何小慧, 石远凯, 杨建良, 韩晓红, 张长弓, 周爱萍, 周生余, 杨晟, 孙燕. 原发纵隔的弥漫大B细胞非霍奇金淋巴瘤34例临床分析[J]. 中国肿瘤临床, 2004, 31(19): 1081-1083.
引用本文: 何小慧, 石远凯, 杨建良, 韩晓红, 张长弓, 周爱萍, 周生余, 杨晟, 孙燕. 原发纵隔的弥漫大B细胞非霍奇金淋巴瘤34例临床分析[J]. 中国肿瘤临床, 2004, 31(19): 1081-1083.
He Xiaohui, Shi Yuankai, Yang Jianliang, Han Xiaohong, Zhang Changgong, Zhou Aiping, Zhou Shengyu, Yang Cheng, Sun Yan. Clinical analysis of Primary Mediastinal Large B-Cell LymPhoma:A report of 34 cases[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(19): 1081-1083.
Citation: He Xiaohui, Shi Yuankai, Yang Jianliang, Han Xiaohong, Zhang Changgong, Zhou Aiping, Zhou Shengyu, Yang Cheng, Sun Yan. Clinical analysis of Primary Mediastinal Large B-Cell LymPhoma:A report of 34 cases[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(19): 1081-1083.

原发纵隔的弥漫大B细胞非霍奇金淋巴瘤34例临床分析

Clinical analysis of Primary Mediastinal Large B-Cell LymPhoma:A report of 34 cases

  • 摘要: 目的 :探讨原发纵隔的弥漫大B细胞非霍奇金淋巴瘤(PMLBL)的临床特征及治疗策略。 方法 :回顾性分析34例原发纵隔的弥漫大B细胞非霍奇金淋巴瘤的临床特点和不同治疗方案对患者生存期的影响。 结果 :临床分期79.4%为Ⅰ-Ⅱ期,50.0%患者起病时出现上腔静脉压迫综合征,47.1%有邻近器官侵犯。采用化、放疗联合治疗29例(85.3%)、单纯化疗5例(14.7%)、自体造血干细胞移植9例(26.4%)。根据寿命表法分析,全组5和10年无瘤生存率(DFS)为47.8%和41.0%,5和10年总生存率(OS)为54.4%和54.4%。自体造血干细胞移植组较常规化、放疗组5年DFS和OS均有所提高,但无显著性差异(P>0.05)。不良预后因素分析显示,具有巨大肿块及治疗后来能获得完全缓解者预后差(P<0.05)。 结论 :原发纵隔的弥漫大B细胞非霍奇金淋巴瘤具有独特的临床和病理特点,治疗以化、放疗为主。具有不良预后因素的患者可考虑自体外周血造血干细胞移植(APBSCT),但最佳的治疗方案尚需进一步的前瞻性随机研究证实。

     

    Abstract: Objective :To analyze the clinical characteri-stics and treatment result in patients with primary mediastinal large B-cell lymphoma (PMLBL). Methods :The authors reviewed the data of 34(PMLBL) patients who were admitted in Cancer Hospital,Chinese Academy Medical Science,Beijing,from July 1985 to June 2001,to evaluate the influence of clinical characteristics and treatment modality on survival. Results :Limited stage disease(I/II) was present in 79.4% of the patients,with superior vena cava syndrome 50% and contiguous infiltration 47.1%.29 of 34 patients were treated with chemotherapy plus radiotherapy,5 of 34 patients with chemotherapy alone.9 of 34 patients were treated with autologous peripheral blood stem cell transplantation (APBSCT).At median follow-up of 69 (range 18-211) months,5-year and 10-year overal l survival were 58.9% and 54.4%.5-year and 10 year disease free survival were 47.8% and 41.0%.The survival for APBSCT was better than conventional chemotherapy and radiotherapy,but the outcome had not significant difference (P>0.05).The survival for CR and bulky disease wer e significantly better than those of PR and or S+P and without bulky disease (P<0.O5). Conclusion :PMLBL is an aggressive NHL with cliniopathologic distinct.The main treatment modality for PMLBL was chemotherapy.The patients with poor prognostic factors can be considered to treat with APBSCT,but the optimal treatment modality for PMLBL 15 necessary to adopt prospective randomized trial.

     

/

返回文章
返回