newest modalities in bone marrow transplantation
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Richard Champlin, M.D., Chair, Dept. of Stem Cell Transplantation and Cellular Therapy, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center - Newest Modalities in Bone Marrow Transplantation Presented at New Frontiers in the Management of Solid and Liquid Tumors hosted by the John Theurer Cancer Center at Hackensack University Medical Center. jtcancercenter.org/CMETRANSCRIPT
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New Modalities in Stem Cell Transplantation
Richard Champlin, M.D.
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Major Innovations SCT-CT
• Nonmyeloablative Conditioning• Alternative Donors
– Cord Blood– Haploidentical Transplants
• Cell Therapy– T-cells– Chimeric Antigen Receptors– NK Cells
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HSCT
DRL
RRL
RR D
DD
D
D
D
DD
Hematopoietic Stem Cell TransplantationPreparativeRegimen
Allogeneic hematopoietic is an effective, but toxic treatment for hematologic malignancies, associated with a high risk of morbidity and mortality (10->50%), restricting its use to young patients withoutcomorbidities
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Goal of Conditioning Regimen
• Provide immune suppression to prevent rejection and create “space” for engraftment
• Eradicate the malignancy– Most effective drugs/radiation treatments
for hematologic malignancies also kill normal myeloid and lymphoid cells
– Kill malignant stem cells
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BMT
Remission
Limit of Detection
High DoseChemoradiotherapy
Unmodified
T-cell depletionIdentical twin
Donor Lymphocyte Infusion
Time
Allogeneic BMT for CMLImportance of GVL
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Graft-vs-Malignancy Allogeneic SCT
• High dose therapy and allogeneic SCT is an effective treatment for hematologic malignancies
• Much of the benefit of alloSCT is due to immune GVL effect; therefore maximally ablative therapy may not be needed.
• Lower dose nonmyeloablative preparative regimens are sufficient to prevent rejection.
• We hypothesized that a reduced intensity, nonmyeloablative allogeneic transplant could reduce toxicity and allow successful treatment of older patients and those with major comorbidities.
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Nonablative and Reduced Intensity Regimens
Myelosuppression
FCRMF
BuCy
TBI/CyT
BuFF-TBI2Gy
Nonablative Reduced Intensity Ablative
Champlin et al 2000
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HSCT +DLI
DTDNK
DRLRL
RRL R
R DBDsc
DT
DNK
DT
DTDT
Dsc
D
DT
DT
DscD
Complete ChimeraRecipient Donor Mixed Chimera
Nonmyeloablative TransplantPreparativeRegimen
R
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AUC
Prob
abilit
y
800 1000 1200 1400 1600 1800
0.0
0.2
0.4
0.6
0.8
AUC
Prob
abilit
y
800 1000 1200 1400 1600 1800
0.0
0.2
0.4
0.6
0.8
AUC
Prob
abilit
y
800 1000 1200 1400 1600 1800
0.0
0.2
0.4
0.6
0.8
AUC
Prob
abilit
y
800 1000 1200 1400 1600 1800
0.0
0.2
0.4
0.6
0.8
1.0
Probability of Mucositis ≥ 3 Probability of GI Toxicity ≥ 3
Probability of Hepatic Toxicity ≥ 2 Probability of GVHD ≥ 2
Busulfan AUC Relative to Toxicity and aGVHD
Andersson et al 2002
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Pathophysiology of Acute GVHD
APC=antigen-presenting cell; CTL=cytotoxic T lymphocyte; IFN=interferon; IL=interleukin; LPS=lipopolysaccharide; Mac=macrophage; NK=natural killer cell; TH=T-helper cell; TNF-α=tumor necrosis factor-alpha.
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Days0 50 100
0.00
0.25
0.50
0.75
1.00
NMA
BUCY/FM
ACUTE
GVHD
HR 3.1 (CI= 1.3-7.2)
Grade 2-4 Acute GVHD
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Nonablative BMT• Reduced toxicity• Reduced GVHD• Similar infections occur, but generally
respond to therapy
• Lower treatment related mortality• Can extend the use of HSCT to patients
up to 75 years of age
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Comparisons Albative vs. RIC SCT• Lack of randomized controlled trials• Non-randomized comparisons always
confounded by different patient populations– Ablative- young, fit patients– RIC- Older patients with comorbidities
• Conclusions– RIC higher relapse, lower NRM, survival not
significantly different. • Can one develop effective anti-tumor
preparative regimens, with acceptable (less) toxicity?
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Time(weeks)
Surv
ival P
robabili
ty
0 20 40 60 80 100 120
0.0
0.2
0.4
0.6
0.8
1.0
In remission, PB.blast=0Active Disease, PB.blast=0Active Disease, PB.blast>0
p<0.0001
Time(weeks)
Eve
nt-
free p
robabili
ty
0 20 40 60 80 100 120
0.0
0.2
0.4
0.6
0.8
1.0
In remission, PB.blast=0Active Disease, PB.blast=0Active Disease, PB.blast>0
p<0.0001
IV Bu-Flu Overall Survivaland Event Free Survival
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Nonablative AlloSCT vs Chemo for Elderly AML
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Opportunities for Cure in CML
Preparative Regimen
Imatinib Donor Lymphocyte Infusion
CM
L C
ell M
ass
Time
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Survival
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Ablative Allo-BMT in Indolent Lymphoma
van Besien et al. Blood. 1998;92:1832-1836. Years
Prob
abili
ty, %
5432100
20
40
60
80
100
6
SurvivalDFSTreatment-related mortalityRelapse
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Rituximab Fludarabine 30 mg/m2 Rituximab375 mg/m2 Cyclophosphamide 750 mg/m2 1000
mg/m2
-13 -6 -5 -4 -3 0 +1 +8
ASCT
Days
NON-MYELOABLATIVE ALLOGENEIC SCT
Conditioning Regimen
•ATG 15 mg/kg daily, was given days –5 to –3 for mismatched or unrelated SCT•Tacrolimus and methotrexate were used for GVHD prophylaxis
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FCR allo SCT for Low Grade Lymphoma
Khouri et al Blood 2008
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Rituximab: Mechanism of Action
Anderson DR, et al. Biochem Soc Trans. 1997;25:705-708, Clynes RA, et al. Nat Med. 2000;6:443-446.
CD20
CELLLYSIS
FcγRI, FcγRII, or FcγRIII
Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC)
Macrophage,Monocyte,
or Natural Killer Cell
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Dendritic Cell
T Cells
Tumor Antigen
RituximabAntigen Presentation and Cross-Priming
Tumor Cell
FcR
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Efficacy of Nonablative HSCT
Highly Effective(better than ablative)
Dose Intensity Important
LGL, CLL CML
Mantle cell lymphoma AML /MDS
Myeloma (tandem)? LCL, Hodgkin’s disease
Renal Cell, OvarianBreast CA-Promising
ALL
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ATG with RIC SCTCIBMTR-Soiffer Blood 2011
• Compare T-replete transplants with no ATG, ATG, Alemtuzumab
• ATG- assoc with decreased cGVHD, increased relapse, worse PFS and survival
• Alemtuzumab- assoc with decreased acute and cGVHD, increased relapse, no change in survival
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Best Available Donor
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MD Anderson Cord Blood BankElizabeth J. Shpall MD
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Cord Blood Transplantation• Rich source of stem cells• ~50,000 units banked, immediately available
for transplantation• Immunologically immature- less prone to
produce GVHD• Less risk of transmitting infection• Can successfully transplant across HLA
mismatch• Major concern- low stem cell dose, longer
time to engraftment- may be overcome by ex vivo expansion
• Results comparable to MUD BMTs
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Mesenchymal Stem Cells (MSC)
• MSC are a stromal componentof the hematopoietic microenvironment.
• They provide cellular and extracellular components of the stem cell “niche”.
• When isolated and used in vitroin combination with cytokines, MSC markedly increase the expansion of CB hematopoietic progenitors.
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Day 14 hematopoietic output from liquid culture of CD133+ (solid bar) vs.co-culture of non-selected CB cells with MSC (striped bar)
x13 x25 x7 x14 x200 x44
Co-culture with MSC significantly enhancesex vivo expansion of CB cells
Robinson et al. Bone Marrow Transplantati
Fold increase
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Median time to engraftment (range)
Neutrophil (>500/µl) 15 days (range 9-42)Platelet (>20,000/µl) 40 days (range 13-62)
Cumulative Incidence of Engraftment
Neutrophil (>500/µl) 97% (n=31)Platelet (>20,000/µl) 81% (n=26)
- One patient died before engraftment
MSC-CB Expansion Trial Engraftment Data
de Lima et al. Blood (ASH Annual Meeting Abstracts), 2010; 116: 362
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Post Transplant Cyclophosphamide for Haploidentical Transplantation
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NST for Haploidentical Transplantation
Luznick et al 2008
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Cell Therapy +/- HSCT
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36
T-cell Immune Response
T-Cell Activation and Proliferation
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Chimeric antigen receptors (CARs)
vL
vH
CH1
CL
Antibody
Fab
vH vL
Chimeric antigen receptor
α βTCR-complex
γ ε ε δ ζ ζ
(Eshhar et al; PNAS 1993)
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Chimeric Antigen Receptors
Cooper et al
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Lysis
Lysisleukemia
DC
NK
DC
DC
NK
NK
Donor alloreactiveNK cells
Lysis
T T T
Kill recipient APCs =protection from GvHD
Kill recipient T cells =improved engraftment
Kill leukemia =GvL effect
Ruggeri et al. Science 2002
Allo NK-based conditioning:Ablation of recipient targets
T T
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Busulfan Fludarabine
HaploidenticalAllo reactive NK Cells
ATG
Allo matchPBPC
Addition of NK cells to HSCT
Phase I/II study to determine toxicity and efficacy of addition of alloreactive NK cells to high dose chemotherapy and allogeneicstem cell transplantation for myeloid leukemias
Champlin et al
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Hematopoiesis
Stem Cells
Granulocytes
Monocytes
Eosinophils
Basophils
Erythrocytes
Megakaryocytes
Platelets
T-lymphocytes
B-lymphocytes
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Immune System
BloodStem Cell
Nervous System
Liver and other organs
MesenchymalBlood vesselsFibrous tissue
GlandsGI tract, islet cells
Heart
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Approach to Abrogate GVHD
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Suicide Switch- Prevention of GVHD
45
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Modified Caspace 9- Self Destruct Switch
46
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If We Can Prevent GVHD • Dramatically expand use of allogeneic
SCT• Bone marrow failure/immune deficiency/metabolic
diseases of hematopoietic cells• Non malignant hematologic/metabolic/immune
mediated diseases– Thalassemia, Hemoglobinapathies– Autoimmune diseases
» Arthritis, Diabetes, Rheumatologic diseases, ……• Tolerance for Organ Transplants• Malignant Diseases
– Eliminates major toxicity of highly effective treatment
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HSCT
Vaccine or ImmuneEffector cells
DD
DRLRLR
RR
R
RLR
R DD
D
D
D DD
D
D
D
D
DD
Complete ChimeraRecipient Donor TolerantMixed Chimera
Ideal Nonablative Hematopoietic Transplant
PreparativeRegimen
No GVHD, Immune Reconstitution, GVL for malignancy