NCT00025662 · STUDY IN CONTEXT
Selective T-Cell Depletion to Reduce GVHD (Patients) Receiving Stem Cell Tx to Treat Leukemia, Lymphoma or MDS
Draft scope assessment: narrower. Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded. The condition was transformed or resolved through the terminology hierarchy to reach this cancer type, so the link itself is a candidate a reviewer must confirm. Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
Read the full study record and all posted results →
Linked outcomes
Proportion of patients with acute GVHD, grade 1 to 4
Acute GVHD (Grade 3 or 4) Using the CIBMTR Grading System.
Nonrelapse mortality in the first 100 days of transplant expressed as a percentage of the total subjects. This is different from outcome measure 3 (Cumulative Nonrelapse Mortality), which is cumulative non relapse mortality till December 2011.
Percent overall survival (actuarial) at analysis in Dec 2011.
Percent non relapse mortality (actuarial) at analysis in Dec 2011
Reported safety
Quality of life and patient-reported measures
No linked quality-of-life measure is recorded for this setting and study.
Full draft applicability and source-link record
- trial
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- trial label
- Selective T-Cell Depletion to Reduce GVHD (Patients) Receiving Stem Cell Tx to Treat Leukemia, Lymphoma or MDS
- applicability
- narrower
- applicability note
- Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded. The condition was transformed or resolved through the terminology hierarchy to reach this cancer type, so the link itself is a candidate a reviewer must confirm.
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- provenance class
- registry-condition-search
- discovery note
- Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
- outcome Count
- 5
- harms Count
- 1
- qol Count
- 0
- outcomes
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0003
- source section id
- NCT00025662-om-0003
- source outcome index
- 3
- endpoint
- Acute GVHD (Any Grade) Using the CIBMTR Grading System.
- endpoint definition
- Proportion of patients with acute GVHD, grade 1 to 4
- time origin
- 100 days from transplant
- analysis role
- exploratory
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- All 22 subjects who received the selectively depleted transplant
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0004
- source section id
- NCT00025662-om-0004
- source outcome index
- 4
- endpoint
- Acute GVHD (Grade 3 or 4) Using the CIBMTR Grading System.
- endpoint definition
- Acute GVHD (Grade 3 or 4) Using the CIBMTR Grading System.
- time origin
- 100 days from transplant
- analysis role
- exploratory
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- All 22 patients who received the selectively depleted transplant
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0000
- source section id
- NCT00025662-om-0000
- source outcome index
- 0
- endpoint
- Treatment-related Mortality
- endpoint definition
- Nonrelapse mortality in the first 100 days of transplant expressed as a percentage of the total subjects. This is different from outcome measure 3 (Cumulative Nonrelapse Mortality), which is cumulative non relapse mortality till December 2011.
- time origin
- 100 days after stem cell infusion
- analysis role
- primary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- all 22 patients who received a selectively depleted allogeneic transplant, including one who was a special exemption for not meeting full eligibility criteria
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0001
- source section id
- NCT00025662-om-0001
- source outcome index
- 1
- endpoint
- Overall Survival
- endpoint definition
- Percent overall survival (actuarial) at analysis in Dec 2011.
- time origin
- Dec 2011.
- analysis role
- secondary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- all patients who received the selectively depleted transplant including one special exemption
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0002
- source section id
- NCT00025662-om-0002
- source outcome index
- 2
- endpoint
- Cumulative Non Relapse Mortality
- endpoint definition
- Percent non relapse mortality (actuarial) at analysis in Dec 2011
- time origin
- Dec 2011.
- analysis role
- secondary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- All patients who received the selectively depleted transplant
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- arms
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0000
- arm key
- OG000
- arm label
- RFT5-SMPT-dgA, an Anti-interleukin, Used in Transplants
- regimen
- Ex vivo selective depletion of alloreactive donor T lymphocytes utilizing RFT5-SMPT-dgA, a specific anti-interleukin-2 receptor immunotoxin in HLA-matched, nonmyeloablative, peripheral blood stem cell transplantation for hematologic malignancies in older adults
- analyzed count
- 22
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00025662-om-0000#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0001
- arm key
- OG000
- arm label
- RFT5-SMPT-dgA, an Anti-interleukin, Used in Transplants
- regimen
- Ex vivo selective depletion of alloreactive donor T lymphocytes utilizing RFT5-SMPT-dgA, a specific anti-interleukin-2 receptor immunotoxin in HLA-matched, nonmyeloablative, peripheral blood stem cell transplantation for hematologic malignancies in older adults
- analyzed count
- 22
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00025662-om-0001#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0002
- arm key
- OG000
- arm label
- RFT5-SMPT-dgA, an Anti-interleukin, Used in Transplants
- regimen
- Ex vivo selective depletion of alloreactive donor T lymphocytes utilizing RFT5-SMPT-dgA, a specific anti-interleukin-2 receptor immunotoxin in HLA-matched, nonmyeloablative, peripheral blood stem cell transplantation for hematologic malignancies in older adults
- analyzed count
- 22
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00025662-om-0002#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0003
- arm key
- OG000
- arm label
- RFT5-SMPT-dgA, an Anti-interleukin, Used in Transplants
- regimen
- Ex vivo selective depletion of alloreactive donor T lymphocytes utilizing RFT5-SMPT-dgA, a specific anti-interleukin-2 receptor immunotoxin in HLA-matched, nonmyeloablative, peripheral blood stem cell transplantation for hematologic malignancies in older adults
- analyzed count
- 22
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00025662-om-0003#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- outcome key
- om-0004
- arm key
- OG000
- arm label
- RFT5-SMPT-dgA, an Anti-interleukin, Used in Transplants
- regimen
- Ex vivo selective depletion of alloreactive donor T lymphocytes utilizing RFT5-SMPT-dgA, a specific anti-interleukin-2 receptor immunotoxin in HLA-matched, nonmyeloablative, peripheral blood stem cell transplantation for hematologic malignancies in older adults
- analyzed count
- 22
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00025662-om-0004#groups/OG000
- harms
- release id
- clinical-indications-draft-1
- disease state id
- ds-myelodysplastic-syndromes
- nct id
- NCT00025662
- harm key
- EG000
- source section id
- NCT00025662-ae
- event group key
- EG000
- event group label
- RFT5-SMPT-dgA, an Anti-interleukin, Used in Transplants
- serious affected
- 22
- serious at risk
- 22
- other affected
- 0
- other at risk
- 22
- frequency threshold
- 5
- collection period
- The adverse event reporting was collected for 7 years.
- event definition
- Source null
- undenominated note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- quality of life
- setting source links
Preserved source evidence · Not medical advice
Triangle