Functional Imaging Using 18-Fluorodeoxyglucose PET in the Management of Primary Mediastinal Large B-Cell Lymphoma: The Contributions of the International Extranodal Lymphoma Study Group

Author(s):  
Franco Cavalli ◽  
Luca Ceriani ◽  
Emanuele Zucca

Primary mediastinal large B-cell lymphoma (PMLBCL) is recognized as a distinct disease entity. Treatment outcomes appear better than in other diffuse large B-cell lymphoma (DLBCL) types, partly because of their earlier stage at presentation and the younger age of most patients. If initial treatment fails, however, the results of salvage chemotherapy and myeloablative treatment are poor. The need to avoid relapses after initial therapy has led to controversy over the extent of front-line therapy, particularly whether consolidation radiotherapy to the mediastinum is always required and whether the 18-fluorodeoxyglucose (18F-FDG) uptake detected by PET-CT scan can be used to determine its requirements. Functional imaging using PET-CT generally allows distinguishing of residual mediastinal masses containing active lymphoma from those with only sclerotic material remaining. The International Extranodal Lymphoma Study Group (IELSG) conducted the prospective IELSG-26 study, which showed that a five-point visual scale can be used to define metabolic response after immunochemotherapy and that a cut point based on liver uptake discriminates effectively between high or low risk of failure, with 5-year progression-free survival (PFS) of 99% versus 68% and 5-year overall survival (OS) of 100% versus 83%. This study also showed that a baseline quantitative PET parameter, namely the total lesion glycolysis describing the metabolic tumor burden, can be a powerful predictor of PMLBCL outcomes and warrants further validation as a biomarker. The ongoing IELSG-37 randomized study addresses the need for consolidation mediastinal radiotherapy in patients in whom a complete metabolic response (CMR) can be seen on PET scans after standard immunochemotherapy.

2009 ◽  
Vol 455 (3) ◽  
pp. 285-293 ◽  
Author(s):  
Naoki Wada ◽  
Junichiro Ikeda ◽  
Masaharu Kohara ◽  
Hiroyasu Ogawa ◽  
Masayuki Hino ◽  
...  

2003 ◽  
Vol 44 (11) ◽  
pp. 1903-1910 ◽  
Author(s):  
James Z. Huang ◽  
Dennis D. Weisenburger ◽  
Julie M. Vose ◽  
Timothy C. Greiner ◽  
Patricia Aoun ◽  
...  

2011 ◽  
Vol 4 (1) ◽  
pp. 14 ◽  
Author(s):  
Takeshi Chihara ◽  
Naoki Wada ◽  
Junichiro Ikeda ◽  
Shigeki Fujita ◽  
Yumiko Hori ◽  
...  

2019 ◽  
Vol 12 (2) ◽  
pp. 595-602 ◽  
Author(s):  
Thomas Bemis ◽  
Jonathan Ioanitescu ◽  
Lynn Mackovick ◽  
Azzam Hammad ◽  
Jascha Rubin

Diffuse Large B Cell Lymphoma (DLBCL) is a heterogeneous disease with a variety of chromosomal abnormalities contributing to differences in management. While it is known that Double Hit Lymphomas (DHL) warrant more aggressive chemotherapy regimens, debate remains on how to treat Double Expresser Lymphomas (DEL). We present a case of a DEL treated with an aggressive regimen of 2 alternating cycles of R-CODOX-M (rituximab, cyclophosphamide, doxorubicin, vincristine and methotrexate) and R-IVAC (rituximab, ifosfamide, etoposide and high dose cytarabine). The regimen resulted in a significant response to treatment with marked reduction in tumor size and avidity, and an acceptable side effect profile. There was, however, residual metabolic activity on repeat PET CT scan. After consolidation with 36 Grey radiotherapy, a PET CT demonstrated a complete metabolic response. Debate remains regarding treatment approaches in DEL. Our case supports the categorization of DEL alongside DHL as resistant lymphomas requiring a more aggressive regimen than standard therapy.


2010 ◽  
Vol 206 (7) ◽  
pp. 439-444 ◽  
Author(s):  
Naoki Wada ◽  
Masaharu Kohara ◽  
Junichiro Ikeda ◽  
Yumiko Hori ◽  
Shigeki Fujita ◽  
...  

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