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Clinical Trials/NCT01374841
NCT01374841
Recruiting
Phase 2

Nonmyeloablative Hematopoietic Stem Cell Transplantation (SCT) for High-Risk Hematologic Malignancies With Related, HLA-Haploidentical Donors: A Phase II Trial of Immunosuppression With Cyclophosphamide Administered Before and After SCT

European Institute of Oncology1 site in 1 country20 target enrollmentAugust 2010

Overview

Phase
Phase 2
Intervention
Cyclophosphamide
Conditions
Hematologic Neoplasms
Sponsor
European Institute of Oncology
Enrollment
20
Locations
1
Primary Endpoint
Donor engraftment
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to determine if engraftment can be achieved safely in patients with high-risk hematologic malignancies who undergo non-myeloablative transplant with peripheral stem cells from Human Leukocyte Antigen (HLA) haploidentical donors with pre and post-transplant cyclophosphamide as immunosuppression.

Detailed Description

It is important to extend the option of nonmyeloablative, hematopoietic stem cell transplantation (HSCT) for potential therapy of hematologic malignancies to patients who do not have an HLA-matched donor. Almost all patients would have a related donor identical for one HLA haplotype (haploidentical) and mismatched at HLA-A, B or DR of the unshared haplotype. Thus far, nonmyeloablative HSCT from HLA-mismatched donors has been associated with a high rate of graft failure and graft-versus-host disease (GVHD). In this protocol, we will use a combination of immunosuppressive agents including cyclophosphamide administered before and after HSCT to facilitate engraftment and to delete highly alloreactive T-cell clones presumably involved in GVHD.

Registry
clinicaltrials.gov
Start Date
August 2010
End Date
December 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
European Institute of Oncology
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients ≤70 years old
  • Eligible diagnoses:
  • CML in AP
  • AML with high-risk cytogenetics \[del(5q)/-5, del(7q)/-7, abnormal 3q, 9q, 11q, 20q, 21q, 17p, t(6:9), t(9;22), complex karyotypes (≥3 abnormalities)\] in CR1
  • AML ≥ CR2; patients should have \<5% marrow blasts at the time of transplant
  • High-risk ALL defined as:
  • CR1 with high-risk cytogenetics t(9;22), t(8;14), t(4;11), t(1;19) for adult patients \>4 wk to achieve CR1
  • ≥ CR2 Patients should have \<5% marrow blasts at the time of transplant
  • MDS (\>int-1 per IPSS) after ≥ 1 prior cycle of induction chemotherapy; should have\<5% marrow blasts at the time of transplant
  • MM Stage II or III patients who have progressed after an initial response to chemotherapy or autologous HSCT or MM patients with refractory disease who may benefit from tandem autologous-nonmyeloablative allogeneic transplant

Exclusion Criteria

  • Patients with suitably matched related or unrelated donors
  • Patients with conventional transplant options (a conventional transplant should be the priority for eligible patients ≤ 50 yr of age who have a related donor mismatched for a single HLA-A, -B or DRB1 antigen)
  • CNS involvement with disease refractory to intrathecal chemotherapy
  • Presence of active, serious infection (e.g., mucormycosis, uncontrolled aspergillosis, tuberculosis)
  • Karnofsky Performance Status \< 60% for adult patients (Appendix A)
  • Patients with the following organ dysfunction:
  • Left ventricular ejection fraction \<35%
  • DLCO \<35% and/or receiving supplemental continuous oxygen
  • Liver abnormalities: fulminant liver failure, cirrhosis of the liver with evidence of portal hypertension, alcoholic hepatitis, esophageal varices, hepatic encephalopathy, uncorrectable hepatic synthetic dysfunction as evidenced by prolongation of the prothrombin time, ascites related to portal hypertension, bacterial or fungal liver abscess, biliary obstruction, chronic viral hepatitis with total serum bilirubin \>3 mg/dL or symptomatic biliary disease.
  • HIV-positive patients

Arms & Interventions

Stem Cell Transplant+Cyclophosphamide

patients with high-risk hematologic malignancies will receive hematopoietic stem cell transplantation from haploidentical donors after treatment with cyclophosphamide

Intervention: Cyclophosphamide

Stem Cell Transplant+Cyclophosphamide

patients with high-risk hematologic malignancies will receive hematopoietic stem cell transplantation from haploidentical donors after treatment with cyclophosphamide

Intervention: Hematopoietic Stem Cell Transplantation,

Outcomes

Primary Outcomes

Donor engraftment

Time Frame: Day +84

percentage of donor engraftment after 84 from baseline

Secondary Outcomes

  • Incidence and severity of graft versus host disease(up to 200 days after the baseline)
  • Non-relapse-related mortality(Incidence and severity of graft versus host disease after 200 days from the baseline)

Study Sites (1)

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