Primary mediastinal large B-cell lymphoma

被引:35
|
作者
Bhatt, Vijaya Raj [1 ]
Mourya, Rajesh [2 ]
Shrestha, Runa [3 ]
Armitage, James O. [1 ]
机构
[1] Univ Nebraska, Med Ctr, Dept Internal Med, Div Hematol Oncol, Omaha, NE 68198 USA
[2] Creighton Univ, Med Ctr, Dept Internal Med, Omaha, NE 68178 USA
[3] SUNY Upstate Med Univ, Dept Internal Med, Syracuse, NY 13210 USA
关键词
Primary mediastinal large B-cell lymphoma; Chemotherapy; Rituximab; Mediastinal radiation; Positron emission tomography; POSITRON-EMISSION-TOMOGRAPHY; CHOP-LIKE CHEMOTHERAPY; NON-HODGKINS-LYMPHOMAS; RESPONSE ASSESSMENT; RADIATION-THERAPY; MACOP-B; RITUXIMAB; EXPRESSION; SCLEROSIS; DOXORUBICIN;
D O I
10.1016/j.ctrv.2015.04.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The management of primary mediastinal large B-cell lymphoma (PMBCL) requires a balance between optimizing chances of cure and reducing risk of long-term toxicities. The combination of rituximab to cyclophosphamide, doxorubicin, vincristine and prednisone (RCHOP) followed by mediastinal radiation results in a plateau in progression-free survival after first few years of follow-up. In rituximab era, a negative positron emission tomography (PET) scan performed after the completion of immunochemotherapy has a high predictive value for durable remission. Consequently, end-of-therapy PET may be utilizable to avoid radiation without compromising survival. Additionally, intensified chemotherapy alone has shown excellent survival. PMBCL is frequently associated with amplification of programmed death ligand (PDL) 1/2 and constitutive activation of JAK-STAT and NFKB pathways; these may serve as promising therapeutic targets. Clinical trials that integrate novel therapies into upfront immunochemotherapy and utilize end-of-therapy PET scan to guide mediastinal radiation have potential to further enhance survival and prevent long-term toxicities. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:476 / 485
页数:10
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