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Beginner 5 min readSource checked

Chronic Myeloid Leukemia (CML): What to Know

Just been diagnosed with CML? Start here instead

A plain-language guide to CML, the Philadelphia chromosome, BCR-ABL testing, and targeted therapy.

This is general education — it cannot tell you what to do in your situation.

Instructions and urgent-contact thresholds vary by treatment and care team. If you are in treatment, follow the instructions your oncology team gave you, and contact them about any new or worsening symptom. If you think you may be having a medical emergency, call your local emergency number.

NCI source

National Cancer Institute - Chronic Myelogenous Leukemia Treatment (PDQ)

A man holds his throat while talking with a female doctor in an exam room
A man holds his throat while talking with a female doctor in an exam room

Key fact

The Philadelphia chromosome, a swap between chromosomes 9 and 22, creates the BCR::ABL1 gene in almost all CML. It is not inherited and cannot be passed to your children.

The short answer

In almost all CML a swap between chromosomes 9 and 22 creates the Philadelphia chromosome and the BCR::ABL1 gene. Daily tyrosine kinase inhibitor pills block the protein it makes, and PCR tests track the response.

  • The Philadelphia chromosome, a swap between chromosomes 9 and 22, creates the BCR::ABL1 gene in almost all CML. It is not inherited and cannot be passed to your children.

  • CML is described by phase from the share of blast cells: under 10% is chronic phase, 10% to 19% accelerated, and 20% or more blastic phase.

  • NCI lists asciminib, imatinib, dasatinib, nilotinib and bosutinib as the tyrosine kinase inhibitors used in CML.

  • Repeat BCR::ABL1 blood testing is how the team judges whether the pill is working.

Choose how you want to understand this

The full explanation.

What it is

Chronic myeloid leukemia, or CML, is a cancer of the blood and bone marrow. Bone marrow is the spongy tissue inside bones where blood cells are made.

In almost all CML, a piece of chromosome 9 swaps places with a piece of chromosome 22. The result is called the Philadelphia chromosome. It creates a new fused gene, BCR::ABL1. That gene makes a protein called a tyrosine kinase, and the protein tells the marrow to make far too many white blood cells. The change is not inherited, and you cannot pass it to your children.

Some people have no symptoms at all, and CML is found on a routine blood test. Others feel very tired, lose weight without trying, run a fever, or have drenching night sweats.

How doctors confirm it

Testing usually includes blood counts, a bone marrow sample, chromosome testing for the Philadelphia chromosome, and a molecular test for BCR::ABL1.

Ask which tests are done and which are still pending. The molecular test matters most. It gives a starting number that later tests are measured against.

Phases

CML is described in three phases. They are based on the share of very young cells, called blasts, in the blood or marrow:

  • Chronic phase. Fewer than 10% blasts. Most people are diagnosed here.
  • Accelerated phase. Between 10% and 19% blasts.
  • Blastic phase. 20% or more blasts. This is sometimes called blast crisis, and it can come with fever, fatigue, and a swollen spleen.

The phase guides treatment. So does how well the disease responds over the first months.

Treatment

Most treatment uses a daily pill called a tyrosine kinase inhibitor, or TKI. It blocks the protein the fused gene makes. Approved TKIs for CML include imatinib, dasatinib, nilotinib, bosutinib, and asciminib. Which one fits you depends on your phase, your other health conditions, and side effects.

Your team will recheck BCR::ABL1 in your blood on a schedule to see how well the drug is working. A stem cell transplant or a different drug may be discussed if the disease resists treatment or reaches an advanced phase.

Do not stop or skip a TKI on your own, even if you feel well. Some people can try stopping later, but only under close monitoring arranged by a specialist. Tell your team about every other medicine you take, and mention if you have had weight-loss surgery, because it can reduce how much of the pill your body absorbs.

What patients often misunderstand

  • Stage or spread does not always mean the same thing in blood cancers as it does in solid tumors.
  • A slow-growing blood cancer is not always harmless; it still needs follow-up.
  • A fast-growing blood cancer is not automatically hopeless; some respond strongly to treatment.
  • A remission still requires monitoring.
  • Supportive care, infection prevention, transfusions, and symptom control are part of treatment, not extras.

Questions to ask

  • What exact subtype do I have?
  • Is it fast-growing or slow-growing?
  • What genetic, chromosome, or molecular results matter?
  • Do I need treatment now, or is observation reasonable?
  • What symptoms or lab changes would make us act sooner?
  • Is a clinical trial worth discussing?

When to get help sooner

CML and its treatment can lower the blood cells that fight infection. An infection can turn serious quickly.

  • Call 911 or go to an emergency department if you have a fever of 100.4°F (38°C) or higher, the threshold CDC gives for infection during cancer treatment, with shaking chills, if you feel confused or very short of breath, or if you have bleeding that will not stop.
  • Call your care team immediately, at any hour, if you have a fever of 100.4°F (38°C) or higher on its own, with no other symptom at all. While you are on a tyrosine kinase inhibitor your white cells can be low, and a temperature is a medical emergency. If nobody answers quickly, go to an emergency department and tell them you are being treated for leukemia.
  • Call your care team the same day if you have new bruising or tiny red spots on your skin, blood in your urine or stool, or sudden severe pain in the upper left side of your belly, where the spleen sits.
  • Call your care team within a day or two if you have new or worsening tiredness, drenching night sweats, unexplained weight loss, or side effects from your pill that are making it hard to keep taking it. Ask what to change rather than stopping on your own.

Start with Leukemia, Lymphoma, Multiple Myeloma, Blood and Marrow Stem Cell Transplant, and CAR T-Cell Therapy.

Sources

Words to know

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Common questions

What causes CML?

In almost all cases a piece of chromosome 9 swaps places with a piece of chromosome 22, creating the Philadelphia chromosome and a fused gene called BCR::ABL1. That gene makes a tyrosine kinase protein that drives the marrow to produce far too many white blood cells. The change is not inherited and you cannot pass it to your children.

What do the three phases mean?

They are based on the share of blast cells in blood or marrow. NCI defines chronic phase as fewer than 10% blasts, accelerated phase as 10% to 19%, and blastic phase as 20% or more. Blastic phase with tiredness, fever and an enlarged spleen is called blast crisis. Most people are diagnosed in chronic phase.

Which tests matter most?

Blood counts, a bone marrow sample, chromosome testing for the Philadelphia chromosome, and a molecular test for BCR::ABL1. The molecular test gives the starting number that later tests are measured against, so ask what yours was and when it is repeated.

Can I ever stop the pill?

Not on your own, even if you feel well. Some people can try stopping later, but only under close monitoring arranged by a specialist. Tell your team about every other medicine you take, and mention any weight-loss surgery, because NCI notes bariatric surgery can block absorption of oral tyrosine kinase inhibitors.

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Sources last checked: 2026-08-13 what this meansLast updated: 2026-08-20Next planned review: 2027-07-20

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How this page was created

Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes. We do not employ clinicians and do not intend to — our work is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.

Editorial status: Source checked This page was written with AI assistance and checked line by line against the sources listed on it. That confirms the sources support what the page says. It is not a medical review, and it does not confirm the page is complete or right for your situation.

Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.

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