An International Study on Pediatric Patients With Rare Tumors.
PARTNER
The PARTNER Study - An International Prospective Observational Study on Pediatric Patients With Very Rare Tumors.
1 other identifier
observational
6,250
1 country
1
Brief Summary
The PARTNER study is an international, prospective, observational study of paediatric patients with very rare tumours.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 25, 2025
CompletedFirst Submitted
Initial submission to the registry
April 15, 2025
CompletedFirst Posted
Study publicly available on registry
July 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 6, 2049
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 6, 2049
July 18, 2025
July 1, 2025
24 years
April 15, 2025
July 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Epidemiology
Evaluate the number of patients (aged 0-18 years) with different Very Rare Tumors in the different countries: observed cases will be compared with expected cases.
through study completion, an average of 1 year
Use of International Recommendations
The study aims to measure the number of patients treated for different neoplasms in different countries, and the proportion of those treated in accordance with the International Recommendations.
through study completion, an average of 1 year
Survival of children and adolescents (0-18 years) affected by Very Rare Tumors
The study will correlate the clinical characteristics of the tumor (size, site, extension) with the treatment, the risk of recurrence and survival.
through study completion, an average of 1 year
Eligibility Criteria
Children and adolescents (0-18 years) with a primary or relapsed Very Rare Tumor (VRT)
You may qualify if:
- Children and adolescents (age 0-18 years) with a primary or relapsed Very Rare Tumor diagnosed and/or treated in a participating country/center.
- Written informed consent from the patient and/or the parent/legal guardian
You may not qualify if:
- Absence of Written informed consent from the patient and/or the parent/legal guardian
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Azienda Ospedaliera di Padovalead
- St. Anna Children's Hospital, Viennacollaborator
- Children's Hospital Zagrebcollaborator
- Centre Hospitalier Universitaire de La Réunion, FRANCEcollaborator
- Klinikum Dortmundcollaborator
- University Children's Hospital Tuebingencollaborator
- Hellenic Oncology Research Groupcollaborator
- Fondazione IRCCS Istituto Nazionale dei Tumori, Milanocollaborator
- Kaplan Medical Center, Rehovot, Israelcollaborator
- Vilnius University hospital Santaros klinikos, Vilnius, Lithuaniacollaborator
- University of Skopjecollaborator
- Gdansk Medical University (Poland)collaborator
- Centro Hospitalar do Portocollaborator
- Bucharest Emergency Hospitalcollaborator
- Institute for Oncology and Radiology Serbia, Belgradecollaborator
- University Hospital Bratislavacollaborator
- University Medical Centre Ljubljanacollaborator
- University of Bilbaocollaborator
- Göteborg Universitycollaborator
- University Hospital, Pariscollaborator
Study Sites (1)
Pediatric Oncology Unit, University Hospital Padova [AOUP Azienda Ospedale Università Padova]
Padua, Italy, 35127, Italy
Related Publications (1)
Orbach D, Ferrari A, Schneider DT, Reguerre Y, Godzinski J, Bien E, Stachowicz-Stencel T, Surun A, Almaraz RL, Dragomir M, Jani D, Ami TB, Roganovic J, Brecht IB, Ladenstein R, Bisogno G. The European Paediatric Rare Tumours Network - European Registry (PARTNER) project for very rare tumors in children. Pediatr Blood Cancer. 2021 Jun;68 Suppl 4:e29072. doi: 10.1002/pbc.29072. Epub 2021 Apr 29.
PMID: 33913610BACKGROUND
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gianni Bisogno, MD
Azienda Ospedale Università Padova - Italy
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Paediatrics
Study Record Dates
First Submitted
April 15, 2025
First Posted
July 18, 2025
Study Start
January 25, 2025
Primary Completion (Estimated)
January 6, 2049
Study Completion (Estimated)
June 6, 2049
Last Updated
July 18, 2025
Record last verified: 2025-07