转移性alk阳性非小细胞肺癌的治疗:单中心研究的真实结果

IF 4 2区 医学 Q2 ONCOLOGY Translational lung cancer research Pub Date : 2024-11-30 Epub Date: 2024-11-12 DOI:10.21037/tlcr-24-396
Caroline Kamali, Georgios Tsakonas, Per Hydbring, Kenbugul Jatta, Anders Berglund, Kristina Viktorsson, Rolf Lewensohn, Luigi De Petris, Simon Ekman
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引用次数: 0

摘要

背景:间变性淋巴瘤激酶(ALK)重排发生在4-7%的非小细胞肺癌(NSCLC)病例中。尽管酪氨酸激酶抑制剂(TKIs)改善了生存率,但治疗耐药性仍然具有挑战性。这项回顾性研究分析了晚期alk阳性NSCLC患者,重点关注临床方面、治疗、耐药性和结局。方法:纳入2009年1月至2021年12月在卡罗林斯卡大学医院诊断并至少接受过一次ALK-TKI治疗的患者。我们评估了克唑替尼或第二代ALK-TKI在一线治疗中的有效性,以及氯拉替尼在后续治疗中的有效性。总生存期(OS)定义为晚期肺癌诊断之日至最后一次随访之日(2022年4月22日)或任何原因死亡之日。无进展生存期(PFS),从开始ALK-TKI之日起至进展、死亡或最后一次随访之日。通过利用下一代测序(NGS)进行再活检评估耐药机制。结果:160例符合条件的患者中,有10例被排除在外。中位随访时间为诊断后54.0个月,初始ALK-TKI治疗后45.0个月。克唑替尼的中位PFS为8.0个月,中位OS为35.0个月。第二代ALK-TKIs显示中位PFS为52.0个月[未达到OS (NR)]。总体而言,中位OS为65.0个月。不良预后因素包括男性、血栓栓塞、克唑替尼治疗和慢性阻塞性肺疾病(COPD)/哮喘。18例患者的再活检显示8例患者继发性ALK突变,与随后ALK- tki治疗的中位PFS缩短相关(1.0个月对7.0个月)。结论:这项跨越十年的综合研究,为中位生存期超过5年的晚期alk阳性NSCLC的临床特征、治疗模式和耐药机制提供了至关重要的见解。治疗期间的再活检对于提高我们对ALK-TKI治疗期间耐药机制和肿瘤动力学演变的理解至关重要。
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Treatment of metastatic ALK-positive non-small cell lung cancer: real-world outcomes in a single center study.

Background: Rearrangement in anaplastic lymphoma kinase (ALK) occurs in 4-7% of non-small cell lung cancer (NSCLC) cases. Despite improved survival with tyrosine kinase inhibitors (TKIs), treatment resistance remains challenging. This retrospective study analyzed advanced ALK-positive NSCLC patients, focusing on clinical aspects, treatments, resistance, and outcomes.

Methods: Patients diagnosed between January 2009 and December 2021 who received at least one ALK-TKI line at the Karolinska University Hospital, were included. We evaluated crizotinib or 2nd generation ALK-TKI effectiveness in first-line treatment and lorlatinib in subsequent lines. Overall survival (OS) was defined as from the date of advanced lung cancer diagnosis until the date of last follow-up (April 22, 2022) or the date of death from any cause. Progression-free survival (PFS), from the date of starting ALK-TKI until the date of progression, death, or last follow-up. Resistance mechanisms were assessed through re-biopsies utilizing next-generation sequencing (NGS).

Results: Out of 160 eligible patients, 10 were excluded. Median follow-up was 54.0 months from diagnosis and 45.0 months from initial ALK-TKI treatment. Crizotinib showed a median PFS of 8.0 months and a median OS of 35.0 months. Second generation ALK-TKIs demonstrated a median PFS of 52.0 months [OS was not reached (NR)]. Overall, the median OS was 65.0 months. Poor prognostic factors included male sex, thromboembolism, crizotinib treatment, and chronic obstructive pulmonary disease (COPD)/asthma. Rebiopsies in 18 cases revealed secondary ALK mutations in 8 patients, correlating with a shorter median PFS in subsequent ALK-TKI treatment (1.0 vs. 7.0 months).

Conclusions: This comprehensive study, spanning over a decade, provides crucial insights into the clinical characteristics, treatment patterns, and resistance mechanisms of advanced ALK-positive NSCLC, where median OS exceeds 5 years. Re-biopsies during treatment are essential for advancing our understanding of resistance mechanisms and the tumor dynamics evolving during ALK-TKI therapy.

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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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