原发性胃肠道弥漫大B细胞淋巴瘤化疗期间并发肺炎的危险因素及其预后

Risk factors for concurrent pneumonia in patients with primary gastrointestinal diffuse large B-cell lymphoma during chemotherapy and their prognosis

  • 摘要: 目的 探讨原发性胃肠道弥漫大B细胞淋巴瘤(PGI-DLBCL)患者接受CHOP/R-CHOP方案化疗期间并发肺炎的危险因素及其对预后的影响。方法 回顾性分析2012年1月-2025年12月南方医科大学珠江医院收治的接受CHOP或R-CHOP方案化疗的PGI-DLBCL患者(n=156)资料。根据化疗期间是否并发肺炎分为感染组(n=57)和非感染组(n=99)。采用单因素及多因素logistic回归分析危险因素。为确保充足随访期,仅将2012年1月-2023年12月确诊的131例患者用于生存分析,采用Kaplan-Meier法及Cox模型分析无进展生存期(PFS)和总生存期(OS)。结果 感染组年龄≥60岁、Lugano分期ⅡE~Ⅳ期、ECOG评分≥2分、乳酸脱氢酶升高及远处淋巴结受累比例均高于非感染组,血清白蛋白水平低于非感染组(P<0.05)。多因素分析显示,ECOG评分≥2分、乳酸脱氢酶升高及年龄≥60岁是化疗期间并发肺炎的独立危险因素,高血清白蛋白是独立保护因素(P<0.05)。感染组PFS和OS均低于非感染组(P<0.001)。结论 年龄≥60岁、ECOG评分≥2分及乳酸脱氢酶升高是PGI-DLBCL化疗期间并发肺炎的独立危险因素,高血清白蛋白为独立保护因素。化疗期间并发肺炎可显著缩短患者PFS和OS。

     

    Abstract: OBJECTIVE To explore the risk factors for concurrent pneumonia in the patients with primary gastrointestinal diffuse large B-cell lymphoma (PGI-DLBCL) during CHOP/R-CHOP chemotherapy and observe the influence on prognosis. METHODS The data were collected from 156 patients with PGI-DLBCL who received CHOP or R-CHOP chemotherapy in Zhujiang Hospital, Southern Medical University from Jan. 2012 to Dec. 2025 and were retrospectively analyzed. The patients were divided into the infection group with 57 cases and the non-infection group with 99 cases. Univariate analysis and multivariate logistic regression analysis were performed for the risk factors. In order to ensure an adequate follow-up period, only 131 patients who were diagnosed from Jan. 2012 to Dec. 2023 were chosen for survival analysis. The progression free survival (PFS) and overall survival (OS) were analyzed by means of Kaplan-Meier method and Cox model. RESULTS The proportions of patients with no less than 60 years of age, Lugano phase ranging between ⅡE and Ⅳ, ECOG score no less than 2 points, rise of lactic dehydrogenase and distant lymph node involvement were higher in the infection group than in the non-infection group, and the serum albumin level of the infection group was lower than that of the non-infection group(P<0.05). Multivariate analysis indicated that ECOG score no less than 2 points, the rise of lactic dehydrogenase and no less than 60 years of age were the independent risk factors for the concurrent pneumonia during the chemotherapy, and the high level of serum albumin was the independent protective factor(P<0.05). The PFS and OS were lower in the infection group than in the non-infection group(P<0.001). CONCLUSIONS The no less than 60 years of age, ECOG score no less than 2 points and the rise of lactic dehydrogenase are the independent risk factors for the concurrent pneumonia in the patients with PGI-DLBCL during the chemotherapy, and the high level of serum albumin is the independent protective factor. The concurrent pneumonia during the chemotherapy may remarkably shorten the PFS and OS of the patients.

     

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