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

7 oktober 2026 uppdaterad av: 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.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Beräknad)

6

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

  • Namn: Knight Cancer Institute Clinical Trials Information
  • Telefonnummer: 503-494-1080
  • E-post: trials@ohsu.edu

Studieorter

    • Oregon
      • Portland, Oregon, Förenta staterna, 97239
        • Rekrytering
        • OHSU Knight Cancer Institute
        • Huvudutredare:
          • Curtis A. Lachowiez
        • Kontakt:
          • Knight Cancer Institute Clinical Trials Information
          • Telefonnummer: 503-494-1080
          • E-post: trials@ohsu.edu

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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

Andra namn:
  • Biologisk provsamling
  • Bioprov insamlat
  • Provsamling
  • Provuppsamling

Undergo bone marrow biopsy/aspiration

Undergo bone marrow biopsy/aspiration

Andra namn:
  • Biopsi av benmärg
  • Biopsi, benmärg

Given PO

Andra namn:
  • Rapamycin
  • Rapamune
  • AY 22989
  • RAPA
  • SILA 9268A
  • WY-090217
  • AY-22989
  • AY22989
  • SILA-9268A
  • SILA9268A
  • WY 090217
  • WY090217

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Incidence of grade 3+ treatment-related adverse events (TRAEs)
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in platelet count
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: 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
Tidsram: 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
Tidsram: 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)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Curtis A Lachowiez, OHSU Knight Cancer Institute

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

5 oktober 2026

Primärt slutförande (Beräknad)

30 juni 2030

Avslutad studie (Beräknad)

31 december 2030

Studieregistreringsdatum

Först inskickad

21 september 2026

Först inskickad som uppfyllde QC-kriterierna

21 september 2026

Första postat (Faktisk)

28 september 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

13 oktober 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

7 oktober 2026

Senast verifierad

1 oktober 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • STUDY00028610
  • P30CA069533 (U.S.S. NIH-anslag/kontrakt)
  • NCI-2026-03902 (Registeridentifierare: CTRP (Clinical Trial Reporting Program))
  • STUDY00028610 (Annan identifierare: OHSU Knight Cancer Institute)

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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