medications. Learn more about your prescriptions by using searchable drug databases .
Stem cell transplantation/bone marrow transplantation
A stem cell transplant is a medical procedure in which bone marrow that contains leukemia is replaced by highly specialized cells, called hematopoietic stem cells, that develop into healthy bone marrow. Hematopoietic stem cells are found both in the bloodstream and in the bone marrow. Today, this procedure is more commonly called a stem cell transplant, rather than bone marrow transplant, because it is the stem cells in the blood that are typically being transplanted, not the actual bone marrow tissue.
Before recommending transplantation, doctors will talk with the patient about the risks of this treatment and consider several other factors, such as the type of leukemia, results of any previous treatment, and patient’s age and general health.
There are two types of stem cell transplantation depending on the source of the replacement blood stem cells: allogeneic (ALLO) and autologous (AUTO). Only ALLO (the stem cells come from a healthy donor) transplants are used to treat CML.
In both types, the goal of transplantation is to destroy cancer cells in the marrow, blood, and other parts of the body and allow replacement blood stem cells to create healthy bone marrow. In most stem cell transplants, the patient received high doses of chemotherapy and/or radiation therapy to destroy as many cancer cells as possible. Learn more about bone marrow and stem cell transplantation .
Immunotherapy (also called biologic therapy) is designed to boost the body's natural defenses to fight the cancer. It uses materials made either by the body or in a laboratory to improve, target, or restore immune system function. Interferon (Roferon-A, Intron A, Alferon, Infergen) is a type of immunotherapy. It can reduce the number of white blood cells and sometimes decrease the number of cells that have the Philadelphia chromosome.
Interferon is given daily or weekly by an injection under the skin and sometimes causes flu-like side effects, such as fever, chills, fatigue, and loss of appetite. When given on an ongoing basis, it can also cause loss of energy and memory changes. Interferon therapy was the primary treatment for chronic phase CML before imatinib became available. A clinical trial showed that imatinib worked better to treat CML than interferon with fewer side effects. Therefore, interferon is no longer recommended as the first treatment for CML. Learn more about immunotherapy .
Getting care for symptoms and side effects
Leukemia and its treatment often cause side effects. In addition to treatment to slow, stop, or eliminate the disease, an important part of care is relieving a person’s symptoms and side effects. This approach is called palliative or supportive care, and it includes supporting the patient with his or her physical, emotional, and social needs.
Palliative care can help a person at any stage of illness. People often receive treatment for the leukemia and treatment to ease side effects at the same time. In fact, patients who receive both often have less severe symptoms, better quality of life, and report they are more satisfied with treatment.
Palliative treatments vary widely and often include medication, nutritional changes, relaxation techniques, and other therapies. You may also receive palliative treatments similar to those meant to eliminate the leukemia, such as chemotherapy, surgery, and radiation therapy. Talk with your doctor about the goals of each treatment in your treatment plan.
Before treatment begins, talk with your health care team about the possible side effects of your specific treatment plan and supportive care options. And during and after treatment, be sure to tell your doctor or another health care team member if you are experiencing a problem so it is addressed as quickly as possible. Learn more about palliative care .
Treatment by phase
The immediate goals of treatment are to reduce any symptoms the patient may have. The longer-term goals are to decrease or get rid of the cells with the Philadelphia chromosome in order to slow down or prevent the disease from moving to blast crisis. Treatment will often first include one of the TKIs mentioned above. An ALLO stem cell transplantation would be considered afterwards only if the TKI treatment is not successful.
The same drugs used for chronic phase CML may also be used in the accelerated phase. Although treatment with a TKI can work well during this stage, it is less likely to work as well as it does for chronic phase CML, and many patients have a recurrence within about two years. Dasatinib or nilotinib are more effective in providing longer remissions. Therefore, an ALLO stem cell transplantation should be considered when possible. If an ALLO stem cell transplantation is not recommended or if a matched donor cannot be found, the treatment plan may include a different TKI or a clinical trial .
Treatment with a TKI only works well for a few months for patients in blast crisis, but it can help to control the CML while a stem cell/bone marrow transplant is being arranged. If the transplant can be done while imatinib or dasatinib is working, then the long-term results are better. Stem cell/bone marrow transplantation in the blast phase is less successful than in chronic phase, but this approach has worked well for some patients. Many people with CML in blastic phase receive imatinib or dasatinib plus chemotherapy similar to that used for patients with acute myeloid leukemia (AML) . The chance of remission from this approach is about 20% to 30%, although the leukemia recurs for most patients within weeks to a few months. Hydroxyurea (see Chemotherapy, above) is often given to patients because it can help control blood cell levels. If stem cell/bone marrow transplantation is not an option, the doctor may recommend a clinical trial .
It is not yet proven whether imatinib, dasatinib, or nilotinib, or the newer drugs bosutinib, ponatinib, or omacetaxine can cure CML. A remission is when leukemia cannot be detected in the body by cytogenetic testing and there are no symptoms. This may also be called “no evidence of disease” or NED.
A remission can be temporary or permanent. This uncertainty leads to many survivors feeling worried or anxious that the leukemia will come back. While many remissions are permanent, it is important to talk with your doctor about the possibility of the disease returning. Understanding the risk of recurrence and the treatment options may help you feel more prepared if the leukemia does return. Learn more about coping with the fear of recurrence .
If the leukemia does return despite the original treatment, it is called recurrent leukemia. When this occurs, a cycle of testing will begin again to learn as much as possible about the recurrence, including whether the leukemia is in a different phase. After testing is finished, you and your doctor will talk about your treatment options. Often the treatment plan will include the therapies described above (such as targeted therapy, chemotherapy, and immunotherapy) but they may be used in a different combination or given at a different dose. Your doctor may also suggest clinical trials that are studying new ways to treat this type of recurrent leukemia.
People with recurrent leukemia often experience emotions such as disbelief or fear. Patients are encouraged to talk with their health care team about these feelings and ask about support services to help them cope. Learn more about dealing with cancer recurrence .
If the leukemia does not respond to treatment, it is called refractory leukemia. Patients with this diagnosis are encouraged to talk with doctors who are experienced in treating this type of leukemia, because there can be different opinions about the best treatment plan. Learn more about seeking a second opinion  before starting treatment, so you are comfortable with the treatment plan chosen. This discussion may include clinical trials . Supportive care will also be important to help relieve symptoms and side effects.
For most patients, a diagnosis of refractory leukemia is very stressful and, at times, difficult to bear. Patients and their families are encouraged to talk about the way they are feeling with doctors, nurses, social workers, or other members of the health care team. It may also be helpful to talk with other patients, including through a support group.
If treatment fails
Recovery from leukemia is not always possible. If treatment is not successful, the disease may be called advanced or terminal leukemia.
This diagnosis is stressful, and this is difficult to discuss for many people. However, it is important to have open and honest conversations with your doctor and health care team to express your feelings, preferences, and concerns. The health care team is there to help, and many team members have special skills, experience, and knowledge to support patients and their families. Making sure a person is physically comfortable and free from pain is extremely important.
Patients who have advanced disease and who are expected to live less than six months may want to consider a type of palliative care called hospice care. Hospice care is designed to provide the best possible quality of life for people who are near the end of life. You and your family are encouraged to think about where you would be most comfortable: at home, in the hospital, or in a hospice environment. Nursing care and special equipment can make staying at home a workable alternative for many families. Learn more about advanced cancer care planning .
After the death of a loved one, many people need support to help them cope with the loss. Learn more about grief and bereavement .
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