Digestive Disease Interventions 2020; 04(03): 260-266
DOI: 10.1055/s-0040-1716739
Review Article

Gastrointestinal Malignancies and Venous Thromboembolic Disease: Clinical Significance and Endovascular Interventions

Xin Li
1   Section of Interventional Radiology, Imaging Institute, Cleveland Clinic Main Campus, Cleveland, Ohio
,
Sasan Partovi
1   Section of Interventional Radiology, Imaging Institute, Cleveland Clinic Main Campus, Cleveland, Ohio
,
Sameer Gadani
1   Section of Interventional Radiology, Imaging Institute, Cleveland Clinic Main Campus, Cleveland, Ohio
,
Charles Martin III
1   Section of Interventional Radiology, Imaging Institute, Cleveland Clinic Main Campus, Cleveland, Ohio
,
Avi Beck
1   Section of Interventional Radiology, Imaging Institute, Cleveland Clinic Main Campus, Cleveland, Ohio
,
Suresh Vedantham
2   Section of Interventional Radiology, Mallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, Missouri
› Author Affiliations
Funding The authors' effort was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Number TL1TR002344 (ST) and by the National Heart Lung and Blood Institute grant UH3-HL138325 for the C-TRACT Clinical Trial. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Abstract

Gastrointestinal malignancy encompasses a wide range of disease processes. Its incidence and mortality rate rank among the highest of all cancers. Venous thromboembolic disease is a common complication of gastrointestinal malignancy. Anticoagulation remains the first-line therapy. However, for patients who cannot tolerate or have failed anticoagulation, inferior vena cava (IVC) filter placement may be an option. Furthermore, to improve symptom resolution and reduce the severity of postthrombotic syndrome, catheter-directed thrombolysis (CDT) may be an option. Recent randomized trials including the ATTRACT (Acute Venous Thrombosis: Thrombus Removal with Adjunctive Catheter-Directed Thrombolysis) trial have shed new light on the efficacy and safety of CDT and related methods. Overall, the decision to proceed with IVC filter placement or CDT must be individualized.



Publication History

Received: 19 June 2020

Accepted: 27 July 2020

Article published online:
22 September 2020

© 2020. Thieme. All rights reserved.

Thieme Medical Publishers
333 Seventh Avenue, New York, NY 10001, USA.

 
  • References

  • 1 Siegel RL, Miller KD, Jemal A. Cancer statistics, 2020. CA Cancer J Clin 2020; 70 (01) 7-30
  • 2 Gaba R, Lokken R. Hepatocellular carcinoma: current practice and new frontiers. Dig Dis Interv 2017; (e-pub ahead of print) DOI: 10.1055/s-0037-1603923.
  • 3 Arellano RS, Sahani DV. Imaging of cholangiocarcinoma. Dig Dis Interv 2017; 1 (01) 8-13
  • 4 Mauri G, Krokidis M. Ablation techniques in liver and pancreatic cancers. Dig Dis Interv 2019; (e-pub ahead of print) DOI: 10.1055/s-0039-1692483.
  • 5 Gennaro N, Mauri G, Varano GM. et al. Thermal ablations for colorectal liver metastases. Dig Dis Interv 2019; (e-pub ahead of print) DOI: 10.1055/s-0039-1688724.
  • 6 Kim K, Shin J, Park JH. Stenting for advanced esophageal carcinoma. Dig Dis Interv 2018; (e-pub ahead of print) DOI: 10.1055/s-0038-1645853.
  • 7 Zhou WZ, Yang ZQ. Minimally invasive interventional management of gastric outlet obstructions. Dig Dis Interv 2018; (e-pub ahead of print) DOI: 10.1055/s-0038-1639335.
  • 8 Singh R, Sousou T, Mohile S, Khorana AA. High rates of symptomatic and incidental thromboembolic events in gastrointestinal cancer patients. J Thromb Haemost 2010; 8 (08) 1879-1881
  • 9 Walker AJ, Card TR, West J, Crooks C, Grainge MJ. Incidence of venous thromboembolism in patients with cancer - a cohort study using linked United Kingdom databases. Eur J Cancer 2013; 49 (06) 1404-1413
  • 10 Blom JW, Vanderschoot JPM, Oostindiër MJ, Osanto S, van der Meer FJM, Rosendaal FR. Incidence of venous thrombosis in a large cohort of 66,329 cancer patients: results of a record linkage study. J Thromb Haemost 2006; 4 (03) 529-535
  • 11 Sista AK, Kuo WT, Schiebler M, Madoff DC. Stratification, imaging, and management of acute massive and submassive pulmonary embolism. Radiology 2017; 284 (01) 5-24
  • 12 Lee AYY. Epidemiology and management of venous thromboembolism in patients with cancer. Thromb Res 2003; 110 (04) 167-172
  • 13 Prandoni P, Lensing AWA, Piccioli A. et al. Recurrent venous thromboembolism and bleeding complications during anticoagulant treatment in patients with cancer and venous thrombosis. Blood 2002; 100 (10) 3484-3488
  • 14 Howlett J, Benzenine E, Cottenet J, Foucher P, Fagnoni P, Quantin C. Could venous thromboembolism and major bleeding be indicators of lung cancer mortality? A nationwide database study. BMC Cancer 2020; 20 (01) 461
  • 15 Khorana AA, Francis CW, Culakova E, Kuderer NM, Lyman GH. Thromboembolism is a leading cause of death in cancer patients receiving outpatient chemotherapy. J Thromb Haemost 2007; 5 (03) 632-634
  • 16 Khorana AA. Venous thromboembolism and prognosis in cancer. Thromb Res 2010; 125 (06) 490-493
  • 17 Galanaud JP, Monreal M, Kahn SR. Epidemiology of the post-thrombotic syndrome. Thromb Res 2018; 164: 100-109
  • 18 Kahn SR, Ginsberg JS. Relationship between deep venous thrombosis and the postthrombotic syndrome. Arch Intern Med 2004; 164 (01) 17-26
  • 19 Galanaud JP, Kahn SR. The post-thrombotic syndrome: a 2012 therapeutic update. Curr Treat Options Cardiovasc Med 2013; 15 (02) 153-163
  • 20 Henke PK, Comerota AJ. An update on etiology, prevention, and therapy of postthrombotic syndrome. J Vasc Surg 2011; 53 (02) 500-509
  • 21 Kahn SR, Hirsch A, Shrier I. Effect of postthrombotic syndrome on health-related quality of life after deep venous thrombosis. Arch Intern Med 2002; 162 (10) 1144-1148
  • 22 Shigemori C, Wada H, Matsumoto K, Shiku H, Nakamura S, Suzuki H. Tissue factor expression and metastatic potential of colorectal cancer. Thromb Haemost 1998; 80 (06) 894-898
  • 23 Khorana AA, Ahrendt SA, Ryan CK. et al. Tissue factor expression, angiogenesis, and thrombosis in pancreatic cancer. Clin Cancer Res 2007; 13 (10) 2870-2875
  • 24 Licciardello JTW, Moake JL, Rudy CK, Karp DD, Hong WK. Elevated plasma von Willebrand factor levels and arterial occlusive complications associated with cisplatin-based chemotherapy. Oncology 1985; 42 (05) 296-300
  • 25 Haenen JH, Janssen MCH, van Langen H. et al. The postthrombotic syndrome in relation to venous hemodynamics, as measured by means of duplex scanning and strain-gauge plethysmography. J Vasc Surg 1999; 29 (06) 1071-1076
  • 26 Roumen-Klappe EM, den Heijer M, Janssen MCH, van der Vleuten C, Thien T, Wollersheim H. The post-thrombotic syndrome: incidence and prognostic value of non-invasive venous examinations in a six-year follow-up study. Thromb Haemost 2005; 94 (04) 825-830
  • 27 Moustafa A, Alim HM, Chowdhury MA, Eltahawy EA. Postthrombotic syndrome: long-term sequela of deep venous thrombosis. Am J Med Sci 2018; 356 (02) 152-158
  • 28 Lee AYY, Levine MN, Baker RI. et al. Randomized Comparison of Low-Molecular-Weight Heparin versus Oral Anticoagulant Therapy for the Prevention of Recurrent Venous Thromboembolism in Patients with Cancer (CLOT) Investigators. Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer. N Engl J Med 2003; 349 (02) 146-153
  • 29 Lee AYY, Kamphuisen PW, Meyer G. et al. CATCH Investigators. Tinzaparin vs warfarin for treatment of acute venous thromboembolism in patients with active cancer: A randomized clinical trial. JAMA 2015; 314 (07) 677-686
  • 30 Francis CW, Kessler CM, Goldhaber SZ. et al. Treatment of venous thromboembolism in cancer patients with dalteparin for up to 12 months: the DALTECAN Study. J Thromb Haemost 2015; 13 (06) 1028-1035
  • 31 Jara-Palomares L, Solier-Lopez A, Elias-Hernandez T. et al. Tinzaparin in cancer associated thrombosis beyond 6months: TiCAT study. Thromb Res 2017; 157: 90-96
  • 32 Raskob GE, van Es N, Verhamme P. et al. Hokusai VTE Cancer Investigators. Edoxaban for the treatment of cancer-associated venous thromboembolism. N Engl J Med 2018; 378 (07) 615-624
  • 33 Young AM, Marshall A, Thirlwall J. et al. Comparison of an oral factor Xa inhibitor with low molecular weight heparin in patients with cancer with venous thromboembolism: Results of a randomized trial (SELECT-D). J Clin Oncol 2018; 36 (20) 2017-2023
  • 34 Kamphuisen PW, Lee AYY, Meyer G. et al. CATCH Investigators. Clinically relevant bleeding in cancer patients treated for venous thromboembolism from the CATCH study. J Thromb Haemost 2018; 16 (06) 1069-1077
  • 35 Ross JA, Miller MM, Rojas Hernandez CM. Comparative effectiveness and safety of direct oral anticoagulants (DOACs) versus conventional anticoagulation for the treatment of cancer-related venous thromboembolism: A retrospective analysis. Thromb Res 2017; 150: 86-89
  • 36 Patel HK, Khorana AA. Anticoagulation in cancer patients: a summary of pitfalls to avoid. Curr Oncol Rep 2019; 21 (02) 18
  • 37 Samuelson Bannow BT, Lee A, Khorana AA. et al. Management of cancer-associated thrombosis in patients with thrombocytopenia: guidance from the SSC of the ISTH. J Thromb Haemost 2018; 16 (06) 1246-1249
  • 38 Khorana AA, Yannicelli D, McCrae KR. et al. Evaluation of US prescription patterns: Are treatment guidelines for cancer-associated venous thromboembolism being followed?. Thromb Res 2016; 145: 51-53
  • 39 Li X, Haddadin I, McLennan G. et al. Inferior vena cava filter – comprehensive overview of current indications, techniques, complications and retrieval rates. J Vasc Med 2020; (e-pub ahead of print) DOI: 10.1024/0301-1526/a000887.
  • 40 Key NS, Khorana AA, Kuderer NM. et al. Venous thromboembolism prophylaxis and treatment in patients with cancer: ASCO clinical practice guideline update. J Clin Oncol 2020; 38 (05) 496-520
  • 41 Ho G, Brunson A, White R, Wun T. Vena cava filter use in cancer patients with acute venous thromboembolism in California. Thromb Res 2015; 135 (05) 809-815
  • 42 Litwin RJ, Huang SY, Sabir SH. et al. Impact of an inferior vena cava filter retrieval algorithm on filter retrieval rates in a cancer population. J Vasc Surg Venous Lymphat Disord 2017; 5 (05) 689-697
  • 43 Mikhail S, Hannan L, Pishvaian MJ, Kessler C. Retrievable inferior vena cava filters in patients with cancer are safe but are they beneficial?. Med Oncol 2015; 32 (06) 622
  • 44 Abtahian F, Hawkins BM, Ryan DP. et al. Inferior vena cava filter usage, complications, and retrieval rate in cancer patients. Am J Med 2014; 127 (11) 1111-1117
  • 45 Decousus H, Leizorovicz A, Parent F. et al. A clinical trial of vena caval filters in the prevention of pulmonary embolism in patients with proximal deep-vein thrombosis. Prévention du Risque d'Embolie Pulmonaire par Interruption Cave Study Group. N Engl J Med 1998; 338 (07) 409-415
  • 46 Decousus H. PREPIC Study Group. Eight-year follow-up of patients with permanent vena cava filters in the prevention of pulmonary embolism: the PREPIC (Prevention du Risque d'Embolie Pulmonaire par Interruption Cave) randomized study. Circulation 2005; 112 (03) 416-422
  • 47 Mismetti P, Laporte S, Pellerin O. et al. PREPIC2 Study Group. Effect of a retrievable inferior vena cava filter plus anticoagulation vs anticoagulation alone on risk of recurrent pulmonary embolism: a randomized clinical trial. JAMA 2015; 313 (16) 1627-1635
  • 48 Barginear MF, Gralla RJ, Bradley TP. et al. Investigating the benefit of adding a vena cava filter to anticoagulation with fondaparinux sodium in patients with cancer and venous thromboembolism in a prospective randomized clinical trial. Support Care Cancer 2012; 20 (11) 2865-2872
  • 49 Brunson A, Ho G, White R, Wun T. Inferior vena cava filters in patients with cancer and venous thromboembolism (VTE) does not improve clinical outcomes: a population-based study. Thromb Res 2017; 153: 57-64
  • 50 Stein PD, Matta F, Lawrence FR, Hughes MJ. Inferior vena cava filters in patients with acute pulmonary embolism and cancer. Am J Med 2018; 131 (04) 442.e9-442.e12
  • 51 Levin JM, Schiff D, Loeffler JS, Fine HA, Black PML, Wen PY. Complications of therapy for venous thromboembolic disease in patients with brain tumors. Neurology 1993; 43 (06) 1111-1114
  • 52 Mansour A, Ismael Y, Abdel-Razeq H. Inferior vena cava filters in patients with advanced-stage cancer. Hematol Oncol Stem Cell Ther 2014; 7 (04) 136-141
  • 53 Enden T, Haig Y, Kløw NE. et al. CaVenT Study Group. Long-term outcome after additional catheter-directed thrombolysis versus standard treatment for acute iliofemoral deep vein thrombosis (the CaVenT study): a randomised controlled trial. Lancet 2012; 379 (9810): 31-38
  • 54 Haig Y, Enden T, Grøtta O. et al. CaVenT Study Group. Post-thrombotic syndrome after catheter-directed thrombolysis for deep vein thrombosis (CaVenT): 5-year follow-up results of an open-label, randomised controlled trial. Lancet Haematol 2016; 3 (02) e64-e71
  • 55 Fleck D, Albadawi H, Shamoun F, Knuttinen G, Naidu S, Oklu R. Catheter-directed thrombolysis of deep vein thrombosis: literature review and practice considerations. Cardiovasc Diagn Ther 2017; 7 (Suppl. 03) S228-S237
  • 56 Vedantham S, Goldhaber SZ, Julian JA. et al. ATTRACT Trial Investigators. Pharmacomechanical catheter-directed thrombolysis for deep-vein thrombosis. N Engl J Med 2017; 377 (23) 2240-2252
  • 57 Kearon C, Gu CS, Julian JA. et al. Pharmacomechanical catheter-directed thrombolysis in acute femoral-popliteal deep vein thrombosis: analysis from a stratified randomized trial. Thromb Haemost 2019; 119 (04) 633-644
  • 58 Comerota AJ, Kearon C, Gu CS. et al. ATTRACT Trial Investigators. Endovascular thrombus removal for acute iliofemoral deep vein thrombosis. Circulation 2019; 139 (09) 1162-1173
  • 59 Kahn SR, Julian JA, Kearon C. et al. Quality of life after pharmacomechanical catheter-directed thrombolysis for proximal deep venous thrombosis. J Vasc Surg Venous Lymphat Disord 2020; 8 (01) 8-23.e18
  • 60 Magnuson EA, Chinnakondepalli K, Vilain K. et al. Cost-effectiveness of pharmacomechanical catheter-directed thrombolysis versus standard anticoagulation in patients with proximal deep vein thrombosis: Results from the ATTRACT trial. Circ Cardiovasc Qual Outcomes 2019; 12 (10) e005659
  • 61 Engelberger RP, Spirk D, Willenberg T. et al. Ultrasound-assisted versus conventional catheter-directed thrombolysis for acute iliofemoral deep vein thrombosis. Circ Cardiovasc Interv 2015; 8 (01) e002027
  • 62 Notten P, Ten Cate-Hoek AJ, Arnoldussen CWKP. et al. Ultrasound-accelerated catheter-directed thrombolysis versus anticoagulation for the prevention of post-thrombotic syndrome (CAVA): a single-blind, multicentre, randomised trial. Lancet Haematol 2020; 7 (01) e40-e49
  • 63 Bjarnason H, Kruse JR, Asinger DA. et al. Iliofemoral deep venous thrombosis: safety and efficacy outcome during 5 years of catheter-directed thrombolytic therapy. J Vasc Interv Radiol 1997; 8 (03) 405-418
  • 64 Watson L, Broderick C, Armon MP. Thrombolysis for acute deep vein thrombosis. Cochrane Database Syst Rev 2016; 11: CD002783
  • 65 Vedantham S, Sista AK, Klein SJ. et al. Society of Interventional Radiology and Cardiovascular and Interventional Radiological Society of Europe Standards of Practice Committees. Quality improvement guidelines for the treatment of lower-extremity deep vein thrombosis with use of endovascular thrombus removal. J Vasc Interv Radiol 2014; 25 (09) 1317-1325
  • 66 Kim HS, Preece SR, Black JH, Pham LD, Streiff MB. Safety of catheter-directed thrombolysis for deep venous thrombosis in cancer patients. J Vasc Surg 2008; 47 (02) 388-394
  • 67 Brailovsky Y, Yeung HM, Lakhter V, Zack CJ, Zhao H, Bashir R. In-hospital outcomes of catheter-directed thrombolysis versus anticoagulation in cancer patients with proximal deep venous thrombosis. J Vasc Surg Venous Lymphat Disord 2020; 8 (04) 538-544.e3