Investigating cancer incidence in Parkinson's patients with a specific gene mutation
Official title: Study on the Incidence of Malignant Neoplasms in Patients With Parkinson's Disease and Heterozygous Mutation of the GBA Gene
Run by Azienda USL Reggio Emilia - IRCCS · NCT06814431 · Data updated 2026-11-12
This study looks at whether people with Parkinson's disease who have a specific gene mutation are more likely to develop cancer compared to those without the mutation and the general population.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 3000 (estimated) |
| Sponsor | Azienda USL Reggio Emilia - IRCCS Government |
| Locations | 4 sites (Brindisi and 3 other locations) |
| Status | Recruiting |
| Started | November 23, 2023 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | July 24, 2026 |
| Trial ID | NCT06814431 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults over 18 years old diagnosed with Parkinson's disease, particularly those with GBA1 mutations.
✕Probably not a fit
Patients with uncertain diagnoses of Parkinson's disease may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This multicenter retrospective observational study examines the incidence of malignant neoplasms in patients with Parkinson's disease (PD) who carry heterozygous mutations in the GBA1 gene. It compares these patients to those with idiopathic PD and the general population using data from local cancer registries. The study aims to determine if there is a higher incidence of cancer among GBA1 mutation carriers and to characterize the types of cancers present. Approximately 3000 PD patients will be included, with a focus on understanding the relationship between genetic factors and cancer risk.
Why it matters
Potential benefit: If successful, this study could provide insights into the cancer risks associated with genetic mutations in Parkinson's disease, potentially leading to improved monitoring and treatment strategies.
How similar studies have gone: While there is growing evidence of increased cancer risk in patients with Gaucher disease, this specific investigation into GBA1 mutations in Parkinson's disease is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * \>18 years * Diagnosis of Parkinson's Disease through the United Kingdom Parkinson's Disease Society Brain Bank Diagnostic Criteria for Parkinson's Disease. Exclusion Criteria: * Uncertain diagnosis
Where it's running
-
Ospedale A. Perrino
Brindisi, Italy Recruiting -
IRCCS Istituto Neurologico Carlo Besta
Milan, Italy Recruiting -
Azienda USL IRCCS di Reggio Emilia
Reggio Emilia, Italy Recruiting -
Ospedale Santa Chiara di Trento
Trento, Italy Recruiting
Study contacts
- Study coordinator: Giulia Di Rauso, MD
- Email: giulia.dirauso@ausl.re.it
- Phone: +39 0522 296494
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.