Siakantaris Marina P, Pangalis Gerassimos A, Dimitriadou Evangelia, Kontopidou Flora N, Vassilakopoulos Theodoros P, Kalpadakis Christina, Sachanas Sotirios, Yiakoumis Xanthi, Korkolopoulou Penelope, Kyrtsonis Marie-Christine, Bobotsis Panayia, Androulaki Athina, Patsouris Eustratios, Panayiotidis Panayiotis, Angelopoulou Maria K
Department of Haematology, National and Kapodistrian University of Athens, Medical School, Laikon General Hospital, Athens, Greece.
Oncologist. 2009 Feb;14(2):148-54. doi: 10.1634/theoncologist.2008-0178. Epub 2009 Feb 9.
Early-stage gastric mucosa-associated lymphoid tissue lymphoma (GML) is considered a localized disease with an indolent course. Circulating malignant cells have been detected in other early-stage indolent lymphomas by molecular methods. We investigated the incidence of occult blood disease in early-stage GML patients, its impact on clinical outcome, and the similarity between blood and gastric lymphocytic clones. Sixty-two patients with localized GML were included in the study; 51 of them had Helicobacter pylori infection. Monoclonality was investigated by leader polymerase chain reaction. Sequencing was performed for the immunoglobulin variable gene (VH) analysis. Blood involvement was absent in all patients by conventional staging methods. In the whole group of 62 patients, the incidence of blood IgH rearrangement was 45%, and this did not correlate with baseline patient characteristics. The monoclonal blood and gastric products of five patients were sequenced and compared with each other. Clonal identity was evident in four of five patients. The VH3 gene was the most frequently used, both in the blood and in the stomach. Early-stage GML is not a truly localized disease because half the patients had a circulating clone, probably identical to the gastric one. The clinical significance of occult blood disease and the potential appropriate intervention need to be further investigated.
早期胃黏膜相关淋巴组织淋巴瘤(GML)被认为是一种病程惰性的局限性疾病。通过分子方法已在其他早期惰性淋巴瘤中检测到循环恶性细胞。我们研究了早期GML患者隐匿性血液疾病的发生率、其对临床结局的影响以及血液和胃淋巴细胞克隆之间的相似性。62例局限性GML患者纳入本研究;其中51例有幽门螺杆菌感染。通过前导聚合酶链反应研究单克隆性。对免疫球蛋白可变基因(VH)进行测序分析。通过传统分期方法,所有患者均未发现血液受累。在62例患者的整个队列中,血液IgH重排的发生率为45%,且这与患者基线特征无关。对5例患者的单克隆血液和胃产物进行测序并相互比较。5例患者中有4例克隆身份明显。VH3基因在血液和胃中都是最常使用的。早期GML并非真正的局限性疾病,因为半数患者有循环克隆,可能与胃克隆相同。隐匿性血液疾病的临床意义以及潜在的适当干预措施有待进一步研究。