A Clinical Study to Investigate Interferon Gamma (IFNɣ) Signature in Patients Post HSCT and in Patients With Impaired HSC Proliferation Pre-transplant

Sobi

Status

Terminated

Conditions

Graft Failure

Treatments

Procedure: blood collection

Study type

Observational

Funder types

Industry

Identifiers

NCT04494061

NI-0501-13

Details and patient eligibility

About

Clinical study designed to collect blood for research purposes in patients after hematopoietic stem cell transplantation (HSCT) or in patients with a medical condition where the blood cells production is impaired. The blood samples will be used to study the role of Interferon gamma (IFNɣ) in graft failure or impairment of hematopoietic stem cell proliferation. The IFNɣ signature will be assessed by measuring primarily IFNɣ and C-X-C Motif Chemokine Ligand 9 (CXCL9).

Full description

This clinical study is designed to investigate IFNγ activity in two cohorts of patients.

First group will include patients post HSCT at risk of graft failure (GF) based on their underlying diseases and on the transplant procedure.
Second group will contain patients with conditions where HSC proliferation is impaired (e.g. aplastic anemia) and with matched controls (healthy volunteers (HV) samples collected outside this clinical protocol).

IFNɣ activity will be assessed by measuring IFNγ and CXCL9 in serum.

For HSCT cohort, the following sampling time points are required: on day -7, pre HSCT on day 0, 1, 3, 5, 9, 13, 17, 21, 28, 31, 38 and one additional sample at the time when primary or secondary GF is suspected if not on the planned schedule. In addition, the following time points are recommended: day 7, 11, 15, 19, 24, 35, 42. It is also suggested to collect a sample when Graft vs Host Disease (GVHD) is diagnosed during any visit that the patients will attend as part of his/her standard treatment during the first 100 days post-transplant. The patient will be followed up until around day 100 post-transplant. This follow up will consist of capturing HSCT outcome information from patient hospital records around day 100.

For IHSCP cohort pre-transplant, it is recommended that, one sample per patient at the time of diagnosis (if possible not more than 1 week from the date of diagnosis) is collected. Age/sex matched control samples should be collected from healthy volunteers or patients with malignant disease outside of this protocol after appropriate consent.

Different sets of data will be collected for the HSCT and IHSCP cohorts respectively as described below:

Data collected for both cohorts

Age and sex
Inflammatory markers
IFNɣ
CXCL9
Other potential relevant exploratory biomarkers
Diagnosis
Date of disease diagnosis
Relevant medical history
Date and time of sample collection

Data collected for HSCT cohort only

Laboratory parameters assessed at the site laboratory on the date of sample collection and between collection dates when available:
Absolute neutrophile count (ANC) and Platelets will be measured as per the schedule of assessment, if possible when routine monitoring of patient health is conducted
Ferritin and Chimerism data will be collected when available (if measured as per site routine practice)
Concomitant medications at the time of sample collection and between collection dates
Presence of infection at the time of sample collection with the date of onset
Presence of donor specific antibodies (DSA)
Transplant information
Date of start of conditioning
Type of conditioning (Reduced Intensity Conditioning (RIC) / Myeloablative Conditioning (MAC) / Non-myeloablative Conditioning (NMAC) and medications
Transplant details (donor type, degree of match, transplant manipulation, stem cell source)
Date of transplant
Date of primary / secondary GF or of confirmed engraftment
GVHD with the date of onset
Post-transplant treatment and date (Donor Lymphocyte Infusion (DLI), Stem Cell (SC) boost, growth factor, GVHD prophylaxis, second HSCT procedure)

Data collected for IHSCP cohort only

Disease severity
In addition, the following data will be recorded for pediatric patients up to 18 years old, if available:
PNH clones
History of hepatitis
Karyotype

Study duration:

The study will be conducted, until the required number of patients is recruited.

HSCT cohort: At patient level, the study will last about 100 days from pre-transplant blood collection to last follow up data collection around day 100 post HSCT, matching the standard HSCT patient care
IHSCP cohort: At patient level the study will last 1 day.

Enrollment

101 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

The patient must have consented to the use of their clinical data and biological samples for research investigations.
In HSCT cohort:
- Patients with underlying:
  
  i. non-malignant hematological disease (e.g. autoimmune and metabolic disorders, aplastic anemia, Sickle cell anemia, Fanconi anemia, Diamond-blackfan anemia, thalassemia, osteopetrosis, Wiskott-Aldrich syndrome, severe combined immunodeficiency) or ii. malignant disease with higher risk of GF, i.e. Acute Myeloid Leukemia (AML) and Acute Lymphoblastic Leukemia (ALL) with primary induction failure, second partial remission or relapse; Chronic Myeloid Leukemia (CML) in blastic phase (circulating blast or blast above 5% in biopsy); Non Hodgkin and Hodgkin Lymphoma and multiple myeloma with primary induction failure, second partial remission or relapse, myelodysplastic syndromes (MDS) and myeloproliferative disorders (MPD) with splenomegaly, myelofibrosis with portal hypertension pre-transplant, MDS/MPD overlap syndromes
- and who received allogeneic HSCT and are at higher risk of graft failure based on at least one of the following criteria: i. Having received reduced intensity conditioning (RIC) or non myeloablative conditioning (NMA) combined with a non-malignant disease or having received graft from Bone Marrow (BM) ii. Ex vivo T cell depleted graft iii. Graft from mismatched unrelated donor or haploidentical donor iv. Graft from Umbilical Cord Blood (UCB)
In the IHSCP cohort:
- Patients with IHSCP pre-transplant (e.g. aplastic anemia)