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Biological Insights of First Relapsed-refractory Patients With Mantle Cell Lymphoma: the MANTLE-FIRST BIO Study.

Recruiting
Conditions
Mantle Cell Lymphoma
Registration Number
NCT04882475
Lead Sponsor
Fondazione Italiana Linfomi - ETS
Brief Summary

Retrospective observational study with a prospective biological evaluation of an historical cohort of first relapsed-refractory patients with mantle cell lymphoma who were relapsed or refractory to rituximab and chemotherapy containing induction regimens with curative intent.

Detailed Description

Biological samples from 80 Mantle Cell Lymphoma (MCL) patients will be collected and analyzed in 30 Italian sites in 36 months.

Patients will be identified and selected both on a clinical base and according to the availability of Formaline-fixed paraffin-embedded (FFPE) material, frozen material or viable cryopreserved cells at Mantle Cell Lymphoma (MCL) diagnosis. They will be analyzed in 4 subgroups, each with different clinical specificity: 1) refractory to Induction Chemoimmunotherapy (CIT); 2) refractory to Bruton Tyrosine kinase (BTK) inhibitors (BTKi); 3) sensitive to induction Induction Chemoimmunotherapy (CIT); 4) sensitive to BTK inhibitors (BTKi).

Each group will undergo central pathology revision with other immunohistochemical studies (Verona, Dr. Parisi; Milano, Prof. Ponzoni; Vicenza, Dr. D'Amore; Brescia, Prof. Facchetti). Formaline-fixed paraffin-embedded (FFPE) diagnostic specimens of Mantle Cell Lymphoma (MCL) will be screened by immunohistochemistry for the expression of immunoglobulin (Ig) heavy chains to identify Mantle Cell Lymphoma (MCL) cases lacking Immunoglobulin (Ig) expression.

Cytofluorimetric and molecular studies will be performed in the laboratories of the Verona University and at IFOM (Istituto FIRC di Oncologia Molecolare (FIRC = Fondazione Italiana per la Ricerca sul Cancro)). Specific methods will be used: Flow cytometry for the status of surface Ig expression and multiplexed phospho-specific flow cytometry, NGS (Next Generation Sequencing), Immunoglobulin (IgH/IgL V(D)J) profiling by BIOMED2 protocol-based, NGS (Next Generation Sequencing) technology in the relapsed-refractory mantle cell lymphoma (R/R MCL) cases, Chromatin accessibility studies by Assay for Transposase-Accessible Chromatin sequencing (ATAC-seq) (on viable cell suspensions or frozen pellets) and Gene Expression Profiling (GEP) by RNA-sequencing and RNA studies of the MALT1-MYC ((Mucosa-associated lymphoid tissue lymphoma translocation protein 1 - MYC) pathway.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Patients with histologically documented diagnosis of Mantle Cell Lymphoma (MCL) as defined in the 2016 edition of the World Health Organization (WHO) classification, with available tissue for revision and additional studies;
  • Diagnosis of Mantle Cell Lymphoma (MCL) between 1st of January 2008 and 30th of June 2020;
  • Adults, 18-80 years at diagnosis;
  • Relapsed or refractory disease after rituximab and chemotherapy containing induction regimens with curative intent.
  • Treatment at relapse or progression on an intention-to-treat basis (ITT): at least one cycle of Chemo-immunotherapy (CIT), Bruton Tyrosine kinase inhibitors (BTKi), or alternative drugs combination;
  • Subject understanding and voluntarily signing an informed consent form approved by an Independent Ethics Committee (IEC), prior to the initiation of any study-specific procedures.
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Exclusion Criteria
  • Unavailability of the samples requested by the study;
  • Any histology other than Mantle Cell Lymphoma (MCL);
  • Patients treated with front line regimens containing only rituximab or with palliative therapy;
  • Untreated patients; patients undergoing watchful waiting approach.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Histopathological characterization of patients with Mantle Cell Lymphoma (MCL)The endpoint will be evaluated from the beginning to the end of the study (up to 36 months)

Histopathological characterization of patients with mantle cell lymphoma (MCL) who were relapsed or refractory to rituximab and chemotherapy containing induction regimens with curative intent. 80 Mantel Cell Lymphoma (MCL) patients stratified according to Chemo-immunotherapy (CIT) or Bruton Tyrosine kinase inhibitors (BTKi) resistance (20 for each of the groups previously identified) will undergo central pathology revision with assessment of Immunoglobulin (Ig) expression and other histopathological studies.

Secondary Outcome Measures
NameTimeMethod
To correlate results of biologic studies with clinical characteristics of patientsThe endpoint will be evaluated from the beginning to the end of the study (up to 36 months)

About 80 cases of Relapsed/Refractory (R/R) Mantle Cell Lymphoma (MCL) with available tissue samples will be considered for correlation between biological studies with clinical characteristics of patients, response to treatment and conventional outcomes (Progression Free Survival, Progression Free Survival at 2 years, Overall Survival, Overall Survival at 2 years)

Mutational analysis of Mantle Cell Lymphoma (MCL) driver genesThe endpoint will be evaluated from the beginning to the end of the study (up to 36 months)

Performed on formalin-fixed paraffin-embedded (FFPE) tissue sections as well as, when available, on frozen material or viable cryopreserved cells at Mantle Cell Lymphoma (MCL) diagnosis. The aim is to perform a mutational analysis for Mantle Cell Lymphoma (MCL) driver genes: Next Generation Sequencing (NGS) on approximately 80 cases of Mantle Cell Lymphoma (MCL), including 20 cases Relapsed/Refractory (R/R) to Bruton Tyrosine kinase inhibitors (BTKi)

Functional study of the B-Cell Receptor (BCR) activity by flow cytometry in Mantle Cell Lymphoma (MCL) cell samplesThe endpoint will be evaluated from the beginning to the end of the study (up to 36 months)

Performed on formalin-fixed paraffin-embedded (FFPE) tissue sections as well as, when available, on frozen material or viable cryopreserved cells at Mantle Cell Lymphoma (MCL) diagnosis. The aim is to perform a functional study of the B-Cell Receptor (BCR) activity: multiplexed phospho-specific flow cytometry on 10-20 Relapsed/Refractory (R/R) Mantle Cell Lymphoma cases.

Unveil the role of the MALT1-MYC (Mucosa-associated lymphoid tissue lymphoma translocation protein 1 - MYC) pathway in Mantle Cell Lymphoma (MCL) cases expressing or not the BCR (B-Cell Receptor)The endpoint will be evaluated from the beginning to the end of the study (up to 36 months)

Performed on formalin-fixed paraffin-embedded (FFPE) tissue sections as well as, when available, on frozen material or viable cryopreserved cells at Mantle Cell Lymphoma (MCL) diagnosis. The aim is to perform RNA studies on 20 cases

To understand the mechanisms of evasion from B-Cell Receptor (BCR) requirement, with particular focus on Mantle Cell Lymphoma (MCL) cases that are resistant to Chemo-immunotherapy (CIT) and/or Bruton Tyrosine kinase (BTK) inhibitionThe endpoint will be evaluated from the beginning to the end of the study (up to 36 months)

Performed on formalin-fixed paraffin-embedded (FFPE) tissue sections as well as, when available, on frozen material or viable cryopreserved cells at Mantle Cell Lymphoma (MCL) diagnosis. The aim is to understand the mechanisms of evasion from B-Cell Receptor (BCR) requirement as follow:

* Immunoglobulin (IgH/IgL V(D)J) profiling by Next Generation Sequencing (NGS) on 80 mantle cell lymphoma (MCL) cases;

* Chromatin accessibility studies (Assay for Transposase-Accessible Chromatin sequencing, ATAC-seq) on approximately 20 cases among the Immunoglobulin (Ig)-negative identified cases or Bruton Tyrosine kinase inhibitors (BTKi) refractory cases, irrespective of their B-Cell Receptor (BCR) status, and on other 20 cases, from the group of patients sensitive to Bruton Tyrosine kinase inhibitors (BTKi);

* Gene Expression Profiling (GEP) by RNA-seq, on about 20 cases selected on the basis of results of the Assay for Transposase-Accessible Chromatin sequencing (ATAC-Seq) analysis;

Trial Locations

Locations (31)

ASST Grande Ospedale Metropolitano Niguarda

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Milano, MI, Italy

P.O. Spirito Santo di Pescara - UOS Dipartimentale - Centro di diagnosi e Terapia dei linfomi

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Pescara, PE, Italy

AOU Senese - U.O.C. Ematologia

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Siena, SI, Italy

A.O. SS. Antonio e Biagio e Cesare Arrigo, SC Ematologia

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Alessandria, Italy

AOU Ospedali Riuniti - Clinica di Ematologia

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Ancona, Italy

Centro Riferimento Oncologico - S.O.C. Oncologia Medica A

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Aviano, Italy

AOU Policlinico Consorziale - U.O. Ematologia con Trapianto

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Bari, Italy

IRCCS Istituto Tumori Giovanni Paolo II - U.O.C Ematologia

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Bari, Italy

ASST Spedali Civili di Brescia - Ematologia

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Brescia, Italy

Ospedale Vito Fazzi - Ematologia

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Lecce, Italy

Ospedale Guglielmo da Saliceto - U.O.Ematologia

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Piacenza, Italy

Azienda Unitа Sanitaria Locale-IRCCS - Arcispedale Santa Maria Nuova - Ematologia - Ematologia

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Reggio Emilia, Italy

A.O. S. Croce e Carle

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Cuneo, Italy

Azienda Ospedaliera Universitaria Careggi- Unità funzionale di ematologia

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Firenze, Italy

Istituto Scientifico San Raffaele - Unità Linfomi - Dipartimento Oncoematologia

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Milano, Italy

Ospedale Maggiore Policlinico - Fondazione IRCCS Ca Granda - Ematologia

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Milano, Italy

AOU Maggiore della Carità di Novara - SCDU Ematologia

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Novara, Italy

AOU di Padova - Ematologia

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Padova, Italy

IRCCS Policlinico S. Matteo di Pavia - Div. di Ematologia

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Pavia, Italy

Ospedale degli Infermi di Rimini - U.O. di Ematologia

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Rimini, Italy

Policlinico Umberto I - Universitа "La Sapienza" - Istituto Ematologia -Dipartimento di Medicina Traslazionale e di Precisione

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Roma, Italy

Universitа Cattolica S. Cuore - Ematologia

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Roma, Italy

A.O.U. Citta della Salute e della Scienza di Torino - S.C.Ematologia

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Torino, Italy

A.O.U. Citta della Salute e della Scienza di Torino- Ematologia Universitaria

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Torino, Italy

Ospedale S. Chiara - S.S. di Ematologia

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Trento, Italy

Ospedale Ca' Foncello - S.C di Ematologia

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Treviso, Italy

Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI) - SC Ematologia

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Trieste, Italy

Azienda Sanitaria Universitaria Friuli Centrale (ASU FC) - SOC Clinica Ematologica

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Udine, Italy

Ospedale di Circolo - U.O.C Ematologia

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Varese, Italy

AOU Integrata di Verona - U.O. Ematologia

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Verona, Italy

ULSS 8 Berica - Ospedale S. Bortolo - Ematologia

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Vicenza, Italy

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