Chronic phase chronic myelogenous leukemia

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Chronic Phase Chronic Myelogenous Leukemia
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Fatigue (medical), Weight loss, Splenomegaly
Complications Progression to accelerated phase or blast crisis
Onset Typically in adulthood
Duration Indefinite without treatment
Types N/A
Causes Genetic mutation (Philadelphia chromosome)
Risks Age, Radiation exposure
Diagnosis Complete blood count, Bone marrow biopsy, Cytogenetic analysis
Differential diagnosis N/A
Prevention N/A
Treatment Tyrosine kinase inhibitors, Stem cell transplantation
Medication N/A
Prognosis Generally good with treatment
Frequency Rare
Deaths N/A


Overview[edit | edit source]

Chronic Phase Chronic Myelogenous Leukemia (CML) is a type of cancer that affects the blood and bone marrow. It is characterized by the overproduction of myeloid cells due to a specific genetic mutation known as the Philadelphia chromosome. This phase is the initial stage of CML and is typically the most manageable with treatment.

Pathophysiology[edit | edit source]

The hallmark of CML is the presence of the Philadelphia chromosome, a result of a translocation between chromosome 9 and chromosome 22, which creates the BCR-ABL fusion gene. This gene encodes a constitutively active tyrosine kinase that leads to uncontrolled cell division and the accumulation of myeloid cells in the bone marrow and peripheral blood.

Clinical Presentation[edit | edit source]

Patients in the chronic phase of CML may be asymptomatic or present with nonspecific symptoms such as fatigue (medical), weight loss, and night sweats. Physical examination may reveal splenomegaly, which can cause discomfort or pain in the left upper quadrant of the abdomen.

Diagnosis[edit | edit source]

The diagnosis of chronic phase CML is typically made through a combination of laboratory tests and clinical findings:

Treatment[edit | edit source]

The mainstay of treatment for chronic phase CML is the use of tyrosine kinase inhibitors (TKIs), which specifically target the BCR-ABL protein. Commonly used TKIs include:

These medications have significantly improved the prognosis of patients with CML, allowing many to achieve long-term remission.

In some cases, stem cell transplantation may be considered, particularly for patients who do not respond to TKIs or who progress to more advanced phases of the disease.

Prognosis[edit | edit source]

With the advent of TKIs, the prognosis for patients with chronic phase CML has improved dramatically. Many patients achieve a complete cytogenetic response and have a normal life expectancy. However, regular monitoring is essential to detect any signs of disease progression.

Complications[edit | edit source]

The primary complication of chronic phase CML is progression to the accelerated phase or blast crisis, which are more aggressive and difficult to treat. Monitoring for resistance to TKIs and managing side effects of treatment are also important aspects of care.

Epidemiology[edit | edit source]

CML is a rare disease, accounting for approximately 15% of all cases of adult leukemia. It is most commonly diagnosed in middle-aged and older adults, with a slight male predominance.

See Also[edit | edit source]

External Links[edit | edit source]

  • [Link to relevant medical resources]


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Contributors: Prab R. Tumpati, MD