A ELN-Multicenter Study on Phenotypic Evolution and Clinical Outcomes
Start Date
12/1/2025
Completion Date
7/31/2026
Summary
International multicenter retrospective observational study consisting of two parts: a nested case-control study (part A) and a comparative retrospective cohort study (part B).
Detailed Description
The study will include ET patients (diagnosed according to "International consensus classification of myeloid neoplasms and acute leukemias - 2022" criteria) who are JAK2V617F positive and have progressed to PV (diagnosed according to "International consensus classification of myeloid neoplasms and acute leukemias - 2022" criteria) by 31/12/2020. The date of PV diagnosis will be defined as the index date and this group of patients will be defined as ET-to-PV cases. Part A - Nested case-control study Controls for ET-to-PV cases will be patients diagnosed with ET, according to the "International consensus classification of myeloid neoplasms and acute leukemias - 2022" criteria, JAK2V617F positive who did not progress to PV after a comparable period of time. This control group will be selected using a 1:1 matched case-control design. For each patient who progressed to PV (case), a control will be selected with the following characteristics: * year of ET diagnosis (+/-2 years as compared to the date of the case); * age at ET diagnosis (+/-3 years as compared to the age of the case); * duration of ET disease (+/-2 years as compared to the period between the diagnosis of ET and the index date of the respective case). Part B - Comparative retrospective cohort study Patients diagnosed with de novo PV (no progression from previous ET) according to the "International consensus classification of myeloid neoplasms and acute leukemias - 2022" data criteria, will be recruited using a 1:1 matching procedure according to the following characteristics: * year of PV diagnosis (+/-2 years as compared to the date of the case); * age at PV diagnosis (+/-3 years as compared to the age of the case); * duration of PV disease (+/-2 years as compared to the period between PV diagnosis and the last follow-up of the respective case). Furthermore, to have at least 5 years of follow-up, de novo PV patients must be diagnosed no later than 2020.
Eligibility Criteria
Age Range: 18 years to 100 years
Conditions
Locations
Mayo Clinic
Rochester, Minnesota 55905-0001
United States
University Hospital Halle
Halle,
Germany
Hannover Medical School
Hanover,
Germany
University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care Johannes Wesling Medical Center
Minden,
Germany
Divisione Ematologia, Fondazione IRCCS Policlinico San Matteo
Pavia, Lombardy 27100
Italy
Divisione Ematologia, Ospedale San Bortolo
Vicenza, Veneto
Italy
A.S.O. SS. Antonio e Biagio e C.Arrigo, SC Ematologia
Alessandria, 15121
Italy
ASST Papa Giovanni XXIII, SC Ematologia
Bergamo,
Italy
ASST-Spedali Civili
Brescia, 25123
Italy
Ospedale Businco
Cagliari,
Italy
AOU Policlinico Vittorio Emanuele - PO Gaspare Rodolico
Catania,
Italy
AOU Careggi, Divisione di Ematologia
Florence,
Italy
ASST Grande Ospedale Metropolitano Niguarda, Divisione di Ematologia
Milan,
Italy
Fondazione IRCCS Cà Grande - Op. Maggiore Policlinico
Milan,
Italy
Ospedale San Raffaele
Milan,
Italy
ASST MONZA Ospedale San Gerardo Clinica Ematologica
Monza, 20900
Italy
Azienda Ospedaliera Universitaria Federico II di Napoli Divisione di Ematologia e Trapianti del Midollo
Naples, 80131
Italy
Azienda Ospedaliero Universitaria Maggiore della Carità di Novara SCDU Ematologia
Novara, 28100
Italy
Presidio Ospedaliero di Pescara
Pescara,
Italy
Fondazione Policlinico Universitario Gemelli
Roma,
Italy
Umberto I Policlinico
Roma,
Italy
Azienda Ospedaliera Universitaria Integrata - Ospedale Borgo Roma, Unità di Ematologia
Verona,
Italy
IDIBAPS, Hospital clinic
Barcelona,
Spain
12 Octubre University Hospital
Madrid,
Spain
Guy's and St. Thomas' NHS Foundation Trust
London,
United Kingdom