Medical Oncology· Topic 12.9 Oncologic emergencies· 12.9.7

Tumor lysis syndrome (TLS)

Tumor lysis syndrome is a metabolic oncologic emergency in which massive tumor cell breakdown, spontaneous or chemotherapy-induced, releases potassium, phosphate, and nucleic acids into the blood, producing hyperuricemia, hyperkalemia, hyperphosphatemia, and secondary hypocalcemia that can precipitate acute kidney injury, arrhythmia, seizure, and death. Risk-stratified prophylaxis with hydration plus allopurinol or rasburicase before chemotherapy, and aggressive correction of electrolytes with renal replacement therapy when needed, are the cornerstones of management.

13 min read5 practice questions8 key factsSubscriber article
  • Topic review
    The full article, organized the way the exam asks it.
  • ABIM-format MCQs
    Vignettes with an explanation for every wrong answer.
  • Key facts
    The numbers and thresholds worth memorizing, up front.
  • AI tutor
    MedBrain answers the question you're stuck on.

What this article covers

  • Overview

    Tumor lysis syndrome (TLS) is a metabolic oncologic emergency caused by the release of tumor cell contents into the bloodstream, either spontaneously or as a result of treatment, producing…

  • Epidemiology

    Occurs most commonly in acute leukemia and high-grade non-Hodgkin lymphoma, particularly Burkitt lymphoma, where the combination of large tumor burden and exquisite chemosensitivity produces rapid, massive cell death.

  • Risk factors

    Large tumor burden and high proliferative rate, the dominant determinant of TLS risk, reflected in bulky disease, high white blood cell count, or elevated lactate dehydrogenase.

  • Pathophysiology

    Rapid lysis of malignant cells, most often triggered by cytotoxic chemotherapy, releases a large intracellular potassium and phosphate load into the bloodstream, directly raising serum potassium and phosphate.

  • Clinical features

    Gastrointestinal symptoms (nausea, vomiting, diarrhea, anorexia): often the earliest nonspecific symptoms, typically emerging within hours to a few days of starting chemotherapy in a high-risk patient.

  • Differential diagnosis

    Cytokine release syndrome (after CAR T-cell therapy or other immunotherapy): fever, hypotension, and tachycardia with a temporal relationship to cellular immunotherapy rather than cytotoxic…

  • Diagnosis

    TLS is confirmed by the laboratory pattern of hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia arising in a patient with a large-burden, chemosensitive tumor around the time of…

  • Management

    First, stratify risk and start prophylaxis before chemotherapy: intermediate-risk: IV hydration plus allopurinol 300 mg PO once daily, starting 1-2 days before chemotherapy, continued 3-7 days after or until values normalize.

  • Complications

    Acute kidney injury, from uric acid and calcium-phosphate crystal precipitation in the renal tubules, the most common organ complication and often the trigger for renal replacement therapy.

  • Prognosis

    Prompt recognition and risk-stratified prophylaxis prevent the great majority of clinically significant TLS, particularly in patients correctly identified as high risk before chemotherapy begins.

  • Prevention

    Risk-stratify every patient before starting chemotherapy for a bulky, chemosensitive hematologic malignancy, and start prophylaxis before, not after, the first dose.

Read the whole article

Subscribing to Internal Medicine opens every article, the full question bank and MedBrain, on the web, iPhone and Android.