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Poor accrual
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The study seeks to compare time from formal search to hematopoietic cell transplantation (HCT) for patients 18 years and older, randomized between haplo-cord search and matched unrelated donor (MUD) search for patients with acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS)
Primary Objectives
To compare time from formal search to hematopoietic cell transplantation (HCT) for patients 18 years and older, randomized between haplo-cord search and matched unrelated donor (MUD) search for patients with acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS)
Secondary Objectives
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Haplo-Cord Search | Other | If subject meets the inclusion criteria and consents, will undergo a haplo-cord transplant. |
|
| Matched Unrelated Donor Search (MUD) | Other | If subject meets the inclusion criteria and consents, will undergo a MUD transplant. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Haplo-Cord Transplant | Biological | For conditioning regimens, haplo-identical grafts will be selected by the Miltenyi Device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Time to Transplant | Time to transplant will be measured from time of date of formal request to stem cell infusion date. Will also capture time from preliminary search to both formal search and transplant date. | Through one year after formal search |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Patients Who Undergo Hematopoietic Cell Transplantation (HCT) | Compare percentage of patients who undergo HCT in each study cohort | Through one year after formal search |
| Estimated Survival Time |
Not provided
Inclusion Criteria for Search Phase:
Diagnosis of acute myeloid leukemia (AML) or high or very high-risk MDS by international prognostic scoring system revised for whom transplant is recommended
18 years of age or older
Subject is likely to be considered for allogeneic transplant in the opinion of the transplant physician (based on age of patient, health, cytogenetics, and/or molecular characteristics).
Karnofsky Performance Status (KPS) >/= 70% at time of enrollment. An exception will be made for those with lower KPS at enrollment with an acute worsening that is likely to resolve in the treating physicians judgment (e.g., reversible infection,trauma, medication reaction, etc)
Ability to understand and the willingness to sign a written informed consent document for the Search Phase.
Patient willing to consider HCT
A preliminary search has identified:
Exclusion Criteria for Search Phase:
Inclusion Criteria for Transplant Phase
High-risk AML for which transplant is recommend based on cytogenetic, molecular and morphologic features. Patients must meet institutional standards for disease control prior to transplant.
For MDS. IPSS-revised criteria of high or very high at diagnosis.
Subject meets institutional criteria for transplant and has acceptable organ and marrow function as defined below:
An adequate graft for the defined donor type
Written informed consent for the transplant phase
Exclusion Criteria for Transplant Phase
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| Name | Affiliation | Role |
|---|---|---|
| Andrew Artz, MD | University of Chicago | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Chicago Cancer Center | Chicago | Illinois | 60637 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Haplo-Cord Search | If subject meets the inclusion criteria and consents, will undergo a haplo-cord transplant. Haplo-Cord Transplant: For conditioning regimens, haplo-identical grafts will be selected by the Miltenyi Device |
| FG001 | Matched Unrelated Donor Search (MUD) |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 16, 2015 |
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| Matched Unrelated Donor Transplant | Procedure |
|
Overall survival time was estimated from date of randomization and from date of transplant using Kaplan-Meier method.
| From date of randomization up to 3 years |
If subject meets the inclusion criteria and consents, will undergo a MUD transplant. Matched Unrelated Donor Transplant |
| COMPLETED |
|
| NOT COMPLETED |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Haplo-Cord Search | If subject meets the inclusion criteria and consents, will undergo a haplo-cord transplant. Haplo-Cord Transplant: For conditioning regimens, haplo-identical grafts will be selected by the Miltenyi Device |
| BG001 | Matched Unrelated Donor Search (MUD) | If subject meets the inclusion criteria and consents, will undergo a MUD transplant. Matched Unrelated Donor Transplant |
| BG002 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Median | Full Range | years |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Time to Transplant | Time to transplant will be measured from time of date of formal request to stem cell infusion date. Will also capture time from preliminary search to both formal search and transplant date. | We analyze only those who went to transplant. | Posted | Median | Full Range | days | Through one year after formal search |
|
|
| ||||||||||||||||||||||||||||
| Secondary | Percentage of Patients Who Undergo Hematopoietic Cell Transplantation (HCT) | Compare percentage of patients who undergo HCT in each study cohort | Posted | Count of Participants | Participants | Through one year after formal search |
|
| |||||||||||||||||||||||||||||||
| Secondary | Estimated Survival Time | Overall survival time was estimated from date of randomization and from date of transplant using Kaplan-Meier method. | We analyzed only those who went transplant. | Posted | Median | 95% Confidence Interval | days | From date of randomization up to 3 years |
|
|
100 days
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Haplo-Cord Search | If subject meets the inclusion criteria and consents, will undergo a haplo-cord transplant. Haplo-Cord Transplant: For conditioning regimens, haplo-identical grafts will be selected by the Miltenyi Device | 1 | 2 | 0 | 2 | 1 | 2 |
| EG001 | Matched Unrelated Donor Search (MUD) | If subject meets the inclusion criteria and consents, will undergo a MUD transplant. Matched Unrelated Donor Transplant | 2 | 3 | 0 | 3 | 2 | 3 |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Anemia | Blood and lymphatic system disorders | Systematic Assessment |
| ||
| Diarrhea | Gastrointestinal disorders | Systematic Assessment |
| ||
| Epistaxis | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
| ||
| Fatigue | General disorders | Systematic Assessment |
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| Nausea | Gastrointestinal disorders | Systematic Assessment |
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| Purpura | Skin and subcutaneous tissue disorders | Systematic Assessment |
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| Weight loss | Investigations | Systematic Assessment |
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| White blood cell decreased | Investigations | Systematic Assessment |
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| Abdominal pain | Gastrointestinal disorders | Systematic Assessment |
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| Anorexia | Metabolism and nutrition disorders | Systematic Assessment |
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| Back pain | Musculoskeletal and connective tissue disorders | Systematic Assessment |
| ||
| Chills | General disorders | Systematic Assessment |
| ||
| Dry mouth | Gastrointestinal disorders | Systematic Assessment |
| ||
| Fever | General disorders | Systematic Assessment |
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| Hypertension | Vascular disorders | Systematic Assessment |
| ||
| Myalgia | Musculoskeletal and connective tissue disorders | Systematic Assessment |
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| Oral hemorrhage | Gastrointestinal disorders | Systematic Assessment |
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| Oral pain | Gastrointestinal disorders | Systematic Assessment |
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| Rash maculo-papular | Skin and subcutaneous tissue disorders | Systematic Assessment |
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| Sinus tachycardia | Cardiac disorders | Systematic Assessment |
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| Tremor | Nervous system disorders | Systematic Assessment |
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| Vomiting | Gastrointestinal disorders | Systematic Assessment |
|
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Hongtao Liu | University of Chicago | 773-834-0589 | hliu2@medicine.bsd.uchicago.edu |
| Feb 10, 2021 |
| Prot_SAP_000.pdf |
| ID | Term |
|---|---|
| D015470 | Leukemia, Myeloid, Acute |
| D009190 | Myelodysplastic Syndromes |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D001855 | Bone Marrow Diseases |
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| Male |
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| Asian |
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| Native Hawaiian or Other Pacific Islander |
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| Black or African American |
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| White |
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| More than one race |
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| Unknown or Not Reported |
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