Ignite Creation Date:
2024-05-05 @ 11:22 AM
Last Modification Date:
2024-10-26 @ 9:06 AM
Study NCT ID:
NCT00014469
Status:
COMPLETED
Last Update Posted:
2013-03-07
First Post:
2001-04-10
Brief Title:
Combination Chemotherapy Followed by Bone Marrow Transplantation in Treating Patients With Advanced Hematologic Cancer
Sponsor:
Memorial Sloan Kettering Cancer Center
Organization:
Memorial Sloan Kettering Cancer Center
Study Overview
Official Title:
A Phase II Trial of IV Busulfan Busulfex and Melphalan as a Preparatory Regimen Prior to Allogeneic Bone Marrow Transplantation for the Treatment of Advanced and High Risk Hematologic Malignancies
Status:
COMPLETED
Status Verified Date:
2013-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
RATIONALE Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die Combining chemotherapy with bone marrow transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells
PURPOSE Phase II trial to study the effectiveness of busulfan and melphalan followed by donor bone marrow transplantation in treating patients who have advanced hematologic cancer
PURPOSE Phase II trial to study the effectiveness of busulfan and melphalan followed by donor bone marrow transplantation in treating patients who have advanced hematologic cancer
Detailed Description:
OBJECTIVES
Determine the antileukemic potential of busulfan and melphalan prior to allogeneic bone marrow transplantation in patients with advanced or high-risk hematologic malignancy
Determine the incidence of transplantation-related morbidity and mortality in patients treated with this regimen
Determine the incidence of acute and chronic graft-versus-host disease in patients treated with this regimen
OUTLINE Patients receive cytoreductive chemotherapy comprising busulfan IV over 2 hours every 6 hours for a total of 16 doses on days -8 to -5 and melphalan IV over 30 minutes on days -4 to -2 Patients undergo T-cell replete allogeneic bone marrow transplantation on day 0 For graft-versus-host disease prophylaxis patients receive tacrolimus IV continuously or every 12 hours beginning on day -1 and continuing for 50 days to 6 months followed by a taper Once oral medications are tolerated patients switch to oral tacrolimus every 12 hours Patients also receive methotrexate IV on days 1 3 6 and 11
Patients are followed weekly through day 100 every 6 weeks for 3 months every 3 months for 1 year and then every 3-6 months for 6 months
PROJECTED ACCRUAL A maximum of 30 patients will be accrued for this study within 3 years
Determine the antileukemic potential of busulfan and melphalan prior to allogeneic bone marrow transplantation in patients with advanced or high-risk hematologic malignancy
Determine the incidence of transplantation-related morbidity and mortality in patients treated with this regimen
Determine the incidence of acute and chronic graft-versus-host disease in patients treated with this regimen
OUTLINE Patients receive cytoreductive chemotherapy comprising busulfan IV over 2 hours every 6 hours for a total of 16 doses on days -8 to -5 and melphalan IV over 30 minutes on days -4 to -2 Patients undergo T-cell replete allogeneic bone marrow transplantation on day 0 For graft-versus-host disease prophylaxis patients receive tacrolimus IV continuously or every 12 hours beginning on day -1 and continuing for 50 days to 6 months followed by a taper Once oral medications are tolerated patients switch to oral tacrolimus every 12 hours Patients also receive methotrexate IV on days 1 3 6 and 11
Patients are followed weekly through day 100 every 6 weeks for 3 months every 3 months for 1 year and then every 3-6 months for 6 months
PROJECTED ACCRUAL A maximum of 30 patients will be accrued for this study within 3 years
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| NCI-H01-0070 | US NIH GrantContract | None | httpsreporternihgovquickSearchP01CA023766 |
| P30CA008748 | NIH | None | None |
| P01CA023766 | NIH | None | None |
| MSKCC-00126 | None | None | None |