期刊文献+

局部晚期NSCLC放化疗联合细胞因子诱导杀伤细胞过继免疫疗法初步研究 被引量:4

Radiochemotherapy combined with adoptive immunotherapy with cytokine-induced killer cells for locally advanced non-small cell lung cancer:a preliminary study
原文传递
导出
摘要 目的比较局部晚期NSCLC采用放化疗与放化疗联合CIK过继免疫疗法治疗的疗效。方法回顾分析2011—2012年间收治的125例未行手术的局部晚期NSCLC 患者资料,其中102例放化疗(对照组)、23例放化疗联合CIK过继免疫治疗(综合治疗组)。采用倾向评分匹配法对两组进行1﹕2匹配,考虑因素包括肿瘤分期、放化疗方案、放化疗后疗效等,匹配后共59例(37、22例)患者入组,比较两组生存及肿瘤控制情况。 Kaplan-Meier法计算生存率并Logrank法检验和单因素预后分析。结果对照组和综合治疗组1、2、3年OS分别为73%、32%、16%和91%、59%、41%( P=0.030),PFS分别为61%、21%、17%和45%、10%、10%( P=0.538);ⅢB 期的3年OS分别为11%和47%( P=0.026),序贯放化疗的3年OS分别为11%和46%( P=0.003);鳞癌患者的3年DMFS分别为22%和73%( P=0.029)。两组不良反应发生率相近,放射性肺炎发生率分别为9%和15%( P=0.889),放射性食管炎发生率分别为12%和7%( P=0.097)。结论放化疗联合CIK有可能使部分局部晚期NSCLC患者生存获益,但其应用人群、时机及剂量安全仍需进一步研究。 Objective To investigate and compare the clinical effects of radiochemotherapy alone or in combination with adoptive immunotherapy with cytokine-induced killer ( CIK) cells in patients with locally advanced non-small cell lung cancer (NSCLC).Methods The clinical data of 125 patients with locally advanced NSCLC who were admitted from 2011 to 2012 and did not undergo surgery were analyzed retrospectively, and among these patients, 102 received radiochemotherapy alone ( control group) , and 23 received radiochemotherapy combined with adoptive immunotherapy with CIK cells ( multimodality therapy group) .The two groups were matched at a ratio of 1:2 using propensity score matching, and the factors considered included tumor stage, radiochemotherapy regimen, and outcome after radiochemotherapy.Then 59 patients ( 22 from the multimodality therapy group and 37 from the control group) were enrolled, and survival and tumor control were compared between the two groups.The Kaplan-Meier method was used to calculate survival rates and the log-rank test was used for survival difference analysis and univariate prognostic analysis.Results The 1-, 2-, and 3-year overall survival ( OS) rates were 73%, 32%, and 16%, respectively, in the control group, and 91%, 59%, and 41%, respectively, in the multimodality therapy group ( P=0.030) .The 1-, 2-, and 3-year progression-free survival rates were 61%, 21%, and 17%, respectively, in the control group, and 45%, 10%, and 10%, respectively, in the multimodality therapy group ( P=0.538) .As for the patients with stage ⅢB NSCLC, those in the multimodality therapy group had a significantly higher 3-year OS rate than those in the control group (47%vs.11%, P=0.026). In the patients receiving sequential chemoradiotherapy, those in the multimodality therapy group had a significantly higher 3-year OS rate than those in the control group ( 46%vs.11%, P=0.003) .As for the patients with squamous cell carcinoma, those in the multimodality therapy group had a significantly higher 3-year distant metastasis-free survival rate than those in the control group ( 73%vs.22%, P=0.029) .The two groups showed similar incidence rates of adverse events, and compared with the control group, the multimodality therapy group had a lower incidence rate of radiation pneumonitis (9%vs.15%, P=0.889) and a higher incidence rate of radiation esophagitis (12%vs.7%, P=0.097).Conclusions Some patients with locally advanced NSCLC can benefit from radiochemotherapy combined with adoptive immunotherapy with CIK cells, but the intended population, timing, and dose safety still need further investigation.
出处 《中华放射肿瘤学杂志》 CSCD 北大核心 2016年第4期345-350,共6页 Chinese Journal of Radiation Oncology
基金 国家自然科学基金(81372429)
关键词 肺肿瘤/放化疗法 肺肿瘤/免疫疗法 预后 Lung neoplasms/radiochemotherapy Lung neoplasms/immunotherapy Prognosis
  • 相关文献

参考文献19

  • 1Jemal A,Bray F,Center MM,et al. Global cancer statistics [J] .CA Cancer J Clin,2011,61(2) :69-90.DOI: 10.3322/caac.20107.
  • 2Ren XB, Yu JP, Liu H, et al. Thl bias in PBMC induced by multicycles of auto-CIKs infusion in malignant solid tumor patients [ J ].Cancer Biother Radiopharm, 2006,21 ( 1 ) : 22-33.DOI : 10.1089/ cbr.2006.21.22.
  • 3Li H, Wang CL, Yu JP, et al. Dendritic cell-activated cytokine- induced killer cells enhance the anti-tumor effect of chemotherapy on non-small cell lung cancer in patients after surgery [J]. Cytotherapy, 2009, 11 ( 8 ) : 1076-1083. DOI: 10. 3109/1465 3240903121252.
  • 4Chang JY, Kestin LL, Barriger RB, et al. ACR Appropriateness Criteria nonsurgical treatment for locally advanced non-small-cell lung cancer: good performance status/definitive intent [J]. Oncology ,2014,28(8) :706-710.
  • 5Bezjak A, Temin S, Franklin G, et al. Definitive and adjuvant radiotherapy in locally advanced non-small-cell lung cancer: American society of clinical oncology clinical practice guideline endorsement of the American Society for radiation oncology evidence-based clinical practice guideline [ J ]. J Clin Oncol, 2015, 33 (18) :2100-2105.DOI : 10.1200/JCO.2014.59.2360.
  • 6Thibodeau J, Bourgeois-Daigneauh MC, Lapointe R. Targeting the MHC Class II antigen presentation pathway in cancer immunotherapy [J] .Oncoimmunology, 2012, 1 ( 6 ) : 908-916. DOI: 10. 4161/onci. 21205.
  • 7Jadus MR,Natividad J,Mai A,et al. Lung cancer:a classic example of tumor escape and progression while providing opportunities for immunological intervention [J], Clin Dev Immunol, 2012, 2012: 160724.DOI : 10.1155/2012/160724.
  • 8Brahmer JR.Harnessing the immune system for the treatment of non- small-cell lung cancer [J] .J Clin Oncol, 2013,31 (8) : 1021-1028. DOI : 10.1200/JCO.2012.45.8703.
  • 9Mery B, Guy JB, Swalduz A, et al. The evolving locally-advanced non-small cell lung cancer landscape: Building on past evidence and experience [ J]. Crit Rev Oncol Hematol, 2015,96 (2) : 319-327. DOI : 10.1016/j.critrevonc.2015.05.020.
  • 10Iyengar P, Gerber DE. Loceally advanced lung cancer: an optimal setting for vaccines and other immunotherapies [ J] .Cancer J, 2013, 19(3) :247-262.DO1 : lO.1097/PPO.0b013e318292e51a.

同被引文献44

引证文献4

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部