Assessment of disease dissemination in gastric compared with extragastric mucosa-associated lymphoid tissue lymphoma using extensive staging:: A single-center experience

被引:139
作者
Raderer, Markus
Woehrer, Stefan
Streubel, Berthold
Troch, Marlene
Turetschek, Karl
Jaeger, Ulrich
Skrabs, Cathrin
Gaiger, Alexander
Drach, Johannes
Puespoek, Andreas
Formanek, Michael
Hoffmann, Martha
Hauff, Wolfgang
Chott, Andreas
机构
[1] Univ Vienna, Dept Internal Med 1, Div Oncol, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Internal Med 4, A-1090 Vienna, Austria
[3] Univ Vienna, Dept Pathol, A-1090 Vienna, Austria
[4] Univ Vienna, Dept Radiol, A-1090 Vienna, Austria
[5] Univ Vienna, Dept Otorhinolaryngol, A-1090 Vienna, Austria
[6] Univ Vienna, Dept Ophthalmol, A-1090 Vienna, Austria
[7] Univ Vienna, Dept Nucl Med, A-1090 Vienna, Austria
[8] Ctr Excellence Clin & Expt Oncol, Vienna, Austria
关键词
D O I
10.1200/JCO.2006.06.0723
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Molecular data and preliminary clinical findings have suggested mucosa-associated lymphoid tissue (MALT) lymphoma as a multifocal disease in a high percentage of patients. We report our findings with an extensive staging routine applied in patients diagnosed with MALT lymphoma at our institution. Patients and Methods A total of 140 consecutive patients (61 with gastric and 79 with extragastric MALT lymphoma) underwent staging according to a standardized protocol. Staging included gastroscopy with multiple biopsies, endosonography of the upper GI tract, computed tomography of thorax and abdomen, lymph node sonography, colonoscopy with multiple biopsies, otorhinolaryngologic assessment, magnetic resonance imaging of salivary and lacrimal glands, and bone marrow biopsy. All lesions suggestive of lymphoma involvement were subjected to biopsy, if accessible, and biopsies were evaluated for MALT lymphoma-specific genetic aberrations by means of reverse transcriptase polymerase chain reaction and/or fluorescent in situ hybridization. Results Fifteen (25%) of 61 patients with gastric MALT lymphoma had multiorgan involvement, with dissemination beyond the GI tract in six patients. By contrast, significantly more patients with extragastric MALT lymphoma had dissemination to another MALT organ (37 of 79 patients, 46%; P=.045). Nine of these 37 patients had dissemination to the stomach. Only three (2%) of 140 patients had bone marrow involvement. Multifocality was significantly associated with t(11;18)(q21;q21) in gastric lymphomas (P=.045) and with trisomy 18 in extragastric lymphomas (P=.011). Conclusion Our findings suggest that MALT lymphoma frequently presents as a multifocal disease. Extragastric MALT lymphomas are significantly more prone to dissemination than gastric MALT lymphomas.
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页码:3136 / 3141
页数:6
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