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    Tumor Lysis Syndrome

    Cardiovascular, Critical Care / Resuscitation, Gastrointestinal, Hematological / Oncological, Metabolic / Endocrine, Neurological

    Last Reviewed on May 21, 2024
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    By Parmveer Brar,Bhavneet Jhajj, Ivjot Samra

    First 5 Minutes

    • Be wary of hyperkalemia.
    • Continuous cardiac monitoring is necessary.
    • Involve intensivist, hematologist, oncologist, and nephrologist early

    Context

    • Tumor lysis syndrome (TLS) is a life-threatening condition that occurs when malignant cells break down rapidly.
    • TLS can occur spontaneously or as a result of a recently started cancer therapy (chemotherapy, radiation, targeted therapy, steroids, hormonal therapy).
    • Mortality rates are up to 20%.
    • TLS risk factors:
      • Tumours with higher turnover, and those with higher responsiveness to therapy.
      • High burden of tumours.
      • Renal impairment.
      • Treatment with cancer therapies.
      • Use of medications/substances that increase uric acid levels (e.g., alcohol, vitamin C, aspirin, caffeine, epinephrine, thiazide diuretics, levadopa).
    • Higher risk malignancies:
      • Acute lymphocytic leukemia (ALL).
      • Acute myeloid leukemia (AML).
      • Burkitt lymphoma.
      • large B-cell lymphoma.
      • T-cell non-Hodgkins lymphoma.

    Diagnostic Process

    • Presentation of TLS is non-specific and may include:
      • Nausea, vomiting, diarrhea, anorexia, seizures, muscle weakness and cramps, tetany, cramps, pain, oliguria/anuria, confusion, kidney injury/failure, abnormal heart rhythms, palpitations.
      • TLS can lead to hyperuricemia, hyperkalemia, hyperphosphatemia, hypocalcemia, and acute kidney injury (AKI).
    • To diagnose TLS, need 2 or more of the following:
      • Uric acid (≥ 476 μmol/L or 25% increase from baseline).
      • Potassium (≥ 6.0 mmol/L or 25% increase).
      • Phosphate (≥ 1.45 mmol/L [adults] or ≥ 2.1 mmol/l [children] or 25% increase).
      • Calcium (≤ 1.75 mmol/L or 25% decrease).

    Recommended Treatment

    • Goal is to manage electrolyte imbalances, improve volume status, and excrete uric acid/phosphate.
    • Aggressive IV fluid hydration (normal saline)
      • Aim for urine output of 100 mL/m2/hr in adults or >4 ml/kg/hr in infants.
      • Deliver fluid at rate of 3 L/m2 per 24 h in adults.
      • Do not add potassium to hydration fluid.
    • Rasburicase if uric acid is elevated
      • 2 mg/kg/day given as a 30-min infusion daily for 3-7 days with electrolyte monitoring.
      • Use allopurinol if patient has G6PD deficiency.
    • Hyperkalemia:
      • Infusion of calcium gluconate
        • Hyperkalemic adults with EKG changes (prolonged PR or QRS) related to hyperkalemia may be given 1000 mg/kg; 100-200 mg/kg for children over 2-3 minutes.
      • IV insulin + glucose can be used for temporary stabilization.
      • NaHCo3.
      • Recommended to administer oral potassium-lowering agents such or AKI and TLS
        • Avoid sodium polystyrene sulfonate (Kayexelate) unless no other options due to adverse effects reported of colonic necrosis.
    • Phosphate binders for hyperphosphatemia
      • 50–150 mg/kg/day PO.
      • Not recommended if poorly tolerated by patient.
    • Calcium for symptomatic hypocalcemia (seizures, arrhythmias, tetany)
      • Calcium administration at lowest possible dose to alleviate symptoms.
      • Do not treat if asymptomatic hypocalcemia.
      • If a patient has hyperphosphatemia and hypocalcemia, do not treat hypocalcemia until hyperphosphatemia is corrected unless there are severe arrhythmias or tetany due to hypocalcemia.

    Hemodialysis is indicated if there is: severe AKI, persistent hyperkalemia, symptomatic hypocalcemia secondary to hyperphosphatemia, calcium-phosphate product ≥70 mg2/dL2 uncontrolled fluid overload.

    Quality Of Evidence?

    Justification

    Although guidelines exist for this topic, gaps remain in treatment protocols. More research is needed to understand the effect of existing treatments.

    Moderate

    Related Information

    OTHER RELEVANT INFORMATION

    Reference List

    1. Grewal K, Herrity E, Pasic I. Tumour lysis syndrome. Canadian Medical Association Journal. 2023;195(14). doi:10.1503/cmaj.221433


    2. Jones GL, Will A, Jackson GH, Webb NJ, Rule S. Guidelines for the management of tumour lysis syndrome in adults and children with haematological malignancies on behalf of the British Committee for Standards in Haematology. British Journal of Haematology. 2015 Apr 15;169(5):661–71. doi:10.1111/bjh.13403


    3. Gupta A, Moore JA. Tumor lysis syndrome. JAMA Oncology. 2018;4(6):895. doi:10.1001/jamaoncol.2018.0613


    4. Zafrani L, Canet E, Darmon M. Understanding tumor lysis syndrome. Intensive Care Medicine. 2019;45(11):1608–11. doi:10.1007/s00134-019-05768-x


    5. Larson RA, Pui C-H. Tumor lysis syndrome: Prevention and Treatment [Internet]. 2023 [cited 2024 Jan 2]. Available from: https://www.uptodate.com/contents/tumor-lysis-syndrome-prevention-and-treatment#H21712100


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