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NCT07372885Toborzás még nem indult1/2. fázis

GRanulocyte Augmented Cord Blood Transplantation for Poor Risk leukaEmia

A Multi-centre Phase I/II Trial of Granulocyte-augmented Cord Blood Transplantation for Young Adults With Very Poor Risk Acute Myeloid Leukaemia.

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. márc. 11.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

Allogeneic stem cell transplantation is the only potentially curative therapy for patients with high-risk Acute Myeloid Leukaemia, but relapse is common and remains the leading cause of death. Patients with certain mutations and those transplanted without first clearing their disease have very poor outcomes with most relapsing soon after transplant, and then surviving only a few months. A recent trial at the Royal Manchester Children's Hospital used cord blood stem cells alongside a type of white blood cell called 'granulocytes' and produced surprisingly good outcomes for children with very resistant leukaemia. GRACE is a clinical trial for adults (<55 years) with Acute Myeloid Leukaemia that has not responded to chemotherapy or harbours mutations that predict a very poor response to conventional transplant. Participants will receive a transplant using umbilical cord blood and be given additional infusions of white blood cells, called granulocytes. The trial will be split into two parts:-The first will study the safety of this new approach. The experience of the investigators in children is that granulocyte infusions cause a fever, rash and expansion of another type of white blood cell called lymphocytes. Children that did not have this reaction did not respond to treatment. The investigators therefore believe that the reaction is necessary for the treatment to work, but the investigators must ensure that it is safe in adult patients. The trial design allows the investigators to determine the dose of granulocytes that is best tolerated and most likely to be effective. The aim of the second part is to demonstrate that the new treatment is more effective than conventional transplantation. The study will be conducted in three NHS transplant centres. Patients will be recruited over 36 months and followed up for a minimum of 1 year. The study is funded by Blood Cancer UK.

Állapot (regiszter)
Toborzás még nem indult
Fázis (regiszter)
1/2. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
50 (tervezett)
Első benyújtás
2025. nov. 20.
Kezdés
2026. febr. 9.
Elsődleges befejezés
2028. dec. 31.
Fő szponzor
University of Manchester
NCT-szám
NCT07372885

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 1/2. fázis
  • Tervezett résztvevők: 50
  • 2026. febr. 9. és az elsődleges befejezés (2028. dec. 31.) között
  • 3 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Prior allogeneic stem cell transplant
  • Participation in another clinical trial that would alter any aspect of the transplant protocol or that aims to reduce the subsequent risk of relapse (discuss with trial team if unsure)
  • Previous history of sensitivity to granulocytes
  • Any other organ dysfunction or co-morbidity that precludes transplant in the opinion of the investigator

Más betegség

  • Active CNS disease
  • History of cardiac arrhythmia
  • Ischaemic heart disease, valvular heart disease or congestive cardiac failure
  • Rheumatologic disease (SLE, RA, polymyositis, mixed CTD or polymyalgia rheumatica)
  • Ulcerative colitis or Crohn's disease
  • Presence of an active second malignancy
  • Uncontrolled infection, including viral reactivation (CMV, EBV)
  • HIV positive
  • Hepatitis B/C active infection with measurable viral load (patients with chronic hepatitis B or C infection require clear documentation of absence of cirrhosis by either fibroscan or biopsy, regardless of viral load)

Egyéb

  • AML Secondary to a myeloproliferative neoplasm
  • Transient ischaemic attack or cerebrovascular accident
  • Liver cirrhosis
  • Pregnancy, breastfeeding, unwilling to use contraception
  • Contraindications to administration of pooled granulocytes
  • Inability of patient to give informed consent
  • Any concern by PI

Kiket keres a vizsgálat

  • Availability of a suitable cord blood unit
  • Age between 16 and 55 years
  • Primary diagnosis of Acute Myeloid Leukaemia (AML) or MDS/AML (as defined by ICC 2022) fitting one or more of the following criteria:
    • TP53 mutation (single- or multi-hit)
    • Presence of inv(3) (q21.3q26.2) or t(3;3)(q21.3;q26.2)
    • Adverse risk (as per ICC 2022) and >0.1% MRD by flow cytometry after 2 cycles of induction
    • AML (any risk) with partial remission (<10% blasts) after 2 cycles induction
    • Early relapse (<6 months) after chemotherapy alone (excluding t(16;16), inv(16) or t(8;21))
  • Bone marrow performed within 28 days of starting conditioning chemotherapy demonstrates either:
    • <10% blasts
    • >10% blasts with a hypocellular background (must be discussed with the trial team)
  • Suitable fitness and organ function as per the following criteria:
    • Glomerular filtration rate >50 mL/min/1.73m2
    • Ejection fraction >50%
    • FEV1 >65% without dyspnoea on mild activity
    • AST/ALT <3 x ULN
    • Bilirubin <1.5 x ULN (excluding Gilbert's syndrome)
    • Performance Status (ECOG) of 0 or 1
  • Females of and male patients of reproductive potential (i.e., not post-menopausal or surgically sterilised) must agree to use appropriate, highly effective, contraception from the point of commencing therapy until 12 months after transplant

Életkor a regiszterben: 16 év – 55 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (3)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
The Royal Marsden Hospital NHS Foundation TrustLondonEgyesült KirályságIsmeretlen állapot
Kings College Hospital NHS TrustLondonEgyesült KirályságIsmeretlen állapot
The Christie NHS Foundation TrustManchesterEgyesült KirályságIsmeretlen állapot

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