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非小细胞肺癌基因突变的治疗结果:一项单机构回顾性队列研究。

Therapeutic outcomes in non-small cell lung cancer with mutations: a single institution, retrospective cohort study.

作者信息

Tan Irena, Stinchcombe Thomas E, Ready Neal E, Crawford Jeffrey, Datto Michael B, Nagy Rebecca J, Lanman Richard B, Gu Lin, Clarke Jeffrey M

机构信息

Department of Internal Medicine, Duke University Medical Center, Durham, NC, USA.

Duke Cancer Institute, Duke University Medical Center, Durham, NC, USA.

出版信息

Transl Lung Cancer Res. 2019 Jun;8(3):258-267. doi: 10.21037/tlcr.2019.04.03.

Abstract

BACKGROUND

Data describing therapeutic outcomes in patients with non-small cell lung cancers (NSCLC) with mutations remains limited.

METHODS

We conducted a retrospective cohort study of 31 patients with metastatic NSCLC treated at Duke University Hospital who had been identified by next-generation sequencing methods to bear a mutation in their tumor in order to evaluate clinical response to immunotherapy and chemotherapy.

RESULTS

Sixty-five percent of patients identified in this cohort were current or former smokers. Fourteen (45.2%) of patients had a V600E mutation and 17 (54.8%) had a non-V600E mutation. Median progression-free survival (PFS) in the 23 patients who received first-line chemotherapy was 6.4 months [95% confidence interval (CI), 2.3 to 13.0]. Overall survival (OS) in patients who received first-line chemotherapy showed a median survival of 18 months (95% CI, 7.4 to 28.6). OS comparing patients who had never received immunotherapy at any point was 18.4 months (95% CI, 4.1 to NE) compared to 19.0 months (95% CI, 9.9 to 28.6) in those who had received immunotherapy. We did not find a statistically significant difference in OS in patients with V600E, amplification, or non-V600E mutations. There was also no difference in OS in patients treated with targeted BRAF inhibitors compared to those who were not treated with targeted BRAF inhibitors.

CONCLUSIONS

We describe therapeutic outcomes for patients with metastatic NSCLC with mutations treated with either cytotoxic chemotherapy or immunotherapy. Although the sample size is small, the survival curves do not suggest improved clinical activity in this population when treated with immunotherapy.

摘要

背景

关于携带 突变的非小细胞肺癌(NSCLC)患者治疗结果的数据仍然有限。

方法

我们对杜克大学医院治疗的 31 例转移性 NSCLC 患者进行了一项回顾性队列研究,这些患者通过下一代测序方法被确定其肿瘤存在 突变,以评估免疫治疗和化疗的临床反应。

结果

该队列中 65%的患者为现吸烟者或既往吸烟者。14 例(45.2%)患者存在 V600E 突变,17 例(54.8%)存在非 V600E 突变。接受一线化疗的 23 例患者的中位无进展生存期(PFS)为 6.4 个月[95%置信区间(CI),2.3 至 13.0]。接受一线化疗患者的总生存期(OS)显示中位生存期为 18 个月(95%CI,7.4 至 28.6)。从未接受过任何免疫治疗的患者的 OS 为 18.4 个月(95%CI,4.1 至未评估),而接受过免疫治疗的患者为 19.0 个月(95%CI,9.9 至 28.6)。我们未发现携带 V600E、 扩增或非 V600E 突变患者的 OS 存在统计学显著差异。接受靶向 BRAF 抑制剂治疗的患者与未接受靶向 BRAF 抑制剂治疗的患者的 OS 也无差异。

结论

我们描述了接受细胞毒性化疗或免疫治疗的携带 突变的转移性 NSCLC 患者的治疗结果。尽管样本量较小,但生存曲线并未表明该人群接受免疫治疗时临床活性有所改善。

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