The utility and limitations of 18F-fluorodeoxyglucose positron emission tomography with computed tomography in patients with primary mediastinal B-cell lymphoma: single institution experience and literature review

被引:19
作者
Cheah, Chan Y. [1 ,3 ]
Hofman, Michael S. [2 ,3 ]
Seymour, John F. [1 ,3 ]
Ritchie, David S. [1 ,3 ]
Dickinson, Michael [1 ,3 ]
Wirth, Andrew [1 ,3 ]
Prince, H. Miles [1 ,3 ,4 ,5 ]
Wolf, Max [1 ,3 ]
Januszcewicz, Elchanan H. [1 ]
Carney, Dennis A. [1 ,3 ]
Herbert, Kirsten E. [1 ,3 ,5 ]
Harrison, Simon J. [1 ,3 ]
Burbury, Kate L. [1 ,3 ]
Tam, Constantine S. [1 ,3 ]
机构
[1] Peter MacCallum Canc Ctr, Dept Haematol, East Melbourne, Vic 8006, Australia
[2] Peter MacCallum Canc Ctr, Ctr Canc Imaging, East Melbourne, Vic 8006, Australia
[3] Univ Melbourne, Melbourne, Vic, Australia
[4] Monash Univ, Clayton, Vic, Australia
[5] Cabrini Hosp, Malvern, Vic, Australia
关键词
Primary mediastinal B-cell lymphoma; PET-CT; interim PET-CT; prognostic factors; risk adapted therapy; non-Hodgkin lymphoma; SUV-BASED ASSESSMENT; F-18-FDG PET; FDG-PET; RITUXIMAB; CYCLOPHOSPHAMIDE; CHEMOTHERAPY; MULTICENTER; VINCRISTINE; DOXORUBICIN; PREDNISONE;
D O I
10.3109/10428194.2014.910656
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There are limited data regarding the role of F-18-fluorodeoxyglucose positron emission tomography with computed tomography (FDG PET-CT) scanning in primary mediastinal B-cell lymphoma (PMBL). We analyzed 28 patients with PMBL treated with chemotherapy, of whom 25 (89%) also received rituximab and 17 (61%) radiotherapy. PET-CT scans were interpreted using visual analysis and a 5-point scale. After a median follow-up of 2.6 years, four patients relapsed and two died. The 2-year progression-free survival and overall survival were 86% and 94%. PET-CT has excellent negative predictive value (interim, 86-87%; end of treatment, 95%) but limited positive predictive value due to the high frequency of positive scans. Several patients with persistent metabolically active masses underwent biopsies, which showed necrosis but no lymphoma. Thus a negative PETCT is an excellent predictor of subsequent outcome. However, residual metabolically active masses after treatment should be biopsied to confi rm viable lymphoma prior to salvage therapy.
引用
收藏
页码:49 / 56
页数:8
相关论文
共 36 条
[21]   Sequential Dose-Dense RCHOP Followed by ICE Consolidation (MSKCC protocol 01-142) without Radiotherapy for Patients with Primary Mediastinal Large B Cell Lymphoma [J].
Moskowitz, Craig ;
Hamlin, Paul A., Jr. ;
Maragulia, Jocelyn ;
Meikle, Jessica ;
Zelenetz, Andrew D. .
BLOOD, 2010, 116 (21) :187-188
[22]   Risk-Adapted Dose-Dense Immunochemotherapy Determined by Interim FDG-PET in Advanced-Stage Diffuse Large B-Cell Lymphoma [J].
Moskowitz, Craig H. ;
Schoeder, Heiko ;
Teruya-Feldstein, Julie ;
Sima, Camelia ;
Iasonos, Alexia ;
Portlock, Carol S. ;
Straus, David ;
Noy, Ariela ;
Palomba, Maria L. ;
O'Connor, Owen A. ;
Horwitz, Steven ;
Weaver, Sarah A. ;
Meikle, Jessica L. ;
Filippa, Daniel A. ;
Caravelli, James F. ;
Hamlin, Paul A. ;
Zelenetz, Andrew D. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (11) :1896-1903
[23]  
Prahladan M, 2012, BLOOD S1, V120
[24]   Interim 18-FDG-PET/CT failed to predict the outcome in diffuse large B-cell lymphoma patients treated at the diagnosis with rituximab-CHOP [J].
Pregno, Patrizia ;
Chiappella, Annalisa ;
Bello, Marilena ;
Botto, Barbara ;
Ferrero, Simone ;
Franceschetti, Silvia ;
Giunta, Francesca ;
Ladetto, Marco ;
Limerutti, Giorgio ;
Menga, Massimo ;
Nicolosi, Maura ;
Priolo, Giorgio ;
Puccini, Benedetta ;
Rigacci, Luigi ;
Salvi, Flavia ;
Vaggelli, Luca ;
Passera, Roberto ;
Bisi, Gianni ;
Vitolo, Umberto .
BLOOD, 2012, 119 (09) :2066-2073
[25]   Primary mediastinal B-cell lymphoma treated with CHOP-like chemotherapy with or without rituximab: results of the Mabthera International Trial Group study [J].
Rieger, M. ;
Osterborg, A. ;
Pettengell, R. ;
White, D. ;
Gill, D. ;
Walewski, J. ;
Kuhnt, E. ;
Loeffler, M. ;
Pfreundschuh, M. ;
Ho, A. D. .
ANNALS OF ONCOLOGY, 2011, 22 (03) :664-670
[26]   Primary mediastinal large cell lymphoma (PMBL):: frontline treatment with autologous stem cell transplantation (ASCT).: The GEL-TAMO experience [J].
Rodriguez, Jose ;
Conde, Eulogio ;
Gutierrez, Antonio ;
Carlos Garcia, Juan ;
Jose Lahuerta, Juan ;
Rosario Varela, Maria ;
Perez, Catalina ;
Albo, Carmen ;
Dolores Caballero, Mana .
HEMATOLOGICAL ONCOLOGY, 2008, 26 (03) :171-178
[27]   Molecular diagnosis of primary mediastinal B cell lymphoma identifies a clinically favorable subgroup of diffuse large B cell lymphoma related to Hodgkin lymphoma [J].
Rosenwald, A ;
Wright, G ;
Leroy, K ;
Yu, X ;
Gaulard, P ;
Gascoyne, RD ;
Chan, WC ;
Zhao, T ;
Haioun, C ;
Greiner, TC ;
Weisenburger, DD ;
Lynch, JC ;
Vose, J ;
Armitage, JO ;
Smeland, EB ;
Kvaloy, S ;
Holte, H ;
Delabie, J ;
Campo, E ;
Montserrat, E ;
Lopez-Guillermo, A ;
Ott, G ;
Muller-Hermelink, HK ;
Connors, JM ;
Braziel, R ;
Grogan, TM ;
Fisher, RI ;
Miller, TP ;
LeBlanc, M ;
Chiorazzi, M ;
Zhao, H ;
Yang, LM ;
Powell, J ;
Wilson, WH ;
Jaffe, ES ;
Simon, R ;
Klausner, RD ;
Staudt, LM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (06) :851-862
[28]   The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse large B-cell lymphomas and shares features with classical Hodgkin lymphoma [J].
Savage, KJ ;
Monti, S ;
Kutok, JL ;
Cattoretti, G ;
Neuberg, D ;
de Leval, L ;
Kurtin, P ;
Dal Cin, P ;
Ladd, C ;
Feuerhake, F ;
Aguiar, RCT ;
Li, SG ;
Salles, G ;
Berger, F ;
Jing, W ;
Pinkus, GS ;
Habermann, T ;
Dalla-Favera, R ;
Harris, NL ;
Aster, JC ;
Golub, TR ;
Shipp, MA .
BLOOD, 2003, 102 (12) :3871-3879
[29]  
Savage KJ, 2012, BLOOD S1, V120
[30]   Treatment of primary mediastinal B-cell lymphoma with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone is associated with a high rate of primary refractory disease [J].
Soumerai, Jacob D. ;
Hellmann, Matthew D. ;
Feng, Yang ;
Sohani, Aliyah R. ;
Toomey, Christiana E. ;
Barnes, Jeffrey A. ;
Takvorian, Ronald W. ;
Neuberg, Donna ;
Hochberg, Ephraim P. ;
Abramson, Jeremy S. .
LEUKEMIA & LYMPHOMA, 2014, 55 (03) :538-543