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OpenTrials
Completed

NCT Number: NCT00491634

Treosulfan-based Conditioning for Transplantation in AML/MDS

The study hypotheses is that the introduction of dose escalated treosulfan, in substitution to busulfan, will reduce toxicity after allogeneic transplantation while improving myeloablation and and disease control in patients with AML and MDS not eligible for standard transplantation.

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Key information

Age range

18 year–68 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Chaim Sheba Medical Center

Tel Litwinsky, Israel

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age less than physiologic 68 years.
  • Patients with AML and MDS not eligible for standard TBI- or Busulfan-based myeloablative conditioning due to age, concurrent medical condition, or extensive prior therapy (e.g. age > 55 years for HLA-matched sibling transplants or > 50 for matched unrelated donor transplants, prior / concomitant pulmonary, liver, or other organ complications).
  • This study will only include patients with chemo-refractory disease or previously untreated active disease.

A. acute myeloid leukemias (AML) according to WHO classification (> 20% myeloblasts in peripheral blood or bone marrow at diagnosis) in induction failure, PR, untreated or chemo-refractory relapse. Patients must have > 10% marrow blasts at the time of transplantation.

B. myelodysplastic syndromes (MDS) according to WHO classification (< 20% myeloblasts in peripheral blood and bone marrow at diagnosis), indicated for allogeneic transplantation:

  • refractory anaemia with excess blasts (RAEB-1 and RAEB-2) with no prior therapy
  • Patients must have an HLA matched related or unrelated donor willing to donate either peripheral blood stem cells or bone marrow. Matching is based on high-resolution class I (HLA-A, -B, -C) and class II (HLA-DRB1, -DQB1) typing. The goal is to transplant > 3 x 106 CD34+ cells per kg body weight of the recipient -

Exclusion criteria

  • Bilirubin > 3.0 mg/dl, transaminases > 3 times upper normal limit
  • Creatinine > 2.0 mg/dl
  • ECOG-Performance status > 2
  • Uncontrolled infection
  • Pregnancy or lactation
  • Abnormal lung diffusion capacity (DLCO < 40% predicted)
  • Severe cardiovascular disease
  • CNS disease involvement
  • Pleural effusion or ascites > 1 liter
  • Known hypersensitivity to fludarabine or treosulfan
  • Psychiatric conditions/disease that impair the ability to give informed consent or to adequately co-operate -

Treatment and study plan

Treosulfan

Drug

12 g/m2 x 3 days

Primary outcomes

  1. disease-free survival

    Time frame: 2 years after transplantation

Secondary outcomes

  1. treatment-related mortality, GVHD, relapse, overall survival

    Time frame: 2 year after transplantation

Sponsors and collaborators

Lead sponsor

Dr. Avichai Shimoni MD

Other Gov

Registry information

Official study title

Phase II Trial of Fludarabine Combined With Intravenous Treosulfan and Allogeneic Hematopoietic Stem-cell Transplantation in Patients With Chemo-refractory or Previously Untreated Acute Myeloid Leukemia and Myelodysplastic Syndrome.

Important dates

Study start
2007
Primary completion
2014
Study completion
2014
First posted
Jun 26, 2007
Registry last updated
Dec 2, 2015

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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