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Allogeneic ORCA-Q Stem Cell Transplant for the Treatment of Relapsed and Refractory High Risk Multiple Myeloma

2026年8月5日 更新者:University of California, Davis

A Phase I Study to Evaluate the Safety and Efficacy of ORCA-Q Allogeneic Hematopoietic Stem Cell Transplantation for the Treatment of Relapsed/ Refractory High Risk Multiple Myeloma

This phase I trial tests the effect of allogeneic Orca-Q stem cell transplant in treating patients with high-risk multiple myeloma that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). An allogeneic (donor) transplant uses blood forming stem cells (graft) from a matched donor. When the healthy blood forming (stem) cells from a donor are infused into a patient, they may help the patient's bone marrow make more healthy cells and platelets and may help destroy any remaining cancer cells. Sometimes the transplanted cells from a donor can attack the body's normal cells (called graft-versus-host disease [GVHD]). Orca-Q includes some T cells (a type a white blood cell) that are thought to help prevent some of the known complications as well as help attack the cancer cells. However, Orca-Q removes a specific type of T cell called naive T lymphocytes. Naive T cells may contribute to GVHD and are not thought to be required for the success of the treatment. Removing these cells may help reduce the frequency or severity of GVHD. Giving chemotherapy, such as thiotepa, busulfan, and fludarabine, before a donor stem cell transplant helps kill cancer cells in the body and prepare the body to receive the transplant graft. Giving allogeneic Orca-Q may be safe, tolerable, and/or effective in treating patients with relapsed or refractory (R/R) high-risk multiple myeloma.

研究概览

详细说明

PRIMARY OBJECTIVE:

I. To evaluate the safety of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

SECONDARY OBJECTIVES:

I. To evaluate the efficacy of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

II. To further evaluate the safety of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

EXPLORATORY OBJECTIVE:

I. To further evaluate the efficacy of allogeneic ORCA-Q transplantation in subjects with R/R multiple myeloma with high-risk features.

OUTLINE:

DONORS: Donors receive granulocyte colony-stimulating factor (G-CSF) or filgrastim subcutaneously (SC) daily (QD) on days -6 to -3 and undergo apheresis on day -2 or -1. Donors may also undergo a second apheresis on day -1 or 0. Additionally, donors undergo blood sample collection at screening.

PATIENTS: Patients receive thiotepa intravenously (IV) over 3 hours on days -7 and -6, busulfan IV over 3 hours on days -5 to -3, fludarabine IV over 30 minutes on days -5 to -2, Orca-Q prime IV on day 0 followed by Orca-Q supplement IV on day 0 or 1 in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo echocardiography or multigated acquisition scan (MUGA) and optional positron emission tomography (PET)/computed tomography (CT) or CT at screening and urine and blood sample collection, as well as bone marrow aspiration and biopsy throughout the study.

After completion of study treatment, patients are followed up on days 1-7, 14, 21, 30, 60, 90, 180, and 365.

研究类型

介入性

注册 (估计的)

20

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • California
      • Sacramento、California、美国、95817
        • University of California Davis Comprehensive Cancer Center
        • 首席研究员:
          • Mehrdad Abedi, MD
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Ability to understand and sign informed consent
  • Age ≥ 18 years and ≤ 65 years
  • Patients should be in very good partial response (VGPR) (5% or less plasma cells in the marrow) or better response status at the time of stem cell transplant with no evidence of central nervous system (CNS) disease. Patients in complete response (CR) should have minimal residual disease (MRD) positivity
  • Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1; or Karnofsky performance status (KPS) of ≥ 70%
  • ≥ 60 days washout period from the last dose of an anti-CD38 antibody before the allogeneic transplant
  • ≥ 6 months washout period from the last autologous transplant before the allogeneic transplant
  • Related or unrelated donors available as follows:

    • Sibling donor who is a 7/8 mismatched or 8/8 matched for human leukocyte antigen (HLA)-A, -B, -C, -DRB1
    • Matched unrelated donor who is a 7/8 mismatched or 8/8 matched for HLA-A, -B, -C, and -DRB1
  • A diagnosis of relapsed or refractory defined as:

    • Primary refractory disease or relapse < 12 months following initial therapy that includes an immunomodulatory agent, proteasome inhibitor, anti-CD38 monoclonal antibody, and corticosteroid
    • Relapse < 12 months after first autologous stem cell transplant
    • Failing to achieve complete response or relapsing after chimeric antigen receptor (CAR)-T treatment or bispecific antibodies; or indicated but ineligible for either bispecific antibodies or CAR-T cells due to low blood counts
    • No appropriate standard of care therapy per investigator
  • A diagnosis of ultra-high risk multiple myeloma defined as having at least one or more of these criteria:

    • Biallelic TP53 inactivation
    • ≥ 2 HRCAs: del(17p), TP53 mutation, t(4;14), t(14;16), t(14;20), gain(1q), amp(1q), del(1p32)
    • Biallelic del(1p32)
    • High-risk gene expression profile signature
    • Extramedullary disease excluding intramedullary plasmacytoma with extraosseous extension and active CNS disease
    • ≥ 2% circulating plasma cells
  • Creatinine clearance of ≥ 50 mL/min as estimated by Cockcroft-Gault
  • Total bilirubin ≤ 1.5 times upper limit of normal (ULN) except in subjects with Gilbert's syndrome in whom total bilirubin ≤ 3 times ULN
  • Alanine transaminase (ALT/serum glutamic pyruvic transaminase [SGPT]) and aspartate aminotransferase (AST/serum glutamic oxaloacetic transaminase [SGOT]) ≤ 3 x the upper limit of normal (ULN) or ≤ 5 x ULN if documented liver involvement by disease
  • Estimated glomerular filtration rate (eGFR) > 50mL/minute. Creatinine clearance of ≥ 30 mL/min is allowed in patients eligible for no tacrolimus immunosuppression
  • Pulmonary function as defined by diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50%
  • Cardiac ejection fraction at rest ≥ 45% or shortening fraction of ≥ 27% by echocardiogram, or radionuclide scan (multigated acquisition scan [MUGA])
  • Corrected diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50%
  • Individuals of childbearing potential or those with partners of childbearing potential must agree to use methods of contraception for the duration of study participation or be surgically sterilized
  • Stated ability and willingness to adhere to the study visit schedule and protocol requirements
  • DONOR: Ability to understand and sign informed consent
  • DONOR: Age ≥ 16 and ≤ 35 years at time of enrollment for unrelated donors and Age ≥ 16 and ≤ 50 years for related donors
  • DONOR: Either one of the following scenarios:

    • Sibling donor who is a 7/8 mismatched or 8/8 matched for HLA-A, -B, -C, and -DRB1, all typed using deoxyribonucleic acid (DNA)-based high-resolution methods
    • Unrelated donor who is 7/8 mismatched or 8/8 matched HLA-A, -B, -C, and -DRB1, all typed using DNA-based high-resolution methods
  • DONOR: Willing to donate stem cell mobilized mononuclear cells for up to two consecutive days
  • DONOR: Able to donate within the continental United States at a site that will employ a Spectra Optia Apheresis System for post-mobilization apheresis
  • DONOR: Meets federal eligibility criteria for donors of viable, leukocyte-rich cells or tissues and all relevant Food and Drug Administration (FDA) Guidance for Industry (Eligibility Determination for Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products, 2007; Use of Donor Screening Tests to Test Donors of Human Cells, Tissues and Cellular and Tissue-Based Products for Infection with Treponema pallidum [syphilis], 2015; Use of Nucleic Acid Tests to Reduce the Risk of Transmission of Hepatitis B Virus from Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products, 2016; Use of Nucleic Acid Tests to Reduce the Risk of Transmission of West Nile Virus from Living Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products [HCT/Ps], 2016)
  • DONOR: Donors determined to be ineligible, based on the results of required testing and/or screening, may nonetheless be included if either applies:

    • The donor is a first-degree blood relative of the recipient
    • Urgent medical need, meaning no comparable human cell product is available, and the recipient is likely to suffer death or serious morbidity without the human cell product, as attested by the investigator
    • Meets any other criteria for donation as specified by standard National Marrow Donor Program (NMDP) guidelines (NMDP donors) or institutional standards (non-NMDP donors)

Exclusion Criteria:

  • Prior allogeneic hematopoietic cell transplantation (HCT)
  • Planned pharmaceutical in vivo or ex vivo T cell depletion, e.g., post-transplant cyclophosphamide (Cy), peri-transplant anti-thymocyte globulin (ATG), or alemtuzumab
  • Positive anti-donor HLA antibodies against a mismatched allele in the selected donor determined by either:

    • A positive crossmatch test of any titer; or
    • The presence of anti-donor HLA antibody to any HLA locus
  • Hematopoietic cell transplantation-specific Comorbidity Index (HCT-CI) > 4
  • Uncontrolled bacterial, viral, or fungal infections (currently taking antimicrobial therapy and with no clinical improvement) at time of enrollment
  • Seropositive for HIV-1 or -2, human T-cell lymphotropic virus (HTLV)-1 or -2
  • Documented allergy or documented hypersensitivity to iron dextran or bovine, murine, algal or Streptomyces avidinii proteins
  • Concurrent malignancies or active disease within 1 year, except non-melanoma skin cancers or any carcinoma in situ that have been curatively resected
  • History of idiopathic or secondary myelofibrosis
  • Individuals who are pregnant or breastfeeding
  • Any condition that would prohibit the understanding or rendering of informed consent
  • Any condition that in the opinion of the investigator would interfere with the subject's safety or compliance while on study
  • A diagnosis of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome
  • DONOR: Evidence of uncontrolled, active infection
  • DONOR: Seropositive for HIV-1 or -2, HTLV-1 or -2
  • DONOR: Positive for hepatitis B (HBV) surface antigen (HBsAg), total anti-hepatitis B core antibody (HBcAb, immunoglobulin [I]gG and IgM), HBV nucleic acid testing (NAT), anti-hepatitis C (HCV) antibody, or HCV NAT
  • DONOR: Aberrant CD45RA isoform expression
  • DONOR: Women who are pregnant or breastfeeding

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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:Treatment (Orca-Q, thiotepa, busulfan, fludarabine)
Recipient participants receive thiotepa IV over 3 hours on days -7 and -6, busulfan IV over 3 hours on days -5 to -3, fludarabine IV over 30 minutes on days -5 to -2, Orca-Q prime IV on day 0, followed by Orca-Q supplement IV on day 0 or 1 in the absence of disease progression or unacceptable toxicity.
鉴于IV
其他名称:
  • 氟多沙
鉴于SC
其他名称:
  • 脑脊液
  • r-metHuG-CSF
  • 纽普生
  • 非格司亭
  • 尼维斯泰姆
  • 重组甲硫氨酰人粒细胞集落刺激因子
  • rG-CSF
  • 替瓦格司亭
  • 非格司亭生物类似药
  • 扎尔西奥
  • 非格司亭XM02
  • 格兰尼克斯
  • 尼维斯汀
  • XM02
  • 非格司亭-sndz
  • 非格司亭生物类似药 Tbo-filgrastim
  • Releuko
  • 纽特罗瓦尔
鉴于IV
其他名称:
  • 白消安
  • 米硫磺
  • 米托生
  • 髓白细胞
  • 骨髓素
  • 1, 4-双[甲磺氧基]丁烷
  • 公共汽车
  • 白舒安
  • CB 2041
  • CB-2041
  • 格列佐酚
  • GT 41
  • GT-41
  • Joacamine
  • 甲磺酸四亚甲基酯
  • 米卢素
  • 米苏班
  • Mylecytan
  • 迈兰
  • 磺胺布丁
  • 四亚甲基双(甲磺酸盐)
  • 四亚甲基双[甲磺酸盐]
  • WR-19508
  • 布西尔维克斯
鉴于IV
其他名称:
  • 铁粉属
  • 奥克替帕
  • 斯泰帕
  • TESPA
  • 特斯帕明
  • TSPA
  • 1,1',1''-Phosphinothioylidynetrisaziridine
  • 吉罗斯坦
  • N,N', N''-三亚乙基硫代磷酰胺
  • 茶胺
  • 硫泰帕
  • 硫磷酰胺
  • 硫菌灵
  • 硫代磷酰胺
  • 噻吩
  • 替福西林
  • 三聚氰胺
  • Tiotef
  • 三乙烯硫磷酰胺
  • 三乙烯硫代磷酰胺
  • 三(1-氮丙啶基)硫化膦
  • WR 45312
  • SH 105
  • SH-105
  • SH105
  • 特吡鲁特
给定SC
其他名称:
  • 脑脊液
  • 粒细胞集落刺激因子
  • GCSF
  • 集落刺激因子 3
  • 集落刺激因子(粒细胞)
  • 脑脊液3
  • 多细胞生成素
Given Orca-Q prime IV
其他名称:
  • Allogeneic Defined HSCs/Immune Cells
  • Allogeneic Defined Stem and Immune Cells
  • Orca-Q
Given Orca-Q supplement IV
其他名称:
  • Allogeneic Defined HSCs/Immune Cells
  • Allogeneic Defined Stem and Immune Cells
  • Orca-Q

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
Incidence of primary graft failure without grade II-IV acute graft-versus-host disease (GVHD)
大体时间:From date of transplant and up to 30 days post-transplant
Frequency and proportions will be obtained.
From date of transplant and up to 30 days post-transplant

次要结果测量

结果测量
措施说明
大体时间
Overall survival
大体时间:From transplant to death from any cause, assessed up to day 365 post-transplant
The Kaplan-Meier (KM) method will be used to estimate the median and percentiles for time-to-event endpoints with 95% confidence intervals (CIs).
From transplant to death from any cause, assessed up to day 365 post-transplant
Progression-free survival
大体时间:From transplant to progressive disease or death, assessed up to 365 days post-transplant
The KM method will be used to estimate the median and percentiles for time-to-event endpoints with 95% CIs.
From transplant to progressive disease or death, assessed up to 365 days post-transplant
Time to relapse
大体时间:From transplant to disease progression, initiation of new anti-multiple myeloma treatment, or death, whichever occurs first, assessed up to 365 days post-transplant
From transplant to disease progression, initiation of new anti-multiple myeloma treatment, or death, whichever occurs first, assessed up to 365 days post-transplant
Non-relapse mortality
大体时间:From transplant to death from any cause not including disease progression, assessed up to 365 days post-transplant
Will be analyzed using the cumulative incidence function to account for the competing risk of disease relapse/progression.
From transplant to death from any cause not including disease progression, assessed up to 365 days post-transplant
Number of treatment-related adverse events (AEs)
大体时间:From date of enrollment up to 100 days post-transplant
Will be classified by severity and graded according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v) 6.0. Frequency and proportions will be obtained.
From date of enrollment up to 100 days post-transplant
Occurrence of grade 3 or 4 treatment-emergent AEs
大体时间:From date of transplant up to 100 days post-transplant
Will be classified by severity and graded according to the NCI CTCAE v 6.0. Frequency and proportions will be obtained.
From date of transplant up to 100 days post-transplant
Incidence of acute GVHD
大体时间:From date of transplant up to 100 days post-transplant
From date of transplant up to 100 days post-transplant
Incidence of chronic GVHD
大体时间:From date of transplant up to 100 days post-transplant
From date of transplant up to 100 days post-transplant
Incidence of GVHD free, relapse free survival
大体时间:From date of transplant up to 365 days post-transplant
The KM method will be used to estimate the median and percentiles for time-to-event endpoints with 95% CIs.
From date of transplant up to 365 days post-transplant
Secondary graft failure rate
大体时间:Up to day 365 post-transplant
Up to day 365 post-transplant

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Mehrdad Abedi、University of California, Davis

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2032年9月1日

研究完成 (估计的)

2033年9月1日

研究注册日期

首次提交

2026年8月5日

首先提交符合 QC 标准的

2026年8月5日

首次发布 (实际的)

2026年8月12日

研究记录更新

最后更新发布 (实际的)

2026年8月12日

上次提交的符合 QC 标准的更新

2026年8月5日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

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