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Treatment types and planning

Treatment for blood cancers and related disorders is tailored to each patient’s specific condition, stage, age, overall health, and genetic factors. A personalized treatment plan often combines different therapies such as chemotherapy, targeted therapy, immunotherapy, stem cell transplant, and supportive care. The goal may range from cure to long-term disease control or symptom management. Planning also involves regular monitoring and adjustments to therapy depending on response and side effects.

Leukaemia

  • Acute forms (ALL, AML): intensive chemotherapy, targeted therapy, and stem cell transplantation in selected patients
  • Chronic forms (CLL, CML): targeted drugs (e.g., TKIs for CML), immunotherapy, chemotherapy for resistant disease

Supportive care includes transfusions, infection prevention, and growth factors


Lymphoma

  • Combination chemotherapy (e.g., CHOP, ABVD) as the backbone of treatment
  • Targeted therapy and monoclonal antibodies (e.g., Rituximab)
  • Radiation therapy for localized disease
  • Stem cell transplantation in relapsed or high-risk cases
  • Emerging role of CAR-T cell therapy in resistant lymphomas

Myeloma

  • Drug therapy: proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, steroids
  • Stem cell transplantation for eligible patients
  • Supportive care: bone-strengthening agents, treatment of kidney problems, infection control, pain management
  • Maintenance therapy to prolong remission

Myelodysplastic Syndromes (MDS)

  • Supportive care: blood transfusions, iron chelation, antibiotics
  • Disease-modifying drugs: hypomethylating agents (azacitidine, decitabine), immunosuppressive therapy
  • Growth factors (EPO, G-CSF) to improve blood counts
  • Allogeneic stem cell transplantation is the only potentially curative option, used in younger/high-risk patients

Myeloproliferative Neoplasms (MPN)

  • Polycythemia Vera & Essential Thrombocythemia: phlebotomy, low-dose aspirin, cytoreductive therapy (e.g., hydroxyurea)
  • Myelofibrosis: JAK inhibitors (e.g., ruxolitinib), transfusions, and in select patients, stem cell transplantation
  • CML: tyrosine kinase inhibitors (imatinib and newer generations) are the mainstay

Careful monitoring for transformation to advanced disease stages

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