Nantes, France.
Paris, France.
Aliment Pharmacol Ther. 2019 Sep;50(6):654-663. doi: 10.1111/apt.15409. Epub 2019 Jul 26.
Gastric mucosa-associated lymphoid tissue (MALT) lymphoma is a rare disease, and most available data on gastric MALT lymphoma (GML) come from clinical studies of selected patients treated in centres of excellence.
To analyse the clinical features, management and survival of GML patients in a population-based study in France METHODS: All new cases of GML diagnosed between 2002 and 2010 in 11 French areas covered by cancer registries were included. Pathology reports were verified and, if necessary, reviewed by an expert pathologist. All clinical data were retrospectively collected from medical files and analysed using stata V. 14 software.
Four hundred and sixteen patients with confirmed GML (50% male, median age 67 years) were identified. Among them, 44 showed an early transformation into diffuse large B cell lymphoma and were considered to have had an initially missed high-grade lymphoma. At diagnosis, 76% of patients were at stage IE/II, and 24% at stage III/IV of the disease. Helicobacter pylori infection was found in 57% of the patients. Eradication treatment was administered to 76% of patients and complete remission (CR) was obtained in 39%. One hundred and ninety patients received at least one other treatment, including 10 already in CR after eradication. Altogether, CR was obtained in 70% of patients and the 5-year overall survival was 79% (95% CI [75-83]).
In comparison to clinical series, in the general population, GMLs are more frequently diagnosed at an advanced stage, their clinical management is heterogeneous, and there is a risk of misdiagnosis and overtreatment. These results highlight the necessity of following currently available guidelines in this field.
胃黏膜相关淋巴组织(MALT)淋巴瘤是一种罕见疾病,大多数关于胃 MALT 淋巴瘤(GML)的可用数据来自于在卓越中心治疗的精选患者的临床研究。
在法国的一项基于人群的研究中分析 GML 患者的临床特征、治疗方法和生存情况。
纳入 2002 年至 2010 年间在 11 个覆盖癌症登记处的法国地区诊断出的所有新的 GML 病例。对病理报告进行了验证,如果有必要,还请专家病理学家进行了审核。所有临床数据均从病历中回顾性收集,并使用 stata V. 14 软件进行分析。
共确定了 416 例确诊的 GML 患者(50%为男性,中位年龄为 67 岁)。其中,44 例患者早期转化为弥漫性大 B 细胞淋巴瘤,被认为最初被漏诊为高级别淋巴瘤。在诊断时,76%的患者处于疾病的 IE/II 期,24%的患者处于 III/IV 期。57%的患者存在幽门螺杆菌感染。76%的患者接受了根除治疗,其中 39%获得完全缓解(CR)。190 例患者接受了至少一种其他治疗,其中 10 例在根除后已处于 CR。总的来说,70%的患者获得了 CR,5 年总生存率为 79%(95%CI[75-83])。
与临床系列相比,在普通人群中,GML 更常被诊断为晚期,其临床管理存在异质性,存在误诊和过度治疗的风险。这些结果突出了在该领域遵循现有指南的必要性。