Leukemia (Blood Cancer)

Leukemia is a cancer of the blood-forming cells, most often originating in the bone marrow, the spongy tissue inside bones responsible for producing blood cells. Leukemia causes the bone marrow to produce abnormal white blood cells that do not function properly and, because they multiply and survive longer than normal cells, gradually crowd out the healthy white blood cells, red blood cells, and platelets the body needs.

Despite the name suggesting an increase in white blood cell numbers, leukemia can sometimes present with a normal or even low white blood cell count, since it is the abnormal function and behaviour of these cells, not simply their number, that defines the disease.

Leukemia is not one disease but several, and the distinction between them matters enormously. Some forms progress rapidly and require treatment to begin within days of diagnosis; others progress so slowly that some patients are simply monitored for years before treatment becomes necessary at all. Treatment for certain types of leukemia has also advanced dramatically over the past two decades, transforming what was once a rapidly fatal diagnosis into a manageable, long-term condition for many patients.


How Leukemia Develops

All blood cells, including white blood cells, red blood cells, and platelets, originate from blood-forming stem cells within the bone marrow, which mature through a carefully regulated process into their final, functioning forms. Leukemia begins when a genetic mutation occurs within one of these developing blood cells, disrupting this normal regulation and allowing the abnormal cell to multiply uncontrollably.

As these abnormal cells accumulate in the bone marrow and bloodstream, they progressively crowd out the space and resources needed for normal blood cell production. This is what drives the core problems seen in leukemia: too few healthy red blood cells causes anaemia and fatigue; too few functioning white blood cells impairs the body's ability to fight infection, even when total white cell counts appear elevated on a blood test; and too few platelets impairs normal blood clotting, causing easy bruising and bleeding.


Types of Leukemia

Leukemia is classified along two dimensions: how quickly it develops and progresses (acute or chronic), and which type of white blood cell is affected (lymphocytic or myelogenous). This produces four main types.

Acute Lymphoblastic Leukemia (ALL)
The most common childhood leukemia, though it also occurs in adults. Involves immature lymphocytes that multiply rapidly, requiring treatment to begin promptly after diagnosis.

Acute myelogenous leukemia (AML)
The most common acute leukemia in adults, involving immature myeloid cells. Progresses quickly and, like ALL, requires urgent treatment initiation.

Chronic lymphocytic leukemia (CLL)
The most common chronic leukemia in adults, involving more mature lymphocytes that accumulate gradually. Many patients feel entirely well for years and are simply monitored (“watch and wait”) before treatment is needed.

Chronic myelogenous leukemia (CML)
Involves more mature myeloid cells, typically progressing slowly over months to years, though it can eventually accelerate into a more aggressive phase if untreated. Almost always associated with a specific genetic change, discussed further below, which has made it one of the most successfully treated cancers in modern medicine.


Why Acute Leukemia Is a Medical Emergency

The distinction between acute and chronic leukemia is not just about speed; it fundamentally changes how urgently treatment is needed.

In acute leukemia, immature blood cells multiply so rapidly that, if left untreated, the disease can become life-threatening within weeks. This is why acute leukemia is generally treated as a medical emergency from the point of diagnosis, with treatment typically beginning within days, not weeks, and often requiring hospital admission for the initial phase of chemotherapy and close monitoring.

Chronic leukemia behaves very differently. Because the abnormal cells are more mature and accumulate more slowly, some patients with early-stage chronic lymphocytic leukemia, for example, may not require any treatment for years, with regular monitoring alone being entirely appropriate. Understanding which category a diagnosis falls into is one of the first and most important pieces of information a patient receives, since it shapes the entire pace and urgency of what follows.


Symptoms of Leukemia

  • Persistent fatigue
  • Fever or night sweats
  • Easy bruising or bleeding
  • Bone or joint pain or tenderness
  • Unexplained weight loss
  • Loss of appetite
  • Frequent or recurrent infections
  • Swollen lymph nodes, or an enlarged liver or spleen
  • Small red spots on the skin (petechiae), reflecting a low platelet count


Risk Factors of Leukemia

  • Exposure to certain chemicals, including benzene, which is linked to an increased risk of certain leukemias
  • Family history of leukemia
  • Certain genetic disorders, including Down syndrome
  • Prior cancer treatment, including certain chemotherapy drugs and radiotherapy, which can increase the risk of developing a different leukemia later in life
  • Smoking, which specifically increases the risk of acute myeloid leukemia
  • Certain blood disorders, which can occasionally progress to leukemia over time


How is Leukemia diagnosed?

  • Complete Blood Count (CBC): Measures the number of red blood cells, white blood cells, and platelets, often the first test to raise suspicion of leukemia, whether through abnormally high, low, or unusual-looking cell counts.
  • Peripheral Blood Smear: A blood sample is examined directly under a microscope, allowing abnormal, immature, or unusual-looking blood cells characteristic of leukemia to be identified.
  • Bone Marrow Aspiration and Biopsy: A sample of bone marrow, usually taken from the hip bone, is examined to confirm the diagnosis, determine the specific type of leukemia, and assess how much of the marrow is affected. This remains the definitive test for confirming a leukemia diagnosis.
  • Cytogenetic and Molecular Testing: Specialised testing of leukemia cells for specific genetic changes, such as the Philadelphia chromosome in CML, or other mutations relevant to certain types of AML and ALL. This information is central to modern leukemia care, since it can identify targeted treatment options and provide important information about prognosis.
  • Imaging: CT scans or other imaging may be used to assess for enlarged lymph nodes, liver, or spleen, or to evaluate the extent of disease in certain situations.


Living with Leukemia

  • Attend all scheduled blood tests and follow-up appointments, since these track treatment response and catch early signs of complications
  • Take infection prevention seriously during periods of low white blood cell counts, including hand hygiene, avoiding crowded places when advised, and reporting fever immediately rather than waiting to see if it settles
  • Ask your care team specifically about your leukemia's genetic and molecular features, since this increasingly shapes treatment choice and expected outcomes
  • If prescribed a targeted therapy such as a TKI, take it consistently as directed, since inconsistent use is one of the most common reasons treatment does not work as well as expected
  • Seek support for the emotional and practical impact of a leukemia diagnosis and its treatment, which is a valid and common part of the experience, not a separate issue from physical treatment

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