Primary Cardiac Lymphoma: Italian Multicenter Experience

Sponsor
Fondazione Italiana Linfomi ONLUS (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05819528
Collaborator
(none)
43
19
10
2.3
0.2

Study Details

Study Description

Brief Summary

The rationale of this study is to provide an overview on PCL (Primary Cardiac Lymphoma) in Italy, trying to shed light on unknown aspects of the disease and on unanswered questions about its management that could be helpful in clinical practice.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Primary cardiac lymphoma (PCL), an extranodal lymphoma involving only the heart (with possible involvement of the pericardium) is a rare entity, accounting for 2% of primary cardiac tumors and 0.5% of extranodal lymphomas. It is more frequent in males; clinical presentation is predominated by cardiac symptoms. The most common histology is Diffuse Large B Cell Lymphoma (DLBCL). Being DLBCL the most frequent histology, patients are usually treated with R-CHOP (rituximab - cyclophosphamide, doxorubicin, vincristine and prednisone) or R-CHOP-like chemoimmunotherapy regimens, with an historically poor outcome, although in the last years survival rates significantly increased. Due to the rarity of this condition, isolated case reports and a few reviews have been published so far, that in most cases included a population collected in a wide period of time, heterogeneously managed both in terms of treatments received and follow-up, and who often did not strictly respect the criteria of PCL. Indeed, while some aspects of PCL are well-known, especially the ones concerning its clinical presentation, a few topics deserve more in-depth analysis. The rationale of this study is to provide an overview on PCL in Italy, trying to shed light on unknown aspects of the disease and on unanswered questions about its management that could be helpful in clinical practice.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    43 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Primary Cardiac Lymphoma: Italian Multicenter Experience
    Anticipated Study Start Date :
    May 1, 2023
    Anticipated Primary Completion Date :
    Dec 31, 2023
    Anticipated Study Completion Date :
    Feb 29, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    Patients enrolled

    Patients with a diagnosis primary cardiac lymphoma. The study includes patients with PCL diagnosed from 01/01/2000 to 31/12/2020.

    Outcome Measures

    Primary Outcome Measures

    1. Overall survival (OS) [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      Overall survival, the percentage of patients alive of the cohort (patients with cardiac lymphoma diagnosed from 01/01/2000 to 31/12/2020).

    Secondary Outcome Measures

    1. Complete remission (CR) [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      The Complete Remission is defined as the lack of detectable evidence of tumor in the cohort of patients (patients with cardiac lymphoma diagnosed from 01/01/2000 to 31/12/2020).

    2. Overall Response Rate (ORR) [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      The Overall Response Rate is defined as the proportion of patients who have a partial or complete response to therapy (patients with cardiac lymphoma diagnosed from 01/01/2000 to 31/12/2020).

    3. Progression-Fee Survival (PFS) [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      The Progression-Free Survival is the length of time during and after the treatment that patients live with the disease, but it does not get worse (patients with cardiac lymphoma diagnosed from 01/01/2000 to 31/12/2020).

    4. Frequencies of the type of chemo(immuno)therapy and of the number of cycles received as first and second line. [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      The numbers of treatment types and numbers of cycles of therapy received by the cohort of patients (patients with cardiac lymphoma diagnosed from 01/01/2000 to 31/12/2020).

    5. Frequencies of the type of Central Nervous System (CNS) prophylaxis [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      The numbers of treatment prophylaxis types for Central Nervous System administered to the cohort of patients (patients with cardiac lymphoma diagnosed from 01/01/2000 to 31/12/2020).

    6. Cumulative incidence rate of Central Nervous System (CNS) relapse detected during treatment or follow-up. [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      The proportion of patients with disease relapse on Central Nervous System (CNS)

    7. Characteristics of patients [The endpoint will be evaluated within 2 months from the end of data collection. The end of data collection is scheduled within the Q4 (fourth quarter) of 2023.]

      Analysis of the following characteristics: Age, gender, disease localization (atria, ventricles, cardiac arteries and veins, pericardium), HIV positivity, type of symptoms at diagnosis.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Diagnosis of PCL (any histotype) defined as an extranodal lymphoma involving only the heart with possible involvement of the pericardium.

    • Age ≥18 years.

    • HIV positive or negative patients.

    • Diagnosis histologically confirmed. Cytofluorimetry analysis of pericardial fluid showing phenotypic features consistent with a primary cardiac lymphoma is permitted if a biopsy sample is not feasible/available for diagnosis; monoclonality is not accepted as a surrogate for diagnosis.

    • Date of diagnosis: from 1st January 2000 to 31st December 2020.

    • Only patients treated in first-line with chemoimmunotherapy regimens including an anti-CD20 monoclonal antibody are eligible for the study.

    Exclusion Criteria:
    • Secondary cardiac involvement from lymphoma; primary mediastinal lymphoma with pericardial infiltration or other lymphomas with involvement of the pericardium/the heart by contiguity and primary effusion lymphoma are not included in this study.

    • Patients treated with chemotherapy regimens that did not include an anti-CD20 monoclonal antibody as first-line therapy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Presidio ospedaliero "A. TORTORA" - U.O. Onco-ematologia Pagani Salerno Italy 84016
    2 AOU di Sassari - Ematologia Sassari SS Italy 07100
    3 Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI) - SC Ematologia Trieste TS Italy 34121
    4 Ospedale Dell'angelo - U.O. Ematologia Mestre Venezia Italy 30174
    5 Azienda Ospedaliera Papa Giovanni XXIII - Ematologia Bergamo Italy 24127
    6 ASST Spedali Civili di Brescia - Ematologia Brescia Italy 25123
    7 Azienda Ospedaliero-Universitaria di Ferrara - Arcispedale Sant'Anna - Ematologia e fisiopatologia della coagulazione Ferrara Italy 44124
    8 Istituto Scientifico San Raffaele - Unitа Linfomi - Dipartimento Oncoematologia Milano Italy 20132
    9 Fondazione IRCCS Istituto Nazionale dei Tumori di Milano - Ematologia Milano Italy 20133
    10 ASST Grande Ospedale Metropolitano Niguarda - SC Ematologia Milano Italy 20162
    11 Ospedale S. Maria della Misericordia - Ematologia Perugia Italy 06129
    12 P.O. Spirito Santo di Pescara - UOS Dipartimentale - Centro di diagnosi e Terapia dei linfomi Pescara Italy 65124
    13 AOU Pisana - U.O. Ematologia Pisa Italy 56126
    14 Roma - Universitа Cattolica S. Cuore - Ematologia Roma Italy 00168
    15 AO Sant'Andrea - Ematologia Roma Italy 00183
    16 A.O. S. Maria di Terni - S.C. Oncoematologia Terni Italy 05100
    17 A.O.U. Città della Salute e della Scienza di Torino - Ematologia Universitaria Torino Italy 10126
    18 Ospedale Ca Foncello - S.C di Ematologia Treviso Italy 31100
    19 AOU Integrata di Verona - U.O. Ematologia Verona Italy 37134

    Sponsors and Collaborators

    • Fondazione Italiana Linfomi ONLUS

    Investigators

    • Principal Investigator: Elisa Lucchini, MD, Trieste - Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI) - SC Ematologia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fondazione Italiana Linfomi ONLUS
    ClinicalTrials.gov Identifier:
    NCT05819528
    Other Study ID Numbers:
    • FIL_Lympho-Heart
    First Posted:
    Apr 19, 2023
    Last Update Posted:
    Apr 21, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Fondazione Italiana Linfomi ONLUS
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 21, 2023