Risk-ADAPTed Conditioning Regimen for Allogeneic Hematopoietic Stem Cell Transplantation

Description

This is a prospective, single-arm, phase II study. Patients will be treated with an allogeneic stem cell transplantation (AHSCT) using fludarabine, melphalan and total body irradiation (TBI) conditioning with different melphalan and TBI doses based on patient- and disease-related risk.

Conditions

Allogeneic Hematopoietic Stem Cell Transplantation, Allogeneic Stem Cell Transplantation, Hematologic Malignancies

Study Overview

Study Details

Study overview

This is a prospective, single-arm, phase II study. Patients will be treated with an allogeneic stem cell transplantation (AHSCT) using fludarabine, melphalan and total body irradiation (TBI) conditioning with different melphalan and TBI doses based on patient- and disease-related risk.

Risk-ADAPTed Conditioning Regimen for Allogeneic Hematopoietic Stem Cell Transplantation (ADAPT)

Risk-ADAPTed Conditioning Regimen for Allogeneic Hematopoietic Stem Cell Transplantation

Condition
Allogeneic Hematopoietic Stem Cell Transplantation
Intervention / Treatment

-

Contacts and Locations

Orange

Chao Family Comprehensive Cancer Center, University of California Irvine, Orange, California, United States, 92868

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Male or female aged 18-70 years
  • 2. Diagnosis of AML, ALL, MDS, CML, NHL, HD, CLL requiring AHSCT
  • 3. Has an HLA-matched related (MRD), HLA-matched unrelated (MUD), haploidentical (HAPLO) or 1-Ag mismatched unrelated donor (MMUD)
  • 4. Karnofsky performance \>70%
  • 5. Adequate major organ system function as demonstrated by:
  • 1. Serum creatinine clearance equal or more than 50 ml/min (calculated with Cockroft-Gault formula).
  • 2. Bilirubin equal or less than 1.5 mg/dl except for Gilbert's disease. ALT or AST equal or less than 200 IU/ml for adults. Conjugated (direct) bilirubin less than 2x upper limit of normal.
  • 3. Left ventricular ejection fraction equal or greater than 40%.
  • 4. Diffusing capacity for carbon monoxide (DLCO) equal or greater than 50% predicted corrected for hemoglobin.
  • 6. Ability to understand and the willingness to sign a written informed consent. a. Both men and women and members of all races and ethnic groups are eligible for this trial. Non-English speaking, deaf, hard of hearing and illiterate individuals are eligible for this trial.
  • 1. Inability to comply with medical recommendations or follow-up
  • 2. Pregnancy
  • 3. Active/uncontrolled bacterial or viral infection (PI is the final arbiter of this criterion.)
  • 4. Has active CNS or ocular disease involvement within 3 months
  • 5. Patients with primary CNS lymphoma
  • 6. Patients who require modifications of the conditional regimen

Ages Eligible for Study

18 Years to 70 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of California, Irvine,

Stefan O. Ciurea, MD, PRINCIPAL_INVESTIGATOR, Chao Family Comprehensive Cancer Center

Study Record Dates

2027-09