AzTrials
AzTrials

Multiple MyelomaROADMAP-MMNCT03405571

Validation of the 4TS RAM in the Prevention of Venous Thromboembolism in Patients With Plasma Cell Dyscrasias.

An observational study of Multiple Myeloma and Venous Thromboembolism, run by University of Athens at 1 site in Greece.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Patients with newly diagnosed symptomatic multiple myeloma per IMWG criteria prior to therapy initiation are enrolled in the study. The aim of the study is to investigate clinical and disease related risk factors for venous thromboembolism (VTE) in these patients as well as possible biomarkers of hypercoagulability… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Multiple Myeloma, Venous Thromboembolism
How many people
800 participants
Where
1 siteGreece
Study dates
1 Jun 2014to 30 Jun 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: Newly diagnosed, treatment naïve patients with MM recruited from the outpatient Hematology and Oncology Unit of the Clinical Therapeutics Department (Alexandra Hospital, Athens, Greece)

Who may be able to join

  • Newly Diagnosed patients with symptomatic multiple myeloma
  • Previously untreated patients

Who cannot join

  • Age younger than 18 years
  • Life expectancy less than 6 months
  • Ongoing pregnancy, major psychiatric disorders
  • Recent (<6 months) episode of VTE or acute coronary syndrome
  • Active anticoagulant treatment (for any indication)
  • Scheduled open elective curative surgery under general anesthesia for abdominal or pelvic or lung cancer last 3 months
  • Hospitalization due to stroke or acute coronary syndrome or congestive heart failure or acute respiratory failure the last 3 months
  • Eligible patients had not undergone any surgery in the preceding 3 months.

Trial locations and contacts

1 site in 1 country.

Despina Fotiou, MD contact

00306946613774

desfotiou@gmail.com

Greece1 site, 1 recruiting
  • Alexandra Hospital , Department of Clinical Therapeutics

    Athens, Attica, 115 28

    Meletios A Dimopoulos, MD, 0030210 3381540, mdimop@med.uoa.gr

    Maria Gavriatopoulou, MD, 0030210 3381556, mgavriat@med.uoa.gr

    Recruiting

Other trials in Greece

About this study

Official title: A Prospective Validation of the 4TS Risk Assessment Model in the Prevention of Venous Thromboembolism in Patients With Plasma Cell Dyscrasias. ROADMAP-MM

Patients with newly diagnosed symptomatic multiple myeloma per IMWG criteria prior to therapy initiation are enrolled in the study. The aim of the study is to investigate clinical and disease related risk factors for venous thromboembolism (VTE) in these patients as well as possible biomarkers of hypercoagulability linked with the occurrence of venous thromboembolism at diagnosis and during the disease course. The purpose is to create a risk assessment model for VTE in newly diagnosed multiple myeloma patients and make the model more accurate by combining relevant clinical and disease characteristics with biomarkers of cellular and plasma hypercoagulability. A standardized clinical research form is completed for all patients at baseline, 3, 6 and 12 month follow up to include relevant clinical, patient-related, disease-related and treatment related data. Blood sampling also takes place at baseline and 3,6,12 months to assess multiple biomarkers of plasma and cellular hypercoagulability. In addition lowe limb ultrasound is performed at baseline, 6 and 12 months. The primary endpoint is VTE occurrence. Following the elaboration of the ROADMAP-CAT-MM risk assessment model we will prospectively validate it. We expect that patients who are classified, as high risk according to the ROADMAP-CAT-MM will experience symptomatic VTE more frequently and will have higher morbidity and mortality rates during the follow-up. The prospective validation of the ROADMAP-CAT-MM will provide guidance for the use and choice of thromboprophylaxis in these patients and will identify high risk patients eligible for thromboprophylaxis with low molecular weight heparin (tinzaparin).

In addition to symptomatic patients with multiple myeloma the study aims to investigate VTE risk in all plasma cell dyscrasias and will recruit patients with monoclonal gammopathy of undetermined significance, asymptomatic multiple myeloma, primary amyloidosis and Waldenström's macroglobulinemia.

Read the detailed description

Hypothesis: We expect that patients who are classified, as high risk according to the ROADMAP-CAT-MM will experience symptomatic VTE more frequently and will have higher morbidity and mortality rates during the follow-up. The prospective validation of the ROADMAP-CAT-MM (combined or not with biomarkers of hypercoagulability) will allow to identify patients eligible for long-term thromboprophylaxis with intermediate dose of tinzaparin.

Objectives of the study Primary objective: using the ROADMAP-CAT-MM we will identify high risk patients who will be eligible for long-term thromboprophylaxis.

Secondary objective: to identify patients with biological resistance to the fixed dose of postoperative thromboprophylaxis LMWH and to evaluate its clinical relevance.

End-points of the study Primary end-point: the occurrence of symptomatic VTE (DVT and/or PE) and asymptomatic DVT, or superficial venous thrombosis of the lower or upper limb, central vein catheter thrombosis or venous thrombosis of rare localization. Venous thrombosis has to be confirmed with any of the following assays: echo-Doppler, CT or MRI angiography, or scintigraphy or CT scan. Occurrence of asymptomatic venous thrombosis found during routine imaging for staging will also be included in the primary end point. Combined end-point including all the above types of venous thrombosis will also be evaluated.

Secondary end-points: mortality, major bleeding, cancer evolution and morbidity during follow-up.

Study design: The proposed project is a prospective observational event driven study. The cohort of multiple myeloma patients will be composed by pre-specified groups (1)Group MM-ASA : patients with plasma cell dyscrasias on treatment with aspirin (2) Group MM-LMWH: patients with plasma cell dyscrasias on treatment with usual prophylactic doses of tinzaparin (3) Group MM-No: patients with plasma cell dyscrasias not receiving any antithrombotic treatment Inclusion criteria: Patients with diagnosis of active multiple myeloma, asymptomatic multiple myeloma, Patients with MGUS, Patients with amyloidosis, Patients with Waldenström's macroglobulinemia, A detailed data base on clinical profile of the patients (stage, previous treatments, etc) and the presence of VTE risk factors will be constructed.

Procedures Clinical assessment and follow up: Clinical data will be recorded in pre-specified CRF: At the inclusion, at 3, 6 and 12 months patient records will be checked.

Assessment of biomarkers of cellular and plasma hypercoagulability Blood samples: At the routine follow up and according to the established practice of the clinical investigation centers and the standardized institutional practice for laboratory monitoring of the patients, blood samples will be obtained after atraumatic vein puncture according to standardized procedure, in order to assess biomarkers of hypercoagulability. No additional blood samples to those routinely taken, will be required. The tests required for the present study will be performed using the residual blood from that required for routine laboratory tests.

Blood will be collected in 2 Vacutainer tubes (5 ml tubes, containing 0.109 mol/L trisodium citrate - 1 volume trisodium citrate to 9 volumes blood). Antecubital vein puncture will be performed using 21G needles, or blood will be withdrawn from a recently (within 2-3 minutes) placed peripheral venous cathether (20G). Following a double centrifugation at 1500 x g for 20 minutes, platelet-poor plasma (PPP) will be prepared within 30 minutes after vein puncture. Plasma will be stored in -80 degrees. Blood samples will be collected at the baseline visit and after 3, 6, and 12 months.

Laboratory assays Platelet activation markers: Flow cytometry : platelet derived microparticles expressing P-Selectin Blood coagulation assays: Thrombin generation in platelet poor and platelet rich plasma (Thrombinoscope assay), PPL-Clotting time Other tests, Fibrinogen, D-Dimers Systematic compression ultrasound examination of external iliac and lower extremity veins: A systematic compression ultrasound examination will be performed by one operator, unaware of the history and treatment assignments, at the following time-points: baseline, at 6 months, at 1 year/ end of the study and at the event. All compression ultrasound examinations will be digitally recorded for further adjudication if needed. Statistics A power calculation is difficult to make because this study concerns a pilot study. The results of the tests will be compared using the Student t-test or a non-parametric test where appropriate.

Ethical consideration: The study will be conducted according to the principles of the last Declaration of Helsinki and in accordance with the Medical Research Involving Human Subjects Act (WMO) and other regulations, guidelines and acts.

Patients recruitment, benefits and risks: Screening and informed consent will be taken by the investigator or the Clinical Research Assistant (CRA). The investigator will be responsible for blood collection. Plasma samples will be prepared and stored at the investigation center under the responsibility of the Investigator. The CRA will visit the Centers weakly, will collect the CRF and will confirm the good quality of the plasma samples. The CRA will be responsible for the follow up of the patients (the telephone interview and files revision). The CRA will centralize the samples at the Institut on Thrombosis and Haemostasis and will be responsible for the expedition to the Core Lab in Paris.The CRA will construct the combined data base of clinical and laboratory data.

No benefits can be expected for individual patients who participate in this study. However, more information on this subject can help in the identification of patients with the highest risk of venous thrombosis. These patients might in the future benefit from prophylactic anticoagulants. If knowledge on this subject becomes incorporated into patient care, it will be in the same group of patients who participate in the present study. Results from this study, i.e. microparticle activity, will not have an influence on regular patient care, because of its experimental character. Patients can refuse to participate in the study for any reason, without consequences for regular treatment. Also, the investigator can decide to withdraw a subject from the study for medical reasons. Risks are not to be expected, because of the observational character of this study. The burden of the study is low, because it only includes a single blood withdrawal. Each patient has to make his or her own comparative assessment and decide on a voluntary base. The Medical Ethical Committee has given us dispensation from the obligation to provide insurance.

ADMINISTRATIVE ASPECTS: All investigators will have access to the research data in a coded form. Patient data will be coded and the code will be stored and taken care of by the responsible investigator. Patient material will be stored in a coded form.

Being tested
No intervention
Medical subject headings
Multiple Myeloma, Venous Thromboembolism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No interventionOther

    No intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Symptomatic venous thromboembolism

    Symptomatic objectively confirmed venous thromboembolism

    Measured: 12 months

Secondary outcomes (3)
  1. Mortality

    deaths per 1000 persons per year

    Measured: 12 months

  2. Major Bleeding

    major bleeding event

    Measured: 12 months

  3. Disease progression

    Progressive disease based on the international myeloma working group criteria

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jan 2018
  2. Study start1 Jun 2014
  3. Primary completion30 Jun 2020
  4. Study completion30 Jun 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
800 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03405571
Sponsor's protocol ID
ROADMAP-MM
Acronym
ROADMAP-MM
Status last verified
Apr 2021
First submitted
12 Jan 2018
Last updated
28 Apr 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Multiple Myeloma and Venous Thromboembolism, run by University of Athens at 1 site in Greece.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 28 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Greece. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Despina Fotiou, MD (00306946613774, desfotiou@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Symptomatic venous thromboembolism (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Apr 2021.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in