首页> 外文期刊>World Journal of Gastroenterology >Primary early-stage intestinal and colonic non-Hodgkin's lymphoma: Clinical features, management, and outcome of 37 patients.
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Primary early-stage intestinal and colonic non-Hodgkin's lymphoma: Clinical features, management, and outcome of 37 patients.

机译:原发性早期肠道和结肠非霍奇金淋巴瘤:37例患者的临床特征,治疗和结局。

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AIM: To analyze the clinical features, management, and outcome of treatment of patients with primary intestinal and colonic non-Hodgkin's lymphoma (PICL). METHODS: A retrospective study was performed in 37 patients with early-stage PICL who were treated in our hospital from 1958 to 1998. Their clinical features, management, and outcome were assessed. Prognostic factors for survival were analyzed by univariate analysis using the Kaplan-Meier product-limit method and log-rank test. RESULTS: Twenty-five patients presented with Ann Arbor stage I PICL and 12 with Ann Arbor stage II PICL. Thirty-five patients underwent surgery (including 31 with complete resection), 22 received postoperative chemotherapy or radiotherapy or both. Two patients with rectal tumors underwent biopsy and chemotherapy with or without radiotherapy. The 5- and 10-year overall survival (OS) rates were 51.9% and 44.5%. The corresponding disease-free survival (DFS) rates were 42.4% and 37.7%. In univariate analysis, multiple-modality treatment was associated with a better DFS rate compared to single treatment (P = 0.001). While age, tumor size, tumor site, stage, histology, or extent of surgery were not associated with OS and DFS, use of adjuvant chemotherapy significantly improved DFS (P = 0.031) for the 31 patients who underwent complete resection. Additional radiotherapy combined with chemo-therapy led to a longer survival than chemotherapy alone in six patients with gross residual disease after surgery or biopsy. CONCLUSION: Combined surgery and chemotherapy is recommended for treatment of patients with PICL. Additional radiotherapy is needed to improve the outcome of patients who have gross residual disease after surgery.
机译:目的:分析原发性肠和结肠非霍奇金淋巴瘤(PICL)患者的临床特征,管理和治疗结果。方法:对1958年至1998年在我院接受治疗的37例早期PICL患者进行回顾性研究,评估其临床特征,治疗和结局。使用Kaplan-Meier乘积极限法和对数秩检验通过单因素分析来分析生存率的预后因素。结果:25例患者患有Ann Arbor I期PICL,12例患有Ann Arbor II期PICL。 35例接受了手术(包括31例完全切除),22例接受了术后化学疗法或放射疗法或两者均接受了手术。两名患有直肠肿瘤的患者在接受或不接受放射治疗的情况下进行了活检和化疗。 5年和10年总生存率分别为51.9%和44.5%。相应的无病生存率分别为42.4%和37.7%。在单因素分析中,与单项治疗相比,多模式治疗与更好的DFS率相关(P = 0.001)。尽管年龄,肿瘤大小,肿瘤部位,分期,组织学或手术范围与OS和DFS无关,但对于31例行完全切除术的患者,辅助化疗显着改善了DFS(P = 0.031)。额外的放疗与化学疗法相结合,使6名在手术或活检后有严重残留疾病的患者比单独化疗具有更长的生存期。结论:推荐合并外科手术和化学疗法治疗PICL患者。需要额外的放射疗法以改善术后严重残留疾病的患者的预后。

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