A Phase II Trial of Erlotinib and Concurrent Palliative Thoracic Radiation for Patients With Non-Small-Cell Lung Cancer

被引:9
作者
Swaminath, Anand [1 ,2 ]
Wright, James R. [1 ,2 ]
Tsakiridis, Theodoros K. [1 ,2 ]
Ung, Yee C. [3 ,4 ]
Pond, Gregory R. [1 ,5 ]
Sur, Ranjan [1 ,2 ]
Corbett, Thomas B. [1 ,2 ]
Okawara, Gordon [1 ,2 ]
Leyine, Mark N. [1 ,2 ,5 ]
机构
[1] McMaster Univ, Dept Oncol, Hamilton, ON, Canada
[2] Hamilton Hlth Sci, Juravinski Canc Ctr, 699 Concess St, Hamilton, ON L8V 5C2, Canada
[3] Odette Canc Ctr, Toronto, ON, Canada
[4] Univ Toronto, Toronto, ON, Canada
[5] Juravinski Hosp, Ontario Clin Oncol Grp, Hamilton, ON, Canada
关键词
Clinical trial; Combined-modality therapy; Palliative radiation; Quality of life; Radiation sensitizer; QUALITY-OF-LIFE; GROWTH-FACTOR RECEPTOR; RADIOTHERAPY; THERAPY; SURVIVAL;
D O I
10.1016/j.cllc.2015.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A phase II trial of combined erlotinib and palliative radiation evaluated the patient-reported quality of life (QoL) in 40 patients with advanced non small-cell lung cancer. Although the combination improved QoL overall, the improvement was not more substantial than that observed with radiation alone. Future trials might identify subgroups of patients with metastatic disease who could benefit from combined targeted therapies and radiation. Background: The downstream signaling pathways of the epidermal growth factor receptor might influence radiation resistance. Data from preclinical work support the hypothesis that erlotinib concurrent with radiation therapy (RT) might increase cancer cell killing. The present trial was designed to examine the efficacy and toxicity of combined erlotinib and palliative chest thoracic RT in non small-cell lung cancer (NSCLC). Materials and Methods: Patients with newly diagnosed stage III-IV (American Joint Committee on Cancer, version 6) or recurrent NSCLC received 3 weeks of erlotinib at a dose of 150 mg daily, starting 1 week before palliative thoracic RT to 30 Gy in 10 fractions within 2 weeks. The primary outcome was a change in the quality of life, as measured by the Lung Cancer Symptom Scale (LOSS) question on the "symptoms of lung cancer" from baseline to 4 weeks after treatment. Results: A total of 40 patients were recruited from 2 institutions. Of the 40 patients, 22 (55%) were men, with an average age of 71 years, and 60% had stage IV disease. A total of 26 patients (65%) completed the full course of erlotinib, and 35 (88%) completed the planned RT. Twenty-five patients (62.5%) reported LCSS scores at 4 weeks after treatment, with an average change (improvement) of -12.5 U (95% confidence interval, -23.0 to -1.9; 2P =.023). This was less than the a priori hypothesis of a change of -17.5 U. The median overall and progression-free survival was 5.2 and 3.2 months, respectively. Conclusion: The present single-arm, phase II trial did not demonstrate additional symptomatic benefit from concurrent erlotinib therapy with standard palliative thoracic RT for patients with locally advanced or metastatic NSCLC. Crown Copyright (C) 2016 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:142 / 149
页数:8
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