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OpenTrials
Completed

NCT Number: NCT00350181

Sirolimus & Mycophenolate Mofetil as GVHD Prophylaxis in Myeloablative, Matched Related Donor HCT

GVHD prophylaxis of sirolimus and mycophenolate mofetil for patients undergoing matched related allogeneic transplant for acute and chronic leukemia, MDS, high risk NHL and HL

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Key information

Age range

2 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Stanford University School of Medicine

Stanford, California, 94305, United States

About this study

To explore the novel combination of sirolimus and mycophenolate mofetil (MMF) as graft versus host disease (GVHD) prevention in HLA matched related donor blood or marrow transplantation (BMT). This study will report the toxicities associated with this drug combination and also explore possible correlations between specific blood cell types and antibody production during this therapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Disease Categories: (one of the following)
  • AML, age 2 - 60 years beyond 2nd remission or relapsed/refractory disease
  • AML, age 51-60 years of age, in first or subsequent remission or relapsed/refractory disease
  • AML with multilineage dysplasia
  • ALL, age 2 - 60 years beyond 2nd remission or relapsed/refractory disease
  • ALL, age 51 - 60 years in first or subsequent remission or relapsed/refractory disease
  • CML Beyond 2nd chronic phase or in blast crisis
  • MDS; Includes World Health Organization classifications of refractory anemia with excess blasts-1 (RAEB-1), RAEB-2 and therapy-related MDS
  • Myeloproliferative disorders; MDS with poor long-term survival including myeloid metaplasia and myelofibrosis
  • High risk NHL in first remission
  • Relapsed or refractory NHL
  • HL beyond first remission
  • Males and females of any ethnic background 2 - 60 years of age
  • Karnofsky Performance Status ≥ 70% or Lansky performance status > 70% for patients < 16 years of age.
  • Matched related donor identified: 6/6 HLA-A, B and DRB1
  • Willingness to take oral medications during the transplantation period
  • Ability to understand and the willingness to sign a written informed consent document

Exclusion criteria

  • Prior myeloablative allogeneic or autologous HCT
  • HIV infection
  • Pregnant
  • Lactating females
  • Evidence of uncontrolled active infection
  • Organ Dysfunction:
  • Serum creatinine > 1.5 mg/dL or 24 hour creatinine clearance < 50 ml/min
  • Direct bilirubin, ALT or AST > 2 x ULN
  • In adults DLCO < 60% predicted and in children room air oxygen saturation < 92%
  • In adults, left ventricular ejection fraction < 45% and in children, shortening fraction < 26%
  • Fasting Cholesterol > 300 mg/dL or Triglycerides > 300 mg/dL while on lipid-lowering agents.
  • Patients receiving investigational drugs unless cleared by the PI.
  • Patients with prior malignancies except basal cell carcinoma or treated carcinoma in-situ.
  • Cancer treated with curative intent > 5 years will be allowed.
  • Cancer treated with curative intent ≤ 5 years will not be allowed with PI approval.

Treatment and study plan

sirolimus

Drug

Immunosuppressant beginning day -3 with 12 mg oral loading dose, 4 mg/day orally for adults

Other names: rapamycin

MMF

Drug

Immunosuppressant given through IV on day 0 at 15 mg/kg twice daily ≥ 2hr after the completion for the donor cell infusion

Other names: Mycophenolate Mofetil

bcnu

Drug

15 mg/kg, IV

Other names: Carmustine, BiCNU

VP-16

Drug

60 mg/kg, IV

Other names: etoposide

CY

Drug

For subjects aged 18-60 with lymphoma 100 mg/kg, IV For subjects aged with AML, ALL or CML 18-50 60 mg/kg, IV For subjects aged 51-60 with MDS, AML or ALL or patients age 18-60 with MDS, secondary AML or non-CML myeloproliferative disease 45 mg/kg

Other names: cyclophosphamide, cytophosphane, Endoxan

FTBI

Drug

1320 cGy delivered in 11 120 cGy fractions over 4 day

Other names: total body irradiation

BU

Drug

BU 1 mg/kg every 6hr x 4 doses, IV

Other names: busulfan

Primary outcomes

  1. To evaluate the incidence of grade II-IV acute GVHD with sirolimus and mycophenolate mofetil GVHD prophylaxis.

    Time frame: D+100 post-transplant

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Official study title

Sirolimus and Mycophenolate Mofetil as GVHD Prophylaxis in Myeloablative, Matched Related Donor Hematopoietic Cell Transplantation

Important dates

Study start
2006
Primary completion
2007
Study completion
2010
First posted
Jul 10, 2006
Registry last updated
Sep 23, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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