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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.
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页码:476 / 485
页数:10
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