Status:

RECRUITING

Upfront Autologous HSCT Versus Immunosuppression in Early Diffuse Cutaneous Systemic Sclerosis

Lead Sponsor:

UMC Utrecht

Collaborating Sponsors:

ZonMw: The Netherlands Organisation for Health Research and Development

Boehringer Ingelheim

Conditions:

Systemic Sclerosis

Systemic Scleroses, Diffuse

Eligibility:

All Genders

18-65 years

Phase:

PHASE4

Brief Summary

HSCT has been implemented in (inter)national treatment guidelines for diffuse cutaneous systemic sclerosis (dcSSc) and is offered in clinical care and reimbursed by national health insurance in severa...

Detailed Description

Rationale: This multicentre, randomized, open label trial aims to compare two treatment strategies used in usual care: upfront autologous HSCT versus usual care with (intravenous (i.v.) cyclophosphami...

Eligibility Criteria

Inclusion

  • Age between 18 and 65 years.
  • Fulfilling the 2013 ACR-EULAR classification criteria for SSc
  • Either: 3.1 or 3.2 3.1. Disease duration ≤ 3 years (from onset of first non-Raynaud's symptoms) and diffuse cutaneous disease with
  • \- progressive skin involvement with a mRSS ≥ 15 (in a diffuse pattern: involvement of skin on the upper limbs, chest and/or abdomen)
  • and/or
  • \- major organ involvement as defined by either:
  • a. clinically significant respiratory involvement = i. DLCO and/or (F)VC ≤ 85% (of predicted) and evidence of interstitial lung disease on HR-CT scan with clinically relevant obstructive disease and emphysema excluded. ii. Patients with a DCLO and/or FVC \> 85%, but with a progressive course of lung disease: defined as rela-tive decline of \>10% in FVC predicted and/or TLC predicted, or \>15% in DLCO predicted and evidence of interstitial lung disease on HR-CT scan with clinically relevant obstructive disease and emphysema ex-cluded, within 12 months. Intercurrent infections excluded.
  • b. clinically significant renal involvement = i. new renal insufficiency (serum creatinine \> upper limit of normal) AND
  • persistent urinalysis abnormalities (proteinuria, haematuria, casts), AND/OR
  • microangiopathic haemolytic anaemia AND/OR
  • hypertension (two successive BP readings of either systolic ≥ 160 mm Hg or diastolic \> 110 mm Hg, at least 12 hours apart), ; non-scleroderma related causes (e.g. medication, infection etc.) must be reasonably excluded.
  • c. clinically significant cardiac involvement = any of the following criteria: i. reversible congestive heart failure, ii. atrial or ventricular rhythm disturbances such as atrial fibrillation or flutter, atrial paroxysmal tachycar-dia or ventricular tachycardia, 2nd or 3rd degree AV block, iii. pericardial effusion (not leading to hemodynamic problems), myocarditis; non-scleroderma related causes must have been reasonably excluded
  • 2. Disease duration ≤ 1 year (from onset of first non-Raynaud's symptoms) and diffuse cutaneous disease with mRSS ≥ 10 and
  • High risk ANA for organ based disease: ATA or ARA positivity and/ or
  • Acute phase response (ESR \> 25 mm/h and/or CRP \> 10.0 mg/L )
  • 4\. Written Informed consent

Exclusion

  • Pregnancy or unwillingness to use adequate contraception during study
  • Concomitant severe disease =
  • respiratory: resting mean pulmonary artery pressure (mPAP) \> 25 mmHg (by right heart catheterisation), DLCO \< 40% predicted, respiratory failure as defined by the primary endpoint
  • renal: creatinine clearance \< 40 ml/min (measured or estimated)
  • cardiac: clinical evidence of refractory congestive heart failure; LVEF \< 45% by cardiac echo or cardiac MR; chronic atrial fibrillation necessitating oral anticoagulation; uncontrolled ventricular arrhythmia; pericardial effusion with hemodynamic consequences
  • liver failure as defined by a sustained 3-fold increase in serum transaminase or bilirubin, or a Child-Pugh score C
  • psychiatric disorders including active drug or alcohol abuse
  • concurrent neoplasms or myelodysplasia
  • bone marrow insufficiency defined as leukocytopenia \< 4.0 x 109/L, thrombocytopenia \< 50x 10\^9/L, anaemia \< 8 gr/dL, CD4+ T lymphopenia \< 200 x 106/L
  • uncontrolled hypertension
  • uncontrolled acute or chronic infection, including HIV, HTLV-1,2 positivity
  • ZUBROD-ECOG-WHO Performance Status Scale \> 2
  • Previous treatments with immunosuppressants \> 12 months including MMF, methotrexate, azathioprine, rituximab, tocilizumab, glucocorticosteroids.
  • Previous treatments with TLI, TBI or alkylating agents including CYC.
  • Significant exposure to bleomycin, tainted rapeseed oil, vinyl chloride, trichlorethylene or silica;
  • eosinophilic myalgia syndrome; eosinophilic fasciitis.
  • Poor compliance of the patient as assessed by the referring physicians.

Key Trial Info

Start Date :

September 17 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 1 2030

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT04464434

Start Date

September 17 2020

End Date

October 1 2030

Last Update

December 6 2024

Active Locations (12)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 3 (12 locations)

1

Gaetano Pini-CTO

Milan, Italy

2

Ospedale San Raffaele

Milan, Italy

3

University Hospital Rome

Roma, Italy

4

Amsterdam Rheumatology Centre

Amsterdam, Netherlands

Upfront Autologous HSCT Versus Immunosuppression in Early Diffuse Cutaneous Systemic Sclerosis | DecenTrialz