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THrombo-Embolic Event in Onco-hematology (THEO)

Primary Purpose

Neoplasms, Thrombosis, Coagulation Disorder

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Blood sample analysis
Sponsored by
Centre Antoine Lacassagne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Neoplasms focused on measuring Neoplasms, Thrombosis, hypocoagulability

Eligibility Criteria

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

Inclusion Criteria:

  1. Patient followed for CAL cancer and admitted to the LTC in the Medicine Department.
  2. Age> to 18 years.
  3. Patient having read the information note and signed the informed consent (including specific consent for genotyping of clotting factors).
  4. Patient receiving social insurance.
  5. Weight> 50kg
  6. Hemoglobin level> 7.0 g / dl

Exclusion Criteria:

  1. Patient not benefiting as part of his treatment from hospitalization, but admitted on an ambulatory basis.
  2. Patient whose age is less than 18 years.
  3. Patient already included in the study.
  4. Patient considered a vulnerable person; Vulnerable people are defined in Article L1121-5 to -8:

    • Pregnant women, parturients and breastfeeding mothers
    • Persons deprived of their liberty by a judicial or administrative decision, persons hospitalized without consent under Articles L. 3212-1 and L. 3213-1 who do not fall under the provisions of Article L. 1121-8
    • and persons admitted to a health or social institution for purposes other than research
    • adults who are legally protected or unable to express their consent

Sites / Locations

  • Centre Antoine Lacassagne

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Experimental arm

Arm Description

Hospitalized patient

Outcomes

Primary Outcome Measures

Evaluation of thrombosis rate in patients hospitalized for cancer
Incidence rate of first occurrence of thromboembolic event in cancer patients, and hospitalized

Secondary Outcome Measures

Comparison of the values of the biological parameters of thrombophilia assessment, blood count and coagulation, at the time of the occurrence of thrombosis, between patients in a situation of hypocoagulability and patients with no hypocoagulability.
These patients in these two situations, will be identified, during the onset of thrombosis, the results of the parameters of their blood count and their intake of antiaggregant or anticoagulant treatment. • Comparison between the hypocoagulable patient group and the non-hypocoagulable patient group of the biological parameters of the thrombophilia balance, blood counts and coagulation counts in patients with cancer at the time of the occurrence of thrombosis o The state of hypocoagulability is defined by: thrombocytopenia <100000 / mm3, abnormality of one or more coagulation factors, platelet antiaggregant treatment, anticoagulant treatment of all kinds.
Determination of thrombosis rate with new oral anticoagulants.
Incidence rate of first occurrence of thromboembolic events in patients with cancer, and treatment with new oral anticoagulants
Comparison of 12-month survival of patients with or without hypocoagulability, with thrombosis.
Survival at 12 months. 12-month survival is defined as the delay between the date of inclusion and the date of death from all causes. Patients lost to follow-up will be censored on the date of the latest news. Patients will be followed for 12 months after inclusion in the study.
• Determination of death rate due to thrombosis.
Death rate due to thrombosis is the number of deaths whose cause is thrombosis.
Determination of the rate of hemorrhagic complications in this population.
Rate of haemorrhagic complications defined by the number of haemorrhagic events, whatever the degree of severity, of biological or medicinal origin. o A haemorrhagic event is defined as the occurrence of bleeding by rupture of a blood vessel or effusion out of a blood vessel. Bleeding may be internal or external, see the examples provided below: Internal haemorrhage: cerebral hematoma, subdural hematoma; intramuscular hematoma - Externalized hemorrhage: epistaxis, gingivorrhagia, externalized digestive bleeding

Full Information

First Posted
January 30, 2019
Last Updated
December 12, 2022
Sponsor
Centre Antoine Lacassagne
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1. Study Identification

Unique Protocol Identification Number
NCT03826043
Brief Title
THrombo-Embolic Event in Onco-hematology
Acronym
THEO
Official Title
"Prospective Study Evaluating the Impact and Treatment of Thrombo-embolic Events in Patients With Cancer"
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
September 9, 2019 (Actual)
Primary Completion Date
September 9, 2022 (Actual)
Study Completion Date
September 9, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Antoine Lacassagne

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The overall incidence of deep vein thrombosis (DVT) and pulmonary embolism (PE) is 1 per 200 cancer patients, about 5 times higher than in the general population. These events are of crucial importance, since nearly 10% of cancer patients died from thromboembolic events (EVT), making them the second leading cause of death in this population. In hospitalized patients, the rate seems to have increase between 1979 and 1990 from 0.6% - 2% before 1990 to 4% since 1990. Thrombotic risk in cancer patients is known and identified. Thrombotic complications affect the survival and quality of life of cancer patients. Chemotherapy is a regular generator of cytopenia, the most prominent of which is thrombocytopenia. In addition, a prospective study of 107 cancer patients in our institution shows that almost 40% of patients over 65 years of age take anticoagulant or antiplatelet therapy. In this specific population (i.e., with cancer and hypocoagulability), the occurrence of thrombosis poses particular problems. The prevalence and incidence of venous thrombosis in this situation is unknown and the behavior to be poorly specified. Based on these considerations, The investigator propose a two-year prospective cohort study to explore the biological parameters of hypocoagulability and to assess the incidence and prevalence of DVT in thrombocytopenic patients on vitamin K antagonists. (AVK), anti-platelet aggregation (AGP) and / or direct oral anticoagulant (AOD). In this study, the investigator means by hypocoagulability any situation modifying the normal coagulation system.
Detailed Description
The overall incidence of deep vein thrombosis (DVT) and pulmonary embolism (PE) is 1 per 200 cancer patients, about 5 times higher than in the general population. These events are of crucial importance, since nearly 10% of cancer patients died from thromboembolic events (EVT), making them the second leading cause of death in this population. In hospitalized patients, the rate seems to have increase between 1979 and 1990 from 0.6% - 2% before 1990 to 4% since 1990. Some studies report an increase in the hospitalization cost of 38%, correlated in part with the increase in hospitalization duration related to venous thromboembolism. Thrombotic risk in cancer patients is known and identified. Thrombotic complications affect the survival and quality of life of cancer patients. Scores were established and validated to establish this risk and to propose prophylaxis in these patients. Guidelines exist for prophylaxis and for the treatment of these patients. Chemotherapy is a regular generator of cytopenia, the most prominent of which is thrombocytopenia. In addition, a prospective study of 107 cancer patients in our institution shows that almost 40% of patients over 65 years of age take anticoagulant or antiplatelet therapy. In this specific population (i.e., with cancer and hypocoagulability), the occurrence of thrombosis poses particular problems. The prevalence and incidence of venous thrombosis in this situation is unknown and the behavior to be poorly specified. Based on these considerations, The investigator propose a two-year prospective cohort study to explore the biological parameters of hypocoagulability and to assess the incidence and prevalence of DVT in thrombocytopenic patients on vitamin K antagonists. (AVK), anti-platelet aggregation (AGP) and / or direct oral anticoagulant (AOD). In this study, the investigator means by hypocoagulability any situation modifying the normal coagulation system, that is to say: The presence of any anti-coagulant or antiplatelet treatment, Or abnormalities of primary or secondary hemostasis causing coagulation disorders. Some studies report an increase in the hospitalization cost of 38%, correlated in part with the increase in hospitalization duration related to venous thromboembolism. Thrombotic risk in cancer patients is known and identified. Thrombotic complications affect the survival and quality of life of cancer patients. Scores were established and validated to establish this risk and to propose prophylaxis in these patients. Guidelines exist for prophylaxis and for the treatment of these patients. Chemotherapy is a regular generator of cytopenia, the most prominent of which is thrombocytopenia. In addition, a prospective study of 107 cancer patients in our institution shows that almost 40% of patients over 65 years of age take anticoagulant or antiplatelet therapy. In this specific population (i.e., with cancer and hypocoagulability), the occurrence of thrombosis poses particular problems. The prevalence and incidence of venous thrombosis in this situation is unknown and the behavior to be poorly specified. Based on these considerations, The investigator propose a two-year prospective cohort study to explore the biological parameters of hypocoagulability and to assess the incidence and prevalence of DVT in thrombocytopenic patients on vitamin K antagonists (AVK), anti platelet aggregation (AGP) and / or direct oral anticoagulant (AOD). In this study the investigator mean by hypocoagulability any situation modifying the normal coagulation system, that is to say: the presence of any anti-coagulant or antiplatelet treatment, or abnormalities of primary or secondary hemostasis causing coagulation disorders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasms, Thrombosis, Coagulation Disorder
Keywords
Neoplasms, Thrombosis, hypocoagulability

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
700 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental arm
Arm Type
Experimental
Arm Description
Hospitalized patient
Intervention Type
Diagnostic Test
Intervention Name(s)
Blood sample analysis
Intervention Description
Thrombophilia, blood count and coagulation count
Primary Outcome Measure Information:
Title
Evaluation of thrombosis rate in patients hospitalized for cancer
Description
Incidence rate of first occurrence of thromboembolic event in cancer patients, and hospitalized
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Comparison of the values of the biological parameters of thrombophilia assessment, blood count and coagulation, at the time of the occurrence of thrombosis, between patients in a situation of hypocoagulability and patients with no hypocoagulability.
Description
These patients in these two situations, will be identified, during the onset of thrombosis, the results of the parameters of their blood count and their intake of antiaggregant or anticoagulant treatment. • Comparison between the hypocoagulable patient group and the non-hypocoagulable patient group of the biological parameters of the thrombophilia balance, blood counts and coagulation counts in patients with cancer at the time of the occurrence of thrombosis o The state of hypocoagulability is defined by: thrombocytopenia <100000 / mm3, abnormality of one or more coagulation factors, platelet antiaggregant treatment, anticoagulant treatment of all kinds.
Time Frame
12 months
Title
Determination of thrombosis rate with new oral anticoagulants.
Description
Incidence rate of first occurrence of thromboembolic events in patients with cancer, and treatment with new oral anticoagulants
Time Frame
12 months
Title
Comparison of 12-month survival of patients with or without hypocoagulability, with thrombosis.
Description
Survival at 12 months. 12-month survival is defined as the delay between the date of inclusion and the date of death from all causes. Patients lost to follow-up will be censored on the date of the latest news. Patients will be followed for 12 months after inclusion in the study.
Time Frame
12 months
Title
• Determination of death rate due to thrombosis.
Description
Death rate due to thrombosis is the number of deaths whose cause is thrombosis.
Time Frame
12 months
Title
Determination of the rate of hemorrhagic complications in this population.
Description
Rate of haemorrhagic complications defined by the number of haemorrhagic events, whatever the degree of severity, of biological or medicinal origin. o A haemorrhagic event is defined as the occurrence of bleeding by rupture of a blood vessel or effusion out of a blood vessel. Bleeding may be internal or external, see the examples provided below: Internal haemorrhage: cerebral hematoma, subdural hematoma; intramuscular hematoma - Externalized hemorrhage: epistaxis, gingivorrhagia, externalized digestive bleeding
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient followed for CAL cancer and admitted to the LTC in the Medicine Department. Age> to 18 years. Patient having read the information note and signed the informed consent (including specific consent for genotyping of clotting factors). Patient receiving social insurance. Weight> 50kg Hemoglobin level> 7.0 g / dl Exclusion Criteria: Patient not benefiting as part of his treatment from hospitalization, but admitted on an ambulatory basis. Patient whose age is less than 18 years. Patient already included in the study. Patient considered a vulnerable person; Vulnerable people are defined in Article L1121-5 to -8: Pregnant women, parturients and breastfeeding mothers Persons deprived of their liberty by a judicial or administrative decision, persons hospitalized without consent under Articles L. 3212-1 and L. 3213-1 who do not fall under the provisions of Article L. 1121-8 and persons admitted to a health or social institution for purposes other than research adults who are legally protected or unable to express their consent
Facility Information:
Facility Name
Centre Antoine Lacassagne
City
Nice
ZIP/Postal Code
06189
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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THrombo-Embolic Event in Onco-hematology

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