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首页> 外文期刊>Journal of Clinical Oncology >Symptom Control and Quality of Life in LUX-Lung 3: A Phase III Study of Afatinib or Cisplatin/Pemetrexed in Patients With Advanced Lung Adenocarcinoma With EGFR Mutations.
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Symptom Control and Quality of Life in LUX-Lung 3: A Phase III Study of Afatinib or Cisplatin/Pemetrexed in Patients With Advanced Lung Adenocarcinoma With EGFR Mutations.

机译:LUX-Lung的症状控制和生活质量3:Afatinib或顺铂/培美曲塞治疗EGFR突变的晚期肺腺癌患者的III期研究。

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摘要

Patient-reported symptoms and health-related quality of life (QoL) benefits were investigated in a randomized, phase III trial of afatinib or cisplatin/pemetrexed.Three hundred forty-five patients with advanced epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma were randomly assigned 2:1 to afatinib 40 mg per day or up to six cycles of cisplatin/pemetrexed. Lung cancer symptoms and health-related QoL were assessed every 21 days until progression using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire C30 and Lung Cancer-13 questionnaires. Analyses of cough, dyspnea, and pain were preplanned, including percentage of patients who improved on therapy, time to deterioration of symptoms, and change in symptoms over time.Questionnaire compliance was high. Compared with chemotherapy, afatinib significantly delayed the time to deterioration for cough (hazard ratio [HR], 0.60; 95% CI, 0.41 to 0.87; P = .007) and dyspnea (HR, 0.68; 95% CI, 0.50 to 0.93; P = .015), but not pain (HR, 0.83; 95% CI, 0.62 to 1.10; P = .19). More patients on afatinib (64%) versus chemotherapy (50%) experienced improvements in dyspnea scores (P = .010). Differences in mean scores over time significantly favored afatinib over chemotherapy for cough (P < .001)
机译:在一项阿法替尼或顺铂/培美曲塞的III期随机试验中研究了患者报告的症状和与健康相关的生活质量(QoL)益处.345例晚期表皮生长因子受体(EGFR)突变阳性的肺每天将腺癌按2:1的比例随机分配给afatinib 40 mg或最多六个周期的顺铂/培美曲塞。每隔21天评估一次肺癌症状和与健康相关的QoL,直至进展为止,使用欧洲研究和治疗癌症生活质量组织问卷C30和Lung Cancer-13问卷进行调查。预先计划了咳嗽,呼吸困难和疼痛的分析,包括接受治疗的患者百分比,症状恶化的时间以及症状随时间的变化。对问卷的依从性很高。与化疗相比,阿法替尼显着延迟了咳嗽(危险比[HR]为0.60; 95%CI为0.41至0.87; P = .007)和呼吸困难(HR为0.68; 95%CI为0.50至0.93; 95%CI为0.50; 0.93)的恶化时间。 P = .015),但不是疼痛(HR,0.83; 95%CI,0.62至1.10; P = .19)。阿法替尼组(64%)比化疗组(50%)更多的患者呼吸困难评分得到改善(P = .010)。随着时间的推移,平均得分的差异明显优于阿法替尼,而不是化疗引起的咳嗽(P <.001)

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