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Progressive Multifocal LeukoencephalopathyMI_PMLNCT06594614

Observational Study on Characteristics and Survival Correlates of Progressive Multifocal Leukoencephalopathy (PML) in Italy

An observational study of Progressive Multifocal Leukoencephalopathy and PML, run by Scientific Institute San Raffaele at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this observational study is to learn about the features of Progressive Multifocal Leukoencephalopathy (PML) at the time of its diagnosis and the factors that may influence the outcome of persons with this disease. Read more about this study

Who is it for?
Any age
How many people
456 participants
Where
1 siteItaly
Study dates
1 Jan 1987to 30 Apr 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients with a diagnosis of PML, achieved by either JCV-DNA identification in the cerebrospinal fluid (CSF) or biopsy/autopsy, or a possible diagnosis based on clinico-radiological data, following revision of magnetic resonance imaging (MRI) exams by a PML expert neuroradiologist

Who may be able to join

  • Definitive PML diagnosis by either JCV-DNA identification in the cerebrospinal fluid (CSF) or biopsy/autopsy, or a possible diagnosis based on clinico-radiological data, following revision of magnetic resonance imaging (MRI) exams by a PML expert neuroradiologist
  • Known year of PML diagnosis
  • Known underlying condition predisposing to PML development

Who cannot join

  • Missing all of the three above-mentioned inclusion criteria

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • San Raffaele Scientific Institute

    Milan, MI, 20127

Other trials in Italy

About this study

Official title: Observational Retrospective Study Describing Demographic, Clinical and Laboratory Characteristics and Survival Correlates of Progressive Multifocal Leukoencephalopathy (PML) in Italy, 1987-2024

The goal of this observational study is to learn about the features of Progressive Multifocal Leukoencephalopathy (PML) at the time of its diagnosis and the factors that may influence the outcome of persons with this disease.

PML is a rare and rapidly progressive disease of the brain, caused by a virus named JC polyomavirus (JCV). This disease almost always occurs in persons with an immune dysfunction. In some people, the underlying immune dysfunction may be the consequence of other conditions, such as certain hematological tumors (for instance, some lymphomas) or the infection with the Human Immune Deficiency Virus (HIV). In other cases it may be associated with other forms of immune deficiency, either present at birth or acquired later in life, or with immunosuppressive or immunomodulant treatments, such as Natalizumab in persons with Multiple Sclerosis.

Read more

Unfortunately, there is no cure for PML, and the only possibility to stop the progression of the disease is to eliminate the cause of the underlying immune dysfunction. This is not always possible, or it may take time, and, therefore, more than half of the persons who developed PML will not survive to the disease.

This study takes advantage of the systematic collection, over a time frame of 37 years, of the characteristics of 456 cases of PML. The main question of this study aims to answer whether and how PML characteristics and outcome have evolved over time and also according to the disease or condition that caused the immune dysfunction leading to PML.

This is important because PML is a rare disease, and, therefore, knowing the context in which it develops can be useful for healthcare providers and families to consider PML as a possible cause of unexpected neurological problems. In fact, an early recognition of PML is associated with a better outcome. On the other hand, there are clinical and laboratory features of PML that can also be associated with different disease outcome. Therefore, it is important that these features are identified, to provide important information for disease management and also for the design of experimental therapeutic interventions.

Participants of this study are persons with a diagnosis of PML who were followed at the Infectious Diseases Unit of San Raffaele Hospital in Milan or referred to the Unit from other Italian clinical centers, between January 1st 1987 and April 30th 2024. We have retrospectively reviewed their clinical charts and collected demographic characteristics, together with the clinical, radiological and laboratory features of PML at the time of its diagnosis. In addition we have also reviewed the evolution of the disease one-year after the date of diagnosis.

The data from the participants have been collected in a custom-made database, which is kept updated with follow-up data and inclusion of new participants. As by April 30th 2024, 456 participants have been included in the database. This is one of the largest existing cohorts and the one with the longest observational window. In addition, and differently from previous cohort studies, it analyzes in detail clinical, radiological, and virological characteristics of PML, providing additional information on their changes over time and possible predictors of disease outcome.

Read the detailed description

This is a retrospective observational study that investigates the features and the correlates of survival of patients with Progressive Multifocal Leukoencephalopathy (PML). The study is based on demographic, clinical and laboratory data stored in an Institutional database

PML is a rare and rapidly progressive demyelinating disease of the central nervous system (CNS), caused by the JC polyomavirus (JCV) that occurs in persons with a primary or acquired immune dysfunction. Common diseases or conditions associated with PML include certain hematological tumors (e.g., some lymphomas), Human Immune Deficiency Virus (HIV) infection, other congenital or acquired forms of immune deficiency, or in people receiving immunosuppressive or immunomodulant treatments, such as Natalizumab in persons with Multiple Sclerosis.

There is no specific effective treatment for PML, and reversion of the underlying immune dysfunction is the only feasible approach to halt disease progression. The overall reported mortality is higher than 50% and most of the persons who survive PML are left with severe neurological sequelae

Being PML a rare disease, knowing the context and the risk factors in which it develops, e.g., specific underlying diseases or treatments and their role in the different time periods, will be key for an early diagnosis of PML, which is usually associated with better outcome. In addition, the identification of variables associated with different disease outcomes will be important in terms of disease management and for the design of experimental therapeutic interventions.

The retrospective assessment of the PML cohort describes and analyzes clinical and laboratory data from 456 PML patients observed in the period 1987-2024. This is one of the largest cohorts and the with the longest observational window ever reported, reflecting an evolving epidemiological context. In addition, differently from previous cohort studies, it analyzes in detail clinical, radiological, and virological variables, providing additional information on the epidemiological changes and determinants of survival.

The cohort includes Italian PML patients who were followed at or referred to the Infectious Diseases Unit of San Raffaele Hospital in Milano, Italy from other Italian clinical centers, between January 1st 1987 and April 30th 2024. Data have been collected in a custom-made database, which is kept updated with follow-up data of cases already included and with inclusion of new cases. We have collected the demographic characteristics and the clinical, radiological and laboratory variables at first observation and at the time of diagnosis and at all the subsequent evaluations until death or up to three years in patients who survive.

More in detail, the following variables have been evaluated for the purpose of this study at the time of PML diagnosis: age, birth sex, year of diagnosis of PML, underlying PML disease, neurological deficits (classified as by presence of motor, cognitive, cerebellar, visual, verbal or cranial nerves problems, headache, seizures or others), presence of contrast enhancement at brain Magnetic Resonance Imaging (MRI), treatment with immunosuppressive or immunomodulant treatments or, in cases with HIV infection, treatment with combination antiretroviral therapy (cART), experimental treatments for PML, JCV-DNA levels in cerebrospinal fluid (CSF) and plasma, with distance in days from the data of diagnosis of PML, CD4 T-cell count.

For assessment of survival we considered either patients' with a date of death or with severe progression at the last observation (i.e., severe deterioration of body functions that would lead to death in a short time span) within the first year from disease onset.

MRI images were qualitatively acquired through either 1.5T or 3T equipments, based on the use of standard protocols that evolved over time. Initial protocols included at least basal axial, sagittal and coronal basal spin echo T1 and proton-density (DP)-T2-weighted sequences, with post-gadolinium T1-weighted sequences. Over time, Fluid Attenuated Inversion Recovery (FLAIR) and Diffusion Weighted Imaging (DWI) sequences were added to most of the protocols. Images were initially acquired on 2D 5 mm-thick sections, and, during most recent periods, by volumetric sequences, such as 3D-FLAIR, which enable standard 5mm-thick section reconstruction.

Quantitative analysis of JCV-DNA in CSF and plasma was performed in the first sample available since the time of diagnosis, by a real-time PCR developed in our laboratory, with a lower detection limit of 100 copies/mL.

Peripheral blood CD4+ T lymphocytes counts were determined by flow cytometry, whereas HIV-RNA was measured in plasma by commercially available assays with a detection limit of 50 copies/mL.

Keywords
Progressive Multifocal Leukoencephalopathy, PML, epidemiology, survival, JCV-DNA, cerebrospinal fluid, JCV, JC virus, JC human polyomavirus, Human polyomavirus 2
Medical subject headings
Leukoencephalopathy, Progressive Multifocal

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06594614
Study groupRoleWhat they receive
Patients with Progressive Multifocal LeukoencephalopathyNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To evaluate the characteristics of PML patients over time and according to the underlying PML condition

    To evaluate the characteristics of PML patients (demographics, clinical, laboratory) over time and according to the underlying PML condition

    Measured: At the time of PML diagnosis

Secondary outcomes (1)
  1. To assess PML patients' survival and associated variables

    To assess PML patients' 1-year survival rates and associated variables

    Measured: One year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Sep 2024
  2. Study start1 Jan 1987
  3. Primary completion30 Apr 2024
  4. Study completion30 Apr 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
456 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06594614
Sponsor's protocol ID
Milano PML cohort
Acronym
MI_PML
Status last verified
Sep 2024
First submitted
10 Sep 2024
Last updated
19 Sep 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Progressive Multifocal Leukoencephalopathy and PML, run by Scientific Institute San Raffaele at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Sep 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To evaluate the characteristics of PML patients over time and according to the underlying PML condition (time frame: At the time of PML diagnosis). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Sep 2024.

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