Wharton Jelly Mesenchymal Stromal Cells as GVHD Prophylaxis

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorCentral Hospital, Nancy, France

About this trial

Despite progress in chemotherapy, targeted therapy and immunotherapy, allogeneic hematopoietic stem cell transplantation (allo-SCT) is still the only curative procedure for some hematological malignancies. The probability of finding a matched sibling donor (MSD) is estimated under the classical 30%, because of the age of patients and their relatives, and a matched unrelated donor (MUD) can take time to identify. Currently in France, 25% of the allo-SCT are performed with an haplo-identical related donor. The Baltimore group developed an approach using haploidentical related donors, RIC, T-replete bone marrow and post-transplant high dose cyclophosphamide (PTCy) in patients with advanced hematological malignancies. PTCy has shown to eradicate alloreactive donor and host T-cells, activated by respective antigens, thereby reducing the incidence of graft versus host disease (GvHD) but delaying hematopoietic recovery. Therefore, the main source of graft is peripheral blood stem cells (PBSC) mobilized by G-CSF in France. Unfortunately, with PBSC we observe a higher cumulative incidence of GvHD (around 50%) and a higher toxicity-related mortality (TRM), especially for recipients \>50 years old. The co-transplantation of Mesenchymal Stem Cells (MSC) at the time of transplantation has previously shown a double interest in GvHD immunomodulation and hematopoiesis support. Pre-clinical studies (in mice) have shown that mesenchymal stromal cells (MSCs) from Wharton's Jelly reduce the incidence of GvHD when the infusions are weekly repeated. We propose a phase I clinical trial to find the maximum tolerated dose (MTD) of a weekly infusion of WJ-MSC administered as GvHD prophylaxis and as a support for a faster hematological reconstitution after haplo-identical allo-SCT.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

With AML/ALL/SMD/SMP or lymphoid neoplasm requiring allogeneic stem cell transplantation

In complete response (CR) for AML/ALL or CR,partial response (PR) or non pre-treated for SMD/SMP and lymphoid neoplasm

Without a HLA matched related donor available and with identification of a haploidentical donor (brother, sister, parents, adult children or cousin)

ECOG ≤ 2

Disqualifiers

History of Cancer in the last 5 years

Uncontrolled infection: Seropositivity for HIV or HTLV-1 or active hepatitis B or C defined by a positive PCR HBV or HCV and hepatic cytolysis due to HBV

Uncontrolled coronary insufficiency, recent myocardial infarction <6 month, current manifestations of heart failure, uncontrolled cardiac rhythm disorders, ventricular ejection fraction <50%

Pulmonary failure with DLCO<50%

Trial design

Design model

Single group

Treatments tested in this trial

  • WJ-MSC infusion

    Biological/Vaccine

    cellular therapy

Treatment groups

12 Participants
are divided into 1 treatment group
Group A: maximum tolerated doseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Maximum Tolerated Dose

The maximum tolerated dose (MTD) will be defined by the highest dose (highest level) where no patient out of 3, or only 1 patient out of 6 presents with dose-limiting toxicity (DLT). The occurrence, within 7 days following one of the three injections, of any adverse event (AE) reasonably related to the injection of CSM-GW grade 3 to 5 according to the NCI-CTCAE classification version 5.0, or part of the "Important Medical Event list", or having a severity criterion The maximum tolerated dose (MTD) will be defined by the highest dose (highest level) where no patient out of 3, or only 1 patient out of 6 presents with dose-limiting toxicity (DLT). The occurrence, within 7 days following one of the three injections, of any adverse event (AE) reasonably related to the injection of CSM-GW grade 3 to 5 according to the NCI-CTCAE classification version 5.0, or part of the "Important Medical Event list", or having a severity criterion

Time frame
7 days

Secondary outcomes

1

acute and chronic GVHD incidence

Time frame
12 months
2

toxicity-related mortality (TRM)

Time frame
12 months
3

relapse incidence (RI)

Time frame
12 months
4

overall surival (OS)

Time frame
12 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Central Hospital, Nancy, France

Lead sponsor

Saint-Louis Hospital, Paris, France

Collaborator

This trial is not recruiting at the moment. You can still explore other options: