[Clinical Efficacy and Safety of R-CDOP Regimen for Treatment of Newly Treated DLBCL Patients with Adverse Prognostic Factors]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Aug;27(4):1143-1148. doi: 10.19746/j.cnki.issn.1009-2137.2019.04.024.
[Article in Chinese]

Abstract

Objective: To investigate the clinical efficacy and Safety of R-CDOP regimen for treatment of newly diagnosed DLBCL patients with adverse prognostic factors.

Methods: The clinical data of 94 patients who suffered from DLBCL and received treatment with R-CDOP regimen, from October 2013 to February 2018 were collected and analyzed retrospectively. The clinical efficacy, survival benifits and safety, as well as the OS and PFS were compared according to clinical features.

Results: After treatment of 94 cases with R-CDOP regimen, 73 cases reachived CR, 14 cases reachived PR, 2 cases were in SD and 4 cases were in PD, the ORR was 92.55% (87/94). The OS rate and PFS rate in followed-up 1 year were 94.68%(89/94) and 85.11%(80/94) separately, However, the median OS and PFS were not reached. There was no significant difference in the followed-up cumulative OS rate and PFS rate between patients with different Age, Ann-Arbor stage, IPI score, number of extranodal tumors, tumor diameter, expression of Ki-67 and LDH level and tissue involvement status(P>0.05). There was no significant difference in the 1 years PFS rate and OS rate between patients with number of extranodal tumors for 0-1 and ≥2(P>0.05). There was no significant difference in the 1 years PFS rate and OS rate between patients with tumor diameter for <7.5 cm and ≥7.5 cm(P>0.05).

Conclusion: The R-CDOP regimen in the treatment of newly diagnosed DLBCL patients with poor prognostic factors can efficiently improve the early clinical efficacy, prolong the survival time and possess good safety, but the clinical prognosis for long-term remains to be observed.

题目: R-CDOP方案治疗初治DLBCL伴预后不良因素患者的疗效及安全性.

目的: 探讨R-CDOP方案对初治DLBCL伴预后不良因素患者临床疗效的影响.

方法: 收集并回顾性分析本院2013年10月-2018年2月收治的初治DLBCL共94例临床资料。均给予患者R-CDOP方案治疗,统计疗效、生存获益及安全性指标,并根据临床特征进行总生存(OS)和无进展生存(PFS)分析.

结果: 94例患者经治疗后,CR共73例,PR共14例,SD 2例,PD 4例,ORR为92.55%;1年OS率和PFS率分别为94.68%(89/94),85.11%(80/94),中位OS和PFS均未达到。不同年龄、Ann-Arbor分期、IPI评分、结外肿物数量、肿物直径、Ki-67、LDH水平及组织受累情况、患者累积OS率和PFS率比较,均无显著性差异(P>0.05);结外肿物0-1个和≥2个患者的1年OS率和PFS率比较差异无显著性(P>0.05);肿物直径<7.5和≥7.5 cm患者1年OS率和PFS率比较差异无显著性(P>0.05).

结论: 对初治DLBCL伴预后不良因素患者采用R-CDOP方案治疗可有效改善早期疗效,延长生存时间,且安全性良好,但远期预后仍有待观察.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Cyclophosphamide
  • Disease-Free Survival
  • Humans
  • Lymphoma, Large B-Cell, Diffuse* / drug therapy
  • Prognosis
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Cyclophosphamide