ESH International Conference
CHRONIC MYELOID LEUKEMIA - Biological Basis of T
herapy
Organizers: J.M. Goldman and J. Cortes
Co-Organizers: A.M. Carella, G. Daley, C. Gambacorti, F. Guilhot,
R. Hehlmann, T. Holyoake, M. Horowitz, T. Hughes,
J.V. Melo, G. Saglio, C. Schiffer, P. Valent, R. Van Etten

5 - 7 September, 2008 - Boston, USA


 Preliminary Programme


 This program is provisional and there will undoubtedly be additional speakers in the final version


Friday, September 5

07:15 - 07:45 Continental Breakfast  
07:50 - 08:00 Welcome J. Goldman
J. Cortes
08:00 - 10:00 Session 1 - Activated kinases in leukemia - Chair: G. Daley (Boston)  
Opening address: Targeting malignant stem cells P. Pandolfi (Boston)
Keynote: Title pending G. Gilliland (Boston)
  JAK2 mutations and MPD pathogenesis T. Green (Cambridge, UK)
  Molecular events involved in initiation and progression of MPDs C. Jamiesson (San Diego)
  Acquired uniparental disomy and novel transforming mutations in atypical CML N. Cross (Southampton)
  Tyrosine kinase inhibitors in eosinophilia-associated myeloproliferative disorders A. Reiter (Mannheim)
  Discussion  
10:00 - 10:30 Break  
10:30 - 12:30 Session 2 - Molecular basis - chronic phase and progression - Chair: F. Frassoni  
 

Analysis of signaling pathways and kinase inhibitors in CML stem/ myeloid progenitors

R.van Etten (Boston)
 

Dissecting the role of GSK3b in CML stem/myeloid progenitors

A.M. Coluccia (Lecce)
 

Genomic determinants of lineage and disease progression in BCR-ABL1 leukemia

C. Mullighan (Memphis)
  More on Ikaros in Ph-positive leukemias I. Iacobucci (Bologna)
  Transcriptional control of ABL.BCR genes in CML: a clue to progression ? C. Gambacorti (Monza)
 

Deregulation of asymmetric division in the progression of chronic myelogenous leukemia

H.Y. Kwon (Durham)
  Mutagenesis to probe kinase regulation M. Azam (Boston)
 

Role of miR in CML

M. Eder (Hannover)
  Discussion  
12:00 - 13:00 Lunch  
13:00 - 15:30 Session 3 - Leukemia stem cells – identification and eradication - Chair: C. Eaves (Vancouver)  
Keynote:

Novel approaches to target cancer stem cells in CML

T. Holyoake (Glasgow)
 

Targeting stem cells and progenitor CML cells by pharmacological restoration of PP2A tumor suppressor activity 

D. Perrotti (Columbus)
 

Properties of CD34+ CML cells that correlate with clinical response to tyrosine kinase inhibitors

X. Jiang
 

Role of FoxO in the persistence of the leukemic progenitors in CML patients treated with TK inhibitors

G. Saglio (Torino)
  Do we need to kill the last CML cell?   J. Melo (Adelaide)
 

Targeting of quiescent leukemia stem cells in chronic myelogenous leukemia by the histone
deacetylase inhibitor LAQ824 in combination with imatinib mesylate

R. Bhatia (Los Angeles)
 

Functional insights of transcriptome analysis of CML stem cells

Y. Zhao (Vancouver)
  Eradication of the leukemia stem cell R. Sackstein (Boston)
  Discussion  
16:00 - 16:30 Break  
16:30 - 18:30 Session 4 - Leukemia stem cells – immune modulation - Chair: Barney Clarkson (New York)  
Keynote:

CTLs and vaccine strategies in CML

K. Rezvani (London)
  Control of the leukaemic stem cell by IFN producing plasmacytoid dendritic cell compartment F. Guilhot (Poitiers)
  IFN-a activates quiescent HSCs in vivo M. Essers (Lausanne)
 

CML stem cells as targets for cellular and immunotherapy

A. Yong (Bethesda)
  Immunotherapy with gene modified T cells H. Stauss (London)
 

PRAME-specific CTLs and transgenic T cells to target CML

F. Pane (Naples)
 

Novel chemical approaches to WT1 vaccines

D. Scheinberg (New York)
 

Expansion of anti-leukemic/anti-host T/NK cells during dasatinib therapy

K. Porkka (Helsinki)
  Discussion  
20:00 Faculty Dinner:
Private Room, Sheraton Boston Hotel 
 

Saturday, September 6

07:30 – 08:00 Continental Breakfast  
08:00 - 09:00 Session 5 - Animal models of leukemia – what can we learn? - Chair: Alan Gewirtz  
Keynote: Murine models of MPD as tools for assessing targeted therapy G. Gilliland (Boston)
  Drosophila model to study BCR-ABL pathway D. Cilloni (Turin)
 

Inducible mouse models of leukemia

S. Koschmieder (Munster

  Molecular basis of HSC and myeloid progenitor compartment expansion induced by junB inactivation E. Passegue (San Francisco)
  Discussion  
09:00 - 11:00

Session 6 - Genomic instability - Chair: TBA               

 

Keynote:

Mechanism of BCR/ABL-induced genomic instability causing resistance to small molecule inhibitors and malignant progression of CML

T. Skorski (Philadelfia)
 

The B-cell lineage specific mutator AID (activation-induced cytidine deaminase)

M. Muschen (Los Angeles)
  Basis and effects of genomic instability M. Sattler (Boston)
  “Back-up” non homologous end-joining (NHEJ) repair: Therapeutic targets in CML? F. Rassool (Baltimore)
  Overcoming drug-resistance to tyrosine-kinase inhibitors in BCR-ABL1 driven leukemia G. Martinelli (Bologna)
 

Application of SNP-array technology to CML

S. Soverini (Bologna)
  Submicroscopic genomic lesions in CML at diagnosis A. Reid (London)
  Inhibiting Abl compromises DNA repair in Bcr-Abl negative cells H. van der Kuip (Stuttgart)
  Discussion  
11:00 - 11:30 Break  
11:30 - 13:00 Session 7 - Targeting tyrosine kinases and signaling pathways - Chair: Nikolas von Bubnoff (Munich)  
Keynote:

Molecular characterization of the BCR-ABL molecular machine as the target of TKIs

G. Superti-Furga (Vienna)
 

Global target profiles for CML TKIs

O. Hantschel (Vienna)
 

Allosteric Bcr-Abl inhibitors: targeting the myristate binding site

N. Gray (Boston)
  Conformational dynamics in wildtype ABL, drug resistant mutants and inhibitor bound complexes John Engen (Boston)
  Gene expression targets for diagnostics and therapy J. Radich (Seattle)
  A novel small molecule disrupts the Bcr-Abl/Jak2/HSP90 network complex leading to apoptosis in blast crisis cells and T3 151 mutant cells R. Arlinghaus (Houston)
  The combination of PHA - 739358 and imatinib is synergistic T. Brümmendorf (Hamburg)
  Discussion  
13:30 - 14:30 Lunch  
13:30 - 15:30 Session 8 - TKIs- how different are they in the clinic? - Chair: R. Stone (Boston)  
Keynote: Outstanding issues with TKIs J. Cortes (Houston)
  Imatinib J. Apperley (London)
  Dasatinib - N. Shah (San Francisco)
  Nilotinib G. Rosti (Bologna)
 

Bosutinib

C. Gambacorti - Passerini (Monza)
  Discussion  
16:00- 16:30 Break  
15:45 - 17:45 Session 9 - Predicting and monitoring responses to imatinib - Chair: R. Silver  (New York)  
Keynote:

Update on predictive assays for de-novo CML patients receiving TKI therapy

T. Hughes (Adelaide)
 

Defining response TKIs and treatment recommendations

M. Baccarani (Bologna) 
  The value of molecular monitoring for imatinib treated patients S. Branford (Adelaide)
  Control of OCT1 expression L. Wang (Liverpool)
  Is it possible to stop imatinib in CML patients? F.-X. Mahon (Bordeaux)
  Interferon after stopping imatinib A. Carella (Genoa)
  Discussion  
18.30 – 19.30

Poster Representations – (3 slides in 3 minutes) - Chairs: Rüdiger Hehlmann (Manheim) and Francisco cervantes (Barcelona)

 
Starting about 19.45 Ending about 22.30   

Conference Gala Dinner – 50th Floor, Prudential Center

 

Sunday, September 7

07:30 - 08:00 Continental Breakfast  
08:00 - 10:00

Session 10 - Resistance to TKIs - Chair: C. Schiffer (Detroit)

 
Keynote: TKI resistance: mutations and more M. Deininger (Portland)
  T3 151 mutated BCR-ABL expression in adult and ES cell derived hematopoiesis A. Turhan (Poitiers)
  Dynamics of mutated clones in vivo A. Hochhaus (Mannheim)
  T3 151 in chronic phase - an epidemiologic study F. Nicolini (Lyon)
  Panale Discussion A. Turhan, M. Scherr, L. Foroni, P. Manley, T. Mughal
10:00 - 10:30 Break  
10:30 - 12:30 Session 11 - Challenges for the next decade - Chair: J. Cortes (Houston)  
Keynote:

Therapeutic thoughts for the future

M. Talpaz (Ann Arbor)
 

What would it take to displace imatinib as first line treatment?

C. Schiffer (Detroit)
  Lessons from clinical trials S. O’Brien (Newscastle)
  Panel Discussion J. Reiffers. P. Vale4nt. J. Cornelissen, A. Quintas Cardama
12:30 - 12:45 Concluding Remarks J. Goldman (London)
     
  Note: This program is still subject to minor changes.