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转移性ALK阳性非小细胞肺癌的治疗:一项单中心研究的真实世界结果

Treatment of metastatic ALK-positive non-small cell lung cancer: real-world outcomes in a single center study.

作者信息

Kamali Caroline, Tsakonas Georgios, Hydbring Per, Jatta Kenbugul, Berglund Anders, Viktorsson Kristina, Lewensohn Rolf, De Petris Luigi, Ekman Simon

机构信息

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

Theme Cancer, Medical Unit Head, and Neck, Lung and Skin Cancer, Thoracic Oncology Center, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Transl Lung Cancer Res. 2024 Nov 30;13(11):2918-2933. doi: 10.21037/tlcr-24-396. Epub 2024 Nov 12.

Abstract

BACKGROUND

Rearrangement in anaplastic lymphoma kinase () 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 2 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 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.

摘要

背景

间变性淋巴瘤激酶(ALK)重排在4%-7%的非小细胞肺癌(NSCLC)病例中出现。尽管酪氨酸激酶抑制剂(TKIs)改善了患者生存率,但治疗耐药性仍然是一个挑战。这项回顾性研究分析了晚期ALK阳性NSCLC患者,重点关注临床情况、治疗、耐药性和结局。

方法

纳入2009年1月至2021年12月期间在卡罗林斯卡大学医院诊断且接受至少一线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洛拉替尼在后续治疗线中的有效性。总生存期(OS)定义为从晚期肺癌诊断日期至最后一次随访日期(2022年4月22日)或任何原因导致的死亡日期。无进展生存期(PFS)定义为从开始ALK-TKI治疗日期至疾病进展、死亡或最后一次随访日期。通过利用二代测序(NGS)的再次活检评估耐药机制。

结果

160例符合条件的患者中,10例被排除。从诊断开始的中位随访时间为54.0个月,从初始ALK-TKI治疗开始的中位随访时间为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的中位PFS为52.0个月[OS未达到(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、克唑替尼治疗以及慢性阻塞性肺疾病(COPD)/哮喘。18例患者的再次活检显示8例患者存在继发性ALK突变,这与后续ALK-TKI治疗中较短的中位PFS相关(1.0至7.0个月)。

结论

这项跨越十多年的综合研究为晚期ALK阳性NSCLC的临床特征、治疗模式和耐药机制提供了关键见解,其中位OS超过5年。治疗期间的再次活检对于增进我们对耐药机制以及ALK-TKI治疗期间肿瘤动态演变的理解至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f55/11632442/9f09e60cf9ea/tlcr-13-11-2918-f1.jpg

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