Output list
Book chapter
Published 2026
Classical Hematology, 371 - 376
The term “thrombophilia” is generally used to designate states of hypercoagulability caused by an inherent abnormality of the coagulation system, resulting in an increased risk of venous thromboembolism (VTE). Various mechanisms can underlie a thrombophilic state, both inherited (i.e., germline genetic alterations) and acquired.
Book chapter
Published 2026
Classical Hematology, 735 - 741
Hematopoietic growth factors (HGFs) and their receptors play essential roles in regulating hematopoiesis. While several HGFs and cytokines have been identified and characterized, three HGFs have had marked impacts on clinical medicine. We will discuss the clinical uses and unique side-effect profiles of erythropoietin, granulocyte colony-stimulating factor, and thrombopoietin mimetics along with current clinical implications of granulocyte-macrophage colony-stimulating factor and Interleukin-1 in this comprehensive chapter.
Book chapter
Management of Thrombocytopenia in Cancer Patients
Published 2019-07-18
Thrombosis and Hemostasis in Cancer, 139 - 150
Chemotherapy-induced thrombocytopenia (CIT) is a frequent complication of cancer therapy, leading to increased risk of bleeding, when the thrombocytopenia is severe (<10,000/mcL). However, the major clinical relevance of CIT is the subsequent delay or dose reduction in chemotherapy. CIT, therefore, leads to reduced relative dose intensity (RDI) of cancer therapy. Reduced RDI has been shown in several studies to impact progression-free survival and other cancer outcomes. While there are a number of factors leading to reduced RDI, CIT is a common cause. We review the causes and clinical manifestations of CIT, the current recommendations for management, and the status of research to develop targeted therapies to treat CIT.
Book chapter
Anticoagulation in the Patient with Cancer
Published 2018-04-17
Anticoagulation Therapy, 425 - 440
The association between malignant neoplasms and venous thromboembolism (VTE) is well recognized, and anticoagulation therapy is commonly administered in the oncological setting. The treatment approach to cancer-associated VTE differs substantially compared to the general population, as chronic low-molecular-weight heparin (LMWH) has been shown to be more effective than vitamin K antagonist (VKA). There are also several challenges specific to the cancer patient. These include an increased risk of bleeding, higher rates of anticoagulation failure, drug interactions, decreased oral intake, chemotherapy-induced thrombocytopenia, and cerebral metastases. Most of the literature in the field concerns the use of LMWH for cancer-associated VTE. Data is accumulating about the use of direct oral anticoagulants (DOACs) in this setting. DOACs offer improved patient quality of life and reduced cost compared to LMWH, although no published randomized trial has directly compared these two classes of anticoagulants in patients with cancer. Even though atrial fibrillation is by far the most common indication for anticoagulation in developed countries, there are little data about the best choice of agent when this arrhythmia occurs in cancer patients. It is unclear if the risk of ischemic stroke or systemic embolization is increased in the presence of malignancy, although the risk of bleeding is likely higher. Notably, VKA are still administered for the treatment of AF despite the difficulties inherent to cancer patients.
Book chapter
Published 2016-08-25
Nonmalignant Hematology, 495 - 502
The term “thrombophilia” is generally used to designate states of hypercoagulability caused by an inherent abnormality of the coagulation system, resulting in an increased risk of thrombosis. Abnormalities of blood flow or the blood vessel wall, the other two components of Virchow’s triad that increase the risk of thrombosis, are not considered a thrombophilia.
Book chapter
Angiostatin: Generation, Structure and Function of the Isoforms
Cytokines and Cancer, 175 - 204