Understanding Childhood Leukemia and Treatments

Sep 30, 2024

Lecture Notes: Leukemia in Children

Overview

  • Leukemia: Malignant transformation and proliferation of hematopoietic cells.
    • Acute Leukemia: Clonal expansion of immature precursors.
    • Chronic Leukemia: Mature bone marrow components becoming clonal.
  • Symptoms: Due to lack of normal bone marrow cell production or accumulation of malignant cells.

Epidemiology

  • Most common pediatric malignancy.
  • 30% of all newly diagnosed children with cancer have leukemia.
  • Higher incidence in boys than girls.

Types of Leukemia in Children

  1. Acute Lymphoblastic Leukemia (ALL)
    • Most common in children.
    • Proliferation of B and T cell lymphocyte precursors.
    • Typically affects children aged 2-5.
    • Higher risk in Caucasian children.
  2. Acute Myelogenous Leukemia (AML)
    • Clonal proliferation of myeloid precursors.
    • Bimodal incidence: peaks in children under 2 and in adolescence.
    • Equal incidence in boys and girls.
    • Strong association with Down syndrome.
  3. Chronic Myelogenous Leukemia (CML)
    • Uncontrolled growth of myeloid cells.
    • Incidence increases with age.
    • Associated with BCR-ABL fusion protein.
  4. Juvenile Myelomonocytic Leukemia (JMML)
    • Rare, usually diagnosed before age 3.
    • Associated with genetic conditions like Down syndrome and neurofibromatosis.

Symptoms of Leukemia

  • Lethargy, fatigue.
  • Respiratory distress, bone pain.
  • Fever, pallor, tachycardia.
  • Bruising, petechiae, lymphadenopathy, hepatosplenomegaly.
  • Testicular enlargement in boys.
  • CNS involvement, especially in ALL.

Diagnosis

  • CBC: Shows abnormal cell lines, presence of blasts.
  • Chemistry panel: Checks for tumor lysis syndrome.
  • Radiology: Chest X-ray for mediastinal mass.
  • Bone Marrow Aspiration/Biopsy: Confirm diagnosis.
  • Lumbar Puncture: Check for CNS involvement in ALL.

High-Risk Factors

  • Age less than 1 year or more than 10 years.
  • Very high white blood cell count.
  • T-cell phenotype.
  • Cytogenic changes in leukemia cells.
  • Poor response to therapy.

Treatment

  • ALL: Multi-agent chemotherapy for 2-3.5 years, prophylactic intrathecal chemotherapy/radiation.
  • AML: Multi-agent chemotherapy for 6-9 months, possible stem cell transplant.
  • CML: Tyrosine kinase inhibitors, possible stem cell transplant.
  • JMML: Often requires a bone marrow transplant.

Prognosis

  • ALL: 80-95% survival in low-risk groups.
  • AML: 50% survival rate, depending on subtype.
  • CML: Lifelong disorder managed with therapy.
  • JMML: 40% survival with bone marrow transplant.

This concludes the review of leukemia in children. The prognosis is generally good for ALL, despite it being a cancer diagnosis.