Prophylaxis of Venous Thromboembolic Disease With Low Molecular Weight (LMWH) (TINzaparin) in Patients With Metastatic Colorectal Cancer Who Start the First Line of Treatment.
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 232
- Locations
- 35
- Primary Endpoint
- Incidence of any VTE
Study Overview
Brief Summary
Patients with metastatic colorectal cancer (mCRC) who are scheduled to receive systemic cancer therapy have an increased risk for venous thromboembolic (VTE) events compared with the general population.
PROTINCOL is a randomized, open label, non placebo-controlled, low intervention, and phase III clinical trial that will recruit patients with mCRC. The study hypothesizes that prophylaxis with Tinzaparin could prevent the appearance of symptomatic and incidental VTE.
All patients will receive the first-line anticancer treatment deemed more appropriate according to the physician criteria. Enrolled patients are randomized in a 1:1 ratio (stratifying by BRAF/RAS, resection of primary tumor, and anti-angiogenic first-line treatment) to: control arm (no interventions related to VTE risk and no placebo) or experimental arm (prophylactic Tinzaparin at a fixed dose of 4500 IU/day in patients with up to 80kg, 6000 IU/day for those between 80-100 kg, or 8000 IU/day for those >100kg). Treatment is scheduled for a maximum period of 4 months. Treatment could be stopped earlier in case of unacceptable toxicity, patient consent withdrawal, physician criteria or end of study. Patients will undergo tumor and VTE assessments according to standard clinical practice.
The main objective of the study is to evaluate the efficacy of tinzaparin for the prevention of symptomatic or incidental VTE events. Secondary objectives include the associations between VTE events and tumor characteristics (i.e. laterality, RAS/BRAF mutations) or management (i.e. surgery or treatment with anti-angiogenic or anti-EGFR agents), cancer-specific survival outcomes, safety, the incidence of bleeding events, and patient-reported quality of life. The trial includes also a translational exploratory analysis to assess the predictive value of risk assessment models and genetic risk scores, their evolution through the study and microsatellite instability or other biomarkers.
Detailed Description
This research study is a prospective, randomized, open label (PROBE), non placebo-controlled, and phase III clinical trial; Investigator Initiated Study (IIS). The study has been considered a low-interventional clinical trial.
The trial will compare the efficacy and safety of tinzaparin with a watch and wait strategy for primary prophylaxis of symptomatic or incidental VTE in adult men and women, 18 years of age and older, with metastatic colorectal cancer who are scheduled to initiate systemic cancer therapy as a component of their standard of care anticancer regimen.
The study consists of 3 periods: a 4-week screening period, a 4 months treatment period and post-treatment follow-up period until the end of treatment (EOT) visit, scheduled 2 months after the last dose of tinzaparin or 6 months from the first dose of tinzaparin (whichever occurs latest). The duration of participation in the study for each subject is approximately 6 months. Further long-term phone follow-up to monitor for progression and survival could be carried out at the end of study. Tumor follow-up assessments will adhere to the standard clinical practice within each site.
All patients will receive the first-line anticancer treatment deemed more appropriate according to the physician criteria and current guideline recommendations. Patients in both groups will receive supportive care as per local practice. No formal recommendations will be issued by the study protocol regarding cancer treatment and supportive care, but the drugs used will be recorded in the clinical report form. Constitutive use of anticoagulant drugs will be prohibited during the treatment period.
Enrolled patients are randomized in a 1:1 ratio to the control arm, or the experimental arm:
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Male or female subjects with age ≥ 18 years.
- •Written informed consent.
- •Patients with a histologically confirmed diagnosis of stage IV colon or rectal adenocarcinoma (mCRC).
- •Locally assessed BRAF and RAS genomic alterations available during screening.
- •Beginning of the first line of treatment for metastatic disease with chemotherapy +/- targeted therapy (i.e. antiangiogenic, anti-EGFR, encorafenib-cetuximab doublet) or immunotherapy.
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0-
- •Life expectancy >6 months.
Exclusion Criteria
- •Contraindication to tinzaparin, or other heparins:
- •Allergy (or hypersensitivity) to heparin, tinzaparin, other LMWHs, or pork products.
- •History or presence of heparin-induced (type II) thrombocytopenia.
- •Have or have had an epidural catheter or a traumatic spinal puncture within the previous 7 days.
- •Prothrombin time (PT) (International normalized ratio [INR] >1.5 for any reason) or aPTT >2 times control value.
- •Active major bleeding or conditions predisposing to major bleeding. a major bleeding is defined as one that meets one of the following three criteria:
- •occurring in a critical area or organ (for example, intracranial, intra-spinal, intraocular, retroperitoneal, intra-articular or pericardial, intrauterine or intramuscular with compartment syndrome),
- •causing a decrease in hemoglobin levels of 2 g/l (1.24 mmol/l) or more, or that requires a transfusion of two or more units of whole blood or packed red blood cells.
- •Lesions or conditions at increased risk of clinically significant bleeding, including:
- •Previously diagnosed/treated VTE ≤ 28 days prior to randomization.
- •Active ulcer disease.
- •Diagnosed cerebral metastases.
- •Stroke within the prior 6 months.
- •History of central nervous system (CNS) or intraocular bleeding.
- •Requirement of other anticoagulant therapy, dual antiplatelet therapy, daily non-steroidal anti-inflammatory drugs, or other medications known to increase the risk of bleeding.
- •Note: A daily dose of ≤100 mg of aspirin and single agent clopidogrel are permitted
- •Acute or chronic renal insufficiency with Creatinine clearance < 30 ml / min.
- •Platelet count < 80.000 /ml at the time of inclusion.
- •Severe liver insufficiency as defined by clinical manifestations of ascites, cirrhosis, encephalopathy and/or jaundice and/or biochemical abnormalities in liver function tests including:
- •elevated levels of total bilirubin (> 2 times the upper limit normal [ULN]),
- •elevated liver transaminases (> 2 times the ULN; > 5 in case of hepatic metastasis).
- •Participating in another study of an investigational agent at the time of enrollment. Note: Use of an experimental regimen of an approved product is not cause for exclusion.
- •Patients who weigh < 50 Kg.
- •Women of childbearing potential (WOCBP), must provide a negative serum or urine pregnancy test at screening. Women breastfeeding are not eligible.
- •Note: A pregnancy test is performed on WOCBP as per standard of care for patients undergoing anticancer treatments.
- •Any underlying medical or psychiatric disorder, which, in the opinion of the investigator, makes the administration of tinzaparin unsafe or interferes with the informed consent process or trial procedures.
Arms & Interventions
Experimental arm
Those patients allocated to the experimental arm will receive prophylactic Tinzaparin at a fixed dose according to their weight:
Patients < 80 kg will receive a fixed dose of 4500 IU daily. Patients between 80-100 kg will receive a fixed dose of 6000 IU daily. Patients > 100 kg will receive a fixed dose of 8000 IU daily.
Accordingly, the effective dose of tinzaparin is estimated to be in the range of 56-90 IU/kg. Tinzaparin dose will be adjusted according to the dose levels specified above in patients who experience changes in body weight greater than 10% during treatment period.
Intervention: Tinzaparin (Drug)
Outcomes
Primary Outcomes
Incidence of any VTE
Time Frame: Throughout the study period, approximately 6 months per patient
The primary efficacy endpoint is the cumulative incidence (percentage of patients) of any VTE event including: Symptomatic non-fatal pulmonary thromboembolism (PE). Symptomatic lower-limb deep vein thromboembolism (sllDVT). Symptomatic upper extremity deep vein thromboembolism (sueDVT). Incidentally diagnosed PE or proximal DVT. Symptomatic central venous catheter thromboembolism. Incidentally visceral vein thrombosis (iVVT). Symptomatic visceral vein thrombosis (sVVT). VTE-related deaths
Secondary Outcomes
- Incidence of VTE-related deaths(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in resected or not resected patients(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in patients with anti-EGFR therapy(Throughout the study period, approximately 6 months per patient)
- Incidence of symptomatic non-fatal PE(Throughout the study period, approximately 6 months per patient)
- Incidence of sueDVT(Throughout the study period, approximately 6 months per patient)
- Incidence of sVVT(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in patients with antiangiogenic therapy(Throughout the study period, approximately 6 months per patient)
- Incidence of incidentally diagnosed PE or proximal DVT(Throughout the study period, approximately 6 months per patient)
- Incidence of sllDVT(Throughout the study period, approximately 6 months per patient)
- Incidence of symptomatic central venous catheter thromboembolism(Throughout the study period, approximately 6 months per patient)
- Incidence of iVVT(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in patients according to tumor laterality(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in patients according to blood type(Throughout the study period, approximately 6 months per patient)
- Incidence of major bleeding (MB) events(Throughout the study period, approximately 6 months per patient)
- Incidence of bleeding events in BRAF/RAS mutated patients(Throughout the study period, approximately 6 months per patient)
- Incidence of bleeding events according to genetic risk(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in BRAF/RAS mutated patients(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in patients according genetic risk scores(Throughout the study period, approximately 6 months per patient)
- Incidence of treatment-related AEs (TRAEs)(Throughout the study period, approximately 2 years)
- Incidence of arterial thromboembolic events (ATE)(Throughout the study period, approximately 6 months per patient)
- Incidence of confirmed VTE events in patients according to progression (PD)(Throughout the study period, approximately 6 months per patient)
- Thrombosis-free survival (TFS)(Throughout the study period, approximately 6 months per patient)
- Mortality rate(Throughout the study period, approximately 2 years)
- Progression-free survival (PFS)(Throughout the study period, approximately 6 months per patient)
- Incidence of relevant adverse events (AE)(Throughout the study period, approximately 2 years)
- Incidence of bleeding events according to tumor laterality(Throughout the study period, approximately 6 months per patient)
- Event-free survival (EFS)(Throughout the study period, approximately 6 months per patient)
- Overall survival (OS)(Throughout the study period, approximately 6 months per patient)
- Quality of life score(Throughout the study period, approximately 6 months per patient)
- Incidence of bleeding events according to antiangiogenic therapy(Throughout the study period, approximately 6 months per patient)
- Incidence of Clinically relevant non-major bleeding (CRNMB)(Throughout the study period, approximately 6 months per patient)
- Incidence of bleeding events according to surgery(Throughout the study period, approximately 6 months per patient)
- Incidence of bleeding events according to anti-EGFR therapy(Throughout the study period, approximately 6 months per patient)