Status:

TERMINATED

Allogeneic Hematopoietic Stem Cell Transplantation (NST) for Patients With Systemic Sclerosis

Lead Sponsor:

Richard Burt, MD

Conditions:

Scleroderma

Eligibility:

All Genders

18-55 years

Phase:

PHASE1

Brief Summary

Scleroderma is disease believed to be due to immune cells, cells which normally protect the body but are now causing damage to the body. There has not been any treatment that has been effective in tre...

Eligibility Criteria

Inclusion

  • Patient
  • Age 18 to 55 years old
  • An established diagnosis of scleroderma (84)
  • Diffuse cutaneous scleroderma with involvement proximal to the elbow or knee and a Rodnan score (see Appendix III) of \> 14 (85)
  • And one of the following:
  • DLCO \< 80% of predicted or decrease in lung function (TLC, DLCO or FEV1) of 10% or more over 12 months
  • Active alveolitis on bronchoalveolar lavage
  • Pulmonary fibrosis or alveolitis on CT scan or CXR
  • Elevated ESR greater than or equal to 25mm/hour confirmed on a second occasion at least two weeks apart without evidence of active infectious process.
  • Abnormal EKG (low QRS voltage, or ventricular hypertrophy) or left ventricle (LV) diastolic dysfunction (expressed by an inverted E/A ratio which represents early and late filling of the LV during atrial contraction) or LV wall thickness
  • Since pulmonary disease independent of skin score (NEJM, 2006, 345:25 2655-2709) carries a poor prognosis, patient may be enroled for only lung involvement defined as active alveolitis on BAL or ground-glass opacity on CT, a DLCO \< 80% predicted or decrease in lung function (TLC), DLCO, FVC) of 10% or more in last 12 months.
  • Patient

Exclusion

  • Poor performance status (ECOG \> or =2) at the time of entry, unless due to disease.
  • Significant end organ damage such as:
  • LVEF \<40% or deterioration of LVEF during exercise test on MUGA or echocardiogram
  • Untreated life-threatening arrhythmia
  • Active ischemic heart disease or heart failure
  • DLCO less than 45% of predicted value, unless due to disease.
  • Pulmonary hypertension (estimated systolic pulmonary arterial pressure \>40 mmHg by Doppler echocardiography or measurement by pulmonary arterial catheter)
  • Serum creatinine \> 2.0 mg/dl
  • Liver cirrhosis, transaminases \>3x of normal limits or bilirubin \>2.0 unless due to Gilberts disease
  • HIV positive
  • Uncontrolled diabetes mellitus or any other illness that in the opinion of the investigators would jeopardize the ability of the patient to tolerate aggressive treatment
  • Prior history of malignancy except localized basal cell or squamous skin cancer. Other malignancies for which the patient is judged to be cured by local surgical therapy, such as (but not limited to) head and neck cancer, or stage I or II breast cancer will be considered on an individual basis.
  • Positive pregnancy test, inability or unable to pursue effective means of birth control, failure to willingly accept or comprehend irreversible sterility as a side effect of therapy
  • Psychiatric illness or mental deficiency making compliance with treatment or informed consent impossible
  • Inability to give informed consent
  • Age \<18 or \> 55 years old
  • Donor Inclusion Criteria:
  • Donor must be a HLA identical sibling or HLA matched cord blood donor
  • If donor is HLA matched sibling, donor must be \> 18 years of age and less than 50 years old
  • If multiple HLA matched donors are available, preference will be given to same sex, same CMV status, or in the case of cord blood higher nucleated cell count
  • If donor is HLA matched cord blood, cord blood stem cells will be obtained from the New York Blood Center Cord Blood Registry (Tel 212-570-3230) which is an internationally recognized registry or, if a match is not available, from Stemcyte (626-821-9860) which is a commercial registry that specializes in minority donors. One unit of HLA matched cord blood unit will be infused on day zero
  • Donor

Key Trial Info

Start Date :

May 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2012

Estimated Enrollment :

8 Patients enrolled

Trial Details

Trial ID

NCT00282425

Start Date

May 1 2005

End Date

December 1 2012

Last Update

December 18 2012

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Northwestern University, Feinberg School of Medicine

Chicago, Illinois, United States, 60611