原发性胃淋巴瘤的治疗及预后分析

Treatment and prognosis of primary gastric lymphoma

  • 摘要: 目的:探讨原发性胃淋巴瘤(PGL)的治疗方法和影响预后的因素。
    方法:回顾性分析2002年7月至2007年12月大连医科大学附属第一医院收治的55例PGL患者的临床资料,根据患者的病理类型,临床分期,是否存在幽门螺旋杆菌感染,以及是否存在合并症(如出血、幽门梗阻等)选择手术、药物、手术联合药物进行治疗,并采用电话方式随访至2013年2月,收集有完整随访资料患者的临床病理资料进行预后分析。KaplanMeier法计算生存率,生存情况的单因素分析采用Logrank检验,对单因素分析中P<0.05的因素进行COX多因素分析。
    结果:肿瘤部位:胃窦部26例、胃体部17例、胃底部5例、贲门部3例、胃体及胃窦部4例。胃镜检查结果:溃疡型46例、结节肿块型5例、弥漫浸润型4例。病理及免疫组织化学特点:B细胞淋巴瘤53例,T细胞淋巴瘤1例,未明确分型1例。53例B细胞淋巴瘤中胃黏膜相关淋巴组织淋巴瘤36例,弥漫大B细胞型淋巴瘤17例。其临床分期:Ⅰ期23例、Ⅱ期23例、Ⅲ期4例、Ⅳ期3例。治疗方法:55例患者中23例采用手术治疗,14例采用药物治疗,17例采用手术联合药物治疗,1例未治疗。53例患者获得随访,中位随访时间为60个月(7~132个月),1、3、5年生存率分别为91%、79%、72%。单因素分析结果表明:肿瘤直径、病理类型以及临床分期是影响PGL患者预后的危险因素(χ 2=9.34,6.59,88.01,P<0.05),而治疗方式不影响PGL患者的预后(χ 2=3.63,P>0.05)。多因素分析结果表明:弥漫大B细胞淋巴瘤和临床分期Ⅲ期和Ⅳ期是影响PGL预后的独立危险因素(OR=5.758,2.231,95%可信区间:2.536~13.073,1.370~3.625,P<0.05)。
    结论:对于PGL患者,治疗应采用多学科团队协作模式。病理类型为弥漫大B细胞淋巴瘤和临床分期Ⅲ期和Ⅳ期是影响PGL患者预后的独立因素。

     

    Abstract: Objective:To investigate the treatment methods for primary gastric lymphoma (PGL) and analyze the prognostic factors. Methods:The clinical data of 55 patients with PGL who were admitted to the First Affiliated Hospital of Dalian Medical University from July 2002 to December 2007 were retrospectively analyzed. Operation, medication or operation combined with medication were applied to patients according to the pathological type, clinical staging, infection of helicobacter pylori and complications. Patients were followed up via phone call till February 2013, and the location, diameter, pathological type, clinical stage of the PGL and the treatment methods were recorded for prognostic analysis. The survival rate was calculated by KaplanMeier method, and the univariate analysis of survival was done by Logrank test. Multivariate analysis was done by COX regression model.
    Results:The PGL located at the gastric antrum in 26 cases, body of the stomach in 17 cases, fundus of the stomach in 5 cases, gastric cardia in 3 cases, body and antrum of the stomach in 4 cases. There were 46 patients with ulcerous PGL, 5 with nodular PGL and 4 with diffused and infiltrated PGL. There were 53 B cell lymphoma, 1 T cell lymphoma and 1 undefined tumor. Of the 53 patients with B cell lymphoma, 36 were with mucosaassociated lymphoid tissue lymphoma (MALTL) and 17 with diffuse large Bcell lymphoma (DLBCL). There were 23 patients in stage Ⅰ, 23 in stage Ⅱ, 4 in stage Ⅲ and 3 in stage Ⅳ. Of the 55 patients, 23 received operation, 14 received medication, 17 received operation+medication, and 1 left untreated. Fiftythree patients had complete followup data. The median time of followup was 60 months (range, 7-132 months). The 1, 3, 5year cumulative survival rates were 91%, 79% and 72%. The results of univariate analysis showed that tumor diameter, pathological type and clinical staging were risk factors influencing the prognosis of PGL patients (χ 2=9.34, 6.59, 88.01, P<0.05), while the treatment methods did not influence the prognosis of PGL patients (χ 2=3.63, P>0.05). The results of multivariate analysis showed that DLBCL, clinical stages Ⅲ and Ⅳ were independent risk factors influencing the prognosis of PGL patients (OR=5.758, 2.231, 95% confidence interval: 2.536-13.073, 1.370-3.625, P<0.05).
    Conclusion:Multidisciplinary team treatment should be recommended for PGL patients. Pathological type (DLBCL) and clinical stages (stage Ⅲ and Ⅳ) are the independent risk factors influencing the prognosis of PGL patients.

     

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