Vol. 3 No. 1: 2006...2009: Now we know T-cell lymphomas better, Bologna, Italy, 16-18 March 2009 | Hematology Meeting Reports (formerly Haematologica Reports)

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Vol. 3 No. 1

11 June 2009

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Vol. 3 No. 1: 2006...2009: Now we know T-cell lymphomas better, Bologna, Italy, 16-18 March 2009

Published: 11 June 2009

Articles

T-cell and natural killer-cell lymphomas An update based on the 2008 WHO classification

E.S. Jaffe

https://doi.org/10.4081/hmr.v3i1.521

253

PDF: 276
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First line therapy for peripheral T-cell lymphoma

D. Sibon

https://doi.org/10.4081/hmr.v3i1.522

195

PDF: 1260
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Treatment of natural killer/T-cell lymphoma

R Liang

https://doi.org/10.4081/hmr.v3i1.523

239

PDF: 1230
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The role of positron emission tomography in T-cell lymphoma and T-cell specific response criteria

BD Cheson

https://doi.org/10.4081/hmr.v3i1.524

241

PDF: 479
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Epigenetic approaches. Histone deacetylase inhibitors: vorinostat. A new treatment option for advanced cutaneous T-cell lymphoma

M Duvic

https://doi.org/10.4081/hmr.v3i1.525

267

PDF: 352
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Panobinostat (LBH589): a novel pan-deacetylase inhibitor with activity in T cell lymphoma

HM Prince, M Prince

https://doi.org/10.4081/hmr.v3i1.526

365

PDF: 4458
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Activity of Belinostat in patients with recurrent or refractory peripheral or cutaneous T-cell lymphoma

F Foss, R Advani, K Hymes, B Pohlman, E Jacobsen, J McDonnell, A Lerner

https://doi.org/10.4081/hmr.v3i1.527

264

PDF: 349
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Gene expression profiling of peripheral T-cell lymphoma: from bench to bedside

PP Piccaluga, M Rossi, A Gazzola, MR Sapienza, C Mannu, S Righi, C Agostinelli, MT Sista, SA Pileri

https://doi.org/10.4081/hmr.v3i1.528

235

PDF: 303
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Angioimmunoblastic T-cell lymphoma: a tumor of follicular helper T cells derivation with clinical and pathological relevance

P Gaulard, Y-L Huang, C Thielen, L de Leval

https://doi.org/10.4081/hmr.v3i1.529

216

PDF: 889
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Anaplastic large cell lymphoma, ALK-positive and anaplastic large cell lymphoma ALK-negative

G Delsol, L Brugières, P Gaulard, E Espinos, L Lamant

https://doi.org/10.4081/hmr.v3i1.530

411

PDF: 872
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Plitidepsin is active in peripheral T-cell lymphoma: a subset analysis from an ongoing multicenter phase II trial

C Ferme, MV Mateos, S Szyldergemajn, E Zucca, S Extremera, J Briones, G Alessandro, V Ribrag

https://doi.org/10.4081/hmr.v3i1.531

215

PDF: 208
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Monoclonal antibody therapy of T cell lymphoma: single agent trials of anti-CD2 (Siplizumab) and anti-CD4 (Humax-CD4)

JE Janik, D O’Mahony, TA Waldmann, JC Morris

https://doi.org/10.4081/hmr.v3i1.532

361

PDF: 385
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Development of LY2334737, an oral gemcitabine prodrug for continuous administration. Perspectives for the therapy of mature T-cell and NK-cell lymphomas

O Shonukan, AH Dantzig, S Kloeker-Rhoades, I Garcia-Ribas

https://doi.org/10.4081/hmr.v3i1.533

316

PDF: 419
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Forodesine

V Gandhi

https://doi.org/10.4081/hmr.v3i1.534

196

PDF: 323
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Pentostatin in peripheral T-cell lymphomas

C Dearden

https://doi.org/10.4081/hmr.v3i1.535

215

PDF: 534
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Preclinical evaluation of sorafenib against B- and T-cell lymphoma

N Schuelper, B Chapuy, T Relander, L Truemper, G Wulf

https://doi.org/10.4081/hmr.v3i1.536

216

PDF: 150
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Immune modulation as a treatment strategy in angioimmunoblastic T-cell lymphoma

R Advani

https://doi.org/10.4081/hmr.v3i1.537

212

PDF: 129
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M. Santucci Cutaneous T-cell lymphomas: histology

M Santucci

https://doi.org/10.4081/hmr.v3i1.538

167

PDF: 1549
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Cutaneous T-cell lymphoma, new insights

MB Wozniak, SM Rodriguez Pinilla, R Villuendas, M Herrera, PL Ortiz, MA Piris

https://doi.org/10.4081/hmr.v3i1.539

210

PDF: 177
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Zanolimumab (Humax-CD4), a fully human monoclonal antibody with significant clinical responses in cutaneous T-cell lymphoma

YH Kim

https://doi.org/10.4081/hmr.v3i1.540

277

PDF: 459
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Forodesine

EA Olsen

https://doi.org/10.4081/hmr.v3i1.541

177

PDF: 135
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Gemcitabine

M Tani, L Alinari, A Broccoli, E Derenzini, M Fina, L Gandolfi, E Marchi, C Pellegrini, V Stefoni, F Venturini, PL Zinzani

https://doi.org/10.4081/hmr.v3i1.542

197

PDF: 187
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Pegylated, liposomal doxorubicin in the treatment of primary cutaneous T-cell lymphoma: an update

S Pulini, S Rupoli, G Goteri, R Alterini, M Cantonetti, A Fabbri, P Quaglino, N Pimpinelli

https://doi.org/10.4081/hmr.v3i1.543

269

PDF: 394
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Innovative treatments: bexarotene

M Duvic

https://doi.org/10.4081/hmr.v3i1.544

205

PDF: 338
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Innovative treatments: bortezomib

PL Zinzani

https://doi.org/10.4081/hmr.v3i1.545

185

PDF: 167
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Lenalidomide (Revlimid®) in patients with cutaneous T-cell lymphoma

C Querfeld, TM Kuzel, J Guitart, ST Rosen

https://doi.org/10.4081/hmr.v3i1.546

334

PDF: 554
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NOTCH1: a therapeutic target for T cell acute lymphoblastic leukemia/lymphoma

V Tosello, A Ferrando

https://doi.org/10.4081/hmr.v3i1.547

156

PDF: 353
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Pediatric T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma therapy

A Pession, R Masetti, R Rondelli

https://doi.org/10.4081/hmr.v3i1.548

326

PDF: 320
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T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma: therapy in adults

M Bonifacio, O Perbellini, G Pizzolo

https://doi.org/10.4081/hmr.v3i1.549

243

PDF: 2412
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Prognostic factors in cutaneous T-cell lymphoma

R Willemze

https://doi.org/10.4081/hmr.v3i1.550

236

PDF: 1533
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High-dose therapy and autotransplantation in peripheral T-cell lymphoma and cutaneous T-cell lymphoma

P Reimer

https://doi.org/10.4081/hmr.v3i1.551

176

PDF: 337
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Allogeneic transplantation for peripheral and cutaneous T-cell lymphomas

P Corradini, A Dodero, G Lambertenghi-Deliliers, F Onida

https://doi.org/10.4081/hmr.v3i1.552

236

PDF: 179
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