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

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.

机构信息

James Chih-Hsin Yang, National Taiwan University Hospital, Taipei, Taiwan; Vera Hirsh, McGill University, Montreal, Quebec, Canada; Martin Schuler, West German Cancer Center, University Duisburg-Essen, Essen; Juliane Lungershausen, Boehringer Ingelheim GmbH, Ingelheim, Germany; Nobuyuki Yamamoto, Shizuoka Cancer Center, Shizuoka, Japan; Kenneth J. O'Byrne, St James' Hospital, Dublin, Ireland; Tony S.K. Mok, State Key Laboratory of Southern China, Hong Kong Cancer Institute, The Chinese University of Hong Kong, Hong Kong; Victoria Zazulina, Mehdi Shahidi, and Dan Massey, Boehringer Ingelheim Limited, Bracknell; Michael Palmer, Keele University, Keele, United Kingdom; and Lecia V. Sequist, Massachusetts General Hospital and Harvard Medical School, Boston, MA.

出版信息

J Clin Oncol. 2013 Sep 20;31(27):3342-50. doi: 10.1200/JCO.2012.46.1764. Epub 2013 Jul 1.

Abstract

PURPOSE

Patient-reported symptoms and health-related quality of life (QoL) benefits were investigated in a randomized, phase III trial of afatinib or cisplatin/pemetrexed.

PATIENTS AND METHODS

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.

RESULTS

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) and dyspnea (P < .001). Afatinib showed significantly better mean scores over time in global health status/QoL (P = .015) and physical (P < .001), role (P = .004), and cognitive (P = .007) functioning compared with chemotherapy. Fatigue and nausea were worse with chemotherapy, whereas diarrhea, dysphagia, and sore mouth were worse with afatinib (all P < .01).

CONCLUSION

In patients with lung adenocarcinoma with EGFR mutations, first-line afatinib was associated with better control of cough and dyspnea compared with chemotherapy, although diarrhea, dysphagia, and sore mouth were worse. Global health status/QoL was also improved over time with afatinib compared with chemotherapy.

摘要

目的

在一项随机、III 期临床试验中,研究了阿法替尼与顺铂/培美曲塞治疗表皮生长因子受体(EGFR)突变阳性晚期肺腺癌患者的患者报告症状和健康相关生活质量(QoL)获益。

患者和方法

345 例晚期 EGFR 突变阳性肺腺癌患者随机分配 2:1 接受阿法替尼 40 mg/天或最多 6 个周期的顺铂/培美曲塞。使用欧洲癌症研究和治疗组织(EORTC)生活质量问卷 C30 和肺癌 13 问卷,每 21 天评估一次肺癌症状和健康相关 QoL,直到疾病进展。咳嗽、呼吸困难和疼痛的分析是预先计划好的,包括治疗后症状改善的患者比例、症状恶化的时间以及随时间推移症状的变化。

结果

调查问卷的依从性很高。与化疗相比,阿法替尼显著延迟了咳嗽(风险比 [HR],0.60;95%CI,0.41 至 0.87;P =.007)和呼吸困难(HR,0.68;95%CI,0.50 至 0.93;P =.015)的恶化时间,但不包括疼痛(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改善(P =.010)。咳嗽(P <.001)和呼吸困难(P <.001)的平均评分随时间的变化差异显著有利于阿法替尼而非化疗。与化疗相比,阿法替尼在全球健康状况/生活质量(P =.015)、身体(P <.001)、角色(P =.004)和认知(P =.007)功能方面的平均评分随时间的改善也更明显。与化疗相比,疲劳和恶心更严重,而腹泻、吞咽困难和口腔疼痛更严重(均 P <.01)。

结论

在 EGFR 突变的肺腺癌患者中,与化疗相比,一线阿法替尼可更好地控制咳嗽和呼吸困难,尽管腹泻、吞咽困难和口腔疼痛更严重。与化疗相比,阿法替尼随时间推移也改善了全球健康状况/生活质量。

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