Controversies in the Front-Line Treatment of Systemic Peripheral T Cell Lymphomas

被引:2
|
作者
Sorigue, Marc [1 ]
Kuittinen, Outi [2 ,3 ,4 ,5 ,6 ]
机构
[1] UAB, Hosp Germans Trias & Pujol, ICO IJC, LUMN,Dept Hematol, Badalona 08916, Spain
[2] Univ Eastern Finland, Inst Clin Med, Fac Hlth Med, Kuopio 70211, Finland
[3] Oulu Univ Hosp, Med Res Ctr & Canc, Oulu 90220, Finland
[4] Oulu Univ Hosp, Canc & Translat Res Unit, Oulu 90220, Finland
[5] Univ Oulu, Oulu 90220, Finland
[6] Kuopio Univ Hosp, Dept Oncol, Kuopio 70210, Finland
关键词
T cell lymphoma; stem cell transplant; etoposide; CHOP; brentuximab; PHASE-2; CLINICAL-TRIAL; NON-HODGKIN-LYMPHOMA; OPEN-LABEL; ALLOGENEIC TRANSPLANTATION; BRENTUXIMAB VEDOTIN; PROGNOSTIC-FACTORS; FINAL REPORT; LENALIDOMIDE; MULTICENTER; ALK;
D O I
10.3390/cancers15010220
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Systemic peripheral T cell lymphomas (PTCL) are a rare and clinically and biologically heterogeneous group of disorders with scarce and generally low-quality evidence guiding their management. In this manuscript, we tackle the current controversies in the front-line treatment of systemic PTCL and give our thoughts vis-a-vis potential developments to come in the next few years. Systemic peripheral T cell lymphomas (PTCL) are a rare and clinically and biologically heterogeneous group of disorders with scarce and generally low-quality evidence guiding their management. In this manuscript, we tackle the current controversies in the front-line treatment of systemic PTCL including (1) whether CNS prophylaxis should be administered; (2) whether CHOEP should be preferred over CHOP; (3) what role brentuximab vedotin should have; (4) whether stem cell transplant (SCT) consolidation should be used and whether autologous or allogeneic; (5) how should molecular subtypes (including DUSP22 or TP63-rearranged ALCL or GATA3 or TBX21 PTCL, NOS) impact therapeutic decisions; and (6) whether there is a role for targeted agents beyond brentuximab vedotin.
引用
收藏
页数:15
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