Initial versus early switch to targeted therapy during first-line treatment among patients with biomarker-positive advanced or metastatic non-small cell lung cancer in the United States

Lisa M. Hess , Patrick Peterson , Tomoko Sugihara , Naleen Raj Bhandari , Peter M. Krein , Anthony Sireci
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Abstract

Objectives

This study compared outcomes between patients with biomarker-positive advanced/metastatic non-small cell lung cancer (a/mNSCLC) who initiated treatment with targeted therapy versus those who initiated chemotherapy-based treatment and switched to targeted therapy during the first ∼3 cycles (defined as the first 56 days) of first-line treatment.

Materials and Methods

This was an observational study of patients with a/mNSCLC who received targeted therapy from a nationwide electronic health record (EHR)-derived de-identified database. Outcomes were compared between those who initiated targeted therapy versus those who switched from chemotherapy to a targeted agent. Time-to-event outcomes were evaluated using Kaplan-Meier method; Cox proportional hazards models (adjusted for baseline covariates) were used to compare outcomes between groups.

Results

Of the 4,244 patients in this study, 3,107 (73.2%) initiated the first line with targeted therapy and 346 (8.2%) switched to targeted therapy. Patients who received initial targeted therapy were significantly more likely to be non-smokers, treated in an academic practice setting, and of slightly older age (all p < 0.05). Patients who received initial targeted therapy also had a significantly longer time to start of first-line treatment (35.8 vs 25.3 days, p < 0.001). No significant differences were observed for clinical outcomes between groups.

Conclusion

In both unadjusted and adjusted analyses, there were no differences in the clinical outcomes observed among patients with a/mNSCLC in this study. This study found that initiating chemotherapy with an early switch to targeted therapy (within 56 days) of receiving biomarker positive results may be an acceptable strategy for a patient for whom immediate care is needed.

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在美国,生物标志物阳性的晚期或转移性非小细胞肺癌患者在一线治疗期间初始与早期切换到靶向治疗
目的本研究比较了在一线治疗的前3个周期(定义为前56天)内开始靶向治疗的生物标志物阳性晚期/转移性癌症(a/mNSCLC)患者与开始化疗治疗并转为靶向治疗患者的结果。材料和方法这是一项观察性研究,研究对象是从全国电子健康记录(EHR)衍生的去识别数据库中接受靶向治疗的a/mNSCLC患者。比较了那些开始靶向治疗的人和那些从化疗转向靶向药物的人的结果。使用Kaplan-Meier方法评估事件发生时间的结果;Cox比例风险模型(根据基线协变量进行调整)用于比较各组之间的结果。结果在本研究的4244名患者中,3107名(73.2%)开始了一线靶向治疗,346名(8.2%)转为靶向治疗。接受初始靶向治疗的患者明显更有可能是在学术实践环境中接受治疗的非吸烟者,年龄稍大(均p<0.05)。接受初始靶向治疗的患者开始一线治疗的时间也明显更长(35.8天vs 25.3天,p<0.001)。两组之间的临床结果没有观察到显著差异。结论在未调整和调整的分析中,本研究中观察到的a/mNSCLC患者的临床结果没有差异。这项研究发现,对于需要立即护理的患者来说,启动化疗并在收到生物标志物阳性结果后(56天内)尽早转向靶向治疗可能是一种可接受的策略。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
148
审稿时长
56 days
期刊介绍: Cancer Treatment and Research Communications is an international peer-reviewed publication dedicated to providing comprehensive basic, translational, and clinical oncology research. The journal is devoted to articles on detection, diagnosis, prevention, policy, and treatment of cancer and provides a global forum for the nurturing and development of future generations of oncology scientists. Cancer Treatment and Research Communications publishes comprehensive reviews and original studies describing various aspects of basic through clinical research of all tumor types. The journal also accepts clinical studies in oncology, with an emphasis on prospective early phase clinical trials. Specific areas of interest include basic, translational, and clinical research and mechanistic approaches; cancer biology; molecular carcinogenesis; genetics and genomics; stem cell and developmental biology; immunology; molecular and cellular oncology; systems biology; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; cancer policy; and integration of various approaches. Our mission is to be the premier source of relevant information through promoting excellence in research and facilitating the timely translation of that science to health care and clinical practice.
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