- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04934930
Adjustment of Chemotherapy Duration in Follicular Lymphoma According to Minimal Residual Disease Status (FLMRD)
Adjustment of Chemotherapy Duration in Follicular Lymphoma Patients According to Peripheral Blood or Bone Marrow Minimal Residual Disease Status
Follicular lymphoma (FL) is a chronic indolent malignancy, where treatment with 6 cycles of bendamustine obinutuzumab (BO) is highly effective but at a cost of increased adverse events.
Tumor specific DNA can be traced in blood and bone marrow of follicular lymphoma patients even after therapy, and when detected after lymphoma treatment it is referred to as minimal residual disease (MRD).
MRD elimination after effective lymphoma treatment is a marker for deep response and correlates with prolonged remission.
In this study we aim to omit chemotherapy after 4 cycles of treatment in patients achieving MRD elimination after 3 months of therapy, as well as complete metabolic response on positron emission computed tomography (PET-CT), hoping to preserve treatment effectiveness while reducing adverse events.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Follicular lymphoma (FL) is the second most common type of non-Hodgkin's lymphoma, with an estimated incidence of 3.18 cases per 100000 people a year in the United States The disease is characterized by an indolent behavior, where often treatment is unnecessary at diagnosis, and a "watch & wait" approach is the standard of care for asymptomatic patients. FL is also a highly responsive disease for immuno-chemotherapeutic combinations, although most patients will eventually relapse. Since the disease is incurable & indolent in nature, the therapeutic strategy should aim for disease control, while using treatments with high safety profile in order to minimize the chance for life threatening adverse events.
Therapy with rituximab cyclophosphamide, doxorubicin, vincristine & prednisone (R-CHOP) combination & subsequent rituximab maintenance therapy for 24 months shows excellent results with a median progression free survival (PFS) of above a decade.
The more recent GALLIUM trial has shown that combining the monoclonal antibody obinutuzumab with chemotherapy is even more efficacious compared to rituximab combinations. When different combinations were examined in this trial the best results were achieved with the bendamustine-obinutuzumab (BO) combination with 3 year PFS of 84%. Unfortunately the trial also revealed a downside for this effective combination with higher rate of fatal adverse events among patients receiving 6 cycles of bendamustine combinations.
In patients with acute leukemia evaluation for minimal residual disease (MRD) is a routine procedure, and the nature & length of treatment are guided by MRD status at different time points during therapy.
Among FL patients treated with obinutuzumab-chemotherapy combinations, it has been shown that after 3 cycles of treatment about 90% of patients were MRD negative. In addition MRD negativity at the end of induction in either peripheral blood or bone marrow was found to be associated with improved outcomes in patients with 1st line treatment for FL as well as in the relapsed setting.
These findings raise the possibility for an MRD based treatment approach, where the duration of chemotherapy could be guided by MRD status at mid-induction. Eliminating chemotherapy while continuing immunotherapy after achievement of MRD negativity & complete metabolic remission on PET-CT at mid-induction could reduce treatment toxicity, while potentially preserving efficacy.
Tipo di studio
Iscrizione (Anticipato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Uri Abadi, MD
- Numero di telefono: 972-9-7472786
- Email: uri.abadi@clalit.org.il
Luoghi di studio
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Kfar Saba, Israele
- Reclutamento
- Meir Medical Center
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Contatto:
- Uri Abadi, MD
- Numero di telefono: 972-9-7472786
- Email: uri.abadi@clalit.org.il
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Age 18 and above.
- FL grade I-IIIa, according to world health organization (WHO) classification, in patients who were not previously treated with chemotherapy, have a high tumor bulk & an indication for treatment, as defined by the Groupe d'Etude des Lymphomes Folliculaires (GELF) criteria.
- Eastern Cooperative Oncology Group (ECOG) performance status grade 0-2.
- The presence of a molecular marker in bone marrow or peripheral blood for MRD assessment.
Exclusion Criteria:
- FL grade IIIb.
- HIV infection.
- HBsAg positivity.
- Active malignancy other than FL
- Pregnancy or lactation.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Reduced number of bendamustine cycles in patients with mid-induction MRD negativity
Patients with follicular lymphoma treated with obinutuzumab bendamustine & achieving MRD negativity as well as complete metabolic response on PET-CT at mid-induction would continue obinutuzumab treatment while omitting bendamustin after 4 cycles.
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Chemotherapy
Altri nomi:
Immunotherapy
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Progression free survival among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
Lasso di tempo: Progression free survival will be assessed 24 months after the end of induction.
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Progression-free survival is defined as the time from randomization to the earliest event of progression, relapse, or death from any cause.
progression-free survival, is assessed by the investigator.
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Progression free survival will be assessed 24 months after the end of induction.
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Progression of disease within 24 months (POD24)
Lasso di tempo: POD24 will be assessed at 24 months after treatment initiation
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POD24 is defined as disease progression or death due to disease progression occurring within 24 months after treatment initiation, as assessed by the investigator.
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POD24 will be assessed at 24 months after treatment initiation
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Overall survival among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
Lasso di tempo: Overall survival will be assessed 24 months after the end of induction.
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Overall survival is defined as the time from study initiation to death from any cause.
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Overall survival will be assessed 24 months after the end of induction.
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The rate of MRD negativity persistence at 12 months among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
Lasso di tempo: Persistence of MRD negativity will be assessed 12 months after study initiation.
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MRD will be assessed at mid-induction, end of induction and subsequently every 6 months.
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Persistence of MRD negativity will be assessed 12 months after study initiation.
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The proportion of adverse events among patients treated with 4 cycles of BO & 2 additional cycles of obinutuzumab.
Lasso di tempo: The proportion of various adverse events will be assessed until 24 months from the end of induction.
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The proportion of various adverse events will be assessed as documented by the investigator.
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The proportion of various adverse events will be assessed until 24 months from the end of induction.
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Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Uri Abadi, MD, Meir Medical Center
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Anticipato)
Completamento dello studio (Anticipato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Processi patologici
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Neoplasie
- Malattie linfoproliferative
- Malattie linfatiche
- Disturbi immunoproliferativi
- Linfoma non Hodgkin
- Processi neoplastici
- Linfoma
- Linfoma, follicolare
- Neoplasia, Residuo
- Meccanismi molecolari dell'azione farmacologica
- Agenti antineoplastici
- Agenti Antineoplastici, Alchilanti
- Agenti Alchilanti
- Agenti antineoplastici, immunologici
- Bendamustina cloridrato
- Obinutuzumab
Altri numeri di identificazione dello studio
- MMC-19-0209
Piano per i dati dei singoli partecipanti (IPD)
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