Acute promyelocytic leukemia medical therapy

Acute promyelocytic leukemia Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Acute promyelocytic leukemia from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms
Physical Examination
Laboratory Findings
Other Imaging Studies
Other Diagnostic Studies
Treatment
Medical Therapy
Interventions
Surgery
Primary PreventionSurgery
Secondary PreventionSurgery
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Acute promyelocytic leukemia medical therapy On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Acute promyelocytic leukemia medical therapy All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Acute promyelocytic leukemia medical therapy
CDC on Acute promyelocytic leukemia medical therapy
Acute promyelocytic leukemia medical therapy in the news
Blogs on Acute promyelocytic leukemia medical therapy
Directions to Hospitals Treating Acute promyelocytic leukemia
Risk calculators and risk factors for Acute promyelocytic leukemia medical therapy

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]

Overview

The treatment of acute promyelocytic leukemia is broadly divided into anti-leukemia therapies and supportive therapies. Anti-leukemia therapies function to eliminate cancer cells, whereas supportive therapies are temporizing measures that can control the disease for a short time until anti-leukemic therapy takes effect. Anti-leukemic therapies include all-trans retinoic acid, arsenic trioxide, gemtuzumab ozogamicin, and cytarabine. Supportive therapies include transfusions (such as cryopreciptate or platelet transfusions) and granulocyte colony stimulating factor.

Medical Therapy

Anti-leukemic Therapies

• All-trans retinoic acid:
  • Acute promyelocytic leukemia is unique among the leukemias distinguished by its sensitivity to all-trans retinoic acid, a derivative of vitamin A. Treatment with all-trans retinoic acid causes differentiation of the immature leukemic promyelocytes into mature granulocytes. This is typically combined with anthracycline-based chemotherapy resulting in a clinical remission in approximately 90% of patients. The introduction of all-trans retinoic acid has revolutionized the treatment paradigm and outcomes in acute promyelocytic leukemia. The 5-year mortality has decreased from 82% to 36% since the introduction of all-trans retinoic acid.
  • Mechanism of action:
    • Induction of differentiation in leukemic blasts
  • Dosing:
    • 45mg/m2 PO daily (typically 22.5mg/m2 PO divided twice daily), given on days 1-14 of a 28-day cycle (2 weeks on, 2 weeks off), for a total of 7 cycles
  • Adverse effects:
    • The most unique adverse effect of all-trans retinoic acid is differentiation syndrome. This was formerly known as retinoic acid syndrome, until it was noted that arsenic trioxide could also result in a similar phenomenon. The etiology of differentiation syndrome has been attributed to capillary leak syndrome from cytokine release from the differentiating promyelocytes. Differentiation syndrome is characterized by the development of dyspnea, fever, weight gain, peripheral edema and is treated with dexamethasone.
• Arsenic trioxide:
  • Arsenic trioxide is commonly used in the treatment of acute promyelocytic leukemia in combination with all-trans retinoic acid.
  • Mechanism of action: Induction of apoptosis via the mitochondrial pathway in leukemic blasts; induction of oxidative stress; induction of DNA damage
  • Dosing:
    • 0.15mg/kg IV daily for days 1-30 of a 60-day cycle (4 weeks on, 4 weeks off), for a total of 4 cycles
  • Adverse effects:
    • The adverse effects of arsenic trioxide include myelosuppression, QT interval prolongation, and liver dysfunction. Liver dysfunction occurs in approximately one-third of patients.
• Gemtuzumab ozogamycin:
• This is an anti-CD33 antibody conjugated to the anti-tumor antibiotic calicheamicin. Gemtuzumab ozogamycin is FDA-approved for the treatment of patients with newly diagnosed acute myeloid leukemia expressing the CD33 antigen. Gemtuzumab ozogamycin shows efficacy in acute promyelocytic leukemia. This medication was originally approved in the year 2000 for relapsed acute myeloid leukemia, then was withdrawn from the marker a few years later, then re-introduced to the marker in 2017.
  • Mechanism of action: Antibody-dependent cell-mediated cytotoxicity towards leukemic blasts expressing the cell surface marker CD33
  • Dosing: 3 mg/m2 IV on days 1, 4, and 7 of the induction regimen
  • Adverse effects: The most unique adverse effect is hepatic venoocclusive disease, which is due to the ozogamycin component.
• Cytarabine:
  • This is a cytotoxic chemotherapy that is used in high-risk acute promyelocytic leukemia along with all-trans retinoic acid. Importantly, cytarabine is not required for the treatment of acute promyelocytic leukemia, as studies from the GIMEMA cooperative group in Italy and the PETHEMA cooperative group in Spain showed that the combination of anthracycline plus all-trans retinoic acid is equally as effective as a cytarabine-containing regimen.
  • Mechanism of action: Incorporation into DNA and disruption of DNA synthesis
  • Dosing: 100 mg/m2 IV infusion continuously for 7 days
  • Adverse effects: Common adverse effects include rash; myelosuppression (infections, fatigue, bleeding); cerebellar dysfunction; conjunctivitis
• Anthacyclines:
  • These are cytotoxic chemotherapy agents that are used in high-risk acute promyelocytic leukemia along with all-trans retinoic acid.
    • Mechanism of action: intercalation into DNA; inhibition of topoisomerase II
    • Dosing: Idarubicin 12mg/m2 IV daily for 3 days, daunorubicin 60 mg/m2 or 90 mfg/m2 IV daily for 3 days
    • Adverse effects: The most unique adverse effect is cardiomyopathy. This can include arrhythmias in the acute setting and heart failure in the long-term setting. Patients who are at highest risk for cardiomyopathy from anthracyclines include those with pre-existing heart disease, diabetes, hypertension, and elderly patients. Mucositis is also a common adverse effect.

Supportive Therapies

• Cryoprecipitate transfusion: Cryoprecipitate is commonly given to patients with acute promyelocytic leukemia who have disseminated intravascular coagulation. Low fibrinogen levels (less than 100 mg/dl) warrant transfusion of cryoprecipitate. Cryoprecipitate contains factor I, factor VIII, and von Willebrand factor.
  • Adverse effects: Risks of cryoprecipitate transfusion include volume overload (low risk) and transfusion reaction. In rare cases, sepsis can occur from contaminated product.
• Packed red blood cell transfusion: Red blood cell transfusion is commonly done in patients with acute promyelocytic leukemia. Transfusion is indicated when the hemoglobin level decreases below 7 g/dl.
  • Adverse effects: Risks of red blood cell transfusion include volume overload, alloimmunization, iron overload, and infection (if the product is contaminated). Alloimmunization is usually prevents with clerical checks and proper blood banking techniques. Iron overload occurs after many repeated transfusion and can be prevented via the use of iron chelators such as deferiprone, deferasirox, and deferoxamine.
• Platelet transfusion: Platelet transfusion is indicated when the platelet count decreases to less than 10,000 cells per microliter. This low platelet count occurs especially when a patient received induction chemotherapy, such as cytarabine or anthacycline.
  • Adverse effects: Risks include sepsis (since platelet units are stored at room temperature and there is a high risk for contamination), volume overload, and thrombosis (less likely).
• Granulocyte colony stimulating factor (G-CSF): G-CSF is sometimes uses to help improve the neutrophil count in patients with acute promyelocytic leukemia. It is important to use G-CSF only when there is no active leukemia, as G-CSF can stimulate the proliferation of leukemic blasts. Patients who receive G-CSF are usually those who have had a favorable anti-tumor response to chemotherapy but have not recovered their normal blood counts. G-CSF helps enhance normal blood cell count recovery.
  • Adverse effects: The most common adverse effects are bone pain, leukocytosis, and injection site erythema and pain. Bone pain can be alleviated via loratadine or other histamine receptor blockers.