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Review
. 2012 Jul;3(4):209-24.

Myeloid toxicity of cancer treatment

Affiliations
Review

Myeloid toxicity of cancer treatment

Sandra Kurtin. J Adv Pract Oncol. 2012 Jul.

Abstract

Myelotoxicity is one of the most common treatment-related adverse events for patients receiving systemic antineoplastic therapy or radiotherapy to bone marrow-producing regions. Myeloid cytopenias, including neutropenia, thrombocytopenia, and anemia, are the most common manifestations of treatment-related myelotoxicity and one of the most common reasons for dose modifications, dose delays, or discontinuation of therapy, potentially limiting therapeutic benefit. Risk factors for myelotoxicity can be broadly categorized into three types: disease-related, host-related, and treatment- related. Familiarity with factors predictive of high-risk febrile neutropenia, bleeding due to thrombocytopenia, and cardiopulmonary compromise due to anemia will provide the advanced practitioner (AP) in oncology with critical tools for rapid identification of patients at risk, prompt implementation of established guidelines for management, and avoidance of clinical deterioration. The AP in oncology is often the primary point of contact for management of cytopenias, including administration of myeloid growth factors, transfusion of blood products, and management of acute events such as neutropenic fevers. Each of these interventions requires familiarity with the risk and benefits of treatment. This article will review the physiology of the bone marrow, risk factors for cytopenias, and current guidelines and recommendations for prevention and treatment of myeloid toxicity of cancer treatment.

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Figures

Figure 1
Figure 1
Bone marrow physiology. G-CSF = granulocyte colony-stimulating factor; GM-CSF = granulocyte-macrophage cology-stimulating factor; IL = interleukin; SCF = stem cell factor. Adapted from NIH (2012), Metcalf (2010), Crea et al. (2009), and Kurtin (2011a).
Table 1
Table 1
Key Elements of the Myeloid Lineage
Table 2
Table 2
Factors Associated With High Risk for Chemotherapy-Induced Myelotoxicity
Table 3
Table 3
Common Chemotherapeutic Regimens for Selected Tumor Types With Intermediate to High Risk for Myelotoxicity3
Table 4
Table 4
National Cancer Institute Common Terminology Criteria for Adverse Events Version 4: Myelotoxicity
Table 5
Table 5
Factors Associated With Poor-Prognosis Febrile Neutropenia
Table 6
Table 6
Recommendations for Prevention and Management of Chemotherapy-Induced Neutropenia and Febrile Neutropenia
Table 7
Table 7
Recommendations for Management of Chemotherapy-Induced Anemia
Table 8
Table 8
Recommendation for Management of Chemotherapy-Induced Thrombocytopenia

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