Kamali Caroline, Tsakonas Georgios, Hydbring Per, Jatta Kenbugul, Berglund Anders, Viktorsson Kristina, Lewensohn Rolf, De Petris Luigi, Ekman Simon
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.
Transl Lung Cancer Res. 2024 Nov 30;13(11):2918-2933. doi: 10.21037/tlcr-24-396. Epub 2024 Nov 12.
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.
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).
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).
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.
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。
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。
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)。
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。