Symptoms and General Pathology

All Conditions

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Leukemia

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Leukemia, B-Cell

Hematologic Diseases

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Disease Attributes

Myelodysplastic-Myeloproliferative Diseases

Myeloid Leukemia

Acute Myeloid Leukemia

Acute Non Lymphoblastic Leukemia

Chronic Myelomonocytic Leukemia

Juvenile Myelomonocytic Leukemia

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Chronic Graft Versus Host Disease

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Chronic Lymphocytic Leukemia

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Acute Graft Versus Host Disease

Chronic Myeloproliferative Disorders

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All Drugs and Chemicals

Antineoplastic Agents

Antirheumatic Agents

Anti-Infective Agents

Tacrolimus

Cyclophosphamide

Fludarabine

Fludarabine phosphate

Melphalan

Mycophenolic Acid

Busulfan

Immunologic Factors

Immunosuppressive Agents

Mesna

Antineoplastic Agents, Alkylating

Alkylating Agents

Calcineurin Inhibitors

Enzyme Inhibitors

Anti-Bacterial Agents

Antibiotics, Antitubercular

Antitubercular Agents

Patients Receive:

Patients receive:

Busulfan (≥ 9 mg/kg total dose) IV or PO on days -6 to -3 Fludarabine (150 mg/m2 total dose) IV on days -6 to -2

Patients receive a peripheral blood stem cell (PBSC) graft infusion from a mismatched unrelated donor on Day 0.

Patients receive a reduced dose of cyclophosphamide (25mg/kg per dose) on Day 3 and Day 4 post-transplant.

First 20 patients with a 4-6/8 mismatched unrelated donor will receive an alternate dose of post-transplant cyclophosphamide of 37.5 mg/kg on Days 3 and Day 4 post-transplant.

Patients receive:

Fludarabine (90 mg/m2 total dose) IV on days -7 to -5 Total body irradiation (TBI) (1200 cGy total dose) on days -4 to -1

Patients receive a peripheral blood stem cell (PBSC) graft infusion from a mismatched unrelated donor on Day 0.

Patients receive a reduced dose of cyclophosphamide (25mg/kg per dose) on Day 3 and Day 4 post-transplant.

First 20 patients with a 4-6/8 mismatched unrelated donor will receive an alternate dose of post-transplant cyclophosphamide of 37.5 mg/kg on Days 3 and Day 4 post-transplant.

Patients receive:

Fludarabine (150-180 mg/m2 total dose) IV on days -6 to -2 Busulfan (less than or equal to 8 mg/kg PO or 6.4 mg/kg IV) on days -5 and -4

Patients receive a peripheral blood stem cell (PBSC) graft infusion from a mismatched unrelated donor on Day 0.

Patients receive a reduced dose of cyclophosphamide (25mg/kg per dose) on Day 3 and Day 4 post-transplant.

First 20 patients with a 4-6/8 mismatched unrelated donor will receive an alternate dose of post-transplant cyclophosphamide of 37.5 mg/kg on Days 3 and Day 4 post-transplant.

Patients receive:

Fludarabine (125-150 mg/m2 total dose) IV on days -7 to -3 Melphalan (100-140 mg/m2) IV on day -1

Patients receive a PBSC graft infusion from a mismatched unrelated donor on Day 0.

Patients receive a reduced dose of cyclophosphamide (25mg/kg per dose) on Day 3 and Day 4 post-transplant.

First 20 patients with a 4-6/8 mismatched unrelated donor will receive an alternate dose of post-transplant cyclophosphamide of 37.5 mg/kg on Days 3 and Day 4 post-transplant.

Patients receive:

Fludarabine (150mg/m2 total dose) IV on days -6 to -2 Cyclophosphamide (29-50mg/kg) IV on days -6 and -5 TBI (200cGy) on day -1

Patients receive a PBSC graft infusion from a mismatched unrelated donor on Day 0.

Patients receive a reduced dose of cyclophosphamide (25mg/kg per dose) on Day 3 and Day 4 post-transplant.

First 20 patients with a 4-6/8 mismatched unrelated donor will receive an alternate dose of post-transplant cyclophosphamide of 37.5 mg/kg on Days 3 and Day 4 post-transplant.

Given IV or PO pre-transplant as part of conditioning regimen

Given IV pre-transplant as part of conditioning regimen

Peripheral blood stem cell graft is infused from a mismatched unrelated donor on Day 0

PBSC Hematopoietic Stem Cell Transplantation (HSCT)

Cyclophosphamide (25mg/kg) is administered on Day 3 and Day 4 post-transplant as an IV infusion over 1-2 hours.

First 20 subjects with a 4-6/8 HLA mismatched unrelated donor will receive an intermediate dose of post-transplant cyclophosphamide of 37.5 mg/kg Day 3 and Day 4 post-transplant.

Post-Transplant Cyclophosphamide

Mesna is given in divided doses IV 30 min pre- and at 3, 6, and 8 hours post cyclophosphamide.

Tacrolimus is given at a dose of 0.05 mg/kg PO or an IV dose of 0.03 mg/kg of ideal body weight (IBW) starting on Day +5 post-transplant with taper recommended at Day + 90 and finished by Day +180.

Mycophenolate mofetil (MMF) is given at a dose of 15 mg/kg three times daily IV or PO from Day +5 to Day +35 post-transplant.

Mycophenolate Mofetil

Survey assessments will be administered to study participants pre transplant, at Day + 100, Day + 180, and Day +365 post transplant.

Patient Reported Outcomes

Given IV pre transplant as part of conditioning regimen

Administered pre-transplant as part of conditioning regimen

Total-body irradiation

Brandan Butler, MBA

OPTIMIZE Study Team

Monzr AlMalki, MD

Hemant Murthy, MD

Antonio M Jimenez Jimenez, MD

Farhad Khimani, MD

Mahasweta Gooptu, MD

Dipenkumar Modi, MD

Mark Juckett, MD

Ramzi Abboud, MD

Brian Shaffer, MD

Katarzyna Jamieson, MD

Rachel J Cook, M.D.

Shannon McCurdy, MD

Betul Oran, MD

Karen Ballen, M.D.

Karen Ballen, MD

Masumi Ueda Oshima, MD

Sameem Abedin, MD

Steven Devine, MD

Jeffery Auletta, MD

The goal of this clinical trial is to determine the effectiveness of Reduced Dose Post-Transplant Cyclophosphamide (PTCy) in patients with hematologic malignancies after receiving an HLA-Mismatched Unrelated Donor (MMUD) . The main question\[s\] it aims to answer are:

* Does a reduced dose of PTCy reduce the occurrence of infections in the first 100 days after transplant?
* Does a reduced dose of PTCy maintain the same level of protection against Graft Versus Host Disease (GvHD) as the standard dose of PTCy?

HLA-Mismatched Unrelated Donor Peripheral Blood Stem Cell Transplantation With Reduced Dose Post Transplantation Cyclophosphamide GvHD Prophylaxis

A Phase II Study of Reduced Dose Post Transplantation Cyclophosphamide as GvHD Prophylaxis in Adult Patients With Hematologic Malignancies Receiving HLA-Mismatched Unrelated Donor Peripheral Blood Stem Cell Transplantation

Survival at 100 days without grades 2-3 infections (per BMT CTN grading criteria)

Defined as time interval between date of transplant and death from any cause

Defined as disease relapse or progression, or death by any cause

Defined as death and grades II-III infection (per BMT CTN criteria)

Defined as relapse or progression of underling disease (by 1 year), grade III-IV acute GvHD (by 6 months), chronic GvHD requiring systemic immune suppression (by 1 year), or death by any cause (by 1 year).

Defined as death without evidence of disease progression or recurrence

Defined as achieving an absolute neutrophil count (ANC) greater than or equal to 500/mm3 for three consecutive measurements on three different days

Defined as platelet count ≥20,000/mm\^3 or ≥50,000/mm\^3 with no platelet transfusions within seven days.

Primary graft failure is defined as no neutrophil recovery to ≥ 500 cells/mm3 by Day 28 post HCT.

Secondary graft failure is defined as as initial neutrophil count recovery followed by subsequent decline in absolute neutrophil counts \<500 cells/mm3, unresponsive to growth factor therapy, but cannot be explained by infection, disease relapse, or medications.

Defined as percent of donor chimerism via peripheral blood

Defined as cumulative incidence of grades II-IV acute GvHD

Defined as grades 2-3 infection as defined by BMT CTN grading criteria.

Defined as incidence of BK virus hemorrhagic cystitis per BMT CTN grading criteria

Defined as disease relapse or progression from Day 0 to 1-year post-HCT

To tabulate adverse events (AEs, experienced by recipients, defined as grade 3-5 unexpected and grade 5 expected AEs according to CTCAE v5

Defined and graded using the ASTCT grading criteria.

National Marrow Donor Program

Center for International Blood and Marrow Transplant Research

Precursor B-Cell Lymphoblastic Leukemia-Lymphoma

Diagnosed as ALL with Philadelphia-negative

Diagnosed as ALL with Philadelphia-positive (including biphenotypic acute leukemia with Philadelphia-positive)

Diagnosed as ALL of other type, including Burkitt leukemia

All patients who will be enrolled in this prospective registry are confined to those who are diagnosed as acute lymphoblastic leukemia at Asan Medical Center, Seoul, Korea, from Jan 2013 till Dec 2047

Diagnosed as ALL

Dae-Young Kim, MD, PhD

The investigators would like to propose a prospective longitudinal observational cohort study for patients who will be diagnosed and/or treated for acute lymphoblastic leukemia at Asan Medical Center, Seoul, Korea, to use the acquired data for fundamentals of other retrospective analysis.

1. Acquisition of informed concent form
2. Data acquisition from medical record including

   * demographic / disease-associated factors
   * details of treatment, and its results
   * complications during treatment
   * genetic data
   * survival outcome (upto 10 years)
3. Accumulation of data for 30 years
4. Use of data for other retrospective analysis (including Asan Medical center Cell Banking basic data)

Bone marrow aspirate or peripheral blood (for its mononuclear cells) will be collected, processed, and cryopreserved for future analysis of DNA or cell culture. Acquisition of biospecimens will be proceeded if patient agree with the informed consent for donation of biospecimen to 'Asan Medical Center Biomaterial Resource Banking Center'. This registry data will be used as a basic demographic and clinical information for the biospecimens.

Acute Lymphoblastic Leukemia Registry at Asan Medical Center

Prospective Observational Cohort Registry for Patients With Acute Lymphoblastic Leukemia at Asan Medical Center

Definition of events will be as 'relapse', 'death from any cause'. Relapse will be defined as hematologic relapse and molecular relapse, respectively when the patient is diagnosed as Philadelphia-positive acute lymphoblastic leukemia

Relapse will be defined as hematologic relapse and molecular relapse, respectively when the patient is diagnosed as Philadelphia-positive acute lymphoblastic leukemia

Asan Medical Center

Assistant Professor

Acute Disease

Acute Leukemia of Ambiguous Lineage

Patients receive:

* Busulfan (≥ 9 mg/kg total dose) IV or PO on days -6 to -3
* Fludarabine (150 mg/m2 total dose) IV on days -6 to -2

Patients receive a peripheral blood stem cell (PBSC) graft infusion from a mismatched unrelated donor on Day 0.

Patients receive:

* Fludarabine (90 mg/m2 total dose) IV on days -7 to -5
* Total body irradiation (TBI) (1200 cGy total dose) on days -4 to -1

Patients receive a PBSC graft infusion from a mismatched unrelated donor on Day 0.

Patients receive:

* Fludarabine (120-180 mg/m2 total dose) IV on days -6 to -2
* Busulfan (less than or equal to 8 mg/kg PO or 6.4 mg/kg IV) on days -5 and -4

Patients receive a PBSC graft infusion from a mismatched unrelated donor on Day 0.

Patients receive:

* Fludarabine (120-180 mg/m2 total dose) IV on days -7 to -3
* Melphalan (100-140 mg/m2) IV on day -1

Patients receive a PBSC graft infusion from a mismatched unrelated donor on Day 0.

Patients receive:

* Fludarabine (150 mg/m2 total dose) IV on days -6 to -2
* Cyclophosphamide (29-50 mg/kg) IV on days -6 and -5
* TBI (200 cGy) on day -1

Patients receive a PBSC graft infusion from a mismatched unrelated donor on Day 0.

Patients receive:

* Busulfan (dosed by age and weight per institutional standards to target goal pharmacokinetic (PK) in range noted in protocol.) on days -6 to -3
* Cyclophosphamide (100 mg/kg total dose) IV on days -2 and -1

Patients receive a bone marrow (BM) graft infusion from a mismatched unrelated donor on Day 0.

Patients receive:

* Cyclophosphamide (100 mg/kg total dose) IV on days -5 and -4
* TBI (1200 cGy total dose) on days -3, -2 and -1

Patients receive a BM graft infusion from a mismatched unrelated donor on Day 0.

Peripheral blood stem cell graft is infused from a mismatched unrelated donor on Day 0.

Bone marrow graft is infused from a mismatched unrelated donor on Day 0.

Bone Marrow Hematopoietic Stem Cell Transplantation

Cyclophosphamide (50 mg/kg) is administered on Day +3 and on Day +4 post-transplant as an IV infusion over 1-2 hours.

Post-transplant Cyclophosphamide

Mesna is given in divided doses IV 30 min pre- and at 3, 6, and 8 hours post-cyclophosphamide.

Tacrolimus is given at a dose of 0.05 mg/kg PO or an IV dose of 0.03 mg/kg of ideal body weight (IBW) starting on Day +5 post-transplant with taper recommended at 90-100 days post HCT.

Survey assessments will be administered to study participants pre- and post-transplant.

Patient-Reported Outcomes

Sarah Smith, RN, BSN

Erin Leckrone

Monzr Al Malki, MD

Aaron Logan, MD

Sally Arai, MD

Alireza Eghtedar, MD

Zenia Al-Mansour, MD

Muna Qayed, MD

Amelia Langston, MD

Kehinde Adekola, MD

Satyajit Kosuri, MD

Nancy Hardy, MD

Javier Bolanos Meade, MD

Zheng (Frank) Zhou, MD

William Hogan, MD

Philip McCarthy, MD

Ran Reshef, MD

Ruby Khoury, MD

Karilyn Larkin, MD

Hannah Choe, MD

Rachel Cook, MD

Alison Loren, MD

Usama Gergis, MD

Michelle Hudspeth, MD

Jeremy Pantin, MD

Haydar Frangoul

Bhagirathbhai Dholaria, MD

Aravind Ramakrishnan

George Carrum

Jose Carlos Cruz, MD

John McCarty, MD

Aric Hall, MD

Medhi Hamadani, MD

This is a prospective, multi-center, Phase II study of hematopoietic cell transplantation (HCT) using human leukocyte antigen (HLA)-mismatched unrelated donors (MMUD) for peripheral blood stem cell transplant in adults and bone marrow stem cell transplant in children. Post-transplant cyclophosphamide (PTCy), tacrolimus and mycophenolate mofetil (MMF) will be used for for graft versus host disease (GVHD) prophylaxis. This trial will study how well this treatment works in patients with hematologic malignancies.

HLA-Mismatched Unrelated Donor Hematopoietic Cell Transplantation With Post-Transplantation Cyclophosphamide

A Multi-Center, Phase II Trial of HLA-Mismatched Unrelated Donor Hematopoietic Cell Transplantation With Post-Transplantation Cyclophosphamide for Patients With Hematologic Malignancies

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization
HLA-Mismatched Unrelated Donor Peripheral Blood Stem Cell Transplantation With Reduced Dose Post Transplantation Cyclophosphamide GvHD Prophylaxis	NCT06001385	Acute Lymphobla... Acute Myeloid L... Acute Leukemia Myelodysplastic... Chronic Myeloid... Chronic Lymphoc... Myeloproliferat... Lymphoma Chronic Myelomo... Pro-Lymphocytic... Myelofibrosis	Busulfan Fludarabine PBSC Hematopoie... Post-Transplant... Mesna Tacrolimus Mycophenolate M... Patient Reporte... Melphalan Total-body irra... Cyclophosphamid...	18 Years -	Center for International Blood and Marrow Transplant Research
Acute Lymphoblastic Leukemia Registry at Asan Medical Center	NCT01761682	Leukemia, Acute... Precursor B-Cel... Leukemia, Biphe... Leukemia, Lymph... Lymphoblastic L...	Diagnosed as AL...	15 Years -	Asan Medical Center
HLA-Mismatched Unrelated Donor Hematopoietic Cell Transplantation With Post-Transplantation Cyclophosphamide	NCT04904588	Acute Lymphobla... Acute Myelogeno... Mixed Phenotype... Acute Leukemia Myelodysplastic... Chronic Myeloge... Chronic Lymphoc... Lymphoma	Busulfan Busulfan Fludarabine Total-body irra... Cyclophosphamid... Melphalan PBSC Hematopoie... Bone Marrow Hem... Post-transplant... Mesna Tacrolimus Mycophenolate M... Patient-Reporte...	1 Year -	Center for International Blood and Marrow Transplant Research

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