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Clinical Trials/NCT01047072
NCT01047072
Withdrawn
Phase 2

Phase II Clinical Trial of Allogeneic Hematopoietic Cell Transplantation After Nonmyeloablative Conditioning for Patients With Severe Systemic Sclerosis

Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium1 site in 1 countryJanuary 12, 2010

Overview

Phase
Phase 2
Intervention
fludarabine phosphate
Conditions
Systemic Scleroderma
Sponsor
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
Locations
1
Primary Endpoint
Event-free survival
Status
Withdrawn
Last Updated
13 years ago

Overview

Brief Summary

The purpose of the study is to see how well reduced intensity conditioning followed by a stem cell transplant from a donor (allogeneic) works in treating patients with severe systemic sclerosis. In an allogeneic stem cell transplant procedure, stem cells are taken from a healthy donor and transplanted into the patient. Stem cells can be donated by a family member or an unrelated donor who is a complete tissue type match.

Detailed Description

PRIMARY OBJECTIVES: I. To evaluate the overall effects of allogeneic hematopoietic cell transplantation (HCT) in systemic sclerosis (SSc). II. To assess the potential efficacy, in terms of event-free survival (EFS) at 2 (part 1) and 5 (part 2) years, of allogeneic HCT as treatment for patients with severe SSc. SECONDARY OBJECTIVES: I. To evaluate the rate of complications of allogeneic HCT after nonmyeloablative conditioning including the incidence of graft rejection, regimen-related toxicities, severe acute and chronic graft-vs-host disease (GVHD), infectious complications, treatment-related mortality (TRM), and overall survival. II. To evaluate treatment effects on disease activation/progression, as indicated by measures of cardiac, pulmonary, gastrointestinal and renal function, as well as skin thickness, overall functional assessment (SHAQ), use of concomitant disease-modifying antirheumatic drugs (DMARDs), and occurrence of myositis. III. To evaluate disease responses after nonmyeloablative conditioning and allogeneic HCT or immunomodulatory therapy, assessing skin disease by modified Rodnan Skin Score (mRSS), pulmonary function as measured by diffusing capacity of the lung for carbon monoxide (DLCO) and forced vital capacity (FVC), Modified Scleroderma Health Assessment Questionnaire (SHAQ), and Quality of Life using Short Form 36 (SF36). IV. To evaluate, by mechanistic studies, of the effect of allogeneic HCT on dermal fibrosis and vasculopathy. V. To evaluate the late complications of allogeneic HCT after nonmyeloablative conditioning including the incidence and prevalence of chronic GVHD and time to discontinue immunosuppression, infectious complications, TRM and overall survival. VI. To evaluate the treatment effects on disease activation/ progression, as indicated by measures of cardiac, pulmonary, gastrointestinal and renal function, as well as skin thickness, overall functional assessment (SHAQ), use of concomitant DMARDs, and occurrence of myositis. VII. To evaluate disease responses after nonmyeloablative conditioning and allogeneic HCT or immunomodulatory therapy, assessing skin disease by modified Rodnan Skin Score (mRSS), pulmonary function as measured by DLCO and FVC, Modified Scleroderma Health Assessment Questionnaire (SHAQ), and Quality of Life using Short Form 36 (SF36). OUTLINE: Patients are assigned to 1 of 2 treatment arms and receive nonmyeloablative conditioning followed by an allogeneic peripheral blood stem cell transplantation. Treatment in both arms continues in the absence of disease progression of unacceptable toxicity. ARM I (transplant): Patients receive fludarabine intravenously (IV) on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus orally (PO) twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper. ARM II (nontransplant): Patients will receive immunosuppressive therapy based on their history. The 3 options that they may receive include 1.)mycophenolate mofetil PO twice daily for 16 months, 2.) Rituximab IV on days 1 and 15 and then repeated at 6 months, and 3.) Cyclophosphamide IV at 28-32 day intervals or orally once daily for 16 months. After completion of study treatment, patients are followed up periodically for 5 years.

Registry
clinicaltrials.gov
Start Date
January 12, 2010
End Date
September 2017
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium

Eligibility Criteria

Inclusion Criteria

  • Patients with severe SSc as defined by the American College of Rheumatology and at high-risk for a fatal outcome based on the following prognostic factors from groups 1-5:
  • Group 1: Patients with 1) both a. and b. below; and 2) at least one of c., d. or e:
  • a. Diffuse cutaneous scleroderma with skin score of \>= 16 (modified Rodnan skin scale)
  • b. Duration of systemic sclerosis =\< 5 years from the onset of first non-Raynaud's symptom
  • c. Presence of interstitial lung disease with FVC or DLCOcorr =\< 70% of predicted and evidence of alveolitis (abnormal bronchoalveolar lavage \[BAL\] or high resolution chest computed tomography \[CT\] scan)
  • d. Left heart failure with left ventricular ejection Fraction (LVEF) \< 50% or pericardial effusion (mild-moderate) or 2nd or 3rd Atrial-Ventricular (AV) block; Myocardial disease not secondary to SSc must be excluded by a cardiologist
  • e. History of SSc-related renal disease that is not active at the time of screening; History of scleroderma hypertensive renal crisis is included in this criterion
  • Group 2: Patients will have progressive pulmonary disease as the primary indication for transplant as defined by a decrease in the FVC or DLCO by 15 percent or greater in the previous 12-month period. In addition, patients may have either less skin involvement than group 1 (mRSS \< 16) if they have a history of diffuse cutaneous disease and the FVC or DLCOcorr is \< 70% or both FVC and DLCOcorr \>= 70% if they have diffuse cutaneous disease (mRSS \> 16) at screening for the study; Patients must also have evidence of alveolitis as defined by abnormal chest CT or BAL
  • Group 3: Have progressive active SSc after prior autologous HCT based on the presence of progressive pulmonary disease; This will be defined by a decrease in the FVC since prior autologous transplant by 10 percent or greater, or DLCO since prior autologous transplant by 15 percent or greater in addition to evidence of alveolitis as defined by chest CT changes or BAL; If patients had prior autologous HCT on the SCOT clinical trial, they must have failed based on the defined study endpoints and be approved by the protocol principal investigator (PI)
  • Group 4: Patients who meet group 1 inclusion criteria but have FVC or DLCO \< 70% plus have had an adverse event to cyclophosphamide preventing its further use (i.e., hemorrhagic cystitis, leucopenia with WBC, 2000 or ANC \< 1000 or platelet count \< 100,000 and other adverse events)

Exclusion Criteria

  • Eligible for the NIH-sponsored randomized clinical trial (SCOT)
  • Fertile men or women unwilling to use contraceptive techniques during and for 12 months or until immunosuppression is discontinued following transplantation
  • Evidence of ongoing active infection
  • Pregnancy
  • Subjects with pulmonary, cardiac, hepatic, or renal impairment that would limit their ability to receive therapy and compromise their survival. This includes but is not restricted to, subjects with any of the following:
  • Severe pulmonary dysfunction defined as:
  • A hemoglobin corrected DLCOcorr \< 30% or FVC \< 40% of predicted; or
  • O2 saturation \< 92% at rest without supplemental oxygen; or
  • PO2 \< 70 mmHg or pCO2 \> 50 mmHg without supplemental oxygen
  • Significant uncontrolled pulmonary hypertension defined as:

Arms & Interventions

Arm I (transplant)

Patients receive fludarabine IV on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus PO twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper.

Intervention: fludarabine phosphate

Arm I (transplant)

Patients receive fludarabine IV on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus PO twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper.

Intervention: total-body irradiation

Arm I (transplant)

Patients receive fludarabine IV on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus PO twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper.

Intervention: tacrolimus

Arm I (transplant)

Patients receive fludarabine IV on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus PO twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper.

Intervention: mycophenolate mofetil

Arm I (transplant)

Patients receive fludarabine IV on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus PO twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper.

Intervention: nonmyeloablative allogeneic hematopoietic stem cell transplantation

Arm I (transplant)

Patients receive fludarabine IV on days -4 to -2. Patients undergo total-body irradiation on day 0. Patients then undergo peripheral blood stem cell transplantation on day 0. Patients receive GVHD prophylaxis comprising tacrolimus PO twice daily on days -3 to 180 and taper and mycophenolate mofetil PO three times daily on days 0-28 and then twice daily until day 180 and taper.

Intervention: peripheral blood stem cell transplantation

Arm II (nontransplant)

Patients receive mycophenolate mofetil PO twice daily for 16 months, rituximab IV on days 1 and 15 and then repeated at 6 months, and cyclophosphamide IV at 28-32 day intervals or orally once daily for 16 months.

Intervention: mycophenolate mofetil

Arm II (nontransplant)

Patients receive mycophenolate mofetil PO twice daily for 16 months, rituximab IV on days 1 and 15 and then repeated at 6 months, and cyclophosphamide IV at 28-32 day intervals or orally once daily for 16 months.

Intervention: rituximab

Arm II (nontransplant)

Patients receive mycophenolate mofetil PO twice daily for 16 months, rituximab IV on days 1 and 15 and then repeated at 6 months, and cyclophosphamide IV at 28-32 day intervals or orally once daily for 16 months.

Intervention: cyclophosphamide

Outcomes

Primary Outcomes

Event-free survival

Time Frame: 2 years

Secondary Outcomes

  • Event-free survival(5 years)
  • Overall survival(5 years)
  • Time to progression(5 years)
  • Incidence of initiation of any SSC disease-modifying therapy other than that specified in the protocol treatment arms(Up to 5 years)
  • Incidence of definite and probable viral, fungal, and bacterial infections(Up to 5 years)
  • Median time to engraftment as defined as having greater than or equal to 5% donor T cells in the peripheral blood (donor T cell chimerism)(From date of transplant to time of engraftment)
  • Rate of primary graft failure(Day 56)
  • Rate of secondary graft failure(1 year)
  • Probability of acute and chronic GVHD(Up to 5 years)

Study Sites (1)

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