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
研究概览
详细说明
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).
研究类型
注册 (估计的)
阶段
- 阶段2
- 第三阶段
联系人和位置
学习联系方式
- 姓名:Paul Rubinstein, MD
- 电话号码:312 413 1300
- 邮箱:paulgr@uic.edu
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
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
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的: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.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Evaluation of Elra consolidation therapy
大体时间: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
大体时间: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
大体时间: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
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Assess event-free survival, progression-free and overall survival of Elra
大体时间: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
大体时间: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
大体时间: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
大体时间:6 months
|
Assess the effects of Elra on CD4 T-cell counts and HIV-1 viral load in people with HIV (PWH).
|
6 months
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 2025-1210
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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