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AL AmyloidosisProDigALItyNCT06383143

Promoting Diagnosis and Management of AL in Italy (ProDigALIty)

An observational study of AL Amyloidosis and Smoldering Multiple Myeloma, run by Fondazione IRCCS Policlinico San Matteo di Pavia at 4 sites in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The investigators plan to establish a dedicated network of Italian Hematologic Departments interconnected with the Amyloidosis Research and Treatment Center in Pavia to: 1. Implement a biomarker-based screening strategy to promote early diagnosis of AL amyloidosis among at-risk patients, including patients with… Read more about this study

Who is it for?
Ages 18 to 99 years
How many people
760 participants
Where
4 sitesItaly
Study dates
1 May 2023to 1 May 2026
How long will I take part?
2 Years
Phase
Observational

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 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The participating Departments of Hematology will be involved in screening at-risk patients with monoclonal gammopathies and refer suspected/confirmed AL cases to the Amyloidosis Center in Pavia.

Who may be able to join

  • diagnosis of MGUS with altered FLCR or SMM;
  • treatment-naïve;
  • age ≥18 years;
  • ability to understand and willingness to sign an informed consent;
  • planned follow-up at participating center.
  • diagnosis of systemic AL amyloidosis;
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  • treatment-naïve;
  • age ≥18 years;
  • ability to understand and willingness to sign an informed consent;
  • planned follow-up at participating center.

Who cannot join

  • Diagnosis of symptomatic monoclonal gammopathies;
  • Previous treatment for monoclonal gammopathies.
  • PART B
  • non-AL amyloidosis;
  • previous treatment for AL amyloidosis.

Trial locations and contacts

4 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Italy4 sites, 4 recruiting
  • Azienda Ospedaliera Policlinico Consorziale

    Bari

    PELLEGRINO MUSTO, MD, 080 5593471, ematologiacontrapianto@policlinico.ba.it

    PELLEGRINO MUSTO, MD

    Recruiting
  • Azienda Ospedaliero Universitaria Policlinico G.Rodolico - San Marco

    Catania

    Francesco Di Raimondo, MD, 095/378.1956, segremat@unict.it

    Francesco Di Raimondo, MD

    Recruiting
  • Fondazione Irccs Policlinico San Matteo

    Pavia

    GIOVANNI PALLADINI, MD, PhD, +390382502994, segreteria.amiloidosi@smatteo.pv.it

    GIOVANNI PALLADINI, MD, PhD

    Recruiting
  • EMATOLOGIA - Città della Scienza e Salute - Torino

    Torino

    FRANCESCA MARIA GAY, MD, PhD, 011.633.5550 - 5935, ematologia@cittadellasalute.to.it

    FRANCESCA MARIA GAY, MD, PhD

    Recruiting

Other trials in Italy

About this study

The investigators plan to establish a dedicated network of Italian Hematologic Departments interconnected with the Amyloidosis Research and Treatment Center in Pavia to:

  1. Implement a biomarker-based screening strategy to promote early diagnosis of AL amyloidosis among at-risk patients, including patients with monoclonal gammopathy of undetermined significance, MGUS, and altered free light chain ratio (aFLCR), and patients with smoldering multiple myeloma (SMM)
  2. Expedite and facilitate patients' referral and their enrollment in ongoing pre-clinical/clinical studies, also to reflect a broader spectrum of the real-world population of patients with AL amyloidosis in Italy;
  3. Investigate the clinical utility of novel diagnostic technologies, including light chain sequencing and N-glycosylation analysis
Read the detailed description

AL amyloidosis (AL) is a rare, severe protein conformational disease caused by misfolding and extracellular deposition of patients-specific monoclonal immunoglobulin light chains in form of amyloid fibrils. This process can affect virtually any body site and result in potentially fatal organ dysfunction.

In a significant proportion of cases, AL is diagnosed late, when advanced, often irreversible organ involvement limits therapeutic options and greatly limits survival. Thus, efforts at promoting early diagnosis are urgently needed.

The presence of a monoclonal protein (M protein) or an abnormally increased concentration of serum free LCs (FLCs) invariably precedes clinically overt AL amyloidosis by several years. Moreover, about 95% of patients with AL have an altered FLC ratio (FLCR) at diagnosis. Yet, AL is often diagnosed late also in patients with known monoclonal gammopathy under hematological follow-up. Screening of at-risk patients with biomarkers of early amyloid organ involvement has been advocated, but not largely implemented.

Diagnosis and management of AL patients require access to sophisticated technologies and expertise available at large tertiary Amyloid Centers. Yet, new models of patients' care are required to intercept those patients who cannot travel to distant, tertiary centers, in order to provide state-of-the-art care to all and to be able to analyze and describe the natural history of the disease in a contemporary, real-world setting.

New molecular features associated with the propensity of light chains to form amyloid are emerging, but their potential clinical utility is unknown. Building on >30 years-experience of the Italian Referral Center for Systemic Amyloidoses and leveraging on an already existing disease registry and a one-of-a-kind biorepository of clinically annotated biological samples, the study plans to extend and corroborate the activity of the Italian Amyloidosis Network, through the involvement of large Hematology Departments strategically distributed across the Country and the establishment of a structured program of patients' referral and sample/data transfer.

The study will be conducted as follows:

Part A: an active biomarker-based surveillance of pre-symptomatic signs of amyloid organ involvement in at-risk subjects (patients with MGUS and aFLCR and patients with SMM) will be implemented in the participating Italian Hematologic Departments. This will enable the verification of the feasibility of such biomarker-based screening, allow the description of baseline characteristics of at-risk patients, and promote early diagnosis of AL amyloidosis.

Part B: newly diagnosed AL amyloidosis patients (either from Part A or from patients with clinically overt AL amyloidosis evaluated in the frame of routine clinical assessments) will be either referred to the Amyloidosis Research and Treatment Center in Pavia or managed locally, with clinical data prospectively entering a disease registry and diagnostic leftovers from biospecimens stored in a biorepository. This will aim to increase referral and increment inclusion of real-world cases of AL amyloidosis in the disease registry and linked biorepositories, as well as patients' enrollment in other already approved and funded pre-clinical and clinical studies on basic disease mechanisms, as well as new diagnostic/therapeutic approaches in AL amyloidosis.

Part C: exploiting data collected from patients enrolled in both part A and part B, the clinical utility of clonal light chain profiling (including light chain sequencing, evaluation of the N-glycosylation status, and artificial intelligence-based amyloidogenicity prediction) will be assessed.

Being tested
no intervention
Medical subject headings
Immunoglobulin Light-chain Amyloidosis, Smoldering Multiple Myeloma, Monoclonal Gammopathy of Undetermined Significance

What participants receive

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

  • no interventionOther

    no intervention

Study groups in NCT06383143
Study groupRoleWhat they receive
Patients with MGUS and aFLCR and with SMMPart A: Patients with MGUS and aFLCR and patients with SMM undergoing an active, biomarker-based screening of presymptomatic amyloid organ involvement. Part B: Newly diagnosed patients with AL amyloidosis identified through Part A or with clinically overt AL amyloidosis evaluated in the frame of routine clinical assessments and referred to the Amyloidosis Research and Treatment Center in Pavia or managed locally at the participating Italian Hematologic Departments
Receives: Other: no intervention

What is being measured

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

  1. Assess proportion of patients with newly diagnosed AL identified through the biomarker-based screening of at-risk patient

    Part A of the study: the proportion of patients with newly diagnosed AL through the biomarker-based screening of at-risk patients with a known monoclonal gammopathy will be identified.

    Measured: 2 years

  2. Assess the proportion of patients with deep haematological response after frontline therapy (best response evaluation) in the new enhanced, contemporary, real-world series of AL patients enrolled during the study.

    Part B of the study: The proportion of patients with deep hematological response after frontline therapy will be assessed

    Measured: 2 years

  3. 3. Identify associations of clonal light chain features with different clinical features at baseline.

    Part C of the study: Associations of clonal light chain features with different clinical features at baseline, including organ tropism and clonal burden, will be assessed.

    Measured: 2 years

Secondary outcomes (6)
  1. Description of the baseline characteristics and 6-months outcome, as well as the time to AL development for patients with AL identified through the biomarker-based screening

    Part A: the baseline characteristics and 6-months outcome, as well as the time to AL development for patients with AL identified through the biomarker-based screening will be evaluated

    Measured: 6 months

  2. Description of the baseline characteristics of MGUS/SMM patients with abnormal FLCR

    Part A: the baseline characteristics of MGUS/SMM patients with abnormal FLCR will be described

    Measured: 2 years

  3. Identification of clinical and biological correlates of hematological response

    part B: clinical and biological correlates of hematological response will be identified

    Measured: 2 years

  4. To verify whether implementing a dedicated pipeline for referral of AL patients to the National Referral Center will increase the proportion of patients from spoke centers

    Part B: it will be verified if implementing a dedicated pipeline for referral of AL patients to the National Referral Center will increase the proportion of patients from spoke centers

    Measured: 2 years

  5. Identification of associations of clonal light chain features with event-free survival

    Part C: associations of clonal light chain features with event-free survival will be identified.

    Measured: 2 years

  6. Validation of existing algorithms for predicting AL amyloidosis status

    Part C: The diagnostic performance of existing algorithms for predicting clonal light chain amyloidogenicity will be evaluated.

    Measured: 2 years

Timeline

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

  1. First posted25 Apr 2024
  2. Study start1 May 2023
  3. Primary completion1 May 2026 (estimated)
  4. Study completion1 May 2026 (estimated)

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
Case only
Time perspective
Prospective
Enrolment
760 participants (estimated)
Target duration
2 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT06383143
Sponsor's protocol ID
AC-020-IT
Acronym
ProDigALIty
Status last verified
Apr 2026
First submitted
19 Apr 2024
Last updated
16 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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