Acute lymphoblastic leukemia

Acute lymphocytic leukaemia (ALL), also known as acute lymphoblastic leukaemia is a cancer of the white blood cells, characterised by the overproduction and continuous multiplication of malignant and immature white blood cells (referred to as lymphoblasts) in the bone marrow. It is a hematological malignancy. It is fatal if left untreated as ALL spreads into the bloodstream and other vital organs quickly (hence "acute"). It mainly affects young children and adults over 50.

Contents

Symptoms

Initial symptoms of ALL are quite aspecific, but worsen to the point that medical help is sought:

The signs and symptoms of ALL result from the lack of normal and healthy blood cells because they are crowded out by malignant and immature white blood cells. Therefore, people with ALL experience symptoms from their red blood cells, white blood cells, and platelets not functioning properly.

Diagnosis

Diagnosing leukemia usually begins with a medical history and physical examination. If there is a suspicion of leukaemia, the patient will then proceed to undergo a number of tests to establish the presence of leukaemia and its type. Patients with this constellation of symptoms will generally have had blood tests, such as a full blood count, renal function, electrolytes and liver enzymes.

These tests may include complete blood count (blasts on the blood film generally lead to the suspicion of ALL being raised). Nevertheless, 10% have a normal blood film, and clinical suspicion alone may be the only reason to perform a bone marrow biopsy, which is the next step in the diagnostic process.

Bone marrow is examined for blasts, cell counts and other signs of disease. Pathological examination, cytogenetics (e.g. presence of the Philadelphia chromosome) and immunophenotyping establish whether the "blast" cells began from the B lymphocytes or T lymphocytes.

If ALL has been established as a diagnosis, a lumbar puncture is generally required to determine whether the malignant cells have invaded the central nervous system (CNS).

Lab tests (mentioned above) and clinical information will also determined if any other medical imaging (such as ultrasound or CT scanning) may be required to find invasion of other organs such as the lungs or liver.

Pathophysiology

The etiology of Acute Lymphocytic Leukaemia remains uncertain although some doctors believe that ALL develops from a combination of genetic and environmental factors. However, there is no definite way of determining the cause of leukaemia.

Scientific research has shown that all malignancies are due to subtle or less subtle changes in DNA that lead to unimpaired cell division and breakdown of inhibitory processes. In leukaemias, including ALL, chromosomal translocations occur regularly. It is thought that most translocations occur before birth during foetal development. These translocations may trigger oncogenes to "turn on", causing unregulated mitosis where cells divide too quickly and abnormally, resulting in leukaemia. There is little indication that propensity for ALL is passed on from parents to children.

There have been indications that excessive exposure to high dose radiation (such as that of nuclear reactors, notably Chernobyl,± and the atomic bombs in Hiroshima, Japan 1945) increases the risk of developing acute leukaemia. There has also been inconclusive evidence suggesting that electromagnetic fields or chemicals such as benzene have an increased risk of developing acute leukaemia.

Classification

Subtyping of the various forms of ALL is done according to the FAB (French-American-British) classification, which is used for all acute leukemias (including acute myelogenous leukemia, AML). As ALL is not a solid tumour, the TxNxMx notation used in those cancers is of little use.

The FAB classification is:

  • ALL-L1: small uniform cells
  • ALL-L2: large varied cells
  • ALL-L3: large varied cells with vacuoles (bubble-like features)

Note: The recent WHO International panel on ALL recommends that this classification be abandoned, since the morphological classification has no clinical or prognostic relevance. It instead, advocates the use of the immunophenotypic classification mentioned below.

Each subtype is then further classified by determining the surface markers of the abnormal lymphocytes, called immunophenotyping. There are three main immunologic types:

  • B-cell
  • pre-B cell
  • T-cell

Subtyping helps determine the prognosis and most appropriate treatment in treating ALL.

Some cytogenetic subtypes have a worse prognosis than others. These include:

  • A translocation between chromosomes 9 and 22, known as the Philadelphia chromosome, occurs in about 20% of adult and 5% in pediatric cases of ALL.
  • A translocation between chromosomes 4 and 11 occurs in about 4% of cases and is most common in infants under 12 months.
  • Not all translocations of chromosomes carry a poorer prognosis. Some translocations are relatively favourable.

Treatment

The earlier acute lymphocytic leukaemia is detected, the more effective the treatment. The aim is to induce a lasting remission, defined as the absence of detectable cancer cells in the body (usually less than 5% blast cells on the bone marrow).

Treatment for acute leukaemia can include chemotherapy, steroids, radiation therapy, intensive combined treatments (including bone marrow or stem cell transplants), and growth factors.

Chemotherapy

Chemotherapy will usually be the treatment of choice but most ALL patients end up receiving a combination of different treatments. There are no surgical options, due to the body-wide distribution of the malignant cells.

As the chemotherapy regimens can be intensive, many patients have an intravenous catheter inserted into a large vein (termed a central line or a Hickman line).

Radiation therapy

Radiation therapy is used on painful bony areas, in high disease burden, or as part of the preparations for a bone marrow transplant (total body irradiation).

Epidemiology

ALL accounts for approximately 80 per cent of all childhood leukaemia cases, making it the most common type of childhood cancer. It has a peak incident rate of 2-5 years old, decreasing in incidence with increasing age before increasing again at around 50 years old. ALL is slightly more common in males than females.

Prognosis

Advancements in medical technology and research over the past four decades in the treatment of ALL has improved the overall prognosis significantly from a zero to 20-75 percent survival rate, largely due to the continuous development of clinical trials and improvements in bone marrow transplantation (BMT) and stem cell transplanation (SCT) technology.

However the prognosis for ALL differs between individuals depending on a wide variety of factors:

  • Sex: females tend to fare better than males.
  • Ethnicity: Caucasians are more likely to develop acute leukaemia than African-Americans, Asians and Hispanics and tend to have a better prognosis than Non-Caucasians.
  • Age at diagnosis: Children between 1-10 years of age are most likely to be cured.
  • Lymphoblast cell count at diagnosis
  • Whether the cancer has spread to the brain or spinal cord
  • Morphological, immunological, and genetic subtypes
  • Response of patient to initial treatment
  • Genetic disorders such as Down's Syndrome

External links

  • The Leukemia & Lymphoma Society (http://www.leukemia-lymphoma.org) - provides information about leukaemia and related diseases, updates on current clinical trials, and discussion forums.
  • Cancer Research UK (http://www.cancerresearchuk.org) - trains and supports scientists for cancer research, offers regional news about current research, and provides ways that individuals can become involved.
  • Children's Cancer Web (http://spade39.ncl.ac.uk/ccw/) - a directory of children's cancer-related resources.
  • Children's Leukaemia and Cancer Research Foundation (INC) (http://www.childcancerresearch.com.au/) (Australia) - provides funding for children's leukaemia, especially to the Princess Margaret Hospital for Children [1] (http://www.pmh.wa.gov.au/).


Health science - Medicine - Hematology
Hematological malignancy and White blood cells
Leukemia (ALL, AML, CLL, CML) - Lymphoma (Hodgkin's disease, NHL) - Multiple myeloma - MDS - Myelofibrosis - Myeloproliferative disease (Essential thrombocytosis, Polycythemia) - Neutropenia
Red blood cells
Anemia - Hemochromatosis - Sickle-cell anemia - Thalassemia - G6PD - other hemoglobinopathies
Coagulation and Platelets
Thrombosis - Deep venous thrombosis - Pulmonary embolism - Hemophilia - ITP - TTP
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