4.7 Review

How I treat microangiopathic hemolytic anemia in patients with cancer

Journal

BLOOD
Volume 137, Issue 10, Pages 1310-1317

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood.2019003810

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Funding

  1. NHLBI NIH HHS [R01 HL133113] Funding Source: Medline

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MAHA with thrombocytopenia in cancer patients can be caused by the malignancy itself, treatment, or separate incidental diagnoses. Prompt differentiation of different types of TMA is crucial for treatment and outcome. The causes and treatment strategies for TMA in cancer patients are complex and diverse.
Microangiopathic hemolytic anemia (MAHA) with thrombocytopenia, suggests a thrombotic microangiopathy (TMA), linked with thrombus formation affecting small or larger vessels. In cancer patients, it may be directly related to the underlying malignancy (initial presentation or progressive disease), to its treatment, or a separate incidental diagnosis. It is vital to differentiate incidental thrombotic thrombocytopenia purpura or atypical hemolytic uremic syndrome in cancer patients presenting with a TMA, as they have different treatment strategies, and prompt initiation of treatment impacts outcome. In the oncology patient, widespread microvascular metastases or extensive bone marrow involvement can cause MAHA and thrombocytopenia. A disseminated intravascular coagulation (DIC) picture may be precipitated by sepsis or driven by the cancer itself. Cancer therapies may cause a TMA, either dose-dependent toxicity, or an idiosyncratic immune-mediated reaction due to drug-dependent antibodies. Many causes of TMA seen in the oncology patient do not respond to plasma exchange and, where feasible, treatment of the underlying malignancy is important in controlling both cancer-TMA or DIC driven disease. Drug-induced TMA should be considered and any putative causal agent stopped. We will discuss the differential diagnosis and treatment of MAHA in patients with cancer using clinical cases to highlight management principles.

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