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Re-administration of Chemotherapy in Patients with Advanced Non-small Cell Lung Cancer Who Recovered from Chemotherapy-induced Interstitial Lung Disease

机译:从化疗引起的间质性肺疾病中恢复的晚期非小细胞肺癌患者的化疗重新给药

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摘要

We reported that epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor re-administration (TKI-R) might be salvage therapy in patients with advanced non-small cell lung cancer after recovery from EGFR-TKI-induced interstitial lung disease (ILD). Here we retrospectively evaluated whether chemotherapy re-administration (CT-R) was effective in patients after chemotherapy-induced ILD. After providing their informed consent due to the risk of severe ILD, five patients received CT-R and six received TKI-R with oral administration of 0.5 mg/kg prednisolone. The overall survival (OS) from the occurrence of drug-induced ILD was shorter in CT-R cases than that in TKI-R cases (7.3 months vs. 25.4 months, p=0.003). The median duration of OS, however, was 7.3 months in cases with CT-R and 1.9 months in cases without CT-R. Multivariate analysis showed that CT-R as well as TKI-R tended to reduce the risk of mortality. CT-R might be salvage therapy in such patients, although the benefit of CT-R was smaller than that of TKI-R.
机译:我们报道表皮生长因子受体(EGFR)酪氨酸激酶抑制剂重新给药(TKI-R)可能是晚期非小细胞肺癌患者从EGFR-TKI诱导的间质性肺病(ILD)恢复后的抢救疗法。在这里,我们回顾性评估在化疗诱导的ILD后,重新给予化疗(CT-R)是否有效。由于严重ILD的风险而征得他们的知情同意后,五名患者接受了CT-R的治疗,六名接受了TKI-R的患者口服了0.5 mg / kg泼尼松龙。在CT-R病例中,由药物引起的ILD发生的总生存期(OS)比TKI-R病例要短(7.3个月对25.4个月,p = 0.003)。然而,CT-R患者的OS中位持续时间为7.3个月,而CT-R患者的OS为1.9个月。多变量分析表明,CT-R和TKI-R倾向于降低死亡风险。尽管CT-R的获益小于TKI-R,但CT-R可能是这类患者的救治方法。

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