Improvement of Immunologic and Molecular Techniques for the Diagnosis and Follow-up of Patients With Thrombotic Thrombocytopenic Purpura

Improvement of Immunologic and Molecular Techniques for the Diagnosis and Follow-up of Patients With Thrombotic Thrombocytopenic Purpura: a Collaborative Study Proposal of the Spanish Apheresis Group (GEA) in Collaboration With the Spanish Foundation of Hematology and Hemotherapy (FEHH)

The lack of ADAMTS13 is the only biological marker that is specific for aTTP diagnosis8 and the assessment of ADAMTS13 is of clinical importance because it is essential for the rapid differential diagnosis between aTTP and other TMA. Furthermore, monitoring of ADAMTS13 activity is useful to ensure biological remission (ADAMTS13 levels > 10%) as well as predicting relapses.

Due to the high mortality rate of aTTP, treatment should be started as soon as the disease is suspected, sometimes even before confirmation with the ADAMTS13 test results. This situation may lead to misdiagnose some patients and leave them without the appropriate treatment. In conclusion, ADAMTS13 activity assay is crucial for an early diagnosis and optimal management of acute aTTP and any delay in ADAMTS13 results will have a negative impact on the diagnosis, treatment and prognosis of the patient.

There are currently 2 techniques available for the ADAMTS13 activity determination, the fluorescence resonance energy transfer (FRET) and the Technozym chromogenic enzyme-linked immunosorbent assay (ELISA). Both are considered reference methods but they require considerable skill because they are highly manual and this increases the risk of error. Furthermore, these methods are time-consuming, not widely available and, in case of the ELISA method, it requires a new calibration at each run. The inter-laboratory variability is also a challenge and therefore a validation and/or interpretation method could be needed.

Recently, a new and first fully automated HemosIL AcuStar ADAMTS13 Activity assay (Instrumentation Laboratory, Bedford, Massachusetts, United States) has been developed. HemosIL AcuStar ADAMTS13 Activity assay is a two steps chemiluminescent immunoassay (CLIA) with an analytical time of 33 minutes for the quantitative measurement of ADAMTS13 activity in human-citrated plasma on the ACL AcuStar analyser. The immunoassay uses the GST-VWF73 substrate in combination with magnetic particles for rapid separation and chemiluminescence technology detection. The ADAMTS13 present in the plasma sample cleavages the GST-VWF73 substrate and the detection of the generated fragments is based upon an isoluminol-labelled monoclonal antibody that specifically reacts with the cleaved peptide. The emitted light is proportional to the ADAMTS13 activity in the sample.

This new ADAMTS13 assay method has been compared with the other two available techniques in two different studies. First, Favresse et al. published the results of the comparison between Technozym activity ELISA assay and the new HemosIL AcuStar chemiluminescent assay. On the other hand, Valsecchi et al. have recently published the results of validation of this new technique in comparison with ELISA and FRETS in 176 samples. Both studies conclude that the new chemiluminescent ADAMTS13 activity assay showed a good correlation and excellent clinical performance for the diagnosis of severe ADAMTS13 deficiency with the FRETS-VWF73 assay and a commercial ELISA when considering only ADAMTS13 activity values below 10% (the internationally accepted cut-off for a diagnosis of severe ADAMTS13 deficiency typical of aTTP). Finally, Stratmann et al. have just published another study comparing the HemosIL AcuStar chemiluminescent assay with two commercially available ADAMTS13 assay kits using 24 paired test samples derived from 10 consecutively recruited patients13 and their results corroborate the previously published data suggesting that the AcuStar assay could be a valuable and accurate tool for ADAMTS13 activity testing and aTTP diagnostic.

In this context, a unique opportunity to validate this new technique is generated, both retrospectively with our already available data from frozen samples and also in the context of a large prospective study. This will be the first study worldwide testing HemosIL AcuStar method in real clinical practice aTTP population (Spanish and Portuguese aTTP populations) with the aim to standardize the diagnosis and follow-up methodology for the disease.

Study Overview

• Status: Recruiting
• Conditions: Acquired Thrombotic Thrombocytopenic Purpura
• Intervention / Treatment: Device: ADAMTS13 Activity Assays

• Study Type: Observational
• Enrollment (Estimated): 500

Contacts and Locations

• Study Contact: Name: Cristina Pascual, MD; Phone Number: +34 91 586 8445; Email: cpascuali@salud.madrid.org
• Study Contact Backup: Name: Jorge Martínez, PhD; Email: adamts13hcsc@gmail.com

Study Locations

• Portugal
  • Coimbra, Portugal, 3004-561
    • Recruiting
    • Centro Hospitalar e Universitário de Coimbra
    • Contact: Teresa Fidalgo, MD
• Spain
  • A Coruña, Spain, 15006
    • Recruiting
    • Complejo Hospitalario Universitario A Coruña
    • Contact: Marta Fernandez Docampo, MD
  • Barcelona, Spain
    • Recruiting
    • Hospital Clínic de Barcelona
    • Contact: Maribel Diaz Ricart
  • Madrid, Spain
    • Recruiting
    • Hospital Gregorio Marañon
    • Contact: Cristina Pascual
  • Madrid, Spain
    • Recruiting
    • Hospital Clinico San Carlos
    • Contact: Jorge Martinez
  • Valencia, Spain
    • Recruiting
    • Hospital La Fe de Valencia
    • Contact: Ines Gomez Segui

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 1 second to 99 years (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

The study population will be all consecutive patients who meet the following inclusion criteria and none of the following exclusion criteria until reaching the number of patients determined for the study.

Description

Inclusion Criteria:

• Patients with confirmed thrombotic microangiopathy (TMA) based on citrated blood samples meeting both of the following criteria:

  • Thrombocytopenia [drop in platelet count ≥50% or platelet count < 100x109/L and
  • Microangiopathic haemolytic anaemia (elevation of lactate dehydrogenase (LDH) >2- fold or by presence or increase of schistocytes in peripheral blood smear)
• Patients that voluntarily sign informed consent. For subjects unable to provide consent, a fully recognized medical proxy may be used according to local laws.
• Patients between 0 to 99 years old at the time of screening.

Exclusion Criteria:

-

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At diagnosis of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At follow up (10 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At follow up (30 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At follow up (60 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At follow up (90 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At follow up (180 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Correlation of a new diagnostic test and standard test	Correlation of a new diagnostic test, HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS in the measurement of activity and antibody of ADAMTS13 in IU/mL	At follow up (365 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients at diagnosis based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At diagnosis of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (10 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (30 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (60 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (90 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (180 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Concordance of classification of aTTP	To evaluate the concordance of classification of aTTP patients based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (365 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At diagnosis of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (10 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (30 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (60 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (90 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (180 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Sensitivity and specificity of classification of aTTP	To evaluate the sensitivity and specificity of classification of aTTP patients visits based on HemosIL AcuStar chemiluminescent assay, in comparison with ELISA and/or FRETS.	At follow up (365 days) of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At diagnosis of patients with acquired thrombotic thrombocytopenic purpura (aTTP).
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At follow up (10 days)
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At follow up (30 days)
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At follow up (60 days)
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At follow up (90 days)
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At follow up (180 days)
Clinical characteristics	Describe clinical characteristics of patients with TMA at the diagnosis and those with aTTP at the diagnosis and follow up based on ADAMTS13 cut-off < 10%.	At follow up (365 days)

Collaborators and Investigators

• Sponsor: Fundación Española de Hematología y Hemoterapía

Study record dates

Study Major Dates

• Study Start (Actual): October 13, 2022
• Primary Completion (Estimated): October 30, 2024
• Study Completion (Estimated): June 30, 2025

Study Registration Dates

• First Submitted: September 8, 2021
• First Submitted That Met QC Criteria: September 8, 2021
• First Posted (Actual): September 16, 2021

Study Record Updates

• Last Update Posted (Estimated): December 20, 2023
• Last Update Submitted That Met QC Criteria: December 19, 2023
• Last Verified: November 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Immune System Diseases; Hematologic Diseases; Hemorrhage; Blood Coagulation Disorders; Skin Manifestations; Thrombocytopenia; Blood Platelet Disorders; Thrombophilia; Thrombotic Microangiopathies; Purpura; Purpura, Thrombocytopenic; Purpura, Thrombotic Thrombocytopenic
• Other Study ID Numbers: INSPIRER

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No