Table 2.

Potential etiologies for cancer-associated anemia

Causes of decreased HbProduction (decreased)Destruction (increased)Loss (overt, occult, or iatrogenic bleeding)
Drugs/therapy Myelosuppressive chemotherapy Antibiotics (eg, β-lactams, dapsone) Anticoagulation (eg, DOACs, LMWHs, warfarin) 
Radiation therapy Chemotherapy (eg, gemcitabine) Antiplatelet agents (eg, clopidogrel, prasugrel, ticagrelor) 
Tyrosine kinase inhibitors (delayed maturation) Immunotherapy (eg, nivolumab, pembrolizumab, ipilimumab) Nonsteroidal anti-inflammatory drugs 
Immunotherapy (inflammation) Intravenous immunoglobulin G Over-the-counter supplements (eg, turmeric) 
Bugs (bacteria, virus, or fungi) Cytomegalovirus HIV Helicobacter pylori 
Parvovirus B19 (in SCT or immunocompromised patients)   
Diseases, disorders, or other Chronic kidney disease (decreased erythropoietin) Microangiopathic hemolytic anemia (may be drug- or disease-related) Gastrointestinal tumors 
Clonal hematopoiesis of indeterminate potential  Frequent phlebotomy 
Iron deficiency (AIDA or FIDA) Autoimmune hemolytic anemia (eg, caused by autoimmune disorders or drug-induced) Arteriovenous malformations 
Leukemia (acute or chronic)  Hemostatic disorders (inherited or acquired) 
De novoor therapy-related myelodysplastic syndromes  Menses 
Myeloproliferative neoplasms Hemophagocytic lymphohistiocytosis Surgery 
Solid tumors Disseminated intravascular coagulation  
Iron overload   
B9 (folate) or B12 (cobalamin) deficiency   
Causes of decreased HbProduction (decreased)Destruction (increased)Loss (overt, occult, or iatrogenic bleeding)
Drugs/therapy Myelosuppressive chemotherapy Antibiotics (eg, β-lactams, dapsone) Anticoagulation (eg, DOACs, LMWHs, warfarin) 
Radiation therapy Chemotherapy (eg, gemcitabine) Antiplatelet agents (eg, clopidogrel, prasugrel, ticagrelor) 
Tyrosine kinase inhibitors (delayed maturation) Immunotherapy (eg, nivolumab, pembrolizumab, ipilimumab) Nonsteroidal anti-inflammatory drugs 
Immunotherapy (inflammation) Intravenous immunoglobulin G Over-the-counter supplements (eg, turmeric) 
Bugs (bacteria, virus, or fungi) Cytomegalovirus HIV Helicobacter pylori 
Parvovirus B19 (in SCT or immunocompromised patients)   
Diseases, disorders, or other Chronic kidney disease (decreased erythropoietin) Microangiopathic hemolytic anemia (may be drug- or disease-related) Gastrointestinal tumors 
Clonal hematopoiesis of indeterminate potential  Frequent phlebotomy 
Iron deficiency (AIDA or FIDA) Autoimmune hemolytic anemia (eg, caused by autoimmune disorders or drug-induced) Arteriovenous malformations 
Leukemia (acute or chronic)  Hemostatic disorders (inherited or acquired) 
De novoor therapy-related myelodysplastic syndromes  Menses 
Myeloproliferative neoplasms Hemophagocytic lymphohistiocytosis Surgery 
Solid tumors Disseminated intravascular coagulation  
Iron overload   
B9 (folate) or B12 (cobalamin) deficiency   

This table represents the authors’ approach to defining etiologies of cancer-associated anemia. The main categories are production defects, destruction, and blood loss. Examples of each category are provided in the columns. This table does not represent a comprehensive list of all possible causes of cancer-associated anemia.

DOAC, direct oral anticoagulant; LMWH, low molecular weight heparin; SCT, stem cell transplantation.

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