Spanish-Portuguese Thrombotic Thrombocytopenic Purpura Registry (RE-PTT)

Development Of Spanish-Portuguese Thrombotic Thrombocytopenic Purpura Registry (REPTT): A Study Proposal Of The Spanish Society Of Hematology And Hemotherapy (SEHH) Whit The Portuguese Society Of Hematology (SPH)

REPTT is an observational, prospective, multi-country, multicentre and non-interventional registry in which at least 300 patients with Thrombotic thrombocytopenic purpura (TTP) in Spain and Portugal will be evaluated.

The study will be carried out in the context of the usual clinical practice conditions, not imposing restrictions on the participating physician or influencing their normal clinical practice.

Study Overview

• Status: Recruiting
• Conditions: Purpura, Thrombocytopenic
• Intervention / Treatment: Other: Standard clinical practice

Detailed Description

TTP is a rare life-threatening haematological disease characterised by thrombotic microangiopathy (TMA) with an average annual prevalence of approximately 10 cases/million people worldwide and an annual incidence between 1.5 and 6.0 cases per million according to different studies conducted in France, the United States and in the United Kingdom. In Spain the incidence is 2,67 cases / million population per year.

Acute TTP episodes cause sequelae like vascular disease or kidney damage along with other symptoms more subtle like small neurocognitive deficits and myocardial infarction.

Thus, prompt resolution of acute episodes along with a better understanding of the cardiac abnormalities may allow to prevent further complications, to develop targeted rehabilitation techniques for TTP patients and to improve their quality of life.

This project will collect a big database capable of providing better answers to questions related with treatment efficacy, associated morbidity and mortality, and the possible neurocognitive and cardiac sequelae derived from relapses and acute episodes. Additionally, this project will be linked to obtaining biological samples for a serum and DNA library from patients with TTP.

Patients will be recruited by medical researchers specialized in haematology or by other investigators specialized in thrombotic microangiopathies disease management. This recruitment will be performed in a competitive manner. The collection period will be at least 3 years with the possibility of extending it.

REPTT aims to evaluate new scores and prognostic factors of morbidity and mortality in TTP patients.

The final aim is to establish guidelines and recommendation to improve the global management, diagnosis and treatment of patients with TTP in real-life.

• Study Type: Observational
• Enrollment (Estimated): 300

Contacts and Locations

• Study Contact: Name: Contact person Designated by the Sponsor; Phone Number: +34934344412; Email: investigacion@mfar.net

Study Locations

• Spain
  • Barcelona, Spain, 08036
    • Recruiting
    • Hospital Clinic Barcelona
    • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
    • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net
  • Guadalajara, Spain, 19002
    • Recruiting
    • Hospital Universitario de Guadalajara
    • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
    • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net
  • Madrid, Spain, 28046
    • Recruiting
    • Hospital Universitario La Paz
    • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
    • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net
  • Murcia, Spain, 30120
    • Recruiting
    • Hospital Virgen de la Arrixaca
    • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
    • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net
  • Valencia, Spain, 46010
    • Recruiting
    • Hospital Clinico Universitario de Valencia
    • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
    • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net
  • Andalucia
    • Sevilla, Andalucia, Spain, 41013
      • Recruiting
      • Hospital Universitario Virgen del Rocio
      • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
      • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net
  • Barcelona
    • L'Hospitalet De Llobregat, Barcelona, Spain, 08907
      • Recruiting
      • Hospital Universitario Bellvitge
      • Principal Investigator: A Principal Investigator Designated by the Sponsor, M.D.
      • Contact: A responsible person Designated by the sponsor; Phone Number: 934344412; Email: investigacion@mfar.net

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: N/A

• Sampling Method: Probability Sample

Study Population

Patients diagnosed with Thrombotic thrombocytopenic purpura (TTP)

Description

Inclusion Criteria:

1. Patients with diagnosis of TTP according to International Consensus criteria from centres in Spain and Portugal.
2. Patients that voluntarily sign the informed consent. For subjects unable to provide informed consent, a fully recognized medical authority may be used according to local laws.
3. Patients between 0 to 99 years old at the time of diagnosis.

Note: Decision was taken to treat the patient with an specific treatment prior and independently of patient inclusion in this non interventional study.

Exclusion Criteria:

1. Inability to comply with study procedures and follow-up exams.
2. Patients with any type of alteration that compromises their ability to grant written informed consent.
3. Patients that do not consent to participate in the study and do not sign informed consent.
4. Patients that do not meet the criteria previously mentioned for TTP.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Thrombotic thrombocytopenic purpura patients; Including all patients enrolled in the study	Other: Standard clinical practice; The study will be carried out in the context of the usual clinical practice conditions, not imposing restrictions on the participating physician or influencing their normal clinical practice.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of TTP in Spain/Portugal	Number of patients diagnosed with TTP and enrolled in the registry per year	Throughout the study period, calculated for the 3 years of expected duration.
Morbidity of TTP in Spain/Portugal	Percentage of patients diagnosed with TTP and enrolled in the registry among spanish / portuguese population per year	Throughout the study period, calculated for the 3 years of expected duration.
Mortality of TTP in Spain/Portugal	Percentage of patients diagnosed with TTP and enrolled in the registry per year who died due to the disease	Throughout the study period, calculated for the 3 years of expected duration.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Clinical response to treatment rate	Defined as sustained normalization of platelet counts above the lower limit of the established reference range and of lactate dehydrogenase (LDH) after cessation of plasma exchange. The number of patients that achieved clinical response and their frequency will be reported.	Throughout the study period, approximately 3 years per patient
TTP Clinical remission rate	Defined as a clinical response after cessation of plasma exchange, maintained for > 30 days. The number of patients that achieved clinical remission and their frequency will be reported	Throughout the study period, approximately 3 years per patient
TTP Exacerbation rate	Defined as a reduction in platelet count to below the lower limit of the established reference range, an increased LDH level, and the need to restart plasma exchange within 30 days of the last plasma exchange after a clinical response to plasma exchange. The number of patients with exacerbations and their frequency will be reported	Throughout the study period, approximately 3 years per patient
TTP Relapse rate	Defined as a fall in platelet count to below the lower limit of the established reference range, with or without clinical symptoms, > 30 days after stopping of plasma exchange for an acute TTP episode, requiring reinitiation of therapy. This is usually associated with a new increase in the LDH level. The number of patients with relapse and their frequency will be reported.	Throughout the study period, approximately 3 years per patient
Refractory TTP rate	defined as persistent thrombocytopenia, lack of a sustained platelet count increment or low platelet counts and a persistently raised LDH level despite five plasma exchanges 44 and steroid treatment. The number of patients with refractory TTP and their frequency will be reported.	Throughout the study period, approximately 3 years per patient
Time-to-response (TTR)	Defined as the time from the date of first administration of treatment until the date of clinical response. Patients who die, are lost to follow-up, or reach the time point of analysis without a known record of response will have the TTR censored at the date of death, last assessment or last contact of a follow-up, whichever occurs last. Patients who received a new treatment for TTP whatever the type of treatment before disease response will be censored at the start date of this new treatment. The cumulative incidence of TTR will be estimated by the method of Kaplan-Meier.	Throughout the study period, approximately 3 years per patient
Duration of response (DoR)	DoR will be calculated among those patients that achieve a clinical response from the time that measurement criteria are first met until the date of exacerbation, relapse, appearance of refractory TTP or death by any cause. Patients who are lost to follow-up, or reach the time point of analysis without a known record of TTP recurrence or death will have the DoR censored at the date of last assessment or last contact of a follow-up, whichever occurs last. Patients who received a new treatment for TTP, whatever the type of treatment, will be censored at the start date of this new treatment.	Throughout the study period, approximately 3 years per patient
Relapse-free survival (RFS)	RFS will be calculated from the date of first administration of treatment until the date of TTP relapse or the date of death due to any cause. Patients who are lost to follow-up, or reach the time point of analysis without a known record of relapse or death will have the RFS censored at the date of last assessment or last contact, whichever occurs last. Patients who received a new treatment for TTP, whatever the type of treatment, before disease relapse or death will be censored at the start date of this new treatment. The cumulative incidence of relapse will be estimated by the method of Kaplan-Meier	Throughout the study period, approximately 3 years per patient
Overall survival (OS)	OS will be calculated from the date of the first episode recorded until the date of death due to any cause. Patients who are lost to follow-up or reach the time point of analysis without a known record of death will have the OS censored at the date of last contact. The cumulative incidence of OS will be estimated by the method of Kaplan-Meier.	Throughout the study period, approximately 3 years per patient
Frequency of serious adverse events (SAEs)	Percentage of patients who experience SAEs during the study	Throughout the study period, approximately 3 years per patient
Rate of complications associated with plasma exchange treatment	Percentage of patients who experience complications associated with plasma exchange	Throughout the study period, approximately 3 years per patient
Frequency of complications associated with plasma exchange treatment	Number of complications associated with plasma exchange per TTP event	Throughout the study period, approximately 3 years per patient

Collaborators and Investigators

• Sponsor: Fundación Española de Hematología y Hemoterapía
• Investigators: Study Chair: Dr. María Eva Mingot Castellano, M.D. Ph.D., Hospital Universitario Virgen del Rocío. Sevilla, España.

Study record dates

Study Major Dates

• Study Start (Actual): March 22, 2024
• Primary Completion (Estimated): September 1, 2026
• Study Completion (Estimated): December 1, 2026

Study Registration Dates

• First Submitted: June 13, 2023
• First Submitted That Met QC Criteria: June 13, 2023
• First Posted (Actual): June 22, 2023

Study Record Updates

• Last Update Posted (Actual): May 29, 2024
• Last Update Submitted That Met QC Criteria: May 27, 2024
• Last Verified: May 1, 2024

More Information

Terms related to this study

• Keywords: registry; observational; real-world; Thrombotic thrombocytopenic purpura
• Additional Relevant MeSH Terms: Pathologic Processes; Immune System Diseases; Hematologic Diseases; Hemorrhage; Blood Coagulation Disorders; Skin Manifestations; Thrombocytopenia; Blood Platelet Disorders; Thrombophilia; Thrombotic Microangiopathies; Cytopenia; Purpura; Purpura, Thrombocytopenic; Purpura, Thrombotic Thrombocytopenic
• Other Study ID Numbers: RE-PTT

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED

Drug and device information, study documents

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