A "Physician & Patient-powered" Cohort Registry (MY MYELOMA)
Study Details
Study Description
Brief Summary
The aim of this observational study is the creation of a national multiple myeloma registry to monitor the current routine clinical practice in Italy and describe the standard of care adopted for the diagnosis and treatment of patients with multiple myeloma in the different Italian hematology centers.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
In Italy, myeloma accounts for 1.3% of all tumour diagnoses in males and for 1.2% of all tumour diagnoses in women. The incidence is 9.5 new cases per 100,000 males and 8.1 cases per 100,000 females. Median age at diagnosis is 68 years and approximately 2% of patients experience onset before the age of 4011. Therefore is to establish a national disease registry to monitor current routine clinical practice in Italy and to describe the standard of care adopted for the diagnosis and treatment of patients with myeloma. National registries have already been established in some countries and a recently-published meta-analysis highlighted certain differences in treatment, survival and the demographic characteristics of patients. An Italian national registry is important for analysing the current situation, in order to deal with the changes that lie ahead. In addition to the standard epidemiological registry - as described in the statistical methods section - a patientpowered registry (PPR) will also be established to encourage patient participation.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Patients registry Non-interventional, multicentre, retrospective and prospective registry. In order to increase the sample size and the validity of the Registry, patients who were diagnosed with myeloma since 1st January 2019 will also be included retrospectively, once their informed consent has been obtained by the enrolling centre. Being a registry, patients will be enrolled consecutively according to their appointments at the centre, at the discretion of their doctor and only once the patient has signed the informed consent form. Also patients participating in interventional or other observational studies can be enrolled. In case of patients enrolled in interventional trials, only baseline and survival data can be collected for the period in with the patient is in interventional trial. The data will be collected using an electronic data capture (EDC) platform. Hospital visits are planned every 6 months. |
Other: Observation
Not applicable-Observational study
|
Outcome Measures
Primary Outcome Measures
- Overall survival (OS) [3 years]
Time between diagnosis and death.
- Time to next treatment (TTNT) [3 years]
Time to next treatment will be measured from the screening to the date of next anti-myeloma therapy, for each treatment regime.
Secondary Outcome Measures
- Patient reported outcomes (PROs) [3 years]
Periodic completion of the EORTC-QLQ-C30 to evaluate the quality of life of the patients.
- Costs incurred by the patients [3 years]
Evaluation of the costs incurred by the patients related to the therapy based on the different treatments.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patients of both sexes
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Age ≥ 18 years
-
Diagnosis of active/symptomatic multiple myeloma (according to CRAB and biological parameters) no earlier than 1st January 2019
-
Able and willing to sign an informed consent form
Exclusion Criteria:
- None considered
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | AOU Ospedali Riuniti Umberto I | Ancona | Italy | ||
| 2 | Policlinico S. Orsola | Bologna | Italy | ||
| 3 | AOU Policlinico Vittorio Emanuele | Catania | Italy | ||
| 4 | Istituto Nazionale Tumori | Milano | Italy | ||
| 5 | Ospedale Maggiore | Novara | Italy | ||
| 6 | Policlinico Umberto I - Università La Sapienza | Roma | Italy | ||
| 7 | IRCCS Ospedale Casa Sollievo della Sofferenza | San Giovanni Rotondo | Italy | ||
| 8 | A.O. Santa Maria | Terni | Italy | ||
| 9 | AOU Città della Salute e della Scienza di Torino | Torino | Italy | ||
| 10 | Policlinico Universitario di Udine | Udine | Italy |
Sponsors and Collaborators
- Fondazione EMN Italy Onlus
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 535/2020