老年套细胞淋巴瘤临床特征及其影响预后因素

张玲玲, 刘宁红,梁 军

武警医学 ›› 2017, Vol. 28 ›› Issue (6) : 560-563.

PDF(589 KB)
PDF(589 KB)
武警医学 ›› 2017, Vol. 28 ›› Issue (6) : 560-563.
论著

老年套细胞淋巴瘤临床特征及其影响预后因素

  • 张玲玲1, 刘宁红2,梁 军1
作者信息 +

Clinical features and prognosis-related factors of mantle cell lymphoma in elderly patients

  • ZHANG Lingling1,LIU Ninghong2,and LIANG Jun1
Author information +
文章历史 +

摘要

目的 分析老年套细胞淋巴瘤(mantle cell lymphoma,MCL)的临床病理特征及其影响预后因素,探讨其合理治疗模式。方法 回顾性分析2005-01至2015-07北京大学国际医院肿瘤内科和北京老年医院肿瘤内科收治的43例老年MCL患者,主要指标如年龄、分期、PS状态、国际预后指数评分等和治疗效果、生存情况。进行生存和预后因素分析。结果 全组患者中位年龄73岁(60~84岁);男女之比为3.3∶1,43例均接受联合化疗。中位随访时间38个月,全组患者的5年总生存率为17.3%,2年无病生存率为27.2%,3年无病生存率为0。中位无进展生存期20个月。单因素分析显示,MCL预后的影响因素包括治疗前PS状态、LDH、B症状、骨髓侵犯、外周血侵犯。而Cox回归多因素分析结果显示,只有PS状态和骨髓侵犯对预后的影响有统计学意义。结论 老年MCL具有临床分期晚、治疗效果欠佳及预后差等特点。PS状态和骨髓侵犯是预后的独立危险因素。目前初治患者多采用以CHOP或R-CHOP为主的方案化疗,不能治愈,需探索新的治疗方法。

Abstract

Objective To study the clinical features as well as therapeutic outcomes of elderly patients with mantle cell lymphoma (MCL) , identify the major prognostic factors and to explore the optimal approach.Methods We retrospectively analyzed 45 patients diagnosed with MCL in two hospitals between 2000 and 2007. Clinical data, including age,stage,performance status,international prognostic index,treatment modalities and clinical outcomes, were evaluated.Results The median age of the patients was 73 years (aged 60 to 84). The ratio of males to females was 3.3∶1. All the patients received combined chemotherapy. With a median follow-up of 38 months, the rates of 5-year overall and 2-year disease-free survivals were 17.3% and 27.2%, respectively. None remained disease-free at year 3. Median progression free survival was 20 months. There was no significant difference between the patients who had received CHOP regimen or R-CHOP regimen. Univariate analysis showed that PS, serum LDH levels, existence of B symptoms, bone marrow and peripheral blood involvement were the prognostic factors of overall survival for MCL patients. Cox regression multivariable analysis showed that only PS and bone marrow involvement were of statistic significance for prognosis.Conclusions Elderly patients with MCL are usually characterized by late staging, poor curative effect, and short survival.PS and bone marrow involvement are independent risk factors which affect the prognosis of elderly patients with MCL.MCL cannot be cured by standard CHOP or R-CHOP regimen. Newly diagnosed patients should be treated with novel modalities in order to improve the outcomes.

关键词

老年患者 / 套细胞淋巴瘤 / 临床特点 / 治疗 / 预后

Key words

elderly patients / mantle cell lymphoma / clinical features / treatment / prognosis

引用本文

导出引用
张玲玲, 刘宁红,梁 军. 老年套细胞淋巴瘤临床特征及其影响预后因素[J]. 武警医学. 2017, 28(6): 560-563
ZHANG Lingling,LIU Ninghong,and LIANG Jun. Clinical features and prognosis-related factors of mantle cell lymphoma in elderly patients[J]. Medical Journal of the Chinese People Armed Police Forces. 2017, 28(6): 560-563
中图分类号: R733   

参考文献

[1] Zhou Y, Wang H, Fang W, et al. Incidence trends of mantle cell lymphoma in the United States between 1992 and 2004[J]. Cancer,2008,113(4):791-798.
[2] 周冬梅,陈 刚,郑雄伟,等.112例套细胞淋巴瘤临床病理分析[J]. 中国肿瘤临床,2015,42(2):82-86.
[3] Sg' korová A, Pytlík R, Móciková H,et al. Staging and treatment response evaluation in malignant lymphomas-czech lymphoma study group recommendations[J]. Klin Onkol,2016,29(4):295-302.
[4] Hagemeister F B. Treatment of relapsed aggressive lymphomas: regimens with and without high-dose therapy and stem cell rescue[J]. Cancer Chemother Pharmacol,2002,49(11):13-20.
[5] Sander B, Quintanilla-Martinez L, Ott G, et al. Mantle cell lymphoma--a spectrum from indolent to aggressive disease[J]. Virchows Arch,2016,468(3):245-257.
[6] Shah B D, Martin P, Sotomayor E M. Mantle cell lymphoma: a clinically heterogeneous disease in need of tailored approaches[J]. Cancer Control,2012,19(3):227-235.
[7] Cheah C Y, Seymour J F, Wang M L. Mantle Cell Lymphoma[J]. J Clin Oncol,2016,34(11):1256-1269.
[8] Lenz G, Dreyling M, Hoster E, et al. Immunochemotherapy with rituximab and cyclophosphamide, doxorubicin, vincristine, and prednisone significantly improves response and time to treatment failure, but not long-term outcome in patients with previously untreated mantle cell lymphoma: Results of a prospective randomized trial of the German Low Grade Lymphoma Study Group (GLSG) [J]. J Clin Oncol, 2005,23(9):1984-1992.
[9] Howard O M, Gribben J G, Neuberg D S, et al. Rituximab and CHOP induction therapy for newly diagnosed mantle-cell lymphoma: Molecular complete responses are not predictive of progression-free survival[J]. J Clin Oncol, 2002,20(5):1288-1294.
[10] Rosenbluth B D, Yahalom J. Highly effective local control and palliation of mantle cell lymphoma with involved-field radiation therapy (IFRT) [J]. Int J Radiat Oncol Biol Phys, 2006,65(4):1185-1191.
[11] Robak T, Huang H Q, Jin J, et al. Bortezomib based therapy for newly diagnosed mantle cell lymphoma[J]. New Engl Med,2015,372(10):944-953.
[12] Kluin H C, Hoster E, Hermine O, et al. Treatment of older patients with mantle cell lymphoma[J]. New Engl J Med,2012,367(6):520-531.
[13] Ruan J, Martin P, Shah B, et al. Lenalidomide plus Rituximab as initial treatment for mantle cell lymphoma[J]. New Engl J Med,2015,373(19):1835-1844.
[14] Tiemann M, Schrader C, Klapper W, et al. Histopathology, cell proliferation indices and clinical outcome in 304 patients with mantle cell lymphoma(MCL):a clinicopathological study from the European MCL Network[J].Br J Haematol, 2005,131(1):29-38.

PDF(589 KB)

Accesses

Citation

Detail

段落导航
相关文章

/