[Serum CYFRA21-1 is Correlated with the Efficacy of Epidermal Growth Factor Receptor-tyrosine Kinase Inhibitor in Non-small Cell Lung Cancer Patients Harboring EGFR Mutations]

Zhongguo Fei Ai Za Zhi. 2016 Aug 20;19(8):550-8. doi: 10.3779/j.issn.1009-3419.2016.08.12.
[Article in Chinese]

Abstract

Background: Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are the standard first-line treatment regimen for EGFR mutated non-small cell lung cancer (NSCLC) patients. However, the efficacy of EGFR-TKIs widely varies. The aim of this study is to determine whether the pretreatment serum cytokeratin-19 fragments (CYFRA21-1) and carcinoembryonic antigen (CEA) are associated with the efficacy of EGFR-TKIs in EGFR-mutated NSCLC patients.

Methods: We retrospectively enrolled 194 NSCLC patients harboring EGFR mutations who received EGFR-TKIs. Clinical characteristics were collected, and the relation between the efficacy of EGFR-TKIs and pretreatment serum CYFRA21-1 and CEA was analyzed.

Results: In all cases, progression-free survival (PFS) in patients with high CYFRA21-1 level was significantly shorter than PFS in patients with normal CYFRA21-1 (7.0 vs 11.9 months, P<0.001). Overall survival (OS) in patients with high CYFRA21-1 was significantly shorter than in the normal-CYFRA21-1 group (12.6 vs 28.0 months, P<0.001). In adenocarcinoma patients, PFS in the high-CYFRA21-1 level group was significantly shorter than in patients with normal CYFRA21-1 (7.0 vs 12.0 months, P<0.001). OS in patients with high CYFRA21-1 was significantly shorter than that in the normal-CYFRA21-1 group (13.1 vs 28.1 months, P<0.001). Among squamous carcinoma patients, CYFRA21-1 level did not affect survival. No significant difference in PFS and OS was observed between patients with high CEA and patients with normal CEA.

Conclusions: EGFR-mutated patients with high CYFRA21-1 had significantly shorter PFS and OS than patients with normal CYFRA21-1 after receiving EGFR-TKIs. Pretreatment serum CYFR21-1 level was a predictive marker of EGFR-TKI treatment in EGFR-mutated NSCLC patients. .

背景与目的 表皮生长因子受体-酪氨酸激酶抑制剂(epidermal growth factor receptor-tyrosine kinase inhibitors, EGFR-TKIs)是EGFR基因突变晚期非小细胞癌(non-small cell lung cancer, NSCLC)患者一线标准治疗方案,但是临床实践中,疗效差异较大。本项实验拟研究治疗前血清细胞角蛋白19片段(cytokeratin-19 fragments, CYFRA21-1)和癌胚抗原(carcinoembryonic antigen, CEA)的水平是否与EGFR-TKIs疗效有关。方法 回顾性分析194例EGFR基因突变阳性且接受EGFR-TKIs治疗的NSCLC患者的治疗前的血清CYFRA21-1和CEA水平与EGFR-TKIs疗效及生存时间的关系。结果 血清水平CYFRA21-1增高和正常的无进展生存时间(progression-free survival, PFS)分别为7.0个月和11.9个月(P<0.001);总生存(overall survival, OS)分别为12.6个月和28.0个月(P<0.001)。腺癌中,血清水平增高和正常的PFS分别为7.0个月和12.0个月(P<0.001),OS分别为13.1个月和28.1个月(P<0.001)。鳞癌中,血清CYFRA21-1水平高低与生存时间无关。治疗前血清CEA水平高低与生存时间无关。结论 在EGFR突变肺腺癌患者,治疗前血清水平CYFRA21-1增高组EGFR-TKIs治疗的PFS和OS均较正常组短。EGFR突变肺腺癌患者,治疗前血清CYFRA21-1水平可以作为预测EGFR-TKIs治疗的疗效指标。.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antigens, Neoplasm / blood*
  • Carcinoma, Non-Small-Cell Lung / blood*
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Disease-Free Survival
  • ErbB Receptors / genetics*
  • Female
  • Humans
  • Keratin-19 / blood*
  • Lung Neoplasms / blood*
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology
  • Male
  • Middle Aged
  • Mutation
  • Neoplasm Staging
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Treatment Outcome

Substances

  • Antigens, Neoplasm
  • Keratin-19
  • Protein Kinase Inhibitors
  • antigen CYFRA21.1
  • ErbB Receptors