Metabolically Fit CD19 CAR T Cells With CD34 Selection Markers in Adults With CD19-Positive B-Cell Acute Lymphocytic Leukemia
A Phase 1B Safety and Feasibility Study of Metabolically Fit CD19 Chimeric Antigen Receptor (CAR)-T Cells With CD34 Selection Markers in Adult Patients With CD19 Positive B-Cell Acute Lymphocytic Leukemia
The goal of this trial is to determine safe dosing of CD19-CD34t metabolically programmed CAR-T cell therapy in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL).
The main questions it aims to answer are to determine the maximum tolerated dose (MTD) of CD19-CD34t metabolically programmed CAR-T cell therapy, to assess the safety of CD19-CD34t metabolically programmed CAR-T cell therapy, and to determine the feasibility of manufacturing CD19-CD34t metabolically programmed CAR-T cell therapy within 15% of the target dose.
調査の概要
状態
詳細な説明
This is an open-label, single-center phase Ib de-escalation safety and feasibility study in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL). The trial will evaluate the safety of autologous peripheral blood mononuclear cell (PBMC) obtained by leukapheresis and then transduced with CD19-CD34t CAR retroviral vector followed by conditioning for a metabolically programmed (TH1/TH17) enhanced CAR-T cell product. The design will follow a 3+3+3 de-escalation design. The starting dose (dose level 1 [DL1]) is 2 x 106 transduced T cells/kg (±15%), based on the RP2D from NCT05702853. A step-down dose (dose level -1 [DL-1]) of 1.4 x 106 transduced T cells/kg (±15%) will be evaluated for safety if DL1 is too toxic. DL1 and DL-1 have demonstrated exceptional safety with therapeutic exposure in the ongoing lymphoma trial (NCT05702853) of this same investigational CAR-T product.
Participants will receive a lymphodepleting preparative regimen of fludarabine and cyclophosphamide followed by infusion of CD19-CD34t metabolically programmed CAR transduced T cells on day 0. Participants will be evaluated sequentially after treatment for toxicity, antitumor effects, and for persistence/expansion of CAR in blood samples and functionality of transduced T cells.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:HCC Clinical Trials Office
- 電話番号:843-792-9321
- メール:hcc-clinical-trials@musc.edu
研究場所
-
-
South Carolina
-
Charleston、South Carolina、アメリカ、29425
- Medical University of South Carolina Hollings Cancer Center
-
コンタクト:
- HCC Clinical Trials Office
- 電話番号:843-792-9321
- メール:hcc-clinical-trials@musc.edu
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
An individual must meet all of the following criteria to be eligible for enrollment:
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Age 18 years or older.
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Willing and able to give written, informed consent to the current study.
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ECOG performance status of 0, 1 or 2.
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Relapsed or refractory CD19-positive B-ALL defined as one of the following:
- Primary refractory disease (not achieving CR after two cycles of induction chemotherapy).
- Relapse after prior complete remission.
- Relapsed or refractory disease after allogeneic transplant provided CAR-T infusion occurs at least 2 months after the stem cell transplant.
NOTE: In patients treated with blinatumomab, CD19 expression on leukemic blasts must be confirmed after blinatumomab therapy has been stopped.
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Cohort-specific inclusion criteria:
a. Cohort Ia: Relapsed/Refractory B-ALL i. Presence of ≥5% blasts in BM at screening, or with isolated extramedullary disease (EMD) (including isolated CNS disease), with or without MRD in the BM ii. Patients with Philadelphia chromosome positive ALL (Ph+ ALL) are eligible if they are intolerant to or have failed two lines of any TKI or one line of second-generation TKI, or if TKI therapy is contraindicated.
b. Cohort Ib: B-ALL in remission with measurable residual disease i. MRD-positive defined as ≥10-6 and <5% blasts in the BM at screening. ii. Patients with Philadelphia chromosome positive ALL (Ph+ ALL) are eligible if they are intolerant to or have failed two lines of any TKI or one line of second-generation TKI, or if TKI therapy is contraindicated.
c. Cohort Ic: B-ALL in remission, indicated but ineligible for or unwilling to undergo allogenic transplant i. B ALL in MRD negative remission, being considered (typically for high-risk B-ALL) for, but ineligible for allogeneic stem cell transplantation due to organ dysfunction, socioeconomic factors or other extraneous reasons as determined by the transplant physician.
ii. B ALL in MRD negative remission, being considered (typically for high-risk B-ALL) for, but unwilling to undergo allogeneic stem cell transplantation for patient's personal reasons.
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For females of childbearing potential (defined as <24 months after last menstruation or not surgically sterile), a negative serum or urine pregnancy test must be documented at screening, prior to pre-conditioning and confirmed before receiving the first dose of study treatment.
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For females who are not postmenopausal (<24 months of amenorrhea) or who are not surgically sterile (absence of ovaries and/or uterus), two methods of contraception comprising of one highly effective method of contraception together with a barrier method must be used during the treatment period and for at least 12 months after the last dose of study treatment. They must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for 12 months after receiving the last dose of study drug (please refer to Appendix F).
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For males, it must be agreed that two acceptable methods of contraception are used (one by the patient - usually a barrier method, and one highly effective method by the patient's partner as defined in Appendix F) during the treatment period and for at least 12 months after the last dose of study treatment and that sperm will not be donated during the treatment period and for at least 12 months after the last dose of study treatment.
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Adequate renal, hematologic, hepatic, pulmonary, and cardiac function defined as:
- Serum alanine aminotransferase/aspartate aminotransferase ≤3 x ULN.
- Creatinine clearance (as estimated by Cockcroft-Gault) ≥50 cc/minute.
- Absolute lymphocyte count (ALC) ≥150 cells/mm3.
- Total bilirubin ≤1.5 x ULN, except in patients with Gilbert's syndrome who must have normal direct bilirubin.
- Baseline oxygen saturation >92% on room air.
- Left ventricular ejection fraction (LVEF) ≥ 45%, no evidence of clinically significant pericardial effusion as determined by an ECHO.
A second CAR-T cell infusion may be considered if the following criteria are met:
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Patient to receive subsequent cell infusion did not experience unacceptable toxicity from the first infusion. Any toxicity (regardless of causality) after the previous CD19-CD34t metabolically programmed CAR-T cell infusion must resolve such that participants meet all the initial eligibility criteria.
AND one or more of the following criteria are also met:
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Loss of B-cell aplasia past 6 months from the date of original CAR-T infusion, defined as either or both:
- CD19+ cells ≥3% of peripheral lymphocytes and absolute CD19 count ≥50/μL.
- Patients with CD19+ cells ≥3% of peripheral lymphocytes, but absolute CD19 count <50 are required to have at least two sets of lymphocyte subsets drawn to confirm stable to up trending absolute CD19 counts.
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Relapse or refractory disease, defined as either or both:
- Emergence or persistence of CD19 expressing MRD positive disease at any time past original CAR-T infusion past 4 weeks after original infusion.
- Frank CD19 positive relapse or refractory disease past 4 weeks after original infusion.
An individual will be excluded from the study if any of the following apply:
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Diagnosis of chronic myelogenous leukemia in lymphoid blast crisis.
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Presence of current CNS 3 disease. Prior CNS 3 disease is allowed if they are treated with residual CNS 1/2 disease.
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Females who are pregnant or lactating.
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Receipt of live vaccine within 6 weeks prior to enrollment.
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Prior CAR-T or Gene Therapy: Previous treatment with any CD19-directed CAR-T cell therapy. (Rationale: prior CAR-T could affect CD19 antigen status and immune response; also, to isolate the effect of this investigational product. However, prior CD19 CAR-T is allowed if it was more than 6 months prior to enrollment and the patient has confirmed CD19+ relapse).
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Uncontrolled Infection: Known active infection including:
- Positive blood cultures for bacteria or fungi with signs of systemic infection that are not controlled.
- Active tuberculosis.
- Opportunistic infections (e.g., Pneumocystis pneumonia, CMV viremia) that are not resolved.
- Fever of unknown origin is a caution; prior to lymphodepletion, a complete evaluation to rule out infection should be done and the treating physician must agree that it is okay to proceed.
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Concurrent Malignancy: Another active malignancy requiring therapy or that is expected to limit survival to <2 years, except certain low-risk cancers (e.g., treated localized prostate cancer on surveillance, adequately treated basal cell carcinoma of skin).
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Autoimmune Disorder: Active autoimmune disease requiring systemic immunosuppressive therapy (e.g. lupus, multiple sclerosis, etc.) especially if the disease or its treatment could be worsened by CAR-T (because steroids or immunosuppressants to control autoimmunity could interfere with CAR-T function, and autoimmunity could flare with immune activation).
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Allogeneic Transplant History: Prior allogeneic hematopoietic stem cell transplant with active graft-versus-host disease (GVHD) of any grade.
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Significant Co-morbid Conditions: For example:
- Unstable angina, myocardial infarction within 6 months, or uncontrolled cardiac arrhythmia.
- No clinically significant signs or symptoms of cardiac dysfunction defined as symptoms consistent with NYHA CHF classification III or IV.
- Acute neurological toxicity > Grade 1 (with the exception of peripheral sensory neuropathy).
- Stroke or seizure disorder not controlled on medication.
- Interstitial lung disease requiring supplemental oxygen.
- Any condition that the investigator deems would make the patient unsuitable (e.g., severe frailty or logistic inability to comply with frequent monitoring).
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Concurrent Therapy: Use of systemic corticosteroids above a physiologic replacement dose (equivalent to >10 mg prednisone daily) within 7 days prior to leukapheresis or planned need for such steroids.
NOTE: Patients who require steroids for disease control must be tapered off before T cell collection, since steroids can impair T cell function for manufacturing and may preclude CAR T expansion after infusion. If emergent steroid use is needed for an indication like brain metastases, patient should be deferred.
- Similarly, any other anti-cancer therapy (chemotherapy, targeted agents, investigational drugs) must be washed out before lymphodepletion (timeframe depends on drug, typically 2 weeks or 5 half-lives, whichever is longer).
- Radiation must have stopped ≥ 2 weeks prior to collection.
- New requirement for oxygen therapy.
A second CAR-T cell infusion will not be considered if any of the following criteria are met:
- All above exclusion criteria apply to a second infusion.
- Grade 3 or higher CRS/ICANS with original infusion at dose level -1.
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:非ランダム化
- 介入モデル:順次割り当て
- 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:Cohort 1a - Relapsed/Refractory B-ALL
Adult patients with relapsed or refractory CD19-positive B-cell acute lymphoblastic leukemia (B-ALL) receiving lymphodepleting chemotherapy followed by CD19-CD34t metabolically programmed CAR-T cell therapy. |
30 mg/m2, IV over 30-60 minutes +/- 10 minutes after cyclo- phosphamide infusion, Days -5, -4, -3 500 mg/m2, IV over 30-60 minutes +/- 10 minutes before Fludarabine, Days -4, -3 (500-750 mg BID) is administered prophylactically starting on Day 0. Autologous CD19 CAR-T cells expressing truncated CD34 (CD34t) administered intravenously following lymphodepleting chemotherapy. Participants receive either Dose Level 1 or Dose Level -1 according to the protocol-defined dose de-escalation design. |
|
実験的:Cohort 1b - B-ALL in remission with measurable residual disease
Adult patients with CD19-positive B-cell acute lymphoblastic leukemia in remission with measurable residual disease (MRD) receiving lymphodepleting chemotherapy followed by CD19-CD34t metabolically programmed CAR-T cell therapy. |
30 mg/m2, IV over 30-60 minutes +/- 10 minutes after cyclo- phosphamide infusion, Days -5, -4, -3 500 mg/m2, IV over 30-60 minutes +/- 10 minutes before Fludarabine, Days -4, -3 (500-750 mg BID) is administered prophylactically starting on Day 0. Autologous CD19 CAR-T cells expressing truncated CD34 (CD34t) administered intravenously following lymphodepleting chemotherapy. Participants receive either Dose Level 1 or Dose Level -1 according to the protocol-defined dose de-escalation design. |
|
実験的:Cohort 1c - B-ALL in Remission, Indicated but Unable to Undergo Allogeneic Transplant
Adult patients with CD19-positive B-cell acute lymphoblastic leukemia in MRD-negative remission who are indicated for but unwilling to undergo or ineligible for allogeneic stem cell transplantation due to organ dysfunction, socioeconomic factors, or other reasons determined by the transplant physician. These patients receive lymphodepleting chemotherapy followed by CD19-CD34t metabolically programmed CAR-T cell therapy. |
30 mg/m2, IV over 30-60 minutes +/- 10 minutes after cyclo- phosphamide infusion, Days -5, -4, -3 500 mg/m2, IV over 30-60 minutes +/- 10 minutes before Fludarabine, Days -4, -3 (500-750 mg BID) is administered prophylactically starting on Day 0. Autologous CD19 CAR-T cells expressing truncated CD34 (CD34t) administered intravenously following lymphodepleting chemotherapy. Participants receive either Dose Level 1 or Dose Level -1 according to the protocol-defined dose de-escalation design. |
|
実験的:Retreatment Cohort - Patients from cohorts 1a - 1c who are retreated
Patients previously treated in Cohort 1a, Cohort 1b, or Cohort 1c who meet protocol-defined eligibility criteria for retreatment and receive lymphodepleting chemotherapy followed by a second infusion of CD19-CD34t metabolically programmed CAR-T cells. |
30 mg/m2, IV over 30-60 minutes +/- 10 minutes after cyclo- phosphamide infusion, Days -5, -4, -3 500 mg/m2, IV over 30-60 minutes +/- 10 minutes before Fludarabine, Days -4, -3 (500-750 mg BID) is administered prophylactically starting on Day 0. Autologous CD19 CAR-T cells expressing truncated CD34 (CD34t) administered intravenously following lymphodepleting chemotherapy. Participants receive either Dose Level 1 or Dose Level -1 according to the protocol-defined dose de-escalation design. |
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 |
|---|---|---|
|
Determine the maximum tolerated dose (MTD) of CD19-CD34t metabolically programmed CAR-T cell therapy in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL).
時間枠:28 days
|
The frequency and percentage of dose limiting toxicities (DLTs) summarized by dose level and overall. |
28 days
|
|
Assess the safety of CD19-CD34t metabolically programmed CAR-T cell therapy
時間枠:28 days
|
The frequency and percentage of adverse events (AEs), serious adverse events (SAEs), and treatment-emergent adverse events (TEAEs) summarized by dose level and overall. |
28 days
|
|
Determine the feasibility of manufacturing CD19-CD34t metabolically programmed CAR-T cell therapy within 15% of the target dose.
時間枠:28 days
|
Proportion of patients for whom their CAR-T cellular product is prepared within 15% of the target dose. Feasibility will be evaluated for initial and second infusion separately. |
28 days
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall remission rate (ORR)
時間枠:28 days
|
Proportion of patients achieving a complete remission (CR) or a complete remission with incomplete recovery (CRi) for Cohort 1a. |
28 days
|
|
Rate of MRD-negative CR in bone marrow
時間枠:28 days
|
by NGS and/or flow cytometry in Cohort 1a, Cohort 1b, Retreatment cohort w/re-emergence of MRD) |
28 days
|
|
Stem cell transplantation prior to leukemia relapse
時間枠:up to 5 years or a disease progression
|
Proportion of patients undergoing stem cell transplantation prior to leukemia relapse in Cohort 1a, Cohort 1b, Retreatment cohort w/relapse of CD19+ ALL |
up to 5 years or a disease progression
|
|
Rate of B cell aplasia reinduction
時間枠:up to 5 years or a disease progression
|
Reinduction of B cell aplasia retreatment cohort w/loss of B cell aplasia |
up to 5 years or a disease progression
|
|
ORR after 2nd infusion
時間枠:up to 5 years or disease progression
|
Proportion of patients achieving a complete remission (CR) or a complete remission with incomplete recovery (CRi) for Retreatment cohort w/relapse of CD19-positive ALL |
up to 5 years or disease progression
|
|
Rate of CR/CRi without stem cell transplantation or other subsequent therapy
時間枠:up to 24 months
|
Proportion of patients in CR/CRi without stem cell transplant or other subsequent therapy at 6-, 12-, and 24-months following CAR-T infusion for Cohort 1a, Cohort 1b, Cohort 1c |
up to 24 months
|
|
Rate of CD19-negative relapse
時間枠:up to 5 years or disease progression
|
Incidence of CD19 negative relapse for Cohort 1a, Cohort 1b, Cohort 1c |
up to 5 years or disease progression
|
|
Progression-free survival (PFS)
時間枠:up to 5 years or disease progression, relapse, or death
|
the time interval from first CAR-T cell infusion to disease progression, relapse, or death due to any cause in Cohort 1a, Cohort 1b, Cohort 1c |
up to 5 years or disease progression, relapse, or death
|
|
Duration of response (DOR)
時間枠:up to 5 years or response to disease progression or death
|
the time interval from first documented response to disease progression or death due to any cause. DOR is defined only among patients who experience a response to the CAR-T cell therapy Cohort 1a, Cohort 1b, Cohort 1c |
up to 5 years or response to disease progression or death
|
|
Overall survival (OS)
時間枠:up to 5 years or death
|
the time interval from first CAR-T cell infusion to death due to any cause in Cohort 1a, Cohort 1b, Cohort 1c |
up to 5 years or death
|
協力者と研究者
捜査官
- 主任研究者:Baratam Praneeth, MD、Medical University of South Carolina
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
- 新生物
- 免疫系疾患
- 感染症
- ウイルス病
- 組織型別の新生物
- DNAウイルス感染症
- リンパ疾患
- リンパ増殖性疾患
- 免疫増殖性疾患
- リンパ腫、非ホジキン
- リンパ腫、B細胞
- リンパ腫
- エプスタイン-バーウイルス感染症
- ヘルペスウイルス感染症
- 腫瘍ウイルス感染症
- ヘミックおよびリンパ疾患
- バーキットリンパ腫
- 有機化学物質
- 複素環化化合物、1リング
- 複素環化化合物
- 炭化水素
- 酸、非環式
- カルボン酸
- アミド
- ホスホルアミドマスタード
- 窒素マスタード化合物
- マスタード化合物
- 炭化水素、ハロゲン化
- ホスホラミド
- 有機リン化合物
- ピロリジン
- アセトアミド
- 酢酸塩
- ピロリジノン
- レベチラセタム
- シクロホスファミド
- フルダラビン
その他の研究ID番号
- 104236
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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