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Low-Dose Sirolimus for the Treatment of RUNX1 Familial Platelet Disorder

2026年10月7日 更新者:Curtis Lachowiez、OHSU Knight Cancer Institute

Low-Dose Sirolimus to Increase Hematopoietic Function in Patients With RUNX1 Familial Platelet Disorder - Part II

This phase I trial studies the safety and side effects of low-dose sirolimus in treating patients with RUNX1 familial platelet disorder (FPD). RUNX1-FPD is a rare inherited disorder with symptoms such as mild to moderately low platelet count, abnormal platelet function, and an increased risk of developing cancers like myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). It is caused by changes (variants) in the RUNX1 gene that is passed down (inherited) from an affected parent. Sirolimus is typically given to help prevent organ rejection in patients receiving kidney transplants. However, sirolimus may also be able to prevent RUNX1-FPD from progressing to cancers like MDS and AML by targeting another protein called mTORC1. Sirolimus may be a safe treatment for patients with RUNX1-FPD.

研究概览

详细说明

PRIMARY OBJECTIVE:

I. Evaluate the safety and tolerability of low-dose sirolimus in patients with RUNX1 familial platelet disorder (RUNX1-FPD).

SECONDARY OBJECTIVES:

I. Evaluate platelet counts. II. Evaluate changes in somatic mutation variant allele frequency (VAF). III. Evaluate somatic mutation acquisition (i.e., mutation burden). IV. Evaluate the change in platelet function. V. Evaluate the change from baseline in bleeding score (International Society on Thrombosis and Haemostasis Bleeding Assessment Tool [ISTH-BAT]).

VI. Evaluate the change in mTORC1 downstream signaling.

EXPLORATORY OBJECTIVES:

I. Evaluate the rescue of elevated cytokine profiles. II. Evaluate the reversal of myeloid skewing using colony formation assay. III. Evaluate monocytes using clinical flow cytometry. IV. Evaluate changes in patient-reported quality of life (QoL) outcomes measures (e.g., Patient-Reported Outcomes-Common Terminology Criteria for Adverse Events [PRO-CTCAE]).

V. Determine the pharmacokinetics of sirolimus in participants with RUNX1-FPD. VI. Evaluate the correlation between sirolimus trough levels and each endpoint. VII. Make bone marrow smears and bone marrow biopsy slides. VIII. Evaluate the cellularity of bone marrow after study treatment.

OUTLINE:

Patients receive sirolimus orally (PO) once daily (QD) on days 1-168 in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and bone marrow biopsy and/or aspiration throughout the study.

After completion of study treatment, patients are followed for 6 months.

研究类型

介入性

注册 (估计的)

6

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

  • 姓名:Knight Cancer Institute Clinical Trials Information
  • 电话号码:503-494-1080
  • 邮箱:trials@ohsu.edu

学习地点

    • Oregon
      • Portland、Oregon、美国、97239
        • 招聘中
        • OHSU Knight Cancer Institute
        • 首席研究员:
          • Curtis A. Lachowiez
        • 接触:
          • Knight Cancer Institute Clinical Trials Information
          • 电话号码:503-494-1080
          • 邮箱:trials@ohsu.edu

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

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Patient has provided signed, informed consent before initiation of any study specific procedures
  • Aged ≥ 18 years at the time of signing the informed consent
  • Confirmed pathogenic/likely pathogenic (P/LP) germline RUNX1 variant per ClinGen Myeloid Malignancy Variant Curation Expert Panel (MM-VCEP) RUNX1-specific variant curation rules
  • Patient must be willing to provide a bone marrow sample at time of screening and at the end of treatment with sirolimus
  • Platelet count of ≥ 50,000/µL
  • Creatinine clearance (CrCl) of ≥ 60 mL/min; estimated using the Cockcroft Gault formula or measured by 24 hour urine collection. Exceptions will be allowed, at the discretion of the investigator, for cases of a concomitant medication that alters renal function
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 3 × upper limit of normal (ULN)
  • Total bilirubin < 1.5 × ULN
  • Left ventricular ejection fraction (EF) > 50% or at the discretion of the investigator

Exclusion Criteria:

  • Known allergy to sirolimus

  • History of major bleeding events that are clinically relevant in the judgement of the investigator or non-major bleeding events that cannot be controlled using SOC practices

  • Any known history of lymphoma, myelodysplastic syndrome (MDS), or other hematologic malignancy using International Working Group criteria

  • Prior treatment with sirolimus or a rapalog, mTOR inhibitor, or B-cell-depleting therapy within 28 days before study day 1

  • Treatment with strong inhibitors of cytochrome P450 3A4 (CYP3A4; e.g., ketoconazole, voriconazole, itraconazole, erythromycin, telithromycin, and clarithromycin), strong inducers of CYP3A4 (e.g., rifampin and rifabutin), other drugs that could increase sirolimus blood concentrations (e.g., bromocriptine, cimetidine, cisapride, clotrimazole, danazol, diltiazem, fluconazole, letermovir, protease inhibitors [e.g., ritonavir, indinavir, boceprevir, and telaprevir], metoclopramide, nicardipine, troleandomycin, and verapamil), other drugs that could decrease sirolimus blood concentrations (e.g., carbamazepine, phenobarbital, phenytoin, rifapentine, St. John's Wort [Hypericum perforatum]), or drugs with blood concentrations that could increase (e.g., verapamil) within 7 days before study day 1, or at the discretion of the investigator

  • Use of cannabidiols that increase blood levels of sirolimus, within 7 days before study day 1 or at the discretion of the investigator

  • Myocardial infarction within 6 months before study day 1, congestive heart failure (New York Heart Association > class II)

  • Total cholesterol > 300 mg/dL or triglyceride > 400 mg/dL

  • Arterial thrombosis (e.g., stroke or transient ischemic attack) within 6 months before study day 1

  • Infection requiring intravenous anti-infective treatment within 1 week of study day 1

  • Live vaccines (e.g., measles, mumps, rubella, oral polio, Bacillus Calmette-Guerin [BCG], yellow fever, varicella, and TY21a typhoid) within 28 days before study day 1

  • Known diagnosis of tuberculosis is exclusionary to provide protection against reactivation of infections by the immunosuppressive activity of the study drug sirolimus

    • The enrollment of a patient with a history of infection with hepatitis B virus (HBV) but with undetectable HBV deoxyribonucleic acid (DNA) by standard institutional testing can be considered after consultation with the investigator
    • Patients with history of chronic hepatitis C virus (HCV) must have documentation of completed curative standard of care (SOC) antiviral therapy
    • Patients with history of HIV infection must be well-managed with SOC antiretroviral therapy (highly active antiretroviral therapy [HAART])
    • Patients with history of Epstein-Barr may be considered after consultation with the treating physician
  • Participants who are pregnant may become pregnant, or who are breastfeeding

    • Because adequate and well-controlled studies of the impact of sirolimus on fetuses currently do not exist, study approved contraception must be used from start of study therapy to 12 weeks after the last dose of sirolimus
    • Adequate and well-controlled studies of infants fed breastmilk from patients undergoing sirolimus therapy do not exist and breastfeeding during study treatment is prohibited

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 (sirolimus)

Patients receive sirolimus PO QD on days 1-168 in the absence of disease progression or unacceptable toxicity. Patients also undergo blood sample collection and bone marrow biopsy and/or aspiration throughout the study.

Ancillary studies

Undergo collection of blood

其他名称:
  • 生物样本采集
  • 收集的生物样本
  • 标本采集
  • 样本收集

Undergo bone marrow biopsy/aspiration

Undergo bone marrow biopsy/aspiration

其他名称:
  • 骨髓活检
  • 活组织检查,骨髓

Given PO

其他名称:
  • 雷帕霉素
  • 拉帕蒙
  • AY 22989
  • 拉帕
  • 西拉9268A
  • WY-090217
  • AY-22989
  • AY22989
  • SILA-9268A
  • SILA9268A
  • 威云090217
  • WY090217

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 grade 3+ treatment-related adverse events (TRAEs)
大体时间:From study day 1 (week 1) to 30 days after the last dose of sirolimus

The incidence of grade 3+ TRAEs and the total proportion of participants who experienced grade 3+ TRAEs will be estimated and presented with the corresponding 95% exact Clopper Pearson confidence intervals.

From study day 1 (week 1) to 30 days after the last dose of sirolimus

次要结果测量

结果测量
措施说明
大体时间
Change in platelet count
大体时间:From screening, pre dose on study day 1 (week 1) to end of treatment (EOT) (week 24, day 168)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to end of treatment (EOT) (week 24, day 168)
Change in variant allele frequency for existing clones
大体时间:From screening to end of study (EOS) (week 52, day 365)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening to end of study (EOS) (week 52, day 365)
Change in number of clonal hematopoiesis of indeterminate potential mutations
大体时间:From screening to EOS (week 52, day 365)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening to EOS (week 52, day 365)
Change in percent positivity based on activated GPIIb IIIa and surface P selectin and CD42b
大体时间:From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
Change in aggregation from baseline based on thromboelastography (TEG)
大体时间:From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to EOT (week 24, day 168)
Change in the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool score
大体时间:From study day 1 (week 1) to EOS (week 52, day 365)

Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From study day 1 (week 1) to EOS (week 52, day 365)
Change in the relative amount of the protein 4eBP1
大体时间:From screening, pre dose on study day 1 (week 1) to EOS (week 52, day 365)

Will be based on flow cytometry and immunohistochemistry assays. Descriptive statistics on continuous data will include means, medians, standard deviations and ranges, while categorical data will be summarized using frequency counts and percentages. Confidence intervals may be included, as appropriate. Graphical summaries of the data may also be presented.

From screening, pre dose on study day 1 (week 1) to EOS (week 52, day 365)

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:Curtis A Lachowiez、OHSU Knight Cancer Institute

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 (实际的)

2026年10月5日

初级完成 (估计的)

2030年6月30日

研究完成 (估计的)

2030年12月31日

研究注册日期

首次提交

2026年9月21日

首先提交符合 QC 标准的

2026年9月21日

首次发布 (实际的)

2026年9月28日

研究记录更新

最后更新发布 (实际的)

2026年10月13日

上次提交的符合 QC 标准的更新

2026年10月7日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

其他研究编号

  • STUDY00028610
  • P30CA069533 (美国 NIH 拨款/合同)
  • NCI-2026-03902 (注册表标识符:CTRP (Clinical Trial Reporting Program))
  • STUDY00028610 (其他标识符:OHSU Knight Cancer Institute)

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

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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