- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07599176
Partial Stem Cell Transplant for Sickle Cell Disease From Matched Donors
Matched Related Donor Non-myeloablative Hematopoietic Cell Transplantation With Alemtuzumab, 400 cGy TBI, and Abatacept for Sickle Cell Disease and Beta-Thalassemia
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Study Description:
Our prior non-myeloablative conditioning regimen (03H0170) included 1mg/kg of alemtuzumab divided over 5 days, 300 cGy total body irradiation (TBI), and sirolimus for immune suppression. Sickle disease-free survival (DFS) and overall survival (OS) were 85% and 94% respectively, graft failure 15%, no transplant related mortality (TRM), and acute or chronic GVHD <5%. A large proportion of patients achieved robust (>=95%) donor myeloid chimerism at day 30, but this proportion decreased quickly to 67.2% at 1, 64.9% at 2, and 60% at 3, and 56.9% at 4 years post-transplant.
A subsequent protocol (000539H) added briquilimab, an antibody targeting CD117 (c-Kit), to alem-300 cGy TBI regimen, but did not reduce the gradual decline in donor myeloid chimerism as originally hypothesized, leading to protocol closure. Rates of graft failure was 20%, no TRM, acute GVHD was 5%, and no chronic GVHD. We now propose to increase TBI to 400 cGy to further deplete host lymphoid and myeloid cells to achieve a higher percentage of donor leukocyte engraftment without substantially increasing toxicity. Since we will continue to use filgrastim to mobilize and collect donor hematopoietic cells, we also add abatacept to preserve the low rates of GVHD.
Objectives:
Primary Objective:
To reduce the proportion of patients with graft failure or donor myeloid chimerism <95%
Secondary Objectives:
- To compare CD14/15 and CD3 chimerism to prior MRD HCT protocols (03-H-0170, 14-H-0077, and 000539H)
- To assess the usual transplant related parameters, such as count recovery, transfusion support, rates of GVHD, viral/bacterial infections, rates of transplant related and overall mortality, and compare to prior MRD HCT protocols
Tertiary Objectives:
- To compare changes in organ function
- To examine neuropsychological functioning, wellbeing, and pain before and after HCT
- To obtain reproductive health related changes before and after HCT
Endpoints:
Primary Endpoint: proportion of participants with graft failure or myeloid chimerism <95% at 1 year post HCT
Secondary Endpoints:
- Percent myeloid (CD14/15) chimerism at day 30, 60, 100, 1 year, 2 years, and 3 years post HCT
- Percent T cell (CD3) chimerism at day 30, 60, 100, 1 year, 2 years, and 3 years post HCT
- Day of neutrophil engraftment per CIBMTR definition
- Day of platelet engraftment per CIBMTR definition
- Rates of viral reactivation or infection to day 100 post HCT
- Rates of acute and chronic GVHD at 1 and 2 years post HCT, respectively
- Rates of graft failure or myeloid chimerism <95% at 1 year post HCT
- Transplant related mortality at 1, 2, and 3 years post HCT
- Non-transplant related mortality at 1, 2 and 3 years post HCT
Exploratory Endpoints:
-Quality of life, neuropsychologic function, reproductive health questionnaires, serial testing or imaging of organ function/status
Studietype
Inschrijving (Geschat)
Fase
- Fase 2
- Fase 1
Contacten en locaties
Studiecontact
- Naam: John F Tisdale, M.D.
- Telefoonnummer: (301) 402-6497
- E-mail: johntis@mail.nih.gov
Studie Contact Back-up
- Naam: Kelly S Norris, R.N.
- Telefoonnummer: (301) 529-7104
- E-mail: kelly.norris@nih.gov
Studie Locaties
-
-
Maryland
-
Bethesda, Maryland, Verenigde Staten, 20892
- Werving
- National Institutes of Health Clinical Center
-
Contact:
- NIH Clinical Center Office of Patient Recruitment (OPR)
- Telefoonnummer: TTY dial 711 800-411-1222
- E-mail: ccopr@nih.gov
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
- INCLUSION CRITERIA
RECIPIENT:
Participants must fulfill one disease category (1 or 2) and 3
Patients with sickle cell disease at high risk for disease related morbidity or mortality, defined by having an end-organ damage (A, B, C, D, OR E) or complication(s) not ameliorated by sickle cell-specific therapies (F):
A. Stroke defined as a clinically significant neurologic event that is accompanied by an infarct on cerebral MRI ORb
B. Abnormal trans-cranial Doppler examination (>=200 cm/s); OR
C. Silent cerebral infarct defined as an infarct-like lesion based on an MRI signal abnormality at least 3 mm in one dimension and visible in two planes on FLAIR or T2- weighted images (or similar image with 3D imaging) and documented neurological examination performed by a neurologist demonstrating the participant has a normal neurologic examination, or an abnormality on examination that could not be explained by the location of the brain lesion(s); OR
D. Sickle cell related renal insufficiency defined by a creatinine level >=1.5 times the upper limit of normal and kidney biopsy consistent with sickle cell nephropathy OR nephrotic syndrome OR creatinine clearance <60mL/min/1.73m2 for patients <16 years of age or <50mL/min for patients >16 years of age OR requiring peritoneal or hemodialysis; OR
Age (Years): <= 5 / Upper limit of normal serum creatinine (mg/dl): 0.8
Age (Years): 5 < age <= 10 / Upper limit of normal serum creatinine (mg/dl): 1.0
Age (Years): 10 < age <= 15 / Upper limit of normal serum creatinine (mg/dl): 1.2
Age (Years): > 15 / Upper limit of normal serum creatinine (mg/dl): 1.3
E. Tricuspid regurgitant jet velocity (TRV) of >=2.5 m/s in patients at least 3 weeks after a vaso-occlusive crisis; OR
F. Recurrent severe priapism defined as at least two episodes of an erection lasting >=4 hours requiring medical intervention (e.g. aspiration, injection of vasoconstrictor, prior penile surgery.); OR
G. Sickle hepatopathy defined as EITHER ferritin >1000mcg/L OR direct bilirubin >0.4 mg/dL at baseline; OR
H. Vaso-occlusive crises: more than 1 hospital admission per year while on a therapeutic dose of sickle cell treatment /medication; OR
I. Acute chest syndrome (ACS): any ACS while on sickle cell treatment /medication
Patients with beta-thalassemia who have grade 2 or 3 iron overload, determined by the presence of 2 or more of the following:
- Portal fibrosis by liver biopsy
- Inadequate chelation history (defined as failure to maintain adequate compliance with chelation with deferoxamine initiated within 18 months of the first transfusion and administered at least 5 days each week)
- Hepatomegaly of greater than 2 cm below the costochondral margin or by other imaging scans
Non disease specific
- Ages >=4 years and less than 65 years old
- Fully matched human leukocyte antigen (HLA) donors at A, B, C, and DR loci (8 of 8 or 10 of 10)
- Ability to comprehend and willing to sign an informed consent, assent obtained from minors when applicable. Negative serum or urine beta-HCG, when applicable
Agree to use birth control throughout the study and 3 months after abatacept or sirolimus administration.
- Female subjects must agree to use a medically acceptable method of birth control such as oral contraceptive, intrauterine device, barrier and spermicide, or implant/injection from start of screening until immunosuppression is stopped.
- Male subjects must agree to use effective contraception (including condoms) from start of screening until immunosuppression is stopped.
DONOR:
- Fully matched human leukocyte antigen (HLA) donors at A, B, C, and DR loci (8 of 8 or 10 of 10) are intended for this study.
- Donors age 4 or older and >=15 kg (or weight deemed acceptable by IR for line placement, DTM for apheresis, and pediatric consult service) eligible to donate hematopoietic stem cells, are eligible for this study.
- Donors will be evaluated in accordance with existing Standard NIH Policies and Procedures for determination of eligibility and suitability for clinical donation. Donors will sign on a separate protocol, 20-H-0099 NHLBI standard of care protocol for the mobilization and collection of HSCs. Note that participation in this study is offered to all eligible donors, but is not required for a donor to make a stem cell donation, so it is possible that not all donors will enroll onto this study.
EXCLUSION CRITERIA
RECIPIENT:
- Karnofsky or Lanksy performance status of <40
- Diffusing capacity of carbon monoxide <35% predicted: DLCO corrected for hemoglobin or KCO (corrected for lung volume). This criterion may be omitted in young children (e.g. near age 5) or other individuals who may have difficulty understanding or complying with instructions of testing.
- Baseline oxygen saturation of <85% or PaO2 <70
- Left ventricular ejection fraction: <35% estimated by ECHO
- Transaminases >5x upper limit of normal for age
- Evidence of uncontrolled bacterial, viral, or fungal infections (currently taking medication and progression of clinical symptoms) within one month prior to starting the conditioning regimen
- Major anticipated illness or organ failure incompatible with survival from HCT
- Pregnant or breastfeeding
DONOR:
- Pregnant or breastfeeding
- Cognitively impaired subjects
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Sequentiële toewijzing
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Ander: Matched related donors
Donors for patients
|
About 5 tablespoons of blood will be collected from donors for research purposes.
|
|
Experimenteel: Transplant recipients
Patients with symptomatic sickle cell disease or beta-thalassemia
|
About 5 tablespoons of blood will be collected from donors for research purposes.
Total Body Irradiation 400 cGy
1 mg/kg
10 mg/kg x 6
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Donor myeloid chimerism
Tijdsspanne: 1 year
|
percentage of donor myeloid chimerism
|
1 year
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Donor CD3 chimerism
Tijdsspanne: 1 year
|
percentage of donor myeloid chimerism
|
1 year
|
|
Overall survival
Tijdsspanne: 1 year
|
percentage of patients surviving at 1 year
|
1 year
|
|
Acute Graft versus Host Disease
Tijdsspanne: 1 year
|
percentage of patients with Grade 2-4 acute GVHD
|
1 year
|
Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: John F Tisdale, M.D., National Heart, Lung, and Blood Institute (NHLBI)
Publicaties en nuttige links
Nuttige links
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Genetische ziekten, aangeboren
- Hematologische ziekten
- Bloedarmoede, hemolytisch, aangeboren
- Bloedarmoede, hemolytisch
- Bloedarmoede
- Hemoglobinopathieën
- Thalassemie
- Aangeboren, erfelijke en neonatale ziekten en afwijkingen
- Hemische en lymfatische ziekten
- Bloedarmoede, sikkelcel
- bèta-thalassemie
- Immunoconjugaten
- Aminozuren, peptiden en eiwitten
- Eiwitten
- Onderzoekstechnieken
- Therapeutica
- Antilichamen, monoklonaal, gehumaniseerd
- Antilichamen, monoklonaal
- Antilichamen
- Immunoglobulinen
- Immunoproteïnen
- Bloedeiwitten
- Serum -globulines
- Globulines
- Radiotherapie
- Abatacept
- Alemtuzumab
- Bestraling van het hele lichaam
Andere studie-ID-nummers
- 10002545
- 002545-H
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .