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International Journal of
Cancer and Clinical Research
ISSN: 2378-3419
REVIEW ARTICLE | VOLUME 4, ISSUE 1 | OPEN ACCESS DOI: 10.23937/2378-3419/1410080

Angiogenesis Inhibitor Induced Thromboembolism in Cancer Patients

Neeharik Mareedu and Carmen P Escalante

Department of General Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA

*Corresponding author: Carmen P Escalante MD, Professor and Chair, Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, 1400 Pressler St. Unit 1465 Houston, TX 77030‐4004, USA, Tel: 713‐792‐2148, Fax: 713‐792‐0365, E-mail: cescalan@mdanderson.org

Received: May 17, 2016 | Accepted: May 29, 2017 | Published: May 31, 2017

Citation: Mareedu N, Escalante CP (2017) Angiogenesis Inhibitor Induced Thromboembolism in Cancer Patients. Int J Cancer Clin Res 4:080. doi.org/10.23937/2378-3419/1410080

Copyright: © 2017 Mareedu N, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract


Therapy with Angiogenesis Inhibitors (AIs) is a newer targeted approach in treating cancers. It gained popularity in the past decade because of better outcomes and fewer side effects when compared to conventional chemotherapeutic agents. These agents act by inhibiting the VEGF pathway and inhibit vasculogenesis, thus shutting off the nutrient supply to the continuously multiplying tumor cells. Growth of blood vessels is a dynamic process in the human body which is required for the various other processes throughout the human life. Thus, apart from their effects on tumor cells, AIs have a unique side effects profile which is quite different from the side effects of traditional chemotherapeutic agents. Thromboembolic Events (TES), both arterial and venous, are part of AIs side effects, which may be life threatening at times and should be diagnosed as soon as possible in patients who are on AI therapy. They need to be taken care of expeditiously to prevent more serious side effects. This review aims to enumerate the risk of TEs with each AI and the current recommendations to be followed in patients with history of TEs or in patients with TEs while on AI therapy. These recommendations will help to prevent more catastrophic events from occurring in these patients.

Keywords


Thromboembolism, Angiogenesis inhibitor, Cancer, Targeted therapy, Side effect

Introduction


With greater advancements in the understanding of the basic pathogenesis of cancer development as well as the molecular basis of the cancer cells, novel approaches in the treatment of various cancers are continuously being developed. In recent years there has been more focus in the development of targeted therapies compared to conventional chemotherapy. Targeted agents are providing better outcomes in patients with cancer and with fewer side effects when compared to conventional agents.

Angiogenesis Inhibitors (AIs) are one of the classes of targeted therapy being used in the treatment of various cancers. Adverse effects profile of AIs is completely different when compared to traditional chemotherapeutic agents owing to their different mechanism of action on tumor cells. Due to more promising results with AIs, an increasing number of oncologists are utilizing these agents in treatment regimens for cancer patients. However, there is an increase in the number of patients being seen by their respective primary care physicians to manage the side effect profile of these agents. Thus, it has become necessary for primary care physicians to be familiar with these agents as well as with the adverse effect profile of these agents.

Methods


A systematic search of Pub med and the NIH website was performed to identify all the United States Food and Drug Administration (FDA) approved AIs as well as to identify all the data regarding the risk factors, incidence, severity and recommendations for thromboembolic events associated with these agents.

Angiogenesis in vivo-brief overview

Human cells essentially derive all of their nutrition from Blood Vessels (BVs), with each cell being at least 100-200 µm in proximity to the nearby BV, allowing them to receive their nutrition via diffusion. This distance is usually the ideal average diffusion range for most of the BVs. Whenever a cell happens to grow beyond this distance range from the nearby BV, it will result in the growth of new BVs for maintenance of its nutrition [1]. Thus, angiogenesis is one of the most vital processes in the human body.

The most essential process for establishment of human life is angiogenesis, as it is required for the implantation of the embryo during establishment of pregnancy as well as throughout the period of embryogenesis and fetal growth until term for meeting the ever increasing demand for nutrition of the developing fetus. Later following birth of a baby, it continues throughout life as a dynamic process required for growth and maturation of the human body and also for the maintenance of homeostasis between various processes in the human body.

Both, insufficient and excessive angiogenesis, can be responsible for multiple disease processes in the human body. Some important conditions caused by aberrations in angiogenesis are listed in Table 1 [2].

Table 1: Conditions resulting from aberrations in angiogenesis. View Table 1

Angiogenesis regulation

Angiogenesis is regulated by both pro- and anti-angiogenic molecules (Table 2) [3]. Vascular Endothelial Growth Factor (VEGF) gene expression is the major rate limiting step in the process of angiogenesis. Oxygen tension, in turn is the major contributor for the expression of the VEGF gene through Hypoxia Inducible Factor-1 (HIF-1) [4,5].

Table 2. Factors involved in angiogenesis. View Table 2

Other cytokines which are responsible for the up regulation of VEGF gene expression are Epidermal Growth Factor (EGF), Transforming Growth Factor - α & β (TGF - α & β), Insulin - Like Growth Factor-1 (IGF-1), Fibroblast Growth Factor (FGF), and Platelet-Derived Growth Factor (PDGF). All are primarily limited to ischemic zones [5,6]. While these factors are essential for VEGF gene expression, angiopoietins play an essential role in regulation of endothelial cell survival and its interactions with other supporting cells [7]. Agents like angiostatin, endostatin, fumagillin and thrombospondin-1 and 2 are involved in the inhibition of VEGF expression [8].

VEGF family, VEGF pathway and cancer chemotherapy

Apart from the above mentioned cytokine signaling pathways, other signaling pathways involved in the process of angiogenesis are notch, Delta Like Ligand-4 (DLL-4), hedgehog and WNT pathways [9]. Among all the pathways, VEGF is a very important factor regulating both physiological and pathological vasculogenesis (angiogenesis and lymph angiogenesis).

The VEGF family consists of VEGF A to D, Placental Growth Factor (PLGF) and homologous sequences in parapoxvirus Orf viruses. VEGF-A (previously known as vascular permeability factor) is the dominant growth factor responsible for the angiogenesis. All of these act via specific tyrosine kinase receptors - VEGF receptors (VEGFR). VEGFR-1 and VEGFR-2 are primarily found on endothelial cells and are associated with the development of BVs, whereas VEGFR-3 is primarily associated with lymph angiogenesis [10].

VEGFs are responsible for vascular hyper permeability, endothelial cell activation, proliferation, invasion and migration as well as their survival. All of these characteristics determine the angiogenic ability of a tumor which in turn primarily defines its basic characteristics like growth, progression, invasion and metastasis. Thus, targeting the angiogenic signaling molecules have shown promising results in controlling the tumor burden. Angiogenesis is targeted at various steps in its pathway. Current AIs in the market act via the following mechanisms,

1) Direct inhibition of VEGF by anti-VEGF Antibodies (ABs), anti VEGFR ABs and small molecule VEGFR inhibitors.

2) Inhibition of other ancillary cytokines stimulating VEGF gene expression - Epidermal Growth Factor (EGF) ABs and Epidermal Growth Factor Receptor (EGFR) inhibitors.

Additional drugs which also act by inhibiting other molecules related to angiogenesis such as PDGF and HIF1s, and drugs targeting antiangiogenic agents in vivo are still in clinical trials.

Many of the AIs approved by the FDA may be used either alone or in conjunction with other chemotherapeutic agents in various solid tumors as well as hematologic malignancies for much better results with the therapy (Table 3 and Table 4). Most common adverse effects of AIs include fatigue, hypertension, proteinuria, abdominal pain and change in bowel habits, stomatitis, impaired wound healing and electrolyte disturbances. More serious adverse effects with the usage of AIs which result in changes in dose or complete discontinuation of treatment with AIs include grade 3 and 4 hypertension, severe (grades ≥ 3) Thromboembolic Events (TEs), hemorrhage, gastrointestinal perforation, cardiac impairment and neutropenia [11].

Table 3: Characteristics of angiogenesis inhibitors. View Table 3

Table 4. FDA approved indications of angiogenesis inhibitors. View Table 4

Angiogenesis inhibitor associated thromboembolism

Endothelial cells play a critical role in the regulation of vascular homeostasis by various mechanisms, one of which is the maintenance of local balance between pro-coagulant and anticoagulant molecules. Any stimulus which disturbs the normal structure of endothelium will also result in a deranged balance between pro- and anti-coagulant molecules locally which in turn leads to either increased clotting or increased bleeding [12]. Cancer patients have an increased predisposition for endothelial disruption due to various local and systemic inflammatory stimuli produced by either the cancer cell themselves of which are derived from the host cells as a secondary response to the underlying neoplastic process. These stimuli include release of cytokines like TNF, interleukin-β (IL-β) or antiangiogenic factors as well as increased expression of tissue factor. Endothelial cell damage leads to the activation of hemostatic mechanisms in the body.

Other risk factors also contribute to the pro-coagulant states in cancer patients. These may be divided into 3 broad categories - Patient related, cancer related or therapy related. Patient related factors may include all the factors which are implicated for increased risk of coagulation as in normal patients like advanced age, underlying comorbidities, family history of coagulation disorders and level of activity. Cancer related factors depend on type of cancer and stage of cancer. Treatment related factors include type of agent, duration of treatment, and long term hospitalizations for treatments.

Therapy with AIs increases the risk of thrombosis in already hyper coagulable patients secondary to cancer. Various mechanisms responsible for increased incidence of thrombosis in cancer patients with AI therapy include, a) Resistance to activated protein C, b) High levels of C-Reactive Protein (CRP), factor VIII, and Von Willebrand Factor (VWF) [13,14]. Another mechanism of thromboses in patients on AIs is due to diminished regenerative capacity of endothelial cells secondary to inhibition of the VEGF pathway which plays a role in the endothelial cell proliferation survival and maintenance of vascular integrity [15]. Disinhibition of pro-coagulant pathways due to inhibition of the VEGF pathway which results in reduction of Nitric Oxide (NO) and Prostacyclin (PGI2) was also considered as one of the mechanisms predisposing to increased Thromboembolic Events (TEs) in patients on AIs. Increased blood viscosity due to over production of hepatic erythropoietin secondary to VEGF inhibition also contributes to increased risk of thrombosis during therapy with AIs [16-18].

AIs, either given alone or in combination with conventional chemotherapeutic drugs have been shown to increase the risk of TEs, both on the arterial as well as venous sides. The most common presentations include peripheral vascular disease, ischemic heart disease, myocardial infarction, deep vein thrombosis, and pulmonary embolism. Less commonly, it may lead to cerebral ischemia, transient ischemic attack, intra-abdominal thrombosis, retinal vein thrombosis, and thrombotic microangiopathy [19].

Incidence of thrombotic events varies depending on various patient demographics like age of the patient, other comorbidities present, and previous history of TEs. They also vary depending on the type of cancer being treated, the total dose and duration of AI treatment, the concomitant use of the other chemotherapies, or the use of other drugs causing thromboembolism [20].

Thromboembolic events with various angiogenesis inhibitors

The very first report highlighting the angiogenesis in tumor growth was published by Dr. Judah Folkman in NEJM, 1971 [21]. He emphasized the importance of angiogenesis in tumor growth and survival and hypothesized that, if the factor responsible (which was not yet determined at that time) for the tumor angiogenesis can be blocked, it will result in the death of the tumor. Actual interest of biopharmaceutical industry to exploit antiangiogenesis for treating tumors was started in the 1980`s, and they started creating new therapeutic compounds. Thirty three years after the famous publication of Dr. Folkman, the first AI, bevacizumab, was approved by the FDA in 2004 for combination use with standard chemotherapy in patients with metastatic colon cancer. After approval of bevacizumab, many more AIs were approved by FDA in the past decade. There are many more in the FDA approval process waiting to appear in the market [22].

Afatinib, bosutinib, ceritinib, cetuximab, crizotinib, dasatinib, gefitinib, ibrutinib, imatinib, lapatinib, ruxolitinib and sunitinib have not been reported to have significant increase in TE`s with their use [23]. Remaining agents may result in various grades of TEs from simple superficial thromboses to severe life-threatening events and even death. Common Terminology Criteria for Adverse Events (CTCAE) grading of TEs is listed in Table 5. Table 6 describes the risks of ATE/VTE and recommendations for each of the following agents.

Table 5: CTCAE grading of thromboembolic events [41]. View Table 5

Table 6.Risk of arterial/venous thromboembolism with AI's and recommendations. View Table 6

Axitinib

Axitinib is a small molecule Tyrosine Kinase Inhibitor (TKI) which was initially approved by the FDA in January 2012 for use as a second line treatment agent in patients with advanced Renal Cell Carcinoma (RCC), in patients who have failed one prior systematic therapy. It acts by inhibiting receptor tyrosine kinases which also includes VEGFR`s.

Axitinib use results in 2% arterial thromboembolic events of all grades with 1% of them being grade 3/4. These include Transient Ischemic Attacks (TIAs), Cerebrovascular Accidents (CVAs), Myocardial Infarction (MI) and retinal artery occlusions [24]. Incidence of all grade Venous Thromboembolic Events (VTEs) in patients receiving axitinib was reported around 3% in controlled clinical trials with most of them being grades 3/4. These include Pulmonary Embolism (PE), Deep Venous Thrombosis (DVT) retinal vein occlusion and retinal vein thrombosis. It has not been studied yet in patients who had an ATE within the previous 12 months or a VTE in the previous 6 months, prior to the start of axitinib therapy, hence caution should be used when administering this agent to these subsets of patients.

Bevacizumab

Bevacizumab (BV) is a recombinant, humanized monoclonal antibody, which specifically binds to VEGF and inhibits its action on endothelial receptors, thereby blocking angiogenesis. It was first approved by the FDA in 2004 for combination use with standard chemotherapy in patients with metastatic colon cancer. Later, it was approved for treatment in various other cancers either alone or in combination with other standard chemotherapeutic regimens. It has also been approved for the treatment of certain eye diseases.

BV usage results in 6% increased incidence of ATEs of any grade with 3% of them being grade 3/4. These events include cerebral infarction, TIAs, MI and angina. Major risk factors for occurrence of ATE in patients receiving BV in combination with other chemotherapeutic agents were observed to be history of previous ATE, diabetes and age ≥ 65 years.

Combination therapy with BV and chemotherapy did show increased risk of TE's in various studies. A meta-analysis performed by Ranpura, et al. published in 2010, concluded that relative risk of ATE was increased by 1.44 (95% CI, 1.08-1.91; p = 0.013) with combination therapy including BV and chemotherapy, when compared to standard anti-neoplastic therapy [25]. Another study performed by Schutz, et al. published in 2011, did show increased relative risk of ATE with BV-based therapy by 1.46 (95% CI 1.11-1.93, P = 0.007) when compared to the controls without BV-based therapy [26]. Similarly, another meta-analysis by Nalluri, et al. showed that the use of BV was also associated with an increased risk [with an RR of 1.33 (95% CI, 1.13-1.56; P < .001) compared with controls] of developing VTE in cancer patients [27].

Thus, BV should be discontinued in all patients who experience a severe ATE. Safety of its resumption has not been studied yet. Any grade VTE occurs with an incidence of 8-14% in patients receiving BV with 5-15% being grade 3/4. These include DVT, intraabdominal thrombosis and PEs. The risk of occurrence of these events still remains elevated (around 21%) with the continuation of BV therapy with the addition of anticoagulants following the initial event of VTE. Thus it is advised to permanently discontinue BV therapy in patients with life-threatening (grade 4) VTEs [28].

Cabozantinib

Cabozantinib is a small molecule TKI which inhibits the activity of multiple tyrosine kinases including MET proto-oncogene, Rearranged during Transfection (RET), VEGFR-1, 2, & 3, TIE-2. It was first approved by the FDA for the treatment of progressive, metastatic Medullary Thyroid Cancer (MTC) in 2012 and is currently undergoing clinical trials for the treatment of various other cancers. Treatment with cabozantinib results in increased incidence of any grade ATE (2%) as well as VTE (6%). It should be discontinued in patients who experience acute MI as well as in patients who develop any other clinically significant arterial thrombotic complications [29].

Erlotinib

Erlotinib is a reversible TKI which inhibits the kinase activity of EGFR. It was first approved by the FDA for use in patients with locally advanced or metastatic Non-Small Cell Lung Cancer (NSCLC), who has failed at least one other prior chemotherapy regimen. Though there are no reports yet suggesting increased incidence of ATEs or VTEs with erlotinib monotherapy, there are reports of increased incidence of these events with erlotinib in combination with other chemotherapeutic regimens. When erlotinib is used in combination with gemcitabine, increased incidence of DVT (4%), MI (2%) and CVAs (2%) were observed when compared to the use of placebo plus gemcitabine usage. Overall grade 3/4 thrombotic events occurred in 11% patients on erlotinib plus gemcitabine combination therapy when compared to gemcitabine plus placebo. There have been no significant studies performed to warrant any specific recommendations for the dose changes or for discontinuation of the drug [30].

Nilotinib

Nilotinib is a selective TKI which specifically targets BCR-ABL kinase by binding to ABL protein and acts by stabilizing the inactive conformation of the kinase domain. It was first approved by the FDA in 2007 for use in the treatment of adult patients with chronic and accelerated phases of Chronic Myelogenous Leukemia (CML) and accelerated resistance or intolerance to prior therapy which includes imatinib. Nilotinib is responsible for various ATEs which are dose dependent. Its use results in 9-15% of ATE`s, incidence varying with the dose of the drug (9% with 300 mg dose and 15% with 400 mg dose). Most of these events are ischemic heart disease, cerebral ischemia, peripheral arterial occlusions and ischemic cerebrovascular events [31].

Panitumumab

Panitumumab is a recombinant human IgG2 monoclonal antibody which specifically binds to the EGFR and competitively inhibits the binding of EGF and other ligands to it. It was originally approved by the FDA in 2006 for the treatment of patients with EGFR - expressing metastatic colorectal cancer with disease progression despite treatment with prior chemotherapy regimens. Panitumumab monotherapy increases the incidence of PE by 1%. In combination with Oxaliplatin + Fluorouracil (5 FU) + Folinic Acid (FOLFOX) chemotherapy regimen, panitumumab increases the incidence of DVT`s by 5% [32].

Pazopanib

Pazopanib is a multi-targeted TKI which acts via inhibiting various cell surface receptors including VEGFR's 1-3, PDGFR's α & β and FGFR's 1 & 3 as well as many other receptor proteins. It was first approved in 2009 by the FDA for the use in the treatment of advanced or metastatic RCC. In patients with RCC receiving pazopanib, MI or ischemia occurred with an increased incidence of 2% along with an incidence of 0.3% cerebrovascular accidents and 1% TIA's. Fatal ATE's were reported in 0.3% of patients. In patients with STS, MI or ischemia and CVA`s occurred with an incidence of 2% and 0.4% respectively with no reported TIAs or fatal ATE`s. Pazopanib should be used with caution in patients with a history of ATEs or who are at increased risk of ATEs. There were no studies done for evaluation of risk of using pazopanib in patients with a history of ATE within 6 months prior to the start of pazopanib therapy, and thus it should be avoided in this subset of patients. Reported incidence for VTE`s were 1% in RCC patients and 5% in STS patients with no fatal PEs in RCC patients and 1% of fatal PEs in STS patients [33].

Ponatinib

Ponatinib is an orally available multi-targeted pan-BCR-ABL TKI first approved by FDA in 2012 for the treatment of adults with CML and Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ ALL). In phase 1 and 2 clinical trials for ponatinib, arterial and venous TEs were reported in at least 27% of patients. Ponatinib is known to cause fatal and life threatening vascular occlusions, and these may be within 2 weeks of initiation of therapy. It can also result in recurrent and multi-site vascular occlusions. These vascular occlusive adverse events were seen more frequently with increasing age and in patients with a prior history of ischemia, hypertension, diabetes or hyperlipidemia. The risk of vascular adverse effects was particularly increased in patients who were sequentially treated with nilotinib and ponatinib.

ATEs including fatal and life threatening events were observed in almost 20% patients. In patients suspected of developing ATEs, it is recommended that the treatment should be discontinued and a benefit-risk re-consideration should guide the decision to restart the therapy with ponatinib. VTEs were observed in 5% of the patients [34].

Ramucirumab

Ramucirumab is a recombinant monoclonal antibody which specifically binds to VEGFR-2 and blocks binding of VEGF ligands to the receptor. It was first approved by the FDA in 2014 for the usage in advanced or metastatic gastric or gastro-esophageal junction adenocarcinoma in patients with disease progression despite prior fluoropyrimidine or platinum-containing chemotherapy. Its use has been associated with 2% increase in ATEs which are serious and sometimes fatal. These events include MI, cardiac arrest, CVAs, and cerebral ischemia [35].

Regorafenib

Regorafenib is a multi-kinase inhibitor acting on various membrane-bound and intracellular kinases involved in the angiogenesis. It was first approved in 2012 by the FDA for use in patients with P(mCRC), who have disease progression despite prior treatment with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF therapy, and anti-EGFR therapy (if KRAS wild type). Increased incidence (1%) of MI or ischemia was observed in patients treated with regorafenib [36].

Sorafenib

Sorafenib is a multikinase inhibitor which inhibits multiple intracellular and cell surface kinase receptors which are thought to be involved in tumor cell signaling, angiogenesis and apoptosis. It was first approved by the FDA for treatment of patients with advanced RCC. There was an increased risk of cardiac ischemia and infarction in patients treated with sorafenib, varying with the type of cancer [Hepatocellular Carcinoma (HCC) 3%, RCC 3% and differentiated thyroid carcinoma 2%]. Patients with unstable Coronary Artery Disease (CAD) or recent MI were not included in the studies performed [37].

Vandetanib

Vandetanib is a multikinase inhibitor which inhibits the activity of tyrosine kinases like EGFR, VEGF, Rearranged during Transfection (RET), Protein Tyrosine Kinase 6 (BRK), tyrosine kinase with immunoglobulin-like and EGF-like domains 2 (TIE-2). It was first approved by FDA in 2011 for the treatment of adult patients with late-stage (metastatic) MTC who are ineligible for surgical therapy and in whom the cancer is growing and causing symptoms. It results in an increased incidence of ischemic cerebrovascular events (1%) [38].

Ziv-aflibercept

Ziv-aflibercept, also known as VEGF-trap is a recombinant fusion protein which acts as a decoy receptor for VEGF-A, VEGF-B, and Placental Growth Factor (PlGF) and thus preventing the activation of VEGFR's by VEGF. It was first approved in 2012 for use in combination with FOLFIRI for treating metastatic colorectal cancer patients who are resistant to or have progressed on other oxaliplatin-based regimens. When used in combination with FOLFIRI regimen, ATE`s were increased by 3% as compared to FOLFIRI alone with 2% being grades 3-4. VTE's were increased by 9% by adding ziv-aflibercept to the FOLFIRI regimen [39].

Summary


Increased incidence of TEs are observed in most of the AIs, which is multifactorial as mentioned in the above review. There are no studies yet to recommend a generalized approach either for prevention or for treatment of these events specific to AIs. Recommendations are based on the rate and severity of occurrence of these events with individual drugs. There are no clinical data yet regarding ATE preventive strategies to date. In terms of VTE, according to the National Comprehensive Cancer Network (NCCN) Practice Guidelines in Oncology, starting of aspirin or anticoagulant prophylaxis in patients with cancer depends on the presence or absence of risk factors for VTE and the use of Angiogenesis Inhibitors as such, was not indicated as a risk factor for VTE in cancer patients as per NCCN [40]. Nevertheless, there should be consideration given to the TE management in patients on AI therapy as mentioned in Table 6 as per the recommendations based on prescribing information of each individual AI. Though the therapy with AIs are initiated by oncologists, dealing with the adverse effects of AIs may be in the hands of primary care physicians. Thus, primary care physicians should be aware of the increase in the incidence of TEs with AIs as well as recommendations for drugs in this class. They should not only suspect an increased risk of TEs in patients, secondary to the cancer diagnosis, but also should think of compounded risk when the cancer patients are being treated with AIs and thus base their management decision. Hematologic events are a common reason for treatment discontinuation with AIs. Collaboration with oncologists, hematologist and primary care physicians is extremely important for the promising results of AI therapies.

References


  1. Carmeliet P, Jain RK (2000) Angiogenesis in cancer and other diseases. Nature 407: 249-257.

  2. Carmeliet P (2003) Angiogenesis in health and disease. Nat Med 9: 653-660.

  3. Timar J, Dome B, Fazekas K, Janovics A, Paku S (2001) Angiogenesis-dependent diseases and angiogenesis therapy. Pathol Oncol Res 7: 85-94.

  4. Ferrara N, Davis-Smyth T (1997) The biology of vascular endothelial growth factor. Endocr Rev 18: 4-25.

  5. Ferrara N, Gerber HP, LeCouter J (2003) The biology of VEGF and its receptors. Nat Med 9: 669-676.

  6. Hidalgo M, Eckhardt SG (2001) Development of matrix metalloproteinase inhibitors in cancer therapy. J Natl Cancer Inst 93: 178-193.

  7. Asahara T, Chen D, Takahashi T, Fujikawa K, Kearney M, et al. (1998) Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization. Circ Res 83: 233-240.

  8. Kunz M, Hartmann A (2002) Angiogenesis--anti-angiogenesis. Significance for tumor growth and metastasis. Hautarzt 53: 373-384.

  9. Zhou W, Wang G, Guo S (2013) Regulation of angiogenesis via Notch signaling in breast cancer and cancer stem cells. Biochim Biophys Acta 1836: 304-320.

  10. Hicklin DJ, Ellis LM (2005) Role of the vascular endothelial growth factor pathway in tumor growth and angiogenesis. J Clin Oncol 23: 1011-1027.

  11. Kamba T, McDonald DM (2007) Mechanisms of adverse effects of anti-VEGF therapy for cancer. Br J Cancer 96: 1788-1795.

  12. Ferroni P, Formica V, Roselli M, Guadagni F (2010) Thromboembolic events in patients treated with anti-angiogenic drugs. Curr Vasc Pharmacol 8: 102-113.

  13. Elice F, Fink L, Tricot G, Barlogie B, Zangari M (2006) Acquired resistance to activated protein C (aAPCR) in multiple myeloma is a transitory abnormality associated with an increased risk of venous thromboembolism. Br J Haematol 134: 399-405.

  14. Elice F, Jacoub J, Rickles FR, Falanga A, Rodeghiero F (2008) Hemostatic complications of angiogenesis inhibitors in cancer patients. Am J Hematol 83: 862-870.

  15. Kilickap S, Abali H, Celik I (2003) Bevacizumab, bleeding, thrombosis, and warfarin. J Clin Oncol 21: 3542.

  16. Zachary I (2001) Signaling mechanisms mediating vascular protective actions of vascular endothelial growth factor. Am J Physiol Cell Physiol 280: 1375-1386.

  17. Spivak JL (2002) Polycythemia vera: myths, mechanisms, and management. Blood 100: 4272-4290.

  18. Tam BY, Wei K, Rudge JS, Hoffman J, Holash J, et al. (2006) VEGF modulates erythropoiesis through regulation of adult hepatic erythropoietin synthesis. Nat Med 12: 793-800.

  19. (2014) Lexi-Comp OnlineTM Lexi-Drugs, Hudson, Ohio: Lexi-Comp, Inc.

  20. Qi WX, Min DL, Shen Z, Sun YJ, Lin F, et al. (2013) Risk of venous thromboembolic events associated with VEGFR-TKIs: a systematic review and meta-analysis. Int J Cancer 132: 2967-2974.

  21. Judah Folkman (1971) Tumor Angiogenesis: Therapeutic Implications. N Engl J Med 285: 1182-1186.

  22. Ribatti D (2007) The history of angiogenesis inhibitors. Leukemia 21: 1606-1609.

  23. DailyMed (2015) National Library of Medicine (US), Bethesda, USA.

  24. Pfizer Laboratories Div Pfizer Inc (2015) Inlyta (Axitinib) tablet, film coated. National Library of Medicine (US), Bethesda, USA.

  25. Ranpura V, Hapani S, Chuang J, Wu S (2010) Risk of cardiac ischemia and arterial thromboembolic events with the angiogenesis inhibitor bevacizumab in cancer patients: a meta-analysis of randomized controlled trials. Acta Oncol 49: 287-297.

  26. Schutz FA, Je Y, Azzi GR, Nguyen PL, Choueiri TK (2011) Bevacizumab increases the risk of arterial ischemia: a large study in cancer patients with a focus on different subgroup outcomes. Ann Oncol 22: 1404-1412.

  27. Nalluri SR, Chu D, Keresztes R, Zhu X, Wu S (2008) Risk of venous thromboembolism with the angiogenesis inhibitor bevacizumab in cancer patients: a meta-analysis. JAMA 300: 2277-2285.

  28. Genentech, Inc (2015) Avastin (bevacizumab injection) solution. National Library of Medicine (US), DailyMed, Bethesda, USA.

  29. Exelixis, Inc (2015) Cometriq (cabozantinib s-malate) capsule. National Library of Medicine (US), DailyMed, Bethesda, USA.

  30. Genentech, Inc (2015) Tarceva (erlotinib hydrochloride) tablet. National Library of Medicine (US), DailyMed, Bethesda, USA.

  31. Novartis Pharmaceuticals Corporation (2015) Tasigna (nilotinib) capsule. National Library of Medicine (US), DailyMed, Bethesda, USA.

  32. Amgen, Inc (2015) Vectibix (panitumumab) solution. National Library of Medicine (US), DailyMed, Bethesda, USA.

  33. GlaxoSmithKline LLC (2015) Votrient (pazopanib hydrochloride) tablet, film coated. National Library of Medicine (US), DailyMed, Bethesda, USA.

  34. ARIAD Pharmaceuticals, Inc (2015) Iclusig (ponatinib hydrochloride) tablet, film coated. National Library of Medicine (US), DailyMed, Bethesda, USA.

  35. Eli Lilly and Company (2015) Cyramza (ramucirumab) solution. National Library of Medicine (US), DailyMed, Bethesda, USA.

  36. Bayer HealthCare Pharmaceuticals, Inc (2015) Stivarga (regorafenib monohydrate) tablet, film coated. National Library of Medicine (US), DailyMed, Bethesda, USA.

  37. Bayer HealthCare Pharmaceuticals, Inc (2015) Nexavar (sorafenib) tablet, film coated. National Library of Medicine (US), DailyMed, Bethesda, USA.

  38. AstraZeneca Pharmaceuticals LP (2015) Caprelsa (vandetanib) tablet. National Library of Medicine (US), DailyMed, Bethesda, USA.

  39. Sanofi-aventis US, LLC (2015) Zaltrap (aflibercept) solution, concentrate. National Library of Medicine (US), DailyMed, Bethesda, USA.

  40. (2015) Common Terminology Criteria for Adverse Events (CTCAE), Version 4.0.

  41. https://www.nccn.org/professionals/physician_gls/pdf/vte.pdf.