胃肠道弥漫性大b细胞淋巴瘤免疫表型、治疗策略与预后的关系

Maoqing Jiang, X. Ruan, Ping Chen, Wenlan Zhou, Hubing Wu, Quanshi Wang
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Kaplan-Meier analysis, log-rank test and Cox regression were performed for statistical analysis. \n \n \nResults \nAmong the 99 patients with GI-DLBCL, 51 patients were treated with chemotherapy alone, and 48 patients were treated with combination of surgery and chemotherapy. Forty-one cases were GCB phenotype and 40 cases were non-GCB phenotype. The median follow-up time was 25 months. The two-year PFS and OS rates were 70.9% and 89.5%, respectively. The two-year PFS and OS rates of chemotherapy alone group were 63.6% and 85.0%, respectively; both were lower than those of combination of surgery and chemotherapy group (79.4% and 94.7%), and the differences were statistically significant (χ2=4.232, P=0.040 and χ2=4.260, P=0.039). The two-year PFS and OS rates of GCB group were 68.8% and 93.9%, respectively. And the two-year PFS and OS rates of non-GCB group were 73.2% and 85.6%, respectively. There were no statistically significant differences between these two groups (both P>0.05). 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引用次数: 0

摘要

目的探讨不同免疫表型胃肠道弥漫性大b细胞淋巴瘤(GI-DLBCL)患者接受不同治疗策略后预后的差异。方法回顾性分析2006年3月至2016年1月广州南方医科大学南方医院病理证实的99例GI-DLBCL患者的临床资料。根据治疗策略将患者分为单纯化疗组和手术化疗联合组。根据免疫表型将患者分为生发中心b细胞样(GCB)型和非GCB型。评估2年无进展生存(PFS)率和总生存(OS)率。采用Kaplan-Meier分析、log-rank检验和Cox回归进行统计学分析。结果99例GI-DLBCL患者中,单纯化疗51例,手术联合化疗48例。GCB型41例,非GCB型40例。中位随访时间为25个月。2年PFS和OS率分别为70.9%和89.5%。单纯化疗组2年PFS和OS分别为63.6%和85.0%;均低于手术加化疗组(79.4%、94.7%),差异均有统计学意义(χ2=4.232, P=0.040; χ2=4.260, P=0.039)。GCB组2年PFS和OS分别为68.8%和93.9%。非gcb组2年PFS和OS分别为73.2%和85.6%。两组间差异无统计学意义(P>0.05)。41例GCB型患者中,手术联合化疗25例,单独化疗16例。手术联合化疗组2年PFS率(83.1%)高于单纯化疗组(49.2%),差异有统计学意义(χ2=5.627, P=0.018)。多因素分析结果显示,治疗策略对所有入组患者和GCB型患者均不是独立的预后因素(均P>0.05)。结论免疫表型对GI-DLBCL患者预后缺乏评价价值。虽然在所有入组患者和GCB型患者中,手术联合化疗患者的预后优于单独化疗患者,但治疗策略并不是独立的预后因素。在选择治疗策略前应综合考虑多种因素。关键词:胃肠道;淋巴瘤,大b细胞,弥漫性;手术;化疗;预后
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Correlation between the immunophenotypes, treatment strategies and prognosis of gastrointestinal diffuse large B-cell lymphoma
Objective To explore the differences in the prognosis of patients with different immunophenotypes gastrointestinal diffuse large B-cell lymphoma (GI-DLBCL) who received different treatment strategies. Methods From March 2006 to January 2016, at Nanfang Hospital, Southern Medical University in Guangzhou, the clinical data of 99 patients with pathologically confirmed GI-DLBCL were retrospectively analyzed. According to treatment strategies, patients were divided into chemotherapy alone group and combination of surgery and chemotherapy group. According to immunophenotypes, patients were divided into germinal center B-cell-like (GCB) type and non-GCB type. The two-year progression-free survival (PFS) rate and overall survival (OS) rate were evaluated. Kaplan-Meier analysis, log-rank test and Cox regression were performed for statistical analysis. Results Among the 99 patients with GI-DLBCL, 51 patients were treated with chemotherapy alone, and 48 patients were treated with combination of surgery and chemotherapy. Forty-one cases were GCB phenotype and 40 cases were non-GCB phenotype. The median follow-up time was 25 months. The two-year PFS and OS rates were 70.9% and 89.5%, respectively. The two-year PFS and OS rates of chemotherapy alone group were 63.6% and 85.0%, respectively; both were lower than those of combination of surgery and chemotherapy group (79.4% and 94.7%), and the differences were statistically significant (χ2=4.232, P=0.040 and χ2=4.260, P=0.039). The two-year PFS and OS rates of GCB group were 68.8% and 93.9%, respectively. And the two-year PFS and OS rates of non-GCB group were 73.2% and 85.6%, respectively. There were no statistically significant differences between these two groups (both P>0.05). Among 41 patients with GCB type, 25 were treated with combination of surgery and chemotherapy and 16 were treated with chemotherapy alone. The two-year PFS rate of patients treated with combination of surgery and chemotherapy (83.1%) was higher than that of patients treated with chemotherapy alone (49.2%), and the difference was statistically significant (χ2=5.627, P=0.018). The results of multivariate analysis indicated that treatment strategy was not an independent prognostic factor for all the enrolled patients and in patients with GCB type (all P>0.05). Conclusions Immunophenotypes may lack evaluation value of prognosis in patients with GI-DLBCL. Although among all the enrolled patients and patients with GCB type, the prognosis of patients treated with combination of surgery and chemotherapy is better than that of patients treated with chemotherapy alone, treatment strategy is not an independent prognostic factor. Multi-factors should be evaluated before selection of treatment strategy. Key words: Gastrointestinal tract; Lymphoma, large B-cell, diffuse; Surgery; Chemotherapy; Prognosis
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