间变性淋巴瘤激酶(ALK)重排非小细胞肺癌(NSCLC)患者接受一种或多种ALK酪氨酸激酶抑制剂(TKIs)的现实世界临床结果趋势:加拿大安大略省的一项队列研究。

IF 3.4 4区 医学 Q2 ONCOLOGY Current oncology Pub Date : 2024-12-27 DOI:10.3390/curroncol32010013
Lara Chayab, Natasha B Leighl, Mina Tadrous, Christine M Warren, William W L Wong
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引用次数: 0

摘要

随着几个ALK TKIs在加拿大获得批准,晚期ALK阳性NSCLC患者的治疗前景迅速发展。然而,ALK TKIs的公共资金主要局限于一线治疗环境。使用相关的省级卫生管理数据库,我们检查了2012年1月1日至2021年12月31日期间安大略省晚期ALK阳性非小细胞肺癌患者接受ALK TKIs的现实结果。用描述性统计方法总结人口学、临床特征和治疗模式。Kaplan-Meier分析各组患者的无进展生存期(PFS)和总生存期(OS)。共确定了413例患者。在一线治疗中,患者接受了阿勒替尼(n = 154)、克唑替尼(n = 80)或姑息性化疗(n = 55)。治疗组间一线PFS有显著差异。阿勒替尼的中位PFS (mPFS)未达到(95% CI, 568天-未达到),而克唑替尼的中位PFS为8.2个月(95% CI, 171-294天)(HR = 0.34, p < 0.0001),化疗的中位PFS为2.4个月(95% CI, 65-100天)(HR = 0.14, p < 0.0001)。治疗组间一线OS无显著差异。在接受一条以上治疗的患者中,与接受一条以上ALK TKI治疗的患者相比,接受两条或两条以上ALK TKI治疗的患者的mOS有显著差异(mOS分别为55个月(95% CI, 400-987天)和26个月(95% CI, 1448-2644天),HR = 4.64, p < 0.0001)。本研究证实了ALK TKI在实际应用中的有效性,并支持多系ALK TKI对ALK阳性NSCLC患者总生存率的潜在益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Trends in Real-World Clinical Outcomes of Patients with Anaplastic Lymphoma Kinase (ALK) Rearranged Non-Small Cell Lung Cancer (NSCLC) Receiving One or More ALK Tyrosine Kinase Inhibitors (TKIs): A Cohort Study in Ontario, Canada.

The treatment landscape for patients with advanced ALK-positive NSCLC has rapidly evolved following the approval of several ALK TKIs in Canada. However, public funding of ALK TKIs is mostly limited to the first line treatment setting. Using linked provincial health administrative databases, we examined real-world outcomes of patients with advanced ALK-positive NSCLC receiving ALK TKIs in Ontario between 1 January 2012 and 31 December 2021. Demographic, clinical characteristics and treatment patterns were summarized using descriptive statistics. Kaplan-Meier analysis was performed to evaluate progression-free survival (PFS) and overall survival (OS) among the treatment groups. A total of 413 patients were identified. Patients were administered alectinib (n = 154), crizotinib (n = 80), or palliative-intent chemotherapy (n = 55) in the first-line treatment. There was a significant difference in first-line PFS between the treatment groups. The median PFS (mPFS) was not reached for alectinib (95% CI, 568 days-not reached), compared to 8.2 months (95% CI, 171-294 days) for crizotinib (HR = 0.34, p < 0.0001) and 2.4 months (95% CI, 65-100 days) for chemotherapy (HR = 0.14, p < 0.0001). There was no significant difference in first-line OS between the treatment groups. In patients who received more than one line of treatment, there was a significant difference in mOS between patients who received two or more lines of ALK TKIs compared to those who received one line of ALK TKI (mOS = 55 months (95% CI, 400-987 days) and 26 months (95% CI, 1448-2644 days), respectively, HR = 4.64, p < 0.0001). This study confirms the effectiveness of ALK TKIs in real-world practice and supports the potential benefit of multiple lines of ALK TKI on overall survival in patients with ALK-positive NSCLC.

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来源期刊
Current oncology
Current oncology ONCOLOGY-
CiteScore
3.30
自引率
7.70%
发文量
664
审稿时长
1 months
期刊介绍: Current Oncology is a peer-reviewed, Canadian-based and internationally respected journal. Current Oncology represents a multidisciplinary medium encompassing health care workers in the field of cancer therapy in Canada to report upon and to review progress in the management of this disease. We encourage submissions from all fields of cancer medicine, including radiation oncology, surgical oncology, medical oncology, pediatric oncology, pathology, and cancer rehabilitation and survivorship. Articles published in the journal typically contain information that is relevant directly to clinical oncology practice, and have clear potential for application to the current or future practice of cancer medicine.
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