- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07647432
HEME-25: Open-Label Feasibility Study of Elranatamab Utilized in Newly Diagnosed Plasmablastic Lymphoma With or Without HIV (HEME-25)
HEME-25: Open-Label Feasibility Study of Elranatamab Utilized in Newly Diagnosed Plasmablastic Lymphoma With or Without HIV in Consolidation After Definitive Therapy
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Patients will receive Elra subcutaneously for up to six 28-day cycles, beginning with a step-up dosing schedule (12 mg on day 1, 32 mg on day 4, followed by 76 mg weekly on days 8, 15, and 22 of Cycle 1). Patients will transition to 76 mg every 2 weeks (days 1 and 15) during Cycles 2 and 3, followed by an interim PET/CT assessment at the end of Cycle 3. During cycles 4 through 6, all patients will receive 76 mg every 4 weeks (on day 1 of each cycle).
Participants will undergo disease assessment with PET/CT at the end of Cycle 3, post-end of treatment (EOT) visit, and every 6 months thereafter (±2 weeks) for up to 2 years to assess recurrence and survival. Routine clinical follow-up will continue every 3 months, as per the standard of care (SOC).
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
- Fase 3
Kontakter og lokationer
Studiekontakt
- Navn: Paul Rubinstein, MD
- Telefonnummer: 312 413 1300
- E-mail: paulgr@uic.edu
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Age ≥ 18 years at time of consent
- ECOG performance status (PS) 0 or 1
- Histologically and immunophenotypically confirmed PBL
- Ann Arbor stage at initial diagnosis: stage I with lactate dehydrogenase (LDH) > upper limit of normal (ULN) and/or bulky disease >7.5 cm or stage II-IV
- Received definitive front-line therapy for PBL with end-of-treatment PR or CR
Adequate bone marrow function with recovery from prior therapy, defined as:
- ANC ≥ 500 cells/mcL
- Platelet count ≥ 50,000 cells/mcL
- Availability of archival tumor tissue (block or unstained slides) for mandatory central pathology review and correlative BCMA testing. Central pathology review and BCMA testing may be completed after enrollment.
- Able to provide written informed consent and HIPAA authorization for release of personal health information, via an approved UIC Institutional Review Board (IRB) informed consent form and HIPAA authorization. If a subject is unable to consent, a LAR may provide consent on their behalf.
- As determined at the discretion of the enrolling physician or protocol designee, the ability of the subject to understand and comply with study procedures for the entire length of the study
- If capable of becoming pregnant: Negative serum or urine pregnancy test
If HIV-positive:
- Receiving effective combined antiretroviral therapy
- CD4+ T-cell count ≥ 50 cells/mcL within 4 weeks before enrollment
Exclusion Criteria:
Key inclusion criteria:
- Age ≥ 18 years at time of consent
- ECOG performance status (PS) 0 or 1
- Histologically and immunophenotypically confirmed PBL
- Ann Arbor stage at initial diagnosis: stage I with lactate dehydrogenase (LDH) > upper limit of normal (ULN) and/or bulky disease >7.5 cm or stage II-IV
- Received definitive front-line therapy for PBL with end-of-treatment PR or CR
Adequate bone marrow function with recovery from prior therapy, defined as:
- ANC ≥ 500 cells/mcL
- Platelet count ≥ 50,000 cells/mcL
- Availability of archival tumor tissue (block or unstained slides) for mandatory central pathology review and correlative BCMA testing. Central pathology review and BCMA testing may be completed after enrollment.
- Able to provide written informed consent and HIPAA authorization for release of personal health information, via an approved UIC Institutional Review Board (IRB) informed consent form and HIPAA authorization. If a subject is unable to consent, a LAR may provide consent on their behalf.
- As determined at the discretion of the enrolling physician or protocol designee, the ability of the subject to understand and comply with study procedures for the entire length of the study
- If capable of becoming pregnant: Negative serum or urine pregnancy test
If HIV-positive:
- Receiving effective combined antiretroviral therapy
- CD4+ T-cell count ≥ 50 cells/mcL within 4 weeks before enrollment
Key exclusion criteria:
- Prior BCMA bispecific therapy
- Stable or progressive disease following front-line therapy as determined by the investigator
- Receiving any other investigational agents
- Expected survival < 2 months
- Known or suspected PBL involvement of the parenchymal brain or spinal cord at diagnosis. Asymptomatic leptomeningeal disease only will be allowed.
- Uncontrolled intercurrent illness, including but not limited to uncontrolled infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Concurrent malignancy requiring active therapy within the last 3 years, except for the following:
- Basal cell carcinoma limited to the skin
- Squamous cell carcinoma limited to the skin
- Carcinoma in situ of the cervix or breast
- Adequately treated lentigo malignant melanoma
- Localized prostate cancer
- Active therapy consists of adjuvant or maintenance therapy to reduce the risk of recurrence of a malignancy that was previously treated with curative intent and with no evidence of active disease within 2 years prior to screening
- Pregnant or nursing
- PWH with a history of AIDS-defining opportunistic infection within the past year
- Receipt of a live vaccine within 28 days prior to the first dose of study treatment
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Single-arm Open label study of Elra of pts with PBL
Patients will receive Elra subcutaneously for up to six 28-day cycles, beginning with a step-up dosing schedule (12 mg on day 1, 32 mg on day 4, followed by 76 mg weekly on days 8, 15, and 22 of Cycle 1).
Patients will transition to 76 mg every 2 weeks (days 1 and 15) during Cycles 2 and 3, followed by an interim PET/CT assessment at the end of Cycle 3.
During Cycles 4 through 6, all patients will receive 76 mg every 4 weeks (on day 1 of each cycle).
|
Elra will be administered subcutaneously on day 1, day 4, then weekly on day 8, 15 and day 22 completing 1 cycle.
Up to 6 cycles may be given.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Evaluation of Elra consolidation therapy
Tidsramme: 12 weeks ( 3 cycles)
|
Evaluation of completion of (Elra) consolidation following definitive therapy in patients with PBL, defined as the proportion of patients completing at least 3 cycles
|
12 weeks ( 3 cycles)
|
|
Estimate the complete response in HIV+/ HIV- patients
Tidsramme: 6 months
|
Estimate the complete response (CR) rate (per 2014 LUGANO criteria)Ref . in HIV-positive and HIV-negative patients after 6 months of consolidation.
|
6 months
|
|
Evaluate the safety and tolerability of Elra consolidation
Tidsramme: 6 months
|
To evaluate the safety and tolerability of Elra consolidation, including the incidence, severity, and management of cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), assessed by ASTCT consensus criteria.
|
6 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Assess event-free survival, progression-free and overall survival of Elra
Tidsramme: 1 year and 2 year
|
Assess event-free survival (EFS), progression-free survival (PFS), and overall survival (OS) at 1- and 2-year post-completion of Elra consolidation
|
1 year and 2 year
|
|
Estimate the conversion rate
Tidsramme: Cycle 3 and cycle 6 (12 weeks and 24 weeks)
|
Estimate the conversion rate from pre-consolidation partial response (PR) to CR at the end of Cycle 3 and Cycle 6.
|
Cycle 3 and cycle 6 (12 weeks and 24 weeks)
|
|
Evaluate quality of life (QoL) outcomes as measured by changes from baseline
Tidsramme: 6 months
|
Evaluate quality of life (QoL) outcomes as measured by changes from baseline in European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 (QLQ-C30) and the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - High-Grade Non-Hodgkin Lymphoma 29 items (EORTC QLQ-NHL-HG29) scores.
|
6 months
|
|
Assess the effects of Elra on CD4 T-cell counts
Tidsramme: 6 months
|
Assess the effects of Elra on CD4 T-cell counts and HIV-1 viral load in people with HIV (PWH).
|
6 months
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Blodbårne infektioner
- Urogenitale sygdomme
- Genitale sygdomme
- Neoplasmer
- Sygdomme i immunsystemet
- Infektioner
- RNA-virusinfektioner
- Virussygdomme
- Neoplasmer efter histologisk type
- Overførbare sygdomme
- Seksuelt overførte sygdomme, virale
- Seksuelt overførte sygdomme
- Lentivirus infektioner
- Retroviridae infektioner
- Immunologiske mangelsyndromer
- Lymfesygdomme
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Lymfom, Non-Hodgkin
- Langsomme virussygdomme
- Lymfom, B-celle
- Lymfom
- HIV-infektioner
- Lymfom, stor B-celle, diffus
- Hemiske og lymfatiske sygdomme
- Plasmablastisk lymfom
- Erhvervet immundefektsyndrom
Andre undersøgelses-id-numre
- 2025-1210
Plan for individuelle deltagerdata (IPD)
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