This site contains promotional information intended only for healthcare professionals resident in the United Kingdom

Visit Pfizer Medical site

Menu

Close

Sign InLog Out
  • EN
Single LinkDropdownLabelLinkLinkLinkLinkLinked DropdownLabelLinkLinkLinkLinkMega MenuHeading

Example of description text sitting alongside header

LabelLinkLinkLinkLinkLabelLinkLinkLinkLinkLabelLinkLinkLinkLink
Linked Mega MenuHeading

Example of description text sitting alongside header

LabelLinkLinkLinkLinkLabelLinkLinkLinkLinkLabelLinkLinkLinkLink
EN - EnglishSelect a languageLanguagesEN - EnglishFR - Françias

Menu

Close

Sign InLog Out
  • EN
Single LinkDropdownLabelLinkLinkLinkLinkLinked DropdownLabelLinkLinkLinkLinkMega MenuHeading

Example of description text sitting alongside header

LabelLinkLinkLinkLinkLabelLinkLinkLinkLinkLabelLinkLinkLinkLink
Linked Mega MenuHeading

Example of description text sitting alongside header

LabelLinkLinkLinkLinkLabelLinkLinkLinkLinkLabelLinkLinkLinkLink
EN - EnglishSelect a languageLanguagesEN - EnglishFR - Françias
Search

Menu

Close

Sign In or RegisterLog Out
Pfizer MedicinesTherapy AreasExplore ContentEventsVideosMaterialsFeatured ArticlesLet’s ConnectSupplyAlliance HealthcareOff-contract claims

Adverse event reporting can be found at the bottom of the page

Therapy AreaHaematologyCancer associated thrombosis patient riskManagement of bleeding and clottingTreating patients and risk factorsAdditional risk factorsSelecting your anticoagulant

Prescribing information for Fragmin® (dalteparin sodium) can be found here. Adverse event reporting can be found at the bottom of the page.

Why patients with cancer are at higher risk of venous thromboembolism (VTE)

The aggressive nature of tumours can increase procoagulant activity, meaning cancer patients are at higher risk of VTE.1 Tumours can compress vessels, alter blood flow or damage the vessel wall increasing the risk of thrombosis.1  

The cancer treatment programme, patient risk factors and cancer type all contribute to VTE risk.  

Read on to understand how they may increase your patients’ risk of cancer-related VTE.  

Epidemiology

VTE is a leading cause of death for patients with cancer.2 


Clinically evident VTE has been noted in up to 15% of patients with cancer which could be even higher if considering subclinical disease.2  


In addition, cancer patients are also more likely to have recurrent VTE, including when they are on appropriate anticoagulants.


In-hospital mortality for patients with cancer and VTE is over twice that of mortality for matched patients without VTE.


However, individual patient risk factors can vary significantly so careful consideration is needed when selecting the best course of treatment to manage VTE risk. 

VTE risk in patients with cancer vs general population

Patients with cancer have a 4-fold higher risk of VTE than individuals without cancer but over the course of a patient’s cancer journey, the risk of VTE can fluctuate based on treatment-related factors.3  

 

Many cancer therapies (including major surgery, aggressive chemotherapy, and hormonal therapy) appear to place patients with cancer at further increased risk for VTE, so it is critical to consider concurrent anticoagulation in patients being treated for cancer.  

 

But VTE is also a marker for occult cancer. In the general population, up to 10% of people with a first-time VTE have a subsequent cancer diagnosis within a year.1  

 

So, if someone presents with VTE and there is no obvious cause, what should you think as a clinician? 

Patient risk of VTE over time

Figure1: Adapted from Lyman GH, 2011.3  

  
VTE in cancer incidence video Virchow’s triad and cancer

Tumours and cancer treatments can cause abnormalities in venous stasis, vessel damage and induce hypercoagulability – which can predispose cancer patients to VTE.1,2,4 

 

Virchow’s triad illustrates how, in cancer patients, these three components contribute to VTE risk.  
 

If anticoagulant treatment can treat hypercoagulability, what about the other two factors? Which anticoagulant should you use in certain circumstances? And when is best to begin treatment?  

 

There are many questions which remain and there is not one rule which fits all circumstances. 

BUT...Choosing the right anticoagulant could be fundamental to minimising VTE risk and a positive outcome in your cancer patients. 

 

Anticoagulation treatment must be tailored to each individual, taking into consideration other potential risk factors.4,6

Virchow's triad of thrombosis adapted from Kwan HC et al. 20074, Rickles FR, Falanga A. 20095; Widick P, et al, 20186
Risk factors

We have explored that VTE risk is heightened in cancer patients. But what is it specifically that puts these patients at risk? 

Cancer, treatment and patient-related factors can all influence VTE risk which requires assessing on an individual basis.7

These may include:*

 Cancer-related
  • ​​​​​​Primary site of cancer  
  • Initial period after diagnosis  
  • Histology  
  • Stage  








 Treatment-related
  • Major surgery and vascular injury 
  • Hospitalisation 
  • Chemotherapy  
  • Some antiangiogenic therapy 
  • Some immunomodulatory agents 
  • Certain hormonal therapy agents 
  • Erythropoiesis-stimulating agents 
  • Central venous access devices 
  • Transfusions 
 Patient-related 
  • Age  
  • Race  
  • Patient comorbidities 
  • Obesity, infection, renal disease, pulmonary disease, arterial thromboembolism 
  • Prior history of thrombosis 
  • Inherited prothrombotic mutations 
  • Performance status 
  • Varicose veins 


Biomarkers 
  • Prechemotherapy leukocyte count 
  • Prechemotherapy platelet count 
  • Haemoglobin <10 g/dL  
  • Tissue factor 
  • D-dimer 
  • C-reactive protein 
  • Soluble P-selectin 
  • Peak thrombin generation 
  • Factor VIII 




You should consider using a risk assessment tool (such as the Khorana tool) to assess your patient’s risk of VTE and always use the anticoagulant SmPC to assess special warnings, precautions for use and interactions.2  

 

Potential drug-drug interactions, cancer treatment regime and type of cancer may influence your choice of anticoagulant.

*Table information is a general guide only. Specific assessment of a patient or interpretation of any results should relate to local guidelines and policies. 

Epidemiology

Incidence of first VTE by cancer type and age ≥18 years (United Kingdom data)1

VTE risk is not evenly spread across all patients with cancer.2  
 

The Khorana risk assessment tool states that stomach and pancreatic cancers are very high risk for VTE and Cohen et al. showed that pancreatic cancer had the highest incidence of VTE closely followed by cancer in the brain and ovaries.2,8  


Patients with haematological malignancies, particularly lymphoma and myeloma are also at increased risk. So, improved survival with anticoagulation may be dependent on tumour type and disease stage.2,3 

Be aware of which types of cancer put patients at most risk of VTE and monitor them closely.

 

The American Society of Haematology state in their recommendations (with moderate certainty) that low molecular weight heparins should be used over direct oral anticoagulants in the immediate, short and long-term treatment in cancer patients with diagnosed VTE.9 


Therefore, emphasis should be placed on considering all risk factors for each individual patient.  
 

It is important to pay close attention to decreasing the risk of VTE while maximising efficacy of treatment in your patients.2 

Methodology5.Cohen et al., reported findings based on an observational cohort study using the Clinical Practice Research Datalink in the United Kingdom. Data include 6,592 active-cancer-associated VTEs with a total of 112,738 cancer-associated person-years of observation between 2001 and 2011. 
References
  1. Sandén P, Svensson PJ, Själander A. Venous thromboembolism and cancer risk. J Thromb Thrombolysis. 2017 Jan;43(1):68–73. 
  2. Guntupalli SR, Spinosa D, Wethington S, Eskander R, Khorana AA. Prevention of venous thromboembolism in patients with cancer. BMJ. 2023 Jun 1;381:e072715 
  3. Lyman GH. Venous thromboembolism in the patient with cancer: focus on burden of disease and benefits of thromboprophylaxis. Cancer. 2011 Apr 1;117(7):1334–49. 
  4. Kwaan HC, Vicuna B. Thrombosis and bleeding in cancer patients. Oncol Rev. 2007;1:14–27.  
  5. Rickles FR, Falanga A. Control of bleeding in cancer. Coagulation in Cancer. New York, NY: Springer, 2009:31–41.  
  6. Widick P, Brunner AM, Schiffman, F. Hematology, Basic Principles and Practice. Hematologic manifestations of malignancy, 7th edition. Philadelphia PA: Elsevier, 2018:2247–2252. 
  7. Lee AYY, Khorana AA. Cancer associated thrombosis. In DeVita, Hellman, and Rosenberg’s Cancer: Principles & Practice of Oncology, 10th Edition. DeVita VT, Lawrence, TS, Rosenberg SA, editors. Philadelphia, PA; Lippincott Williams & Wilkins, 2015. 
  8. Cohen AT, Katholing A, Rietbrock S, et al. Epidemiology of first and recurrent venous thromboembolism in patients with active cancer. A population-based cohort study. Thromb Haemost 2017;117(1):57–65. 
  9. Gary H. Lyman, Marc Carrier, Cihan Ay, Marcello Di Nisio, Lisa K. Hicks, Alok A. Khorana, Andrew D. Leavitt, Agnes Y. Y. Lee, Fergus Macbeth, Rebecca L. Morgan, Simon Noble, Elizabeth A. Sexton, David Stenehjem, Wojtek Wiercioch, Lara A. Kahale, Pablo Alonso-Coello; American Society of Hematology 2021 guidelines for management of venous thromboembolism: prevention and treatment in patients with cancer. Blood Adv 2021;5(4):927–974 
PP-UNP-GBR-8036. January 2024

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

PfizerPro Account

To access further materials, resources and receive communication about medicines and vaccines promoted by Pfizer.

Sign In or RegisterAccountSign Out

This site is intended only for healthcare professionals resident in the United Kingdom. If you are a member of the public wishing to access information on a specific medicine, please visit www.medicines.org.uk/emc

 

This website is brought to you by Pfizer Limited, a company registered in England 

and Wales under No. 526209 with its registered office at Ramsgate Road, Sandwich, Kent, CT13 9NJ

 

Copyright © 2024 Pfizer Limited. All rights reserved.

 

VAT registration number GB201048427

PP-UNP-GBR-7866. January 2024
For UK Healthcare Professionals*

These pages are not intended for patients or for members of the general public. The healthcare professional web pages contain promotional content.

I confirm that I am a healthcare professional* resident in the United Kingdom.

If you select 'No', you will be redirected to Pfizer.co.uk where you will be able to access reference information on Pfizer's prescription medicines.

*The ABPI Code definition for healthcare professional is members of the medical, dental, pharmacy and nursing professionals and any other persons who in the course of their professional activities may administer, prescribe, purchase, recommend or supply a medicine.

PP-UNP-GBR-7812. January 2024

YesNo
You are now leaving PfizerPro​​​​​

​​​​​​​You are now leaving www.pfizerpro.co.uk. Links to external websites are provided as a resource to the viewer. This website is neither owned or controlled by Pfizer Ltd. 

Pfizer accepts no responsibility for the content or services of the linked site.​​​​​​​​​​​​​​

​​​​​​​PP-PFE-GBR-3858. November 2021​​​​​​​
​​​​​​​
You are now leaving PfizerPro
​​​​​​​
​​​​​​​You are now leaving www.pfizerpro.co.uk. Links to external websites are provided as a resource to the viewer. This website is neither owned nor controlled by Pfizer Ltd. 

Pfizer accepts no responsibility for the content or services of the linked site other than the information or other materials relating to ​​​​​Pfizer medicines or 
business which it has provided or reviewed.

PP-PFE-GBR-3859. November 2021
​​​​​​​