Fludarabine Based Conditioning for Allogeneic Transplantation for Advanced Hematologic Malignancies

NACompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

February 29, 2000

Primary Completion Date

May 31, 2013

Study Completion Date

May 31, 2013

Conditions
Acute Myeloid LeukemiaAcute LeukemiaChronic Myelogenous LeukemiaMalignant LymphomaHodgkin's DiseaseMultiple MyelomaLymphocytic LeukemiaMyeloproliferative DisorderPolycythemia VeraMyelofibrosisAplastic Anemia
Interventions
DRUG

fludarabine/busulfan

All patients below age 55, should receive fludarabine/busulfan, and ATG in case of unrelated or mismatched donor, unless there is significant pulmonary, hepatic or cardiac damage: (E.g FEV1 \<40%, DLCO\<50%, LVEF\<40, Serum bilirubin \>1.5 mg% or serum transaminases \> 2x nl) and/or specific medical conditions such as preventing a standard myeloablative treatment, as per discussion with the PI.

DRUG

fludarabine/ melphalan

All patients above age 55 or below age 65, should receive fludarabine/melphalan, and ATG, unless there is significant pulmonary, hepatic or cardiac damage: (E.g FEV1 \<40%, DLCO\<50%, LVEF\<40, Serum bilirubin \>1.5 mg% or serum transaminases \> 2x nl).

DRUG

ATG

Patients receiving a transplant from a matched unrelated or mismatched related/unrelated donor would receive ATG in the conditioning regimen.

Trial Locations (1)

60612

University of Illinois at Chicago Medical Center, Chicago

All Listed Sponsors
lead

University of Illinois at Chicago

OTHER

NCT01499147 - Fludarabine Based Conditioning for Allogeneic Transplantation for Advanced Hematologic Malignancies | Biotech Hunter | Biotech Hunter