A retrospective analysis of primary gastric diffuse large B-cell lymphoma with or without concomitant mucosa-associated lymphoid tissue (MALT) lymphoma components

被引:22
作者
Li, Xiaowu [1 ]
Xia, Bing [1 ]
Guo, Shanqi [1 ]
Zhan, Zhongli [2 ]
Zhang, Lianyu [2 ]
Zhao, Dandan [3 ]
Wu, Xiaoxiong [3 ]
Zhang, Yizhuo [1 ]
机构
[1] Tianjin Canc Inst & Hosp, Dept Hematol, Tianjin 300060, Peoples R China
[2] Tianjin Canc Inst & Hosp, Dept Pathol, Tianjin 300060, Peoples R China
[3] Chinese Peoples Liberat Army, Gen Hosp, Affiliated Hosp 1, Dept Hematol, Beijing 100853, Peoples R China
基金
中国国家自然科学基金;
关键词
Gastric; Diffuse large B-cell lymphoma; Mucosa-associated lymphoid tissue; Treatment; Prognostic factor; NON-HODGKINS-LYMPHOMA; HELICOBACTER-PYLORI; CLINICOPATHOLOGICAL FEATURES; MANAGEMENT; PROGNOSIS; RITUXIMAB; TRANSFORMATION; CHEMOTHERAPY; ERADICATION; WORKSHOP;
D O I
10.1007/s00277-013-1701-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary gastric diffuse large B-cell lymphoma (DLBCL) is a heterogeneous disease entity that includes patients with (DLBCL/MALT) and without detectable mucosa-associated lymphoid tissue (MALT) lymphoma components (de novo DLBCL). We sought to evaluate the clinical characteristics and outcome of this disease in a large number of cases. Patients with primary gastric DLBCL (n = 162) seen on 2001-2011 at the Tianjin Medical University Cancer Institute and Hospital and the First affiliated Hospital of Chinese PLA General Hospital were retrospectively reviewed. The distribution of sex, age, Lugano staging, and other main clinical characteristics was similar between the de novo DLBCL and DLBCL/MALT groups (p > 0.05). However, the proportion of patients with a stage-modified international prognostic index (m-IPI) a parts per thousand yenaEuro parts per thousand 2 was higher in the de novo DLBCL (34 %) than the DLBCL/MALT group (17 %) (p = 0.026). In addition, the Helicobacter pylori infection rates were higher in the DLBCL/MALT (75 %) than the de novo DLBCL group (36 %) (p < 0.001). Five-year progression-free survival (PFS) and overall survival (OS) estimates were similar for patients in the de novo DLBCL (p = 0.705) and DLBCL/MALT groups (p = 0.846). Surgical treatment did not offer survival benefits when compared with chemotherapy for 5-year PFS (p = 0.607) and OS estimates (p = 0.554). There were no significant differences in 5-year PFS and OS estimates for patients treated with rituximab-chemotherapy (p = 0.261) or conventional chemotherapy (p = 0.227). Non-GCB subtype and m-IPI a parts per thousand yenaEuro parts per thousand 2 were independently associated with shorter OS, and advanced stages of lymphoma were independently associated with shorter PFS.
引用
收藏
页码:807 / 815
页数:9
相关论文
共 33 条
[1]   Gastrointestinal lymphomas: Pattern of distribution and histological subtypes: 10 years experience in a tertiary centre in South India [J].
Arora, Neeraj ;
Manipadam, Marie Therese ;
Pulimood, Anna ;
Ramakrishna, B. S. ;
Chacko, Ashok ;
Kurian, Susy S. ;
Nair, Sheila .
INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY, 2011, 54 (04) :712-719
[2]   Surgical resection plus chemotherapy versus chemotherapy alone:: comparison of two strategies to treat diffuse large B-cell gastric lymphoma [J].
Binn, M ;
Ruskoné-Fourmestraux, A ;
Lepage, E ;
Haioun, C ;
Delmer, A ;
Aegerter, P ;
Lavergne, A ;
Guettier, C ;
Delchier, JC .
ANNALS OF ONCOLOGY, 2003, 14 (12) :1751-1757
[3]   Evaluation of the international index in the prognosis of high grade gastric MALT lymphoma [J].
Castrillo, JM ;
Montalban, C ;
Abraira, V ;
Carrion, R ;
Cruz, MA ;
Larana, JG ;
Menarguez, J ;
Bellas, C ;
Piris, MA ;
GomezMarcos, F ;
Serrano, M ;
Rivas, C .
LEUKEMIA & LYMPHOMA, 1996, 24 (1-2) :159-163
[4]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[5]   Stage-modified international prognostic index effectively predicts clinical outcome of localized primary gastric diffuse large B-cell lymphoma [J].
Cortelazzo, S ;
Rossi, A ;
Roggero, E ;
Oldani, E ;
Zucca, E ;
Tondini, C ;
Ambrosetti, A ;
Pasini, F ;
Pinotti, G ;
Bertini, M ;
Vitolo, U ;
Busetto, M ;
Gianni, L ;
Cavalli, F ;
Barbui, T .
ANNALS OF ONCOLOGY, 1999, 10 (12) :1433-1440
[6]   Primary gastric lymphoma pathogenesis and treatment: what has changed over the past 10 years? [J].
Ferrucci, Pier Francesco ;
Zucca, Emanuele .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 136 (04) :521-538
[7]   Current Aspects of the Pathology and Differentiation of Extranodal Marginal Zone B-Cell Lymphoma, MALT-Type, and Gastrointestinal Diffuse Large B-Cell Lymphoma [J].
Flossbach, L. ;
Kestler, H. A. ;
Gress, T. M. ;
Moeller, P. ;
Barth, T. F. E. .
ZEITSCHRIFT FUR GASTROENTEROLOGIE, 2010, 48 (08) :833-838
[8]  
Freedman Arnold S, 2005, Hematology Am Soc Hematol Educ Program, P314
[9]   Primary gastrointestinal lymphoma [J].
Ghimire, Prasanna ;
Wu, Guang-Yao ;
Zhu, Ling .
WORLD JOURNAL OF GASTROENTEROLOGY, 2011, 17 (06) :697-707
[10]   Confirmation of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray [J].
Hans, CP ;
Weisenburger, DD ;
Greiner, TC ;
Gascoyne, RD ;
Delabie, J ;
Ott, G ;
Müller-Hermelink, HK ;
Campo, E ;
Braziel, RM ;
Jaffe, ES ;
Pan, ZG ;
Farinha, P ;
Smith, LM ;
Falini, B ;
Banham, AH ;
Rosenwald, A ;
Staudt, LM ;
Connors, JM ;
Armitage, JO ;
Chan, WC .
BLOOD, 2004, 103 (01) :275-282