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Prognostic Study of Markers of Angiogenesis and Coagulability in Patients With Monoclonal Gammopathy

Prognostic Study of Markers of Angiogenesis and Coagulability in Patients With Monoclonal Gammopathy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01543100
Acronym
PACMoG
Enrollment
60
Registered
2012-03-02
Start date
2010-11-30
Completion date
2014-01-31
Last updated
2014-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Monoclonal Gammopathy, Monoclonal Gammopathy of Undetermined Signification, Myeloma

Keywords

MGUS

Brief summary

Blood circulating endothelial cells (CEC) and microparticles (MPs) are described in the literature to be associated with vascular failures and dysfunction that reflect neo-angiogenesis and risk of thrombosis, respectively. There a few number of CEC in healthy patients although they significantly increase in several cancers including myeloma. However, no study explored to date a correlation of CEC and/or circulating endothelial progenitors (CEP) and MPs with the tumoral growth of monoclonal gammopathy. On the other hand, there is no study measuring the CEC and CEP directly in the bone marrow. The investigators aim is to evaluate these 2 original features in patients with monoclonal gammopathy: monoclonal gammopathy of undetermined signification (MGUS) and myeloma. This is a preliminary multicentric study.

Detailed description

Principal objective : Research of a correlation of blood CEC and MPs with the tumoral volume and the clinico-biological staging of monoclonal gammopathies. Secondary objectives : Research of a correlation of bone marrow endothelial cells and MPs, both measured by flow cytometry, with the tumoral volume and the clinico-biological staging of monoclonal gammopathies. Principal analyses : Blood levels of CEC and its progenitors, soluble parameters of angiogenesis and of coagulability, and microparticles versus classical indicators of tumoral growth of monoclonal gammopathies (beta2-microglobulin and Ig peak). Secondary analyses : Bone marrow levels of endothelial cells and its progenitors, soluble parameters of angiogenesis and of coagulability, and microparticles versus classical indicators of tumoral growth of monoclonal gammopathies (beta2-microglobulin and Ig peak). Methodology : PACMoG is an interventional, prospective and multicentric pilot study. Biologic parameters will be determined at the diagnosis of monoclonal gammopathy. Results will be compared to the monoclonal gammopathy international staging and the clinical follow-up. Procedures : Specific tests of the study will be realized from : * Blood samples: 2 EDTA tubes and 1 tube without anticoagulant per included patient. * Bone marrow: 3 ml collected during of myelogram punction made for the diagnosis. In all cases, no additional sampling will be performed. Specific analyses : \- Specific biological assays in blood and bone marrow will be: * Endothelial and progenitor cells levels * Number and cellular origin of MPSs * Levels of phospholipid-dependant coagulability * Soluble parameters of angiogenesis (VEGF, soluble CD146, endostatin) * Soluble parameters of coagulability (Levels of thrombomodulin, tissue factor and D-Dimer)

Interventions

OTHERblood and bone marrow samples

Specific tests of the study will be realized from : * Blood samples: 2 EDTA tubes and 1 tube without anticoagulant per included patient. * Bone marrow: 3 ml collected during of myelogram punction made for the diagnosis. In all cases, no additional sampling will be performed.

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with monoclonal gammopathy either MGUS or myeloma at diagnosis or more than 3 months after a first myeloma treatment with chemotherapy and/or antiangiogenic drugs. * Patient's age ≥ 18 years old, * Patients having signed the specific consent of the study.

Exclusion criteria

* Treatment with chemotherapy and/or antiangiogenic drugs at the inclusion * Age \< 18 years old * No specific consent of the study

Design outcomes

Primary

MeasureTime frameDescription
Blood levels of CEC and its progenitorsDay 1Blood levels of CEC and its progenitors
Blood levels of soluble parameters of angiogenesis and of coagulabilityDay 1Blood levels of soluble parameters of angiogenesis and of coagulability
Blood levels of microparticles versus classical indicators of tumoral growth of monoclonal gammopathies (beta2-microglobulin and Ig peak).Day 1Blood levels of microparticles versus classical indicators of tumoral growth of monoclonal gammopathies (beta2-microglobulin and Ig peak).

Secondary

MeasureTime frameDescription
Bone marrow levels of endothelial cells and its progenitorsDay 1Bone marrow levels of endothelial cells and its progenitors
Bone Marrow levels of soluble parameters of angiogenesis and of coagulabilityDay 1Bone Marrow levels of soluble parameters of angiogenesis and of coagulability
Bone Marrow levels of microparticles versus classical indicators of tumoral growth of monoclonal gamopathies (beta2-mcicroglobulin and Ig peak).Day 1Bone Marrow levels of microparticles versus classical indicators of tumoral growth of monoclonal gamopathies (beta2-mcicroglobulin and Ig peak).

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026