RRMS: Disease PROgression and Myeloid Profiling After Bone Marrow TRANSPLANTation and Second Line Therapies

Multiple Sclerosis Clinical Trial

— TRANSPLANTPRO  

Official title:

Biomarkers of Disease PROgression and Myeloid Profiling in Patients With Relapsing Remitting Multiple Sclerosis Treated With Autologous Hematopoietic Stem Cell TRANSPLANTation and Second Line Therapies.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06267781
• Other study ID #: TRANSPLANT-PRO
• Status: Recruiting
• Start date: September 2, 2022
• Est. completion date: September 2, 2027

Study information

• Verified date: February 2024
• Source: IRCCS San Raffaele
• Contact: Angela Genchi
• Phone: +390226452846
• Email: genchi.angela[@]hst.it
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

To study whether highly effective therapies can halt disease progression in people with multiple sclerosis by modulating the peripheral myeloid landscape.

Description:

Due to the limited availability of treatment in progressive multiple sclerosis (PMS), an in-depth analysis to better understand (1) the effect of disease-modifying therapies (DMTs) in preventing transition to secondary PMS (SPMS) and (2) the progression-related pathogenetic mechanisms, is essential. This could contribute to change the MS therapeutic perspective halting the progression independent of relapse activity putative processes, beside the prevention of relapse-associated worsening. Myeloablative autologous haematopoietic stem cell transplantation (aHSCT) in relapsing remitting multiple sclerosis (RRMS), differently from other widely used highly effective DMTs such as ocrelizumab and alemtuzumab, could modulate the myeloid activity inducing - after the depletion induced by conditioning regimen - a homeostatic expansion and enhanced immune regulation of monocytes/macrophages and dendritic cells. Currently used DMTs do not primarily target microglia/macrophage-mediated inflammation, and the effect on the abovementioned immune population could account for the advantage of aHSCT, compared to ocrelizumab and alemtuzumab, on progression free survival (PFS). Indeed, alemtuzumab and ocrelizumab achieve a long-term PFS lower than aHSCT. The results of such analyses could guide clinical decisions that will have a long-term impact, given the chronicity of the diseases, the duration of therapies, and the long-lasting effects of some treatments.

Given this premise, by evaluating n.10 consecutively recruited patients with RRMS treated with myeloablative aHSCT in comparison with patients (n.10 per group) treated with anti-cluster of differentiation (CD) 52 monoclonal antibody (alemtuzumab) and anti-CD20 monoclonal antibody (ocrelizumab or ofatumumab), the aims of this longitudinal study are the following:

Aim 1: To evaluate the impact of the studied treatments (myeloablative aHSCT, alemtuzumab and ocrelizumab/ofatumumab) on biomarkers of disease progression in MS. Since to clinically evaluate conversion to SPMS a long follow-up is required, the evaluation of progression's surrogate biomarkers (clinical, neuroradiological and biological) will allow a better and faster identification of the disease course.

Aim 2: To characterize the myeloid compartments' longitudinal changes induced by each treatment (aHSCT, alemtuzumab and ocrelizumab/ofatumumab) in the enrolled patients.

Aim 3: To explore a correlation between characteristics of the myeloid profile and surrogate endpoints of disease progression, assessing whether the treatment-induced homeostatic expansion and enhanced immune regulation of the myeloid compartment are related to surrogate endpoints of progression.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: September 2, 2027
• Est. primary completion date: September 2, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age =18 years;

• Signed written informed consent;

• A diagnosis of RRMS according to the 2017 Revisions of the McDonald Criteria;

• High clinical and magnetic resonance imaging (MRI) inflammatory disease activity (at least 2 clinical relapses, or one clinical relapse with gadolinium (Gd)- enhancing or new T2 MRI lesions at a separate time point, in the previous 12 months)

• Patients referred for pharmacological treatment with aHSCT, alemtuzumab or ocrelizumab /ofatumumab, according to clinical practice following the Italian pharmacological regulatory agency (AIFA) criteria and guidelines and recommendations from the European Society for Blood and Marrow Transplantation (EBMT) Autoimmune Diseases Working Party (ADWP) and the Joint Accreditation Committee of EBMT and ISCT (JACIE);

Exclusion Criteria:

• Diagnosis of PPMS or SPMS according to the 2017 McDonald criteria

• Known intolerances/allergies to the active substance or the excipients contained in the DMT and/or contraindications according to product information

Related Conditions & MeSH terms

• Disease Progression
• Multiple Sclerosis
• Sclerosis

Locations

Country	Name	City	State
Italy	IRCCS San Raffaele	Milan

Sponsors (1)

Lead Sponsor	Collaborator
IRCCS San Raffaele

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of fading/disappearing paramagnetic rim lesions (PRLs)	Evolution of the paramagnetic rim lesions (PRLs), main biomarker of progression, evaluated longitudinally (proportion of stable vs. fading/disappearing PRLs in each group of patients)	2 years (baseline and at 6, 12 and 24 months after study treatment )
Secondary	Surrogate biomarkers of disease progression (MSFC)	Changes in multiple sclerosis functional composite score (MSFC) evaluated longitudinally	2 years (baseline and at 6, 12 and 24 months after study treatment)
Secondary	Surrogate biomarkers of disease progression (sNfL)	Changes in serum neurofilament light chain (sNfL) evaluated longitudinally	2 years (baseline and at 6, 12 and 24 months after study treatment)
Secondary	Surrogate biomarkers of disease progression (RNFL)	Changes in retinal nerve fibre layer (RNFL) thickness evaluated longitudinally	2 years (baseline and at 6, 12 and 24 months after study treatment)
Secondary	Surrogate biomarkers of disease progression (cortical lesions)	Number of new cortical lesions	2 years (baseline and at 6, 12 and 24 months after study treatment)
Secondary	Surrogate biomarkers of disease progression (atrophy)	Changes of brain volumes evaluated longitudinally	2 years (baseline and at 6, 12 and 24 months after study treatment)
Secondary	Changes in myeloid landscape	Peripheral blood myeloid line subpopulations changes induced by each therapy studied by cytofluorometric analysis	2 years (baseline and at 3, 6, 12 and 24 months after study treatment)