The Catheter Study: Central Venous Catheter Survival in Cancer Patients Using Low Molecular Weight Heparin (Dalteparin) for the Treatment of Deep Vein Thrombosis
Information source: Lawson Health Research Institute
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Embolism and Thrombosis
Intervention: Dalteparin (Drug); Warfarin (Drug)
Phase: Phase 2
Status: Completed
Sponsored by: Lawson Health Research Institute Official(s) and/or principal investigator(s): Michael J Kovacs, MD, FRCPC, Principal Investigator, Affiliation: University of Western Ontario, Canada
Summary
The purpose of this study is to obtain an estimate of catheter survival in the setting of
upper extremity deep vein thrombosis (UEDVT) in patients treated with dalteparin and
warfarin.
Anticoagulation with dalteparin and warfarin in patients with UEDVT secondary to central
venous catheters in patients with an active malignancy is an effective therapy as quantified
by the success of catheter preservation. A prolonged line salvage rate without a recurrence
of UEDVT will improve the management of cancer patients who develop upper extremity deep
venous thrombosis in the setting of a central venous (CV) catheter.
Clinical Details
Official title: A Pilot Study of Central Venous Catheter Survival in Cancer Patients Using Low Molecular Weight Heparin (Dalteparin) for the Treatment of Deep Vein Thrombosis of the Upper Extremity
Study design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Primary outcome: The primary endpoint of the study will be rate of central line failure, defined as infusion failure that does not respond to 2mg tissue plasminogen activator (tPA), within the 3 months of study follow-up.
Secondary outcome: The secondary endpoints include recurrence of deep vein thrombosis (DVT) or pulmonary embolism (PE), major bleeding and death, time to central line failure.
Detailed description:
Deep venous thrombosis (DVT) is a serious disorder with an annual incidence of approximately
0. 1% and increasing with age to 1% in the elderly. Deep venous thrombosis of the upper
extremity (UEDVT) is estimated to constitute 1-5% of all cases of DVT.
The therapy of UEDVT has not been standardized. Therapeutic options include anticoagulation
with unfractionated heparin followed by warfarin, treatment with a thrombolytic agent, or a
thrombectomy. Recently, treatment with low molecular weight heparin has been shown to be a
safe and effective treatment for patients with verified UEDVT.
In patients with cancer, treatment of UEDVT associated with central venous catheters is even
less standardized. Some groups advocate removal of the catheter as the sole treatment for the
DVT, others remove the catheter and treat the DVT. A major disadvantage to removing the line
is that often re-insertion in the opposite limb is then required to avoid disruption of
chemotherapeutic treatment. This reinsertion again puts the patient at risk for thrombosis
and pulmonary embolism. Another therapy is treatment only with systemic thrombolytic therapy.
The disadvantage of thrombolytic therapy in persons with cancer is that there is a high risk
for major bleeding at the doses used.
A treatment regimen that has been adopted by the London Health Sciences Centre, and others
across Canada, is to leave the catheter in place and treat the DVT with low molecular weight
heparin and warfarin. This regimen is believed to halt the progression of thrombi, prevent
embolism and allow natural thrombolytic mechanisms to work effectively. By leaving the
central line in situ and appropriately treating the thrombosis there is no disruption in the
delivery of life-prolonging or life-saving treatment in the form of chemotherapy.
Preliminary data has been collected over the past 24 months at the London Health Sciences
Centre; the results suggest that this approach to treatment will prove to be beneficial to
the patient. Thirteen (13) patients with cancer and an UEDVT associated with a central venous
catheter were treated with dalteparin and warfarin with an intention to leave the central
line in situ. Of the 13, 1 patient had the line removed after 3 days at a peripheral hospital
against recommendation. The UEDVT was treated successfully and without the need for line
removal in 9 (75%) of the remaining 12 patients. Two (2) of the 12 had lines removed at 1
week and 1 had the line removed at 4 weeks due to worsening symptoms of UEDVT.
Therefore, UEDVT is a more common and less benign disease than previously reported and
generally arises in the presence of recognizable risk factors such as central venous
catheters and cancer. Treatment of the UEDVT with dalteparin and warfarin will treat the
thrombosis while preserving the central venous access for continued use. Hence, the need for
additional catheters and subsequent risk of bilateral UEDVT will be minimized.
Result of the CLOT (Clot in Cancer) Trial have shown the superiority of treatment with
dalteparin for 6 months as compared to the conventional treatment with short-term dalteparin
and extended warfarin for cancer patients with acute symptomatic DVT or PE. Extended
anticoagulant therapy may be beneficial in patients with UEDVT as well, however, there are
currently no estimates of clinical outcomes for either conventional (dalteparin followed by
warfarin) or extended therapy with dalteparin in this patient population.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Males or females greater than or equal to 18 years of age, inclusive.
- Symptomatic acute upper limb thrombosis with or without pulmonary embolism
associated with central venous catheter objectively documented by compression
ultrasonography, venogram or computed tomography (CT) scan.
- Diagnosis of active malignancy, as defined by patients who are either receiving active
treatment, or have metastatic disease or who have been diagnosed within the past two
years.
- Willing to provide written informed consent.
Exclusion Criteria:
- Dialysis catheters.
- Active bleeding or high risk for major bleeding.
- Platelet count < 100 x 10x9/L.
- Serum creatinine > 177umol/L
- Currently on warfarin with therapeutic intent (does not include minidose warfarin used
as prophylaxis for CV catheter thrombosis).
- Pulmonary embolism accompanied by hemodynamic instability or oxygen requirement.
- Inability to infuse through the catheter after a trial of intraluminal thrombolytic
therapy.
- Patients with acute myelogenous leukemia (AML) or acute lymphoblastic leukemia (ALL)
with a bone marrow or stem cell transplant pending in next 3 months.
Locations and Contacts
Queen Elizabeth II Health Care Centre, Halifax, Nova Scotia B3H 1Y8, Canada
Ottawa General Hospital, Ottawa, Ontario KiY 4B1, Canada
Ottawa Civic Hospital, Ottawa, Ontario KiY 4E9, Canada
London Health Sciences Centre, London, Ontario N6A 4G5, Canada
St. Joseph's Healthcare, Hamilton, Ontario L8N 4A6, Canada
Sir Mortimer B. Davis Jewish General Hospital, Montreal, Quebec H3T 1E2, Canada
Additional Information
Related publications: Kommareddy A, Zaroukian MH, Hassouna HI. Upper extremity deep venous thrombosis. Semin Thromb Hemost. 2002 Feb;28(1):89-99. Review. Kooij JD, van der Zant FM, van Beek EJ, Reekers JA. Pulmonary embolism in deep venous thrombosis of the upper extremity: more often in catheter-related thrombosis. Neth J Med. 1997 Jun;50(6):238-42. Monreal M, Raventos A, Lerma R, Ruiz J, Lafoz E, Alastrue A, Llamazares JF. Pulmonary embolism in patients with upper extremity DVT associated to venous central lines--a prospective study. Thromb Haemost. 1994 Oct;72(4):548-50. Volturo GA, Repeta RJ Jr. Non-lower extremity deep vein thrombosis. Emerg Med Clin North Am. 2001 Nov;19(4):877-93, vi. Review. Monreal M, Davant E. Thrombotic complications of central venous catheters in cancer patients. Acta Haematol. 2001;106(1-2):69-72. Review. Elliott G. Upper-extremity deep vein thrombosis. Lancet. 1997 Apr 26;349(9060):1188-9. No abstract available. Baarslag HJ, van Beek EJ, Koopman MM, Reekers JA. Prospective study of color duplex ultrasonography compared with contrast venography in patients suspected of having deep venous thrombosis of the upper extremities. Ann Intern Med. 2002 Jun 18;136(12):865-72. Erratum in: Ann Intern Med. 2003 Mar 4;138(5):438. Summary for patients in: Ann Intern Med. 2002 Jun 18;136(12):I-30. Savage KJ, Wells PS, Schulz V, Goudie D, Morrow B, Cruickshank M, Kovacs MJ. Outpatient use of low molecular weight heparin (Dalteparin) for the treatment of deep vein thrombosis of the upper extremity. Thromb Haemost. 1999 Sep;82(3):1008-10. Kovacs MJ, Anderson DA, Wells PS. Prospective assessment of a nomogram for the initiation of oral anticoagulation therapy for outpatient treatment of venous thromboembolism. Pathophysiol Haemost Thromb. 2002 May-Jun;32(3):131-3.
Starting date: September 2002
Ending date: March 2006
Last updated: September 6, 2006
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