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
調査の概要
詳細な説明
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).
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 3
連絡先と場所
研究連絡先
- 名前:Paul Rubinstein, MD
- 電話番号:312 413 1300
- メール:paulgr@uic.edu
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Evaluation of Elra consolidation therapy
時間枠: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
時間枠: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
時間枠: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
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Assess event-free survival, progression-free and overall survival of Elra
時間枠: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
時間枠: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
時間枠: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
時間枠:6 months
|
Assess the effects of Elra on CD4 T-cell counts and HIV-1 viral load in people with HIV (PWH).
|
6 months
|
協力者と研究者
協力者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 2025-1210
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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