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首页> 外文期刊>Clinical lung cancer >Subsequent chemotherapy improves survival outcome in advanced non-small-cell lung cancer with acquired tyrosine kinase inhibitor resistance.
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Subsequent chemotherapy improves survival outcome in advanced non-small-cell lung cancer with acquired tyrosine kinase inhibitor resistance.

机译:随后的化疗通过获得性酪氨酸激酶抑制剂的耐药性改善了晚期非小细胞肺癌的生存结果。

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BACKGROUND: Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) provide promising effect against non-small-cell lung cancer (NSCLC), although most tumors acquire resistance. Our objective was to assess the survival outcome of patients with NSCLC with or without subsequent chemotherapy after acquired TKI resistance. PATIENTS AND METHODS: A total of 114 patients with pathologically confirmed stage IIIB or IV NSCLC who had had disease control with TKIs were retrospectively reviewed. After acquired TKI resistance, patients received either best supportive care (BSC) only or BSC plus subsequent chemotherapy. Both groups were well balanced in regard to performance status, age, sex, histology subtype, and smoking status. RESULTS: Sixty-seven patients (58.8%) received subsequent chemotherapy, and 47 patients (41.2%) received BSC only. The median overall survival (OS) and progression-free survival (PFS) from the time of TKI resistance in the subsequent-chemotherapy group (11.2 months and 3.5 months, respectively) were longer than those of the BSC group (3.8 months and 1.5 months, respectively; P < .01). Patients who subsequently received taxane-based chemotherapy exhibited higher a response rate and disease control rate (48.7% and 79.5%, respectively) than patients treated with a nontaxane regimen (21.4% and 53.5%, respectively; P < .05). Overall survival and PFS in patients after taxane-based subsequent chemotherapy (12.7 months and 5.1 months, respectively) were longer than those of patients given a nontaxane regimen (7 months and 1.8 months, respectively; P < .01). CONCLUSION: This study suggests that acquired TKI resistance should be managed aggressively. The higher antitumor response and survival outcome with a taxane-based regimen in this retrospective study could encourage further prospective investigation to confirm the efficacy of taxane over nontaxane chemotherapy in patients with NSCLC whose disease progresses with EGFR TKI treatment.
机译:背景:表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)对非小细胞肺癌(NSCLC)具有很好的疗效,尽管大多数肿瘤都具有耐药性。我们的目标是评估获得性TKI耐药后有或没有后续化疗的NSCLC患者的生存结局。患者和方法:回顾性回顾了114例经病理证实的IIIB或IV期NSCLC患者,这些患者已通过TKI进行了疾病控制。获得TKI抵抗后,患者仅接受最佳支持治疗(BSC)或接受BSC加后续化疗。两组在表现状态,年龄,性别,组织学亚型和吸烟状态方面均保持平衡。结果:67例患者(58.8%)接受了后续化疗,47例患者(41.2%)仅接受了BSC。在随后的化学治疗组中,从TKI抵抗开始到发生TKI抵抗时的中位总体生存期(OS)和无进展生存期(PFS)分别比BSC组的中位生存期(3.8个月和1.5个月)长(分别为11.2个月和3.5个月)。分别; P <0.01)。随后接受紫杉烷类化学疗法的患者显示出更高的反应率和疾病控制率(分别为48.7%和79.5%),比接受非紫杉烷方案的患者(分别为21.4%和53.5%; P <0.05)。以紫杉烷为基础的后续化疗后患者的总生存期和PFS(分别为12.7个月和5.1个月)比接受非紫杉醇方案的患者(分别为7个月和1.8个月; P <0.01)更长。结论:这项研究表明,应积极控制获得性TKI耐药性。在这项回顾性研究中,以紫杉类为基础的方案具有更高的抗肿瘤应答和生存结果,这可能会鼓励进一步的前瞻性研究,以证实紫杉烷在非EGFR化疗中对EGFR TKI治疗进展的NSCLC患者的疗效。

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