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Erschienen in: Current Hematologic Malignancy Reports 4/2017

01.06.2017 | B-cell NHL, T-cell NHL, and Hodgkin Lymphoma (D Persky, Section Editor)

Therapeutic Options for Aggressive T-Cell Lymphomas

verfasst von: Jennifer K. Lue, Anna Kress, Jennifer E. Amengual

Erschienen in: Current Hematologic Malignancy Reports | Ausgabe 4/2017

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Abstract

T-cell lymphomas (TCL) are a rare, heterogeneous group of non-Hodgkin lymphomas associated with very poor prognosis with standard cytotoxic chemotherapy. Epigenetic-based therapy, such as with histone deacetylase inhibitors, was initially discovered to be efficacious in TCL. In recent years, our understanding of the mechanisms driving T-cell lymphomagenesis has validated the use of epigenetic-based drugs and has also led to the development of novel agents with promising efficacy in pre-clinical and early clinical trials. These new treatments play upon the prominent existence of epigenetic and immune dysfunction present in T-cell lymphomas. With these advances, novel therapeutic regimens combining traditional chemotherapy as well as epigenetic and/or immunotherapy serve as promising future treatment options for TCL. In this review, we discuss the traditional methods of treatment for TCL as well as novel agents and combinations that will likely change the treatment paradigms resulting in better clinical outcomes.
Literatur
1.
Zurück zum Zitat • Iqbal J, Wright G, Wang C, et al. Gene expression signatures delineate biological and prognostic subgroups in peripheral T-cell lymphoma. Blood. 2014;123:2915–23. Iqbal et al elucidated that diferential expression of IDH2, GATA3 or TBX21 can characterize PTCL-NOS into futher catergories which in turn can be linked to clinical outcomes. • Iqbal J, Wright G, Wang C, et al. Gene expression signatures delineate biological and prognostic subgroups in peripheral T-cell lymphoma. Blood. 2014;123:2915–23. Iqbal et al elucidated that diferential expression of IDH2, GATA3 or TBX21 can characterize PTCL-NOS into futher catergories which in turn can be linked to clinical outcomes.
2.
Zurück zum Zitat Gascoyne RD, Aoun P, Wu D, et al. Prognostic significance of anaplastic lymphoma kinase (ALK) protein expression in adults with anaplastic large cell lymphoma. Blood. 1999;93:3913–21.PubMed Gascoyne RD, Aoun P, Wu D, et al. Prognostic significance of anaplastic lymphoma kinase (ALK) protein expression in adults with anaplastic large cell lymphoma. Blood. 1999;93:3913–21.PubMed
3.
Zurück zum Zitat Sibon D, Fournier M, Briere J, et al. Long-term outcome of adults with systemic anaplastic large-cell lymphoma treated within the Groupe d’Etude des Lymphomes de l’Adulte trials. J Clin Oncol. 2012;30:3939–46.CrossRefPubMed Sibon D, Fournier M, Briere J, et al. Long-term outcome of adults with systemic anaplastic large-cell lymphoma treated within the Groupe d’Etude des Lymphomes de l’Adulte trials. J Clin Oncol. 2012;30:3939–46.CrossRefPubMed
4.
Zurück zum Zitat Vose J, Armitage J, Weisenburger D, International TCLP. International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol. 2008;26:4124–30.CrossRefPubMed Vose J, Armitage J, Weisenburger D, International TCLP. International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol. 2008;26:4124–30.CrossRefPubMed
5.
Zurück zum Zitat Schmitz N, Trumper L, Ziepert M, et al. Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group. Blood. 2010;116:3418–25.CrossRefPubMed Schmitz N, Trumper L, Ziepert M, et al. Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group. Blood. 2010;116:3418–25.CrossRefPubMed
6.
Zurück zum Zitat Ellin F, Landstrom J, Jerkeman M, Relander T. Real-world data on prognostic factors and treatment in peripheral T-cell lymphomas: a study from the Swedish Lymphoma Registry. Blood. 2014;124:1570–7.CrossRefPubMed Ellin F, Landstrom J, Jerkeman M, Relander T. Real-world data on prognostic factors and treatment in peripheral T-cell lymphomas: a study from the Swedish Lymphoma Registry. Blood. 2014;124:1570–7.CrossRefPubMed
7.
Zurück zum Zitat Reimer P, Rudiger T, Geissinger E, et al. Autologous stem-cell transplantation as first-line therapy in peripheral T-cell lymphomas: results of a prospective multicenter study. J Clin Oncol. 2009;27:106–13.CrossRefPubMed Reimer P, Rudiger T, Geissinger E, et al. Autologous stem-cell transplantation as first-line therapy in peripheral T-cell lymphomas: results of a prospective multicenter study. J Clin Oncol. 2009;27:106–13.CrossRefPubMed
8.
Zurück zum Zitat d’Amore F, Relander T, Lauritzsen GF, et al. Up-front autologous stem-cell transplantation in peripheral T-cell lymphoma: NLG-T-01. J Clin Oncol. 2012;30:3093–9.CrossRefPubMed d’Amore F, Relander T, Lauritzsen GF, et al. Up-front autologous stem-cell transplantation in peripheral T-cell lymphoma: NLG-T-01. J Clin Oncol. 2012;30:3093–9.CrossRefPubMed
9.
Zurück zum Zitat Mak V, Hamm J, Chhanabhai M, et al. Survival of patients with peripheral T-cell lymphoma after first relapse or progression: spectrum of disease and rare long-term survivors. J Clin Oncol. 2013;31:1970–6.CrossRefPubMed Mak V, Hamm J, Chhanabhai M, et al. Survival of patients with peripheral T-cell lymphoma after first relapse or progression: spectrum of disease and rare long-term survivors. J Clin Oncol. 2013;31:1970–6.CrossRefPubMed
10.
Zurück zum Zitat Zelenetz AD, Hamlin P, Kewalramani T, Yahalom J, Nimer S, Moskowitz CH. Ifosfamide, carboplatin, etoposide (ICE)-based second-line chemotherapy for the management of relapsed and refractory aggressive non-Hodgkin’s lymphoma. Ann Oncol : Off J Eur Soc Med Oncol / ESMO. 2003;14(Suppl 1):i5–10.CrossRef Zelenetz AD, Hamlin P, Kewalramani T, Yahalom J, Nimer S, Moskowitz CH. Ifosfamide, carboplatin, etoposide (ICE)-based second-line chemotherapy for the management of relapsed and refractory aggressive non-Hodgkin’s lymphoma. Ann Oncol : Off J Eur Soc Med Oncol / ESMO. 2003;14(Suppl 1):i5–10.CrossRef
11.
Zurück zum Zitat Yao YY, Tang Y, Zhu Q, et al. Gemcitabine, oxaliplatin and dexamethasone as salvage treatment for elderly patients with refractory and relapsed peripheral T-cell lymphoma. Leukemia & lymphoma. 2013;54:1194–200.CrossRef Yao YY, Tang Y, Zhu Q, et al. Gemcitabine, oxaliplatin and dexamethasone as salvage treatment for elderly patients with refractory and relapsed peripheral T-cell lymphoma. Leukemia & lymphoma. 2013;54:1194–200.CrossRef
12.
Zurück zum Zitat Lopez A, Gutierrez A, Palacios A, et al. GEMOX-R regimen is a highly effective salvage regimen in patients with refractory/relapsing diffuse large-cell lymphoma: a phase II study. Eur J Haematol. 2008;80:127–32.CrossRefPubMed Lopez A, Gutierrez A, Palacios A, et al. GEMOX-R regimen is a highly effective salvage regimen in patients with refractory/relapsing diffuse large-cell lymphoma: a phase II study. Eur J Haematol. 2008;80:127–32.CrossRefPubMed
13.
Zurück zum Zitat Connors JM, Sehn LH, Villa D, et al. Gemcitabine, dexamethasone, and cisplatin (GDP) as secondary chemotherapy in relapsed/refractory peripheral T-cell lymphoma. Blood. 2013;122:4345.CrossRef Connors JM, Sehn LH, Villa D, et al. Gemcitabine, dexamethasone, and cisplatin (GDP) as secondary chemotherapy in relapsed/refractory peripheral T-cell lymphoma. Blood. 2013;122:4345.CrossRef
14.
Zurück zum Zitat Chihara D WC, Duvic M, Medeiros L, Oki Y. T-cell lymphomas. In: Kantarjian HM WR, ed. The MD Anderson manual of medical oncology. Third ed: McGraw-Hill; 2016. Chihara D WC, Duvic M, Medeiros L, Oki Y. T-cell lymphomas. In: Kantarjian HM WR, ed. The MD Anderson manual of medical oncology. Third ed: McGraw-Hill; 2016.
15.
17.
Zurück zum Zitat Lemonnier F, Couronne L, Parrens M, et al. Recurrent TET2 mutations in peripheral T-cell lymphomas correlate with TFH-like features and adverse clinical parameters. Blood. 2012;120:1466–9.CrossRefPubMed Lemonnier F, Couronne L, Parrens M, et al. Recurrent TET2 mutations in peripheral T-cell lymphomas correlate with TFH-like features and adverse clinical parameters. Blood. 2012;120:1466–9.CrossRefPubMed
18.
Zurück zum Zitat Couronne L, Bastard C, Bernard OA. TET2 and DNMT3A mutations in human T-cell lymphoma. N Engl J Med. 2012;366:95–6.CrossRefPubMed Couronne L, Bastard C, Bernard OA. TET2 and DNMT3A mutations in human T-cell lymphoma. N Engl J Med. 2012;366:95–6.CrossRefPubMed
19.
20.
Zurück zum Zitat Losman JA, Looper RE, Koivunen P, et al. (R)-2-hydroxyglutarate is sufficient to promote leukemogenesis and its effects are reversible. Science. 2013;339:1621–5.CrossRefPubMed Losman JA, Looper RE, Koivunen P, et al. (R)-2-hydroxyglutarate is sufficient to promote leukemogenesis and its effects are reversible. Science. 2013;339:1621–5.CrossRefPubMed
21.
Zurück zum Zitat Rohle D, Popovici-Muller J, Palaskas N, et al. An inhibitor of mutant IDH1 delays growth and promotes differentiation of glioma cells. Science. 2013;340:626–30.CrossRefPubMedPubMedCentral Rohle D, Popovici-Muller J, Palaskas N, et al. An inhibitor of mutant IDH1 delays growth and promotes differentiation of glioma cells. Science. 2013;340:626–30.CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Davis MI, Gross S, Shen M, et al. Biochemical, cellular, and biophysical characterization of a potent inhibitor of mutant isocitrate dehydrogenase IDH1. J Biol Chem. 2014;289:13717–25.CrossRefPubMedPubMedCentral Davis MI, Gross S, Shen M, et al. Biochemical, cellular, and biophysical characterization of a potent inhibitor of mutant isocitrate dehydrogenase IDH1. J Biol Chem. 2014;289:13717–25.CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat Stein EM, Altman JK, Collins R, et al. AG-221, an oral, selective, first-in-class, potent inhibitor of the IDH2 mutant metabolic enzyme, induces durable remissions in a phase I study in patients with IDH2 mutation positive advanced hematologic malignancies. Blood. 2014;124:115. Stein EM, Altman JK, Collins R, et al. AG-221, an oral, selective, first-in-class, potent inhibitor of the IDH2 mutant metabolic enzyme, induces durable remissions in a phase I study in patients with IDH2 mutation positive advanced hematologic malignancies. Blood. 2014;124:115.
24.
Zurück zum Zitat Ji M. Histone-modifying gene mutations are related to tumor progression and response to histone deacetylase inhibitors in patients with peripheral T-cell lymphoma not otherwise specified. Blood. 2016;128:4110.CrossRef Ji M. Histone-modifying gene mutations are related to tumor progression and response to histone deacetylase inhibitors in patients with peripheral T-cell lymphoma not otherwise specified. Blood. 2016;128:4110.CrossRef
25.
Zurück zum Zitat Bates SE, Zhan Z, Steadman K, et al. Laboratory correlates for a phase II trial of romidepsin in cutaneous and peripheral T-cell lymphoma. Br J Haematol. 2010;148:256–67.CrossRefPubMed Bates SE, Zhan Z, Steadman K, et al. Laboratory correlates for a phase II trial of romidepsin in cutaneous and peripheral T-cell lymphoma. Br J Haematol. 2010;148:256–67.CrossRefPubMed
26.
Zurück zum Zitat Sandor V, Senderowicz A, Mertins S, et al. P21-dependent g(1)arrest with downregulation of cyclin D1 and upregulation of cyclin E by the histone deacetylase inhibitor FR901228. Br J Cancer. 2000;83:817–25.CrossRefPubMedPubMedCentral Sandor V, Senderowicz A, Mertins S, et al. P21-dependent g(1)arrest with downregulation of cyclin D1 and upregulation of cyclin E by the histone deacetylase inhibitor FR901228. Br J Cancer. 2000;83:817–25.CrossRefPubMedPubMedCentral
27.
Zurück zum Zitat Kelly WK, Richon VM, O’Connor O, et al. Phase I clinical trial of histone deacetylase inhibitor: suberoylanilide hydroxamic acid administered intravenously. Clin Cancer Res : Off J Am Assoc Cancer Res. 2003;9:3578–88. Kelly WK, Richon VM, O’Connor O, et al. Phase I clinical trial of histone deacetylase inhibitor: suberoylanilide hydroxamic acid administered intravenously. Clin Cancer Res : Off J Am Assoc Cancer Res. 2003;9:3578–88.
28.
Zurück zum Zitat Kelly WK, O’Connor OA, Krug LM, et al. Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J Clin Oncol. 2005;23:3923–31.CrossRefPubMedPubMedCentral Kelly WK, O’Connor OA, Krug LM, et al. Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J Clin Oncol. 2005;23:3923–31.CrossRefPubMedPubMedCentral
29.
Zurück zum Zitat Olsen EA, Kim YH, Kuzel TM, et al. Phase IIb multicenter trial of vorinostat in patients with persistent, progressive, or treatment refractory cutaneous T-cell lymphoma. J Clin Oncol. 2007;25:3109–15.CrossRefPubMed Olsen EA, Kim YH, Kuzel TM, et al. Phase IIb multicenter trial of vorinostat in patients with persistent, progressive, or treatment refractory cutaneous T-cell lymphoma. J Clin Oncol. 2007;25:3109–15.CrossRefPubMed
30.
Zurück zum Zitat Duvic M, Talpur R, Ni X, et al. Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL). Blood. 2007;109:31–9.CrossRefPubMedPubMedCentral Duvic M, Talpur R, Ni X, et al. Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL). Blood. 2007;109:31–9.CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Whittaker SJ, Demierre MF, Kim EJ, et al. Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma. J Clin Oncol. 2010;28:4485–91.CrossRefPubMed Whittaker SJ, Demierre MF, Kim EJ, et al. Final results from a multicenter, international, pivotal study of romidepsin in refractory cutaneous T-cell lymphoma. J Clin Oncol. 2010;28:4485–91.CrossRefPubMed
32.
33.
Zurück zum Zitat Coiffier B, Pro B, Prince HM, et al. Results from a pivotal, open-label, phase II study of romidepsin in relapsed or refractory peripheral T-cell lymphoma after prior systemic therapy. J Clin Oncol. 2012;30:631–6.CrossRefPubMed Coiffier B, Pro B, Prince HM, et al. Results from a pivotal, open-label, phase II study of romidepsin in relapsed or refractory peripheral T-cell lymphoma after prior systemic therapy. J Clin Oncol. 2012;30:631–6.CrossRefPubMed
34.
Zurück zum Zitat O’Connor OA, Horwitz S, Masszi T, et al. Belinostat in patients with relapsed or refractory peripheral T-cell lymphoma: results of the pivotal phase II BELIEF (CLN-19) study. J Clin Oncol. 2015;33:2492–9.CrossRefPubMedPubMedCentral O’Connor OA, Horwitz S, Masszi T, et al. Belinostat in patients with relapsed or refractory peripheral T-cell lymphoma: results of the pivotal phase II BELIEF (CLN-19) study. J Clin Oncol. 2015;33:2492–9.CrossRefPubMedPubMedCentral
35.
Zurück zum Zitat Sirotnak FM, DeGraw JI, Chello PL, Moccio DM, Dorick DM. Biochemical and pharmacologic properties of a new folate analog, 10-deaza-aminopterin, in mice. Cancer treatment reports. 1982;66:351–8.PubMed Sirotnak FM, DeGraw JI, Chello PL, Moccio DM, Dorick DM. Biochemical and pharmacologic properties of a new folate analog, 10-deaza-aminopterin, in mice. Cancer treatment reports. 1982;66:351–8.PubMed
36.
Zurück zum Zitat Marchi E, Mangone M, Zullo K, O’Connor OA. Pralatrexate pharmacology and clinical development. Clin Cancer Res: Off J Am Assoc Cancer Res. 2013;19:6657–61.CrossRef Marchi E, Mangone M, Zullo K, O’Connor OA. Pralatrexate pharmacology and clinical development. Clin Cancer Res: Off J Am Assoc Cancer Res. 2013;19:6657–61.CrossRef
37.
Zurück zum Zitat O’Connor OA, Pro B, Pinter-Brown L, et al. Pralatrexate in patients with relapsed or refractory peripheral T-cell lymphoma: results from the pivotal PROPEL study. J Clin Oncol. 2011;29:1182–9.CrossRefPubMedPubMedCentral O’Connor OA, Pro B, Pinter-Brown L, et al. Pralatrexate in patients with relapsed or refractory peripheral T-cell lymphoma: results from the pivotal PROPEL study. J Clin Oncol. 2011;29:1182–9.CrossRefPubMedPubMedCentral
38.
Zurück zum Zitat O’Connor OA, Marchi E, Volinn W, Kim WS. Case match control analysis of propel reveals survival advantage for patients with relapsed/refractory (R/R) peripheral T-cell lymphoma (PTCL) treated with pralatrexate. Blood. 2016;128:4149. O’Connor OA, Marchi E, Volinn W, Kim WS. Case match control analysis of propel reveals survival advantage for patients with relapsed/refractory (R/R) peripheral T-cell lymphoma (PTCL) treated with pralatrexate. Blood. 2016;128:4149.
40.
Zurück zum Zitat Pro B, Advani R, Brice P, et al. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol. 2012;30:2190–6.CrossRefPubMed Pro B, Advani R, Brice P, et al. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol. 2012;30:2190–6.CrossRefPubMed
41.
Zurück zum Zitat Horwitz SM, Advani RH, Bartlett NL, et al. Objective responses in relapsed T-cell lymphomas with single-agent brentuximab vedotin. Blood. 2014;123:3095–100.CrossRefPubMedPubMedCentral Horwitz SM, Advani RH, Bartlett NL, et al. Objective responses in relapsed T-cell lymphomas with single-agent brentuximab vedotin. Blood. 2014;123:3095–100.CrossRefPubMedPubMedCentral
42.
Zurück zum Zitat • Dupuis J, Morschhauser F, Ghesquieres H, et al. Combination of romidepsin with cyclophosphamide, doxorubicin, vincristine, and prednisone in previously untreated patients with peripheral T-cell lymphoma: a non-randomised, phase 1b/2 study. Lancet Haematol. 2015;2:e160–5. Phase I study in treatment naïve PTCL investigating the combination of epigenetic therapy (romidepsin) with cytotoxic therapy (CHOP). The combination was tolerable with 51% of the patients achieving a complete response. This regimen is currently being further investigated in Phase III trial ((NCT0196002). • Dupuis J, Morschhauser F, Ghesquieres H, et al. Combination of romidepsin with cyclophosphamide, doxorubicin, vincristine, and prednisone in previously untreated patients with peripheral T-cell lymphoma: a non-randomised, phase 1b/2 study. Lancet Haematol. 2015;2:e160–5. Phase I study in treatment naïve PTCL investigating the combination of epigenetic therapy (romidepsin) with cytotoxic therapy (CHOP). The combination was tolerable with 51% of the patients achieving a complete response. This regimen is currently being further investigated in Phase III trial ((NCT0196002).
43.
Zurück zum Zitat • Johnston PB, Cashen AF, Nikolinakos PG, et al. Safe and effective treatment of patients with peripheral T-cell lymphoma (PTCL) with the novel HDAC inhibitor, belinostat, in combination with CHOP: results of the bel-CHOP phase 1 trial. Blood. 2015;126:253. Phase I trial investigating the combination of belinostat and CHOP in PTCL which demonstrated an ORR of 89%, with CR of 72%. • Johnston PB, Cashen AF, Nikolinakos PG, et al. Safe and effective treatment of patients with peripheral T-cell lymphoma (PTCL) with the novel HDAC inhibitor, belinostat, in combination with CHOP: results of the bel-CHOP phase 1 trial. Blood. 2015;126:253. Phase I trial investigating the combination of belinostat and CHOP in PTCL which demonstrated an ORR of 89%, with CR of 72%.
44.
Zurück zum Zitat Fanale MA, Horwitz SM, Forero-Torres A, et al. Brentuximab vedotin in the front-line treatment of patients with CD30+ peripheral T-cell lymphomas: results of a phase I study. J Clin Oncol. 2014;32:3137–43.CrossRefPubMedPubMedCentral Fanale MA, Horwitz SM, Forero-Torres A, et al. Brentuximab vedotin in the front-line treatment of patients with CD30+ peripheral T-cell lymphomas: results of a phase I study. J Clin Oncol. 2014;32:3137–43.CrossRefPubMedPubMedCentral
45.
Zurück zum Zitat Fanale MA, Horwitz SM, Forero-Torres A, et al. Four-year survival and durability results of brentuximab vedotin in combination with CHP in the frontline treatment of patients with CD30-expressing peripheral T-cell lymphomas. Blood. 2016;128:2993. Fanale MA, Horwitz SM, Forero-Torres A, et al. Four-year survival and durability results of brentuximab vedotin in combination with CHP in the frontline treatment of patients with CD30-expressing peripheral T-cell lymphomas. Blood. 2016;128:2993.
46.
Zurück zum Zitat Advani RH, Ansell SM, Lechowicz MJ, et al. A phase II study of cyclophosphamide, etoposide, vincristine and prednisone (CEOP) alternating with pralatrexate (P) as front line therapy for patients with peripheral T-cell lymphoma (PTCL): final results from the T- cell consortium trial. Br J Haematol. 2016;172:535–44.CrossRefPubMed Advani RH, Ansell SM, Lechowicz MJ, et al. A phase II study of cyclophosphamide, etoposide, vincristine and prednisone (CEOP) alternating with pralatrexate (P) as front line therapy for patients with peripheral T-cell lymphoma (PTCL): final results from the T- cell consortium trial. Br J Haematol. 2016;172:535–44.CrossRefPubMed
47.
Zurück zum Zitat Shustov AR OY, Barta SK, Johnston PB, Sharma P, Song T, and Mourya S. CHOP in combination with pralatrexate, a novel folate analogue metabolic inhibitor in patients with previously untreated peripheral T-cell lymphoma (PTCL): interim results of the phase I trial. ASH Annual Conference San Diego, California: American Society of Hematology; 2016:5355. Shustov AR OY, Barta SK, Johnston PB, Sharma P, Song T, and Mourya S. CHOP in combination with pralatrexate, a novel folate analogue metabolic inhibitor in patients with previously untreated peripheral T-cell lymphoma (PTCL): interim results of the phase I trial. ASH Annual Conference San Diego, California: American Society of Hematology; 2016:5355.
48.
Zurück zum Zitat Kluin-Nelemans HC, van Marwijk KM, Lugtenburg PJ, et al. Intensified alemtuzumab-CHOP therapy for peripheral T-cell lymphoma. Ann Oncol : Off J Eur Soc Med Oncol / ESMO. 2011;22:1595–600.CrossRef Kluin-Nelemans HC, van Marwijk KM, Lugtenburg PJ, et al. Intensified alemtuzumab-CHOP therapy for peripheral T-cell lymphoma. Ann Oncol : Off J Eur Soc Med Oncol / ESMO. 2011;22:1595–600.CrossRef
49.
Zurück zum Zitat Gallamini A, Zaja F, Patti C, et al. Alemtuzumab (Campath-1H) and CHOP chemotherapy as first-line treatment of peripheral T-cell lymphoma: results of a GITIL (Gruppo Italiano Terapie innovative nei Linfomi) prospective multicenter trial. Blood. 2007;110:2316–23.CrossRefPubMed Gallamini A, Zaja F, Patti C, et al. Alemtuzumab (Campath-1H) and CHOP chemotherapy as first-line treatment of peripheral T-cell lymphoma: results of a GITIL (Gruppo Italiano Terapie innovative nei Linfomi) prospective multicenter trial. Blood. 2007;110:2316–23.CrossRefPubMed
50.
Zurück zum Zitat Foss FM, Sjak-Shie N, Goy A, et al. A multicenter phase II trial to determine the safety and efficacy of combination therapy with denileukin diftitox and cyclophosphamide, doxorubicin, vincristine and prednisone in untreated peripheral T-cell lymphoma: the CONCEPT study. Leukemia & lymphoma. 2013;54:1373–9.CrossRef Foss FM, Sjak-Shie N, Goy A, et al. A multicenter phase II trial to determine the safety and efficacy of combination therapy with denileukin diftitox and cyclophosphamide, doxorubicin, vincristine and prednisone in untreated peripheral T-cell lymphoma: the CONCEPT study. Leukemia & lymphoma. 2013;54:1373–9.CrossRef
51.
Zurück zum Zitat Shen L, Au WY, Guo T, et al. Proteasome inhibitor bortezomib-induced apoptosis in natural killer (NK)-cell leukemia and lymphoma: an in vitro and in vivo preclinical evaluation. Blood. 2007;110:469–70.CrossRefPubMed Shen L, Au WY, Guo T, et al. Proteasome inhibitor bortezomib-induced apoptosis in natural killer (NK)-cell leukemia and lymphoma: an in vitro and in vivo preclinical evaluation. Blood. 2007;110:469–70.CrossRefPubMed
52.
Zurück zum Zitat Iwata S, Yano S, Ito Y, et al. Bortezomib induces apoptosis in T lymphoma cells and natural killer lymphoma cells independent of Epstein-Barr virus infection. Int J Cancer J Int du Cancer. 2011;129:2263–73.CrossRef Iwata S, Yano S, Ito Y, et al. Bortezomib induces apoptosis in T lymphoma cells and natural killer lymphoma cells independent of Epstein-Barr virus infection. Int J Cancer J Int du Cancer. 2011;129:2263–73.CrossRef
53.
Zurück zum Zitat Evens AM, Rosen ST, Helenowski I, et al. A phase I/II trial of bortezomib combined concurrently with gemcitabine for relapsed or refractory DLBCL and peripheral T-cell lymphomas. Br J Haematol. 2013;163:55–61.CrossRefPubMed Evens AM, Rosen ST, Helenowski I, et al. A phase I/II trial of bortezomib combined concurrently with gemcitabine for relapsed or refractory DLBCL and peripheral T-cell lymphomas. Br J Haematol. 2013;163:55–61.CrossRefPubMed
54.
Zurück zum Zitat Kim SJ, Yoon DH, Kang HJ, et al. Bortezomib in combination with CHOP as first-line treatment for patients with stage III/IV peripheral T-cell lymphomas: a multicentre, single-arm, phase 2 trial. Eur J Cancer. 2012;48:3223–31.CrossRefPubMed Kim SJ, Yoon DH, Kang HJ, et al. Bortezomib in combination with CHOP as first-line treatment for patients with stage III/IV peripheral T-cell lymphomas: a multicentre, single-arm, phase 2 trial. Eur J Cancer. 2012;48:3223–31.CrossRefPubMed
55.
Zurück zum Zitat • Amengual JE, Lichtenstein R, Rojas C, et al. The pralatrexate-romidepsin doublet: a well tolerated and highly effective combination for patients with relapsed or refractory peripheral T-cell lymphoma. Blood. 2016;128:1824. Novel combination of pralatrexate and romidepsin demonstrated promising results in PTCL cohort, and is now being investigated in a Phase II trial. • Amengual JE, Lichtenstein R, Rojas C, et al. The pralatrexate-romidepsin doublet: a well tolerated and highly effective combination for patients with relapsed or refractory peripheral T-cell lymphoma. Blood. 2016;128:1824. Novel combination of pralatrexate and romidepsin demonstrated promising results in PTCL cohort, and is now being investigated in a Phase II trial.
56.
Zurück zum Zitat Jain S, Jirau-Serrano X, Zullo KM, et al. Preclinical pharmacologic evaluation of pralatrexate and romidepsin confirms potent synergy of the combination in a murine model of human T-cell lymphoma. Clin Cancer Res: Off J Am Assoc Cancer Res. 2015; Jain S, Jirau-Serrano X, Zullo KM, et al. Preclinical pharmacologic evaluation of pralatrexate and romidepsin confirms potent synergy of the combination in a murine model of human T-cell lymphoma. Clin Cancer Res: Off J Am Assoc Cancer Res. 2015;
57.
Zurück zum Zitat Delarue R, Dupuis J, Sujobert P, et al. Treatment with hypomethylating agent 5-azacytidine induces sustained response in angioimmunoblastic T cell lymphomas. Blood. 2016;128:4164. Delarue R, Dupuis J, Sujobert P, et al. Treatment with hypomethylating agent 5-azacytidine induces sustained response in angioimmunoblastic T cell lymphomas. Blood. 2016;128:4164.
58.
Zurück zum Zitat O’Connor OA, Marchi E, Zullo K, et al. The combination of hypomethylating agents and histone deacetylase inhibitors (HDACi) are synergistically cytotoxic and reverse the malignant phenotype in preclinical models of T-cell lymphoma. 2013. O’Connor OA, Marchi E, Zullo K, et al. The combination of hypomethylating agents and histone deacetylase inhibitors (HDACi) are synergistically cytotoxic and reverse the malignant phenotype in preclinical models of T-cell lymphoma. 2013.
59.
Zurück zum Zitat Mehta-Shah NLM, Boruchov AM, et al. . A phase I/II trial of the combination of romidepsin and lenalidomide in patients with relapsed/refractory lymphoma and myeloma: activity in T-cell lymphoma. 2015 ASCO Annual Meeting. Chicago, Illnois2015. Mehta-Shah NLM, Boruchov AM, et al. . A phase I/II trial of the combination of romidepsin and lenalidomide in patients with relapsed/refractory lymphoma and myeloma: activity in T-cell lymphoma. 2015 ASCO Annual Meeting. Chicago, Illnois2015.
60.
Zurück zum Zitat Mehta-Shah N, Moskowitz AJ, Lunning M, et al. A phase Ib/IIa trial of the combination of romidepsin, lenalidomide and carfilzomib in patients with relapsed/refractory lymphoma shows complete responses in relapsed and refractory T-cell lymphomas. Blood. 2016;128:2991. Mehta-Shah N, Moskowitz AJ, Lunning M, et al. A phase Ib/IIa trial of the combination of romidepsin, lenalidomide and carfilzomib in patients with relapsed/refractory lymphoma shows complete responses in relapsed and refractory T-cell lymphomas. Blood. 2016;128:2991.
61.
Zurück zum Zitat Reiman T, Savage KJ, Crump M, et al. A phase I study of romidepsin, gemcitabine, dexamethasone and cisplatin combination therapy in the treatment of peripheral T-cell and diffuse large B-cell lymphoma: Canadian Cancer Trials Group Study LY.15. Blood. 2016;128:4162. Reiman T, Savage KJ, Crump M, et al. A phase I study of romidepsin, gemcitabine, dexamethasone and cisplatin combination therapy in the treatment of peripheral T-cell and diffuse large B-cell lymphoma: Canadian Cancer Trials Group Study LY.15. Blood. 2016;128:4162.
62.
Zurück zum Zitat Yan J, Ng S-B, Tay JL-S, et al. EZH2 overexpression in natural killer/T-cell lymphoma confers growth advantage independently of histone methyltransferase activity. Blood. 2013;121:4512–20.CrossRefPubMed Yan J, Ng S-B, Tay JL-S, et al. EZH2 overexpression in natural killer/T-cell lymphoma confers growth advantage independently of histone methyltransferase activity. Blood. 2013;121:4512–20.CrossRefPubMed
63.
Zurück zum Zitat Fujikawa D, Nakagawa S, Hori M, et al. Polycomb-dependent epigenetic landscape in adult T-cell leukemia. Blood. 2016;127:1790–802.CrossRefPubMed Fujikawa D, Nakagawa S, Hori M, et al. Polycomb-dependent epigenetic landscape in adult T-cell leukemia. Blood. 2016;127:1790–802.CrossRefPubMed
64.
Zurück zum Zitat Ishida T, Inagaki H, Utsunomiya A, et al. CXC chemokine receptor 3 and CC chemokine receptor 4 expression in T-cell and NK-cell lymphomas with special reference to clinicopathological significance for peripheral T-cell lymphoma, unspecified. Clin Cancer Res: Off J Am Assoc Cancer Res. 2004;10:5494–500.CrossRef Ishida T, Inagaki H, Utsunomiya A, et al. CXC chemokine receptor 3 and CC chemokine receptor 4 expression in T-cell and NK-cell lymphomas with special reference to clinicopathological significance for peripheral T-cell lymphoma, unspecified. Clin Cancer Res: Off J Am Assoc Cancer Res. 2004;10:5494–500.CrossRef
65.
Zurück zum Zitat Wang T, Feldman AL, Wada DA, et al. GATA-3 expression identifies a high-risk subset of PTCL, NOS with distinct molecular and clinical features. Blood. 2014;123:3007–15.CrossRefPubMedPubMedCentral Wang T, Feldman AL, Wada DA, et al. GATA-3 expression identifies a high-risk subset of PTCL, NOS with distinct molecular and clinical features. Blood. 2014;123:3007–15.CrossRefPubMedPubMedCentral
66.
Zurück zum Zitat Nakagawa M, Schmitz R, Xiao W, et al. Gain-of-function <em>CCR4</em> mutations in adult T cell leukemia/lymphoma. The Journal of Experimental Medicine 2014. Nakagawa M, Schmitz R, Xiao W, et al. Gain-of-function <em>CCR4</em> mutations in adult T cell leukemia/lymphoma. The Journal of Experimental Medicine 2014.
67.
Zurück zum Zitat Ishida T, Iida S, Akatsuka Y, et al. The CC chemokine receptor 4 as a novel specific molecular target for immunotherapy in adult T-cell leukemia/lymphoma. Clin Cancer Res : Off J Am Assoc Cancer Res. 2004;10:7529–39.CrossRef Ishida T, Iida S, Akatsuka Y, et al. The CC chemokine receptor 4 as a novel specific molecular target for immunotherapy in adult T-cell leukemia/lymphoma. Clin Cancer Res : Off J Am Assoc Cancer Res. 2004;10:7529–39.CrossRef
68.
Zurück zum Zitat Duvic M, Pinter-Brown LC, Foss FM, et al. Phase 1/2 study of mogamulizumab, a defucosylated anti-CCR4 antibody, in previously treated patients with cutaneous T-cell lymphoma. Blood. 2015;125:1883–9.CrossRefPubMedPubMedCentral Duvic M, Pinter-Brown LC, Foss FM, et al. Phase 1/2 study of mogamulizumab, a defucosylated anti-CCR4 antibody, in previously treated patients with cutaneous T-cell lymphoma. Blood. 2015;125:1883–9.CrossRefPubMedPubMedCentral
69.
Zurück zum Zitat Phillips AA FP, Hermine O, et al. A prospective, multicenter, randomized study of anti-CCR4 monoclonal antibody mogamulizumab (moga) vs investigator’s choice (IC) in the treatment of patients (pts) with relapsed/refractory (R/R) adult T-cell leukemia-lymphoma (ATL). J Clin Oncol 2016; 34 (suppl; abstr 7501) 2016. Phillips AA FP, Hermine O, et al. A prospective, multicenter, randomized study of anti-CCR4 monoclonal antibody mogamulizumab (moga) vs investigator’s choice (IC) in the treatment of patients (pts) with relapsed/refractory (R/R) adult T-cell leukemia-lymphoma (ATL). J Clin Oncol 2016; 34 (suppl; abstr 7501) 2016.
70.
Zurück zum Zitat Ansell SM, Lesokhin AM, Borrello I, et al. PD-1 blockade with nivolumab in relapsed or refractory Hodgkin’s lymphoma. N Engl J Med. 2015;372:311–9.CrossRefPubMed Ansell SM, Lesokhin AM, Borrello I, et al. PD-1 blockade with nivolumab in relapsed or refractory Hodgkin’s lymphoma. N Engl J Med. 2015;372:311–9.CrossRefPubMed
71.
Zurück zum Zitat Khodadoust M, Rook AH, Porcu P, et al. Pembrolizumab for treatment of relapsed/refractory mycosis fungoides and Sezary syndrome: clinical efficacy in a Citn multicenter phase 2 study. Blood. 2016;128:181. Khodadoust M, Rook AH, Porcu P, et al. Pembrolizumab for treatment of relapsed/refractory mycosis fungoides and Sezary syndrome: clinical efficacy in a Citn multicenter phase 2 study. Blood. 2016;128:181.
72.
Zurück zum Zitat Lesokhin AM, Ansell SM, Armand P, et al. Nivolumab in patients with relapsed or refractory hematologic malignancy: preliminary results of a phase Ib study. J Clin Oncol. 2016;34:2698–704.CrossRefPubMedPubMedCentral Lesokhin AM, Ansell SM, Armand P, et al. Nivolumab in patients with relapsed or refractory hematologic malignancy: preliminary results of a phase Ib study. J Clin Oncol. 2016;34:2698–704.CrossRefPubMedPubMedCentral
73.
Zurück zum Zitat Weber J, Salgaller M, Samid D, et al. Expression of the MAGE-1 tumor antigen is up-regulated by the demethylating agent 5-aza-2′-deoxycytidine. Cancer Res. 1994;54:1766–71.PubMed Weber J, Salgaller M, Samid D, et al. Expression of the MAGE-1 tumor antigen is up-regulated by the demethylating agent 5-aza-2′-deoxycytidine. Cancer Res. 1994;54:1766–71.PubMed
74.
Zurück zum Zitat Yang H, Bueso-Ramos C, DiNardo C, et al. Expression of PD-L1, PD-L2, PD-1 and CTLA4 in myelodysplastic syndromes is enhanced by treatment with hypomethylating agents. Leukemia. 2014;28:1280–8.CrossRefPubMed Yang H, Bueso-Ramos C, DiNardo C, et al. Expression of PD-L1, PD-L2, PD-1 and CTLA4 in myelodysplastic syndromes is enhanced by treatment with hypomethylating agents. Leukemia. 2014;28:1280–8.CrossRefPubMed
75.
Zurück zum Zitat Kim K, Skora AD, Li Z, et al. Eradication of metastatic mouse cancers resistant to immune checkpoint blockade by suppression of myeloid-derived cells. Proc Natl Acad Sci U S A. 2014;111:11774–9.CrossRefPubMedPubMedCentral Kim K, Skora AD, Li Z, et al. Eradication of metastatic mouse cancers resistant to immune checkpoint blockade by suppression of myeloid-derived cells. Proc Natl Acad Sci U S A. 2014;111:11774–9.CrossRefPubMedPubMedCentral
76.
77.
Zurück zum Zitat Xue L, Chiang L, Kang C, Winoto A. The role of the PI3K-AKT kinase pathway in T-cell development beyond the beta checkpoint. Eur J Immunol. 2008;38:3200–7.CrossRefPubMedPubMedCentral Xue L, Chiang L, Kang C, Winoto A. The role of the PI3K-AKT kinase pathway in T-cell development beyond the beta checkpoint. Eur J Immunol. 2008;38:3200–7.CrossRefPubMedPubMedCentral
78.
Zurück zum Zitat Okkenhaug K, Vanhaesebroeck B. PI3K in lymphocyte development, differentiation and activation. Nat Rev Immunol. 2003;3:317–30.CrossRefPubMed Okkenhaug K, Vanhaesebroeck B. PI3K in lymphocyte development, differentiation and activation. Nat Rev Immunol. 2003;3:317–30.CrossRefPubMed
79.
Zurück zum Zitat Jones RG, Parsons M, Bonnard M, et al. Protein kinase B regulates T lymphocyte survival, nuclear factor κb activation, and Bcl-X<sub>L</sub> levels in vivo. J Exp Med. 2000;191:1721–34.CrossRefPubMedPubMedCentral Jones RG, Parsons M, Bonnard M, et al. Protein kinase B regulates T lymphocyte survival, nuclear factor κb activation, and Bcl-X<sub>L</sub> levels in vivo. J Exp Med. 2000;191:1721–34.CrossRefPubMedPubMedCentral
80.
Zurück zum Zitat Carlo-Stella C, Delarue R, Barde PJ, et al. Clinical activity and safety of RP6530, a dual PI3Kδ/γ inhibitor, in patients with advanced Hematologic malignancies: final analysis of a phase 1 multicenter study. Blood. 2016;128:3011.CrossRef Carlo-Stella C, Delarue R, Barde PJ, et al. Clinical activity and safety of RP6530, a dual PI3Kδ/γ inhibitor, in patients with advanced Hematologic malignancies: final analysis of a phase 1 multicenter study. Blood. 2016;128:3011.CrossRef
81.
Zurück zum Zitat Oki Y, Huen A, Barde PJ, et al. A dose escalation study of RP6530, a novel dual PI3K δ/γ inhibitor, in patients with relapsed/refractory T-cell lymphoma. Blood. 2016;128:3004. Oki Y, Huen A, Barde PJ, et al. A dose escalation study of RP6530, a novel dual PI3K δ/γ inhibitor, in patients with relapsed/refractory T-cell lymphoma. Blood. 2016;128:3004.
82.
Zurück zum Zitat Pardee TS, Lee K, Luddy J, et al. A phase I study of the first-in-class antimitochondrial metabolism agent, CPI-613, in patients with advanced hematologic malignancies. Clin Cancer Res. 2014;20:5255–64.CrossRefPubMedPubMedCentral Pardee TS, Lee K, Luddy J, et al. A phase I study of the first-in-class antimitochondrial metabolism agent, CPI-613, in patients with advanced hematologic malignancies. Clin Cancer Res. 2014;20:5255–64.CrossRefPubMedPubMedCentral
83.
Zurück zum Zitat Lamar ZS, Isom S, Vaidya R, Beaven AW, ZA MI. Phase I dose-escalation study of Cpi-613, in combination with bendamustine, in relapsed or refractory T-cell non-Hodgkin lymphoma. Blood. 2016;128:4163. Lamar ZS, Isom S, Vaidya R, Beaven AW, ZA MI. Phase I dose-escalation study of Cpi-613, in combination with bendamustine, in relapsed or refractory T-cell non-Hodgkin lymphoma. Blood. 2016;128:4163.
Metadaten
Titel
Therapeutic Options for Aggressive T-Cell Lymphomas
verfasst von
Jennifer K. Lue
Anna Kress
Jennifer E. Amengual
Publikationsdatum
01.06.2017
Verlag
Springer US
Erschienen in
Current Hematologic Malignancy Reports / Ausgabe 4/2017
Print ISSN: 1558-8211
Elektronische ISSN: 1558-822X
DOI
https://doi.org/10.1007/s11899-017-0389-7

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