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Screening for Occult Malignancy in Patients With Idiopathic Venous Thromboembolism (SOME)

Primary Purpose

Venous Thromboembolism, Deep Vein Thrombosis, Pulmonary Embolism

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Comprehensive computed tomography of the abdomen/pelvis
Limited Malignancy Screening
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Venous Thromboembolism focused on measuring Cancer, Screening

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a new diagnosis of unprovoked proximal deep vein thrombosis (DVT) or pulmonary embolism (PE) will be eligible to participate into the study:

    • Unprovoked VTE is defined as the absence of any of the following predisposing factors:

      1. known active cancer;
      2. recent (less than 3 months) paralysis, paresis or plaster immobilization of the lower extremities;
      3. recently bedridden for period of 3 or more days, or major surgery, within the previous 12 weeks requiring general or regional anaesthesia;
      4. previous unprovoked VTE;
      5. known thrombophilia (hereditary or acquired)
    • Proximal DVT is defined as a non-compressibility of any vein segment from the common femoral vein to the trifurcation of the popliteal vein or a persistent intra-luminal filling defect of the iliac, common femoral, superficial femoral or popliteal veins on contrast venography.
    • Pulmonary embolism is defined as:

      1. patients with a high/intermediate pre-test probability (Wells' model > 4) + high probability V/Q scan;
      2. positive pulmonary angiogram; or
      3. spiral CT demonstrating intraluminal filling defect in a vessel larger than a segmental artery

Exclusion Criteria:

Patients will be excluded from the study if they have any of the following criteria:

  • Age < 18 years-old;
  • Refusal or inability to provide informed consent;
  • Greater than 21 days post diagnosis of idiopathic VTE
  • Index VTE event of UEDVT or unusual site DVT
  • Diagnosis of SSPE in the absence of above or below knee DVT
  • Allergy to contrast media;
  • Creatinine clearance < 60 ml/min;
  • Claustrophobia or agoraphobia;
  • Weight > 130 kg;
  • Diagnosis of ulcerative colitis; and
  • Diagnosis of glaucoma
  • Current pregnancy

Sites / Locations

  • St. Boniface Hospital
  • Capital Health Centre for Research
  • St. Joseph's Healthcare Hamilton
  • London Health Sciences Center
  • Ottawa Hospital
  • Montreal General Hospital
  • Sacre-Coeur Hospital
  • Sir Mortimer B. Davis Jewish General Hospital
  • St. Mary's Hospital Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Limited Malignancy Screening

Extensive Malignancy Screening

Arm Description

Limited screen as described above in combination with comprehensive computed tomography of the abdomen/pelvis

Outcomes

Primary Outcome Measures

Previously undiagnosed malignancy "missed" by malignancy screening defined as biopsy proven tissue diagnosis of malignancy diagnosed from the time of malignancy screening completion to the end of the 1 year follow-up period.

Secondary Outcome Measures

Overall mortality
Recurrent VTE
Early malignancy: T1-2N0M0 as per the World Health Organization TNM classification system
QALYs gained
Incremental cost-effectiveness ratio
Adverse events with cCT

Full Information

First Posted
October 14, 2008
Last Updated
July 2, 2015
Sponsor
Ottawa Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00773448
Brief Title
Screening for Occult Malignancy in Patients With Idiopathic Venous Thromboembolism
Acronym
SOME
Official Title
Screening for Occult Malignancy in Patients With Idiopathic Venous Thromboembolism: an Open Randomized Controlled Trial Using a Comprehensive Abdomen/Pelvis Computed Tomography
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ottawa Hospital Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Blood clots in leg veins (deep vein thrombosis) or lung arteries (pulmonary embolism) that happen for no reason (i.e. unexplained) are both called "unprovoked venous thromboembolism" (VTE). These unexplained blood clots can be the first symptom of cancer. Up to 10% of patients with unexplained blood clots will be diagnosed with cancer within one year of their blood clot diagnosis. These cancers can be found anywhere in the body although the relationship appears stronger with the pancreas, ovary and liver. Cancer testing in patients with blood clots is controversial. There is presently a wide variety of expert opinions and practices. Previous studies showed that a limited cancer screen including a medical history, physical examination, basic blood work and chest X-ray, will find about 90% of cancers. More recent and better designed studies showed that the limited cancer screen misses many cancers and needs to be improved. More extensive cancer testing may find more cancers but is potentially uncomfortable for patients, costs a lot of money and involves a lot of people. The "comprehensive computed tomography" is less uncomfortable, inexpensive, radiological test made to find many cancers at once. Thus, the scientific question to be asked is: Does a "comprehensive computed tomography" miss less cancers than a limited cancer screen in patients with blood clots? The main goal of this study is to find out if a "comprehensive computed tomography" misses less cancers than a limited cancer screen in patients with unexplained blood clots. The second goal of the study is 1) to find out if a "comprehensive computed tomography" finds more "curable" cancers than the limited cancer screen; 2) to find out if the patients diagnosed with cancer are still alive and cancer-free after one year (i.e. the patients with curable cancer were treated and are doing well); 3) to prove that a negative "comprehensive computed tomography" means that the patient will not have cancer and; 4) to find out if a "comprehensive computed tomography" is well tolerated and safe for patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thromboembolism, Deep Vein Thrombosis, Pulmonary Embolism
Keywords
Cancer, Screening

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
862 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Limited Malignancy Screening
Arm Type
Active Comparator
Arm Title
Extensive Malignancy Screening
Arm Type
Experimental
Arm Description
Limited screen as described above in combination with comprehensive computed tomography of the abdomen/pelvis
Intervention Type
Device
Intervention Name(s)
Comprehensive computed tomography of the abdomen/pelvis
Intervention Description
Virtual colonoscopy and gastroscopy, a biphasic enhanced CT for hepatoma and renal cell carcinoma, parenchymal pancreatogram with minimum intensity projection (MinIP) reformation for pancreatic carcinoma, and finally uniphasic enhanced CT of distended bladder for bladder and ovarian carcinomas.
Intervention Type
Other
Intervention Name(s)
Limited Malignancy Screening
Intervention Description
1) A complete medical history and physical examination; 2) complete blood count; 3) liver function tests (AST, ALT, ALP, bilirubin, LDH); 4) renal function test (creatinine); 5) chest X-ray (if not performed in the past year) In women, a pap smear/pelvic examination (if > 18 and < 70 years old and not performed during the past year),a mammogram (> 50 years old) will be performed if not conducted in last year. Similarly for men, prostate examination +/- PSA testing (>40 years old) will be performed if not conducted in the past year.
Primary Outcome Measure Information:
Title
Previously undiagnosed malignancy "missed" by malignancy screening defined as biopsy proven tissue diagnosis of malignancy diagnosed from the time of malignancy screening completion to the end of the 1 year follow-up period.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Overall mortality
Time Frame
1 year
Title
Recurrent VTE
Time Frame
1 year
Title
Early malignancy: T1-2N0M0 as per the World Health Organization TNM classification system
Time Frame
1 year
Title
QALYs gained
Time Frame
1 year
Title
Incremental cost-effectiveness ratio
Time Frame
1 year
Title
Adverse events with cCT
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a new diagnosis of unprovoked proximal deep vein thrombosis (DVT) or pulmonary embolism (PE) will be eligible to participate into the study: Unprovoked VTE is defined as the absence of any of the following predisposing factors: known active cancer; recent (less than 3 months) paralysis, paresis or plaster immobilization of the lower extremities; recently bedridden for period of 3 or more days, or major surgery, within the previous 12 weeks requiring general or regional anaesthesia; previous unprovoked VTE; known thrombophilia (hereditary or acquired) Proximal DVT is defined as a non-compressibility of any vein segment from the common femoral vein to the trifurcation of the popliteal vein or a persistent intra-luminal filling defect of the iliac, common femoral, superficial femoral or popliteal veins on contrast venography. Pulmonary embolism is defined as: patients with a high/intermediate pre-test probability (Wells' model > 4) + high probability V/Q scan; positive pulmonary angiogram; or spiral CT demonstrating intraluminal filling defect in a vessel larger than a segmental artery Exclusion Criteria: Patients will be excluded from the study if they have any of the following criteria: Age < 18 years-old; Refusal or inability to provide informed consent; Greater than 21 days post diagnosis of idiopathic VTE Index VTE event of UEDVT or unusual site DVT Diagnosis of SSPE in the absence of above or below knee DVT Allergy to contrast media; Creatinine clearance < 60 ml/min; Claustrophobia or agoraphobia; Weight > 130 kg; Diagnosis of ulcerative colitis; and Diagnosis of glaucoma Current pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Carrier, MD MSc FRCPC
Organizational Affiliation
The Ottawa Hospital Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Boniface Hospital
City
Winnipeg
State/Province
Manitoba
Country
Canada
Facility Name
Capital Health Centre for Research
City
Halifax
State/Province
Nova Scotia
Country
Canada
Facility Name
St. Joseph's Healthcare Hamilton
City
Hamilton
State/Province
Ontario
Country
Canada
Facility Name
London Health Sciences Center
City
London
State/Province
Ontario
Country
Canada
Facility Name
Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada
Facility Name
Montreal General Hospital
City
Montreal
State/Province
Quebec
Country
Canada
Facility Name
Sacre-Coeur Hospital
City
Montreal
State/Province
Quebec
Country
Canada
Facility Name
Sir Mortimer B. Davis Jewish General Hospital
City
Montreal
State/Province
Quebec
Country
Canada
Facility Name
St. Mary's Hospital Center
City
Montreal
State/Province
Quebec
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
18765702
Citation
Carrier M, Le Gal G, Wells PS, Fergusson D, Ramsay T, Rodger MA. Systematic review: the Trousseau syndrome revisited: should we screen extensively for cancer in patients with venous thromboembolism? Ann Intern Med. 2008 Sep 2;149(5):323-33. doi: 10.7326/0003-4819-149-5-200809020-00007.
Results Reference
background
PubMed Identifier
26095467
Citation
Carrier M, Lazo-Langner A, Shivakumar S, Tagalakis V, Zarychanski R, Solymoss S, Routhier N, Douketis J, Danovitch K, Lee AY, Le Gal G, Wells PS, Corsi DJ, Ramsay T, Coyle D, Chagnon I, Kassam Z, Tao H, Rodger MA; SOME Investigators. Screening for Occult Cancer in Unprovoked Venous Thromboembolism. N Engl J Med. 2015 Aug 20;373(8):697-704. doi: 10.1056/NEJMoa1506623. Epub 2015 Jun 22.
Results Reference
result
PubMed Identifier
34597414
Citation
Robertson L, Broderick C, Yeoh SE, Stansby G. Effect of testing for cancer on cancer- or venous thromboembolism (VTE)-related mortality and morbidity in people with unprovoked VTE. Cochrane Database Syst Rev. 2021 Oct 1;10(10):CD010837. doi: 10.1002/14651858.CD010837.pub5.
Results Reference
derived
PubMed Identifier
26817957
Citation
Ihaddadene R, Corsi DJ, Lazo-Langner A, Shivakumar S, Zarychanski R, Tagalakis V, Solymoss S, Routhier N, Douketis J, Le Gal G, Carrier M. Risk factors predictive of occult cancer detection in patients with unprovoked venous thromboembolism. Blood. 2016 Apr 21;127(16):2035-7. doi: 10.1182/blood-2015-11-682963. Epub 2016 Jan 27.
Results Reference
derived

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Screening for Occult Malignancy in Patients With Idiopathic Venous Thromboembolism

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