Overview
- Background
Sickle cell disease (SCD) is an inherited disorder of the blood. It can damage a person s organs and cause serious illness and death. A blood stem cell transplant is the only potential cure for SCD. Treatments that improve survival rates are needed.
- Objective
To find out if a new antibody drug (briquilimab, JSP191) improves the success of a blood stem cell transplant
- Eligibility
People aged 13 or older who are eligible for a blood stem cell transplant to treat SCD. Healthy family members over age 13 who are matched to transplant recipients are also needed to donate blood.
- Design
Participants receiving transplants will undergo screening. They will have blood drawn. They will have tests of their breathing and heart function. They may have chest x-rays. A sample of marrow will be collected from a pelvic bone.
Participants will remain in the hospital about 30 days for the transplant and recovery. They will have a large intravenous line inserted into the upper arm or chest. The line will remain in place for the entire transplant and recovery period. The line will be used to draw blood as needed. It will also be used to administer the transplant stem cells as well as various drugs and blood transfusions. Participants will also receive some drugs by mouth.
Participants must remain within 1 hour of the NIH for 3 months after transplant. During that time, they will visit the clinic up to 2 times a week.
Follow-up visits will include tests to evaluate participants mental functions. They will have MRI scans of their brain and heart.
Description
Study Description:
We propose to add briquilimab, an antibody targeting CD117 (c-Kit), to the 03-H-0170 regimen to improve myeloid chimerism, in patients considered at high risk for complications from or ineligible from standard myeloablative HSCT. Given the preclinical and clinical data, the addition of briquilimab has the potential to further deplete host lymphoid and myeloid cells to achieve a higher percentage of donor leukocyte engraftment without increased toxicity. Our prior non-myeloablative conditioning (NMA) regimen includes 1 mg/kg of alemtuzumab divided over 5 days, 300 cGy total body irradiation (TBI), and sirolimus for immune suppression. This regimen demonstrated a disease-free survival (DFS) and overall survival (OS) of 87% and 94% respectively, a 13% graft failure rate, no treatment related mortality (TRM), and no acute or chronic GVHD. A large proportion of patients achieves robust (>=98%) donor myeloid chimerism early, but this proportion decreases to 57% at 1, 54% at 2, and 49% at 3, and 50% at 4 years post-transplant. Monoclonal antibodies (mAb) targeting human stem cells (HSCs) is one strategy to improve DFS and may have synergy when combined with TBI as part of transplant conditioning regimen.
- Objectives
Primary Objective:
-To determine if addition of CD117 antibody (briquilimab) would increase proportion of patients with donor myeloid chimerism >=98% at 1 year post transplant
Secondary Objectives:
- To measure briquilimab and alemtuzumab clearance at 1 and 2 years post transplant:
- To compare CD14/15 and CD3 chimerism to protocol 03-H-0170
- Estimate the proportion of patients with donor myeloid chimerism at or above 75%
- To assess the usual transplant related parameters, such as count recovery, transfusion
support, rates of GVHD, viral/bacterial infections, and rates of transplant related and
overall mortality, and compare to those results in 03-H-0170
- Endpoints
Primary Endpoint:
-Percent myeloid (CD14/15) chimerism
Secondary Endpoints:
- Briquilimab antibody PK levels
- Alemtuzumab levels
- Percent T cell (CD3) chimerism
- Day of neutrophil engraftment
- Day of platelet engraftment
- Rates of viral infection and/or reactivation
- Rates of bacterial infection
- Rates of acute and chronic GVHD
- Transplant related mortality
- Non-transplant related mortality
- Rates of graft failure
- Quality of life and neuropsychologic function
Eligibility
- INCLUSION CRITERIA:
Recipient: patients must fulfill one disease category under inclusion criteria 1 and all of
criteria 2
1. 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-SPECIFC THERAPIES (F):
A. Stroke defined as a clinically significant neurologic event that is accompanied by an
infarct on cerebral MRI OR an abnormal trans-cranial Doppler examination (>=200 m/s); OR
B. Sickle cell related renal insufficiency defined by a creatinine level >=1.5 times the
upper limit of normal (see table below) 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) Upper limit of normal serum creatinine (mg/dl)
<= 5 0.8
5 < age <= 10 1.0
10 < age <= 15 1.2
> 15 1.3
C. Tricuspid regurgitant jet velocity (TRV) of >=2.5 m/s in patients >=18 years of age at
least 3 weeks after a vaso-occlusive crisis; OR
D. Recurrent tricorporal priapism defined as at least two episodes of an erection lasting
>=4 hours involving the corpora cavernosa and corpus spongiosa; OR
E. Sickle hepatopathy defined as EITHER ferritin >1000mcg/L OR direct bilirubin >0.4 mg/dL
at baseline in patients >18 years of age; OR
F. Any one of the below complications:
- Complication || Eligible for HSCT
- Vaso-occlusive crises || More than 1 hospital admission per year while on a
therapeutic dose of sickle cell treatment /medication
- Acute chest syndrome (ACS) || Any ACS while on sickle cell treatment /medication
- Osteonecrosis of 2 or more joints || And on sickle cell treatment /medication where
total hemoglobin increase less than 1 g/dL or fetal hemoglobin increases <2.5 times
the baseline level
- Red cell alloimmunization || Total hemoglobin increase <1 g/dL while on therapeutic
doses of 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 subcutaneously for 8-10 hours at least 5 days each week)
- hepatomegaly of greater than 2 cm below the costochondral margin or by other imaging
scans
2. Non disease specific
- Ages >=4 years (>=18 years for phase 1 portion of the study)
- 6/6 HLA matched family donor available
- Ability to comprehend and willing to sign an informed consent, assent obtained
from minors
- Negative serum or urine beta-HCG, when applicable
- Agree to use birth control throughout the study and 12 months after drug product
infusion.
- Female subjects must agree to use a medically acceptable method of birth control such
as oral contraceptive, intrauterine device, barrier and spermicide, or contraceptive
implant/injection from start of screening through 12 months after drug product
infusion.
- Male subjects must agree to use effective contraception (including condoms) from start
of screening through 12 months after drug product infusion.
3. Patients and Capacity to Consent
- Subject provides informed consent prior to initiation of any study procedures.
- Subject understands and agrees to comply with planned study procedures.
4. 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 >=20 kg, eligible to donate
hematopoietic stem cells, who are additionally willing to donate blood for research 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. 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 exclusion criteria:
- ECOG performance status of 3 or more, or Lanksy performance status of <40 (See
Appendix A).
- Diffusion capacity of carbon monoxide (DLCO) <35% predicted (corrected for hemoglobin
and alveolar 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 PBSC
transplant.
- Pregnant or breastfeeding
Donor exclusion criteria:
- Pregnant or breastfeeding
- Cognitively impaired subjects
