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Liothyroniini BIT-hoidon yhdistelmänä medulloblastoomalle, jossa on tai ei ole vähäisiä jäljellä olevia taudinalueita (PNOC044)

torstai 24. syyskuuta 2026 päivittänyt: Sabine Mueller, MD, PhD

PNOC044: Liothyroniini (L-T3) yhdistettynä bevatsimumabiin, irinotekaaniin ja temostolomiidiin (BIT) etenevälle tai uusiutuneelle medulloblastoomalle (Kohortti 1) tai monoterapiana medulloblastoomalle, jossa on minimaalinen jäännöstauti (Kohortti 2)

This is a Phase 1/Phase 2 study assessing liothyronine (L-T3) immunotherapy and in combination with standard chemotherapy (bevacizumab, irinotecan and temozolomide (BIT)) in children and young adults with medulloblastoma that is relapsed or progressive after standard upfront therapy.

Tutkimuksen yleiskatsaus

Tila

Rekrytointi

Ehdot

Interventio / Hoito

Yksityiskohtainen kuvaus

OUTLINE: This is an intra-patient dose escalation (Phase 1 (Cohort 1)) followed by a Phase 2 (Cohort 2) study.

Cohort 1: Children and young adults with relapsed or progressive disease following standard upfront therapy (including craniospinal radiation or high dose chemotherapy with autologous stem cell rescue). evaluating the safety and efficacy of combination L-T3 with BIT. Cohort 2: Children and young adults with medulloblastoma and CSF cell-free deoxyribonucleic acid (cf-DNA) positivity without radiographic disease progression/recurrence following standard upfront therapy. This is a Phase 2 study to evaluate clearance of Circulating free DNA (cfDNA) positive disease in CSF in response to L-T3 monotherapy at the RP2D (established as part of Cohort 1; Phase 1) as single agent.

Participants may continue therapy for up to 12 cycles if there is no evidence of unacceptable toxicity, disease progression, or withdrawal of consent. For participants that are benefiting from therapy, they may continue L-T3 monotherapy for one additional year (24 cycles total therapy). Treatment beyond that specified in the protocol should be discussed with the study chairs. Duration of Follow up Participants will enter follow up after the 30-day toxicity period.

Follow-up procedures are to be captured under the Pediatric NeuroOncology Consortium (PNOC) COMP protocol with the exception of protocol defined follow up procedures. Participants will be followed under the PNOC COMP protocol until death or withdrawal from study.

The study will complete enrollment within 5 years from the time the study opens to accrual (including 3 years for enrollment and 2 years of long term follow up).

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

69

Vaihe

  • Vaihe 2
  • Vaihe 1

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

  • Nimi: Kelly Hitchner
  • Puhelinnumero: 877-827-3222
  • Sähköposti: PNOC044@ucsf.edu

Opiskelupaikat

    • California
      • San Francisco, California, Yhdysvallat, 94143
        • Ei vielä rekrytointia
        • University of California, San Francisco
        • Ottaa yhteyttä:
          • cancertrials@ucsf.edu
        • Ottaa yhteyttä:
          • PNOC Operations Office
          • Puhelinnumero: 877-827-3222
          • Sähköposti: PNOC044@ucsf.edu
    • District of Columbia
    • Washington

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

1 vuosi - 25 vuotta (Lapsi, Aikuinen)

Hyväksyy terveitä vapaaehtoisia

Ei

Sukupuolet, jotka voivat opiskella

Kaikki

Kuvaus

Inclusion Criteria:

  1. Phase 1 and Phase 2, Cohort 1:

    Participants must have histologically confirmed medulloblastoma that is relapsed/progressive following standard upfront therapy. Tissue confirmation of medulloblastoma diagnosis is required at diagnosis and not required at the time of relapse for entry into the study.

  2. Phase 2, Cohort 2: Participants must have cerebrospinal fluid (CSF) with cell-free deoxyribonucleic acid (cf-DNA) + assessed in a Chemiluminescent immunoassay (CLIA)-certified or protocol-approved laboratory. After entry into the study, another CSF sample will be collected and analyzed centrally prior to initiation of protocol therapy to verify cf-DNA positivity.

  3. Evidence of Disease:

    Phase 1 and Phase 2, Cohort 1:

    Participants may have either Measurable or Evaluable Disease Measurable Disease: Participants must have clear residual disease at the time of enrollment, defined as tumor that is measurable in two perpendicular dimensions on MRI Evaluable Disease: Diffuse leptomeningeal disease OR clear MRI evidence of disease that may not be measurable in two perpendicular dimensions.

    Phase 2, Cohort 2:

    For cf-DNA positive cohort: Participants are not required to have measurable or evaluable disease but must have cf-DNA positivity in a CLIA-certified or protocol-approved laboratory, as above.

  4. Prior Therapy: Participants must have received standard upfront therapy for medulloblastoma (either with craniospinal radiation or high dose chemotherapy and autologous stem cell rescue. If other therapy utilized, must be discussed with study chairs prior to participation). Participants for Phase 1 and Phase 2 cohort 1 may have received further chemotherapy and/or radiation therapy beyond standard upfront therapy prior to trial enrollment. Participants within the Phase 2 cohort 1 must have experienced at least one, and at most, two relapses prior to study enrollment.

  5. Age 1-25 years old.

  6. Performance Score: Karnofsky ≥ 50 for participants > 16 years of age and Lansky ≥ 50 for participants ≤16 years of age (See Appendix A). Participants who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.

  7. For those participants currently treated with levothyroxine (Synthroid) they must have stable dosing for a minimum of 3 months prior to enrollment.

  8. Organ Function Requirements

    1. Peripheral absolute neutrophil count (ANC) ≥ 1000/cubic millimeters (mm3)

    2. Platelet count ≥ 75,000/microliter (uL) (transfusion independent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment).

    3. A serum creatinine < 1.5 institutional/reference range upper Limit normal (ULN) based on age and gender

    4. Total bilirubin ≤ 3 x upper limit of normal (ULN); in presence of Gilbert's syndrome, total bilirubin ≤ 6 x ULN or direct bilirubin ≤ 3 x ULN

      • Alanine aminotransferase (ALT) ≤ 5 x upper limit of normal (ULN)
      • Aspartate aminotransferase (AST) ≤ 5 x ULN. 3.3.7.4 Adequate Neurologic Function Defined as:
      • Participants with seizure disorder may be enrolled if well controlled. Participants on non-enzyme inducing anticonvulsants may be excluded pending interaction(s) with study drug. 3.3.7.5 Adequate Cardiac Function Defined as:
      • Normal left ventricular systolic function on baseline transthoracic echocardiogram (TTE)
      • Normal left ventricular systolic function is defined as left ventricular ejection fraction (LVEF) >55% or shortening fraction (SF) >28%.

    AND

    • No clinically significant arrhythmia on baseline ECG (sinus arrhythmia, sinus tachycardia, sinus bradycardia, early repolarization and 1st degree atrioventricular block when partial response (PR) interval < 300 millisecond (ms) are not considered clinically significant arrhythmias).
    • In addition, the following ECG findings are not considered clinically significant in the setting of a normal echocardiogram:
    • Left axis deviation
    • Left atrial enlargement
    • Right atrial enlargement
    • Possible left ventricular hypertrophy
    • Possible right ventricular hypertrophy
    • Non-specific T wave abnormality 3.3.7.6 For the Phase 1 cohort, normal adrenal axis function is required. For those participants in the Phase 2 cohort, must have controlled adrenal insufficiency >3 months (no change in steroid replacement or stress dose plan for at least 3 months).
    • Normal adrenal axis function as defined as:
    • Morning (AM) cortisol >11mcg/deciliter (dL)
    • If AM cortisol is <11 microgram (mcg)/dL, cosyntropin stimulation test with rise to >18
  9. Endocrine conditions: Participants with diabetes insipidus, diabetes melitus, or being treated with levothyroxine, must have stable dosing and control for minimum of 3 months prior to enrollment

  10. For Cohort 1 only: participants must have recovered from any surgical procedure before enrolling on this study (see below for examples of major, intermediate, and minor surgical procedures):

    1. Participants with a major surgical procedure within 28 days prior to enrollment should be excluded.
    2. Participants with an intermediate surgical procedure within 14 days prior to enrollment should be excluded.
    3. For minor surgical procedures (including Broviac line or infusaport placement), participants should not receive the first planned dose of bevacizumab until the wound is healed and at least 7 days have elapsed.
    4. There should be no anticipation of need for major surgical procedures during the course of the study.
  11. The effects of L-T3 with chemotherapy on the developing human fetus are unknown. For this reason and because chemotherapy agents as well as other therapeutic agents used in this trial are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation and 4 months after completion of L-T3 and chemotherapy administration. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.

  12. Participants must be enroll on PNOC COMP if PNOC COMP is open to accrual at the enrolling institution.

  13. A legal parent/guardian or participant must be able to understand, and willing to sign, a written informed consent and assent document, as appropriate.

Exclusion Criteria:

  1. For Cohort 1 only: participants who have previously been treated with BIT in combination. Treatment with individual bevacizumab, irinotecan or TMZ is not an exclusion criteria.
  2. Participants who have had myelosuppressive chemotherapy within 3 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier. (Participants receiving chemotherapy directly into the CSF at doses not expected to be myelosuppressive may have received therapy up to 7 days prior to enrollment).
  3. Participants must be at least 7 days since the completion of therapy with a biologic or small molecule agent or non-myelosuppressive chemotherapy agent. For any agent with known adverse events that can occur beyond 7 days after administration, the period prior to enrollment must be beyond the time during which adverse events are known to occur. Such participants should also be discussed with study chairs.
  4. Radiation: For participants on the Phase 1 and Phase 2 Cohort 1, the tumor designated as "measurable" for protocol purposes must not have received radiation within 6 weeks prior to study entry and focal radiation to areas of symptomatic metastatic disease must not be given within 14 days of study entry. If a new lesion occurs outside the radiation field, the participant is eligible to enroll at any time point from completion of radiation. For Cohort 2 participants, there is no required washout for radiation therapy.
  5. Participants who are receiving any other investigational agents.
  6. History of allergic reactions attributed to compounds of similar chemical or biologic composition to L-T3 or other agents used in study.
  7. Participants receiving any medications or substances that are strong inhibitors or strong inducers of CYP450 enzymes are ineligible. Because the lists of these agents are constantly changing, it is important to regularly consult a frequently updated list such as http://medicine.iupui.edu/clinpharm/ddis/table.aspx; medical reference texts such as the Physicians' Desk Reference may also provide this information. As part of the enrollment/informed consent procedures, the participant and/or legal parent or guardian will be counseled on the risk of interactions with other agents, and what to do if new medications need to be prescribed or if the participant is considering.
  8. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection.
  9. Women of childbearing potential must not be pregnant or breast-feeding.
  10. Human immunodeficiency virus- (HIV) positive participants will be ineligible if HIV therapy regimen has not been stable for at least 4 weeks or there is intent to change the regimen within 8 weeks following enrollment, or if they are severely immunocompromised.
  11. Diagnosis of Graves' Disease or other pre-existing hyperthyroid disease.
  12. Participants with severe protein calorie malnutrition that in the opinion of the investigator may not tolerate protocol therapy.
  13. Participants with previous or active clinical cardiovascular disease, including the history of heart failure, myocardial infarction, cardiomyopathy, or ventricular systolic dysfunction on TTE (LVEF <55% or SF <28%), clinically significant arrhythmia (including atrial fibrillation, atrial flutter, frequent ventricular ectopy), clinically significant peripheral vascular disease.
  14. Participants with uncontrolled systemic hypertension (systolic blood pressure > 95th percentile for age and height if participant is ≤ 17 years old)
  15. Participants with uncontrolled diabetes mellitus (HbA1c >8%) or uncontrolled diabetes insipidus

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Ei satunnaistettu
  • Inventiomalli: Peräkkäinen tehtävä
  • Naamiointi: Ei mitään (avoin tarra)

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: Phase 1 Cohort (Cohort 1)

Participants will be treated with a backbone of BIT. L-T3 will be administered on day 1 of each cycle at planned dose levels (DL). Once the Recommended Phase 2 Dose (RP2D) is established with dosing days 1-7, an additional cohort of 6 participants will be treated at the maximum tolerated DL for 14 days of the cycle, Dose level escalation (DLE), which, if tolerated, will become the RP2D. If DLE is not tolerated, the RP2D will become the highest tolerated DL from the prior cohort.

Given IV

Muut nimet:
  • Camptosar

Given orally (PO)

Muut nimet:
  • L-T3

Given IV

Muut nimet:
  • verisuonten endoteliaalisen kasvutekijän (VEGF) estäjä
  • VEGF-estäjä

Given PO

Muut nimet:
  • TMZ
Kokeellinen: Phase 2 Cohort 1- Relapsed/Progressive Disease

Participants will be treated at the RP2D of L-T3 based on the results of the safety Phase 1 cohort. Participants may continue therapy for up to 12 cycles if there is no evidence of unacceptable toxicity, disease progression, or withdrawal of consent. For participants that are benefiting from therapy, they may continue L-T3 monotherapy for one additional year (24 cycles total therapy). Treatment beyond that specified in the protocol should be discussed with the study chairs. Duration of Follow up Participants will enter follow up after the 30-day toxicity period.

Follow-up procedures are to be captured under the PNOC COMP protocol with the exception of protocol defined follow up procedures. Participants will be followed under the PNOC COMP protocol until death or withdrawal from study.

Given IV

Muut nimet:
  • Camptosar

Given orally (PO)

Muut nimet:
  • L-T3

Given IV

Muut nimet:
  • verisuonten endoteliaalisen kasvutekijän (VEGF) estäjä
  • VEGF-estäjä

Given PO

Muut nimet:
  • TMZ
Kokeellinen: Phase 2 Cohort 2 - cfDNA positive in CSF

Children and young adults with medulloblastoma and CSF cf-DNA positivity without radiographic disease progression/recurrence following standard upfront therapy. will include children and young adults with medulloblastoma and positive cf-DNA in CSF following initial standard therapy and will involve a Phase 2 to evaluate clearance of cf-DNA positive disease in CSF in response to L-T3 monotherapy at the RP2D. Cohort 2 will begin enrolling once the RP2D of L-T3 is established.

Given orally (PO)

Muut nimet:
  • L-T3

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Proportion of participants experienced an Adverse Event
Aikaikkuna: Up to 28 days

Proportion of participants with adverse events of L-T3 as graded by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE version 5.0)

Up to 28 days
Proportion of participants who experience dose-limiting toxicity (DLT) (Dose Escalation)
Aikaikkuna: Up to 28 days

The DLT evaluable analysis set includes all participants in the dose-finding part of the study who have received the target doses of L-T3, and who have either experienced a DLT or were followed for the full DLT evaluation period. DLT is defined as L-T3-related toxicity at a frequency ≥33% in any treatment arm.

Up to 28 days
Maximum Tolerated Dose (MTD) (Dose Escalation)
Aikaikkuna: Up to 28 days

The DLT evaluable analysis set includes all participants in the dose-finding part of the study who have received the target doses of L-T3, and who have either experienced a DLT or were followed for the full DLT evaluation period. The MTD is defined as the dose level given for 14 days which ≤ 1/6 participants experience a DLT.

Up to 28 days
Percentage Progressive Free Survival (PFS) at month 9
Aikaikkuna: up to 9 months

Cohort 1 Phase 2, PFS at 9 months is defined as the proportion of patients alive and progression-free 9 months from start of treatment. Any patient lost-to-follow-up prior to 9 months will be considered an event (i.e., progression/death) for the purposes of the analysis.

up to 9 months
Percentage of cf-DNA clearance
Aikaikkuna: Up to 30 days after last dose of L-T3.

Participants in Cohort 2 Phase 2 will be assessed in two serial measurements of at least one month apart to determine cf-DNA clearance in cerebrospinal fluid (CSF). Percentage of participants with cf-DNA clearance will be reported.

Up to 30 days after last dose of L-T3.

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Sponsori

Tutkijat

  • Päätutkija: Sabine Mueller, University of California, San Francisco

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Todellinen)

Perjantai 21. elokuuta 2026

Ensisijainen valmistuminen (Arvioitu)

Maanantai 31. maaliskuuta 2031

Opintojen valmistuminen (Arvioitu)

Maanantai 31. maaliskuuta 2031

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Keskiviikko 14. tammikuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Keskiviikko 14. tammikuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Perjantai 16. tammikuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Maanantai 28. syyskuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Torstai 24. syyskuuta 2026

Viimeksi vahvistettu

Tiistai 1. syyskuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muut tutkimustunnusnumerot

  • 250812
  • NCI-2025-08554 (Rekisterin tunniste: NCI Clinical Trials Reporting Program (CTRP))

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

JOO

IPD-suunnitelman kuvaus

De-identified datasets will be shared with research collaborators during the course of the study.

IPD-jakamista tukeva tietotyyppi

  • STUDY_PROTOCOL
  • MAHLA
  • ICF

Lääke- ja laitetiedot, tutkimusasiakirjat

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Joo

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Ei

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