UNRELATED DONOR TRANSPLANTS A Bacigalupo, Ospedale San Martino, Genova, Italy.

Slides:



Advertisements
Similar presentations
台北榮總血液腫瘤科 楊元豪 / 高志平大夫. 2 Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the only potentially curative treatment in patients.
Advertisements

Hematopoietic Stem Cell Transplantation Lynn Savoie September 30, 2006.
Congenital Neutropenia: Making the Decision to Transplant John E. Levine, MD, MS University of Michigan Blood and Marrow Transplantation Program.
G. S / AIH 2006 Aplastic anemia; treatment options Gérard Socié, MD PhD Hospital Saint Louis.
A single centre study of the efficacy of extracorporeal photopheresis in Acute Graft Versus Host Disease Lynne Watson Nottingham University Hospital NHS.
High Resolution HLA Matching in Bone Marrow Transplantation
Haploidentical Hematopoietic Stem Cell Transplantation for Hematological Malignancies Xiao-Jun Huang M.D. Ph.D. Peking University Institute of Hematology,
Hematopoietic stem cell transplantation
Dao-Pei Lu May 2010, Shanghai Hematopoietic Stem Cell Transplantation (HSCT) in China (2010)
Blood and marrow stem cell transplantation A.Basi ADULT HEMATOLOGIST,ONCOLOGIST IRAN UNIVERSITY OF MEDICAL SCIENCES.
Peking University People’s Hospital & Institute of Hematology Beijing Key Laboratory of HSCT, Beijing, P.R.China Xiao-Jun Huang M.D Donor Lymphocyte Infusion.
The role of transplant for CML in the imatinib era Dr Wendy Ingram Consultant Haematologist University Hospital of Wales.
Current Uses and Outcomes of Hematopoietic Stem Cell Transplantation 2010 CIBMTR Summary Slides SUM10_1.ppt.
Current Uses and Outcomes of Hematopoietic Stem Cell Transplantation 2011 Summary Slides Worldwide SUM-WW11_1.ppt.
Advances in SCT in Acute Leukemia 충남대학교병원 혈액종양내과 조 덕 연.
New Strategies for the Prevention and Treatment of Graft vs. Host Disease (GVHD) Simrit Parmar, MD Stem Cell Transplant & Cellular Therapy BTG2013, Hong.
Therapeutic Response to Azacitidine (AZA) in Patients with Secondary Myelodysplastic Syndromes (sMDS) Enrolled in the AVIDA Registry 1 Prospective Trial.
Graft vs Host Disease Remains the major cause of treatment related morbidity and mortality in allogeneic HCT. Caused by donor derived alloreactive T cells.
DR. YETUNDE T. ISRAEL-AINA PAEDIATRICIAN, UNIVERSITY OF BENIN TEACHING HOSPITAL, BENIN CITY BENIN BLOOD AND MARROW TRANSPLANT WORKSHOP, UNIVERSITY OF BENIN.
1 Transplant and Cellular Therapy Unit Institut Paoli Calmettes Inserm U599 Université de la Méditerranée Marseille, France ALLOGENEIC STEM CELL TRANSPLANTATION.
林建廷 April 28,  IPSS for MDS (FAB classification) ◦ Greenberg P et al. International scoring system for evaluating prognosis in myelodysplastic.
What about stem cell transplantation? Dr Catherine Flynn Consultant Haematologist St James’s Hospital 17/06/2011.
Cord blood selection, release, and transplantation 6th World Congress Tissue Banking Barcelona, Spain, 10 November 2011 Guillermo Sanz Hospital Universitari.
Role of ATG in Allogeneic HSCT ZiYi Lim National University Cancer Institute Singapore 3rd BTG – Hong Kong 24th Feb 2012.
5-Azacitidine For Myelodysplasia Before Allogeneic Hematopoietic Cell Transplantation Field T et al. Bone Marrow Transplant 2009:[Epub ahead of print].
DONOR LYMPHOCYTE INFUS I ON (DLI) Dr. Serdar ŞIVGIN February 2011 Kayseri.
Reduced-Intensity Conditioning (RIC) and Allogeneic Stem Cell Transplantation (allo-SCT) for Relapsed/Refractory Hodgkin Lymphoma (HL) in the Brentuximab.
G. S / AIH 2006 Graft-versus-Host disease Physiopathology Gérard Socié, MD PhD Hospital Saint Louis Translating experimental into clinical knowledge.
Improved Survival in Patients with First Relapsed or Refractory Acute Myeloid Leukemia (AML) Treated with Vosaroxin plus Cytarabine versus Placebo plus.
Low Dose Decitabine Versus Best Supportive Care in Elderly Patients with Intermediate or High Risk MDS Not Eligible for Intensive Chemotherapy: Final Results.
N ATIONAL M ARROW D ONOR P ROGRAM ® Entrusted to operate the C.W. Bill Young Cell Transplantation Program, including the Be The Match Registry SM Advances.
Daunorubicin VS Mitoxantrone VS Idarubicin As Induction and Consolidation Chemotherapy for Adults with Acute Myeloid Leukemia : The EORTC and GIMEMA Groups.
Safety Review. 2 Sources of Safety Information BLA (Applicant’s data) – : Voluntary questionnaires –2008-present: SCTOD FDA Dockets Literature.
HAPLOIDENTICAL STEM CELL TRANSPLANT
Hematopoietic Stem Cell Current Status and Future Directions
Abstract Immune Reconstitution and Clinical Outcome After Donor Lymphocyte Infusion for Relapsed Disease After Reduced-Intensity Allogeneic Hematopoietic.
Pavan Kumar Bhamidipati 1, John F. DiPersio 1, Keith Stockerl-Goldstein 1, Geoffrey L. Uy 1, Peter Westervelt 1, Feng Gao 2, Ravi Vij 1, Mark A. Schroeder.
New Approaches for Transplant Patients Linda J Burns, MD Medical Director, Health Services Research Program National Marrow Donor Program (NMDP)/Be the.
Peripheral-Blood Stem Cells versus Bone Marrow from Unrelated Donors N Engl J Med 2012;367: R3 Sunhee park/Prof. Kyung-sam cho.
(Donor T-Cells Transduced with iC9 Suicide Gene)
Biostatistical Sciences and Pharmacometrics, Novartis
RIC UCBT Transplantation of Umbilical Cord Blood from Unrelated Donors in Patients with Haematological Diseases using a Reduced Intensity Conditioning.
Maury S et al. Proc ASH 2015;Abstract 1.
Slide set on: McCarthy PL, Owzar K, Hofmeister CC, et al
Haploidentical Transplantation with Post-transplant Cyclophosphamide and Melphalan-based Conditioning– A retrospective Analysis of the First 100 Patients.
Supplemental table 1 Patients' characteristics Variables Number
M. Bregni, M. Bernardi, P. Servida,
Il trapianto allogenico da donatore alternativo dopo condizionamento a ridotta intensità Alessandro Rambaldi.
Whom should you refer for allogeneic transplantation?
Ematologia, Ospedali Riuniti, Bergamo
Assessment of Allogeneic HCT in Older Patients with AML and MDS: A CIBMTR Analysis McClune B et al. ASCO/ASH Symposium 2009;The Best of ASH Special & Plenary.
ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION for MULTIPLE MYELOMA
Haploidentical BMT with Post Transplant Cyclophosphamide
Cord blood transplantation and stem cell regenerative potential
Qualitative and quantitative PCR monitoring of minimal residual disease (MRD) in relapsed poor-risk chronic lymphocytic leukemia (CLL): early assessment.
Comparison of Outcomes after HLA-Matched Sibling and Unrelated Donor Transplantation for Children with High-Risk Acute Lymphoblastic Leukemia  Mei-Jie.
Significance of Ethnicity in the Risk of Acute Graft-versus-Host Disease and Leukemia Relapse after Unrelated Donor Hematopoietic Stem Cell Transplantation 
Peripheral Blood Grafts from Unrelated Donors Are Associated with Increased Acute and Chronic Graft-versus-Host Disease without Improved Survival  Mary.
Comparison of Cord Blood Transplantation with Unrelated Bone Marrow Transplantation in Patients Older than Fifty Years  Masatsugu Tanaka, Koichi Miyamura,
Twenty Years of Unrelated Donor Bone Marrow Transplantation for Pediatric Acute Leukemia Facilitated by the National Marrow Donor Program  Margaret L.
Dynamic Detection of Anti–Human Leukocyte Antigen (HLA) Antibodies but not HLA-DP Loci Mismatches Can Predict Acute Graft-versus-Host Disease and Overall.
Successful Prevention of Acute Graft-versus-Host Disease Using Low-Dose Antithymocyte Globulin after Mismatched, Unrelated, Hematopoietic Stem Cell Transplantation.
Higher CD34+ and CD3+ Cell Doses in the Graft Promote Long-Term Survival, and Have No Impact on the Incidence of Severe Acute or Chronic Graft-versus-Host.
Hematopoietic cell transplant for acute myeloid leukemia and myelodysplastic syndrome: conditioning regimen intensity by Mary Eapen, Ruta Brazauskas, Michael.
Graft-versus-Host Disease Induced Graft-versus-Leukemia Effect: Greater Impact on Relapse and Disease-Free Survival after Reduced Intensity Conditioning 
Is KIR- typing relevant to HCT donor selection?
Introduction. Title: Activities and Outcomes of Hematopoietic Cell Transplantation in Japan.
Stem Cell Transplant for Myeloid Neoplasms
Clinical Lymphoma, Myeloma and Leukemia
A pilot study of tacrolimus and mycophenolate mofetil graft-versus-host disease prophylaxis in childhood and adolescent allogeneic stem cell transplant.
Presentation transcript:

UNRELATED DONOR TRANSPLANTS A Bacigalupo, Ospedale San Martino, Genova, Italy

Donor Safety

death BM PB /36317 RELATED 0/14706 UNRELATED

One additional death in Unrelated Donor Age = Gender= Cause = repiratory insufficiency after attempted insertion of CVC, and bilateral pneumothorax

SAE BM PB

DONOR SAFETY 1.HSC donations carries a small, but proven hazard: we must be cautious (VERY) in selecting HSC donor 2. PB donations are not safer than BM Higher death rate and signficantly higher SAE rate for PB vs BM donations. Informed consent should say so 3. Accurate donor screening will reduce risk of lethal complications Lower death risk occurred in UNRELATED donations

Donor Safety Graft versus Host Disease

Preventing acute GvHD II-IV Blood 2000 BBMT 2008;BJH : :920 Lancet Onc 2009:10march 8

Reduction of GvHD in alternative donor TX for 402 Myeloid Leukemias: Genova San Martino P<0.0001

Preventing Chronic GvHD Blood 2000 BBMT 2008;BJH : :920 march 8

Biol Blood Marrow Transpl ; 2006 ; 12: 560 Lancet Oncol 2009; 10:855 Same results with ATG Thymo Or ATG Fresenius Chronic GvHD P<0.0001

Day BU 3.2 mg/kg x4 CY 50 mg/kg x2 UD or SIB BM Tx CY 50 mg /kg

GvHD 1.Prophylaxis with 2 drugs (C+M, T+M) is associated with significant acute+chronic GvHD 2. A third agent (ATG or CAMPATH or SIROLIMUS) signifanctly REDUCES acute +GvHD 3. ATG significantly reduces chronic GvHD 4. High dose CY post-Transplant may be a promising new option with or without C+M

Donor Safety Graft versus Host Disease Does reduction of GvHD translate in better OS?

GITMO trial (Thymo) BBMT 2006; 12:560 German trial (Thymo) Lancet Onc ; 2009 OS not significantly different (not inferior) with ATG vs no ATG

Very long follow up (over 10 years), may allow for late complications of chronic GvHD (in particular lung complications) to become clinically relevant

Donor Safety Graft versus Host Disease Does eduction of GvHD translate in better OS? HLA matching criteria

Worse outcomes with

Early Stage Disease: Adverse impact of HLA mismatch HLA-A,B, C, DR Lee et al, 2007 Each mm yield 10-11% worse survival

Advanced Disease: Limited impact of HLA mismatch HLA-A,B, C, DR Lee et al, 2007 Delay had worse consequences than MM

StudyReferenceN.patientsDiagnosis Survival disadvantage in mismatched pairs Type of mismatch One should avoid Seattlle Petersdorf Blood 2004; 104: LeukemiaEarly disC locus NMDP CIBMTR Lee Blood AML ALL MDS CML Early disA or DRB1 JMDP Takakazu Blood ; Malignant and non malignant All patients C locus Non permissive mismatches positions 9,77,80,99,116,156 Seattle Petersdorf Plos Med 2007; 4: LeukemiaAll patients Haplotype Mismatched GITMO Crocchiolo, Blood 2009, 114: LeukemiaAll patients DP non permissive mismacth CIBMTRCooley, Blood 2010, 116: LeukemiaAMLDonor B gene content <2

KIR genes on Chromosome 19 Segregate indep. From HLA A group (inhibitory receptors) B group (activating receptors) A/A= homozygous for A B/x (at least one B)

Lancet February 15, 2012

HLA 10/10 match DP permiss mm # same TRM as DP= # lower TRM as DP non perm mm # lower Relapse as DP=

V V

Faster Registration on International Donor Registries and Shorter Time to Allogeneic Hematopoietic Stem Cell Transplantation After Having Found a Donor Confers Better Outcome In Acute Leukemia Patients Mauricette Michallet 1, Lyon Abstract 2371 ASH 2010; Patients = 251 with acute leukemia and active donor search The 3years OS for SD allo-HSCT59% UD allo-HSCT early registration: 47% UD allo-HSCT late registration: 29%

Donor selection EARLY DISEASE 1.Choose 8/8 = A,B,C,DRB1 donors 2. permissive DP mm should be preferred of non permissive mm 3.In AML patients, if possible, with a NK -B cent haplotype ADVANCED DISEASE The earlier, the better

Donor Registries Donor Safety Graft versus Host Disease Does eduction of GvHD translate in better OS? HLA matching criteria Stem cell source

Patient Selection  Transplants in  PB = 451  BM = 781  Age, yrs  ALL, AML, MDS and CML  Excluded:  T-cell depleted grafts  Reduced Intensity Conditioning  Median follow-up:  PB, 34 months  BM, 38 months PBG05_3.ppt Eapen et al, Biol Blood Marrow Transplant, 2007

Months Cumulative Incidence, % PB (N=451; 45%) BM (N=781; 46%) Transplant-Related Mortality Eapen et al, Biol Blood Marrow Transplant, 2007

Months Cumulative Incidence, % BM (N=777; 40%) PB (N=447; 54%) Chronic GVHD

Months Cumulative Incidence, % BM (N=781; 24%) PB (N=451; 26%) Relapse Eapen et al, Biol Blood Marrow Transplant, 2007

Probability, % PB (N=451; 29%) BM (N=781; 31%) Months: No at Risk PB: BM: Leukemia-free Survival Eapen et al, Biol Blood Marrow Transplant, 2007

Randomized CTN trial (Anasetti et al ASH 2011) Median follow up 36 months Peripheral BLOODMARROWP Overall survival51%46%0.3 OS transplanted52%48%0.3 DFS transplanted47%44%0.6 Relapse28%28%0.8 NRM26%27%0,6 ANC 500 day 10095%86%0.09 aGvHD II-IV47%46%0.8 aGvHD III-IV16%14%0.3 cGvHD53%40%0.02 Ext cGvHD46%31%0.01

Stem cell source 1.Same TRM /relapse / LFS 2.More chronic GvHD Both in retrospective and prospective trials

PERIPHERAL BLOOD TRANSPLANTS DONORS # more SAE for PB donations (significant) # more deaths (ns) # should be stated in the informed consent PATIENTS # no protection against relapse # same TRM; same LFS # more chronic GvHD Should we continue to use PB grafts routinely? ??

Donor Registries Donor Safety Graft versus Host Disease HLA matching criteria Stem cell source Outcome

ACUTE LEUKAEMIA REGISTRY ADULTS TRANSPLANTED FROM 2000 TO 2010 MATCHED UNRELATED DONOR / OS at 5 years AML n=2901ALL n= %±1 40%±2 21%±2 46%±2 28%±2 13%±2 CR1 (n=1117) CR2 (n=879) ADV (n=905) CR1 (n=804) CR2 (n=510) ADV (n=341)

Matched Unrelated Transplants for SAA Effect of transplant era 10 year OS >2000 (752)67% >1990 (230)44% >1980 (27)29% (1)0% P=0.1 P< > days from transplant

Conclusions 1.Caution required for donor harvest (BM and especially PB) 2.Several options for HLA /non HLA donor selection 3.Three agents (C+M+other) for appropriate GvHD prophylaxis 4.Time to transplant= crucial factor 5. Should we continue to use PB??

Donor Registries

Activations BMT Tx 3445 (8%) 3574 (8%) PB Tx 8162 (18%) 9248 (20%) CB 3792 (9%) 4036 (9%) TOTtranspl (35%) (37%) WMDA 2012

REGISTRIES: Large Donor pool Searches Activated : UD Transplants = : = We are transplanting 1/3 of patients who activate a donor search (optimistically 50%)