Trakya University, Faculty of Medicine, Department of Medical Oncology, Balkan Oncology Hospital, 22030 Edirne, Turkey.
Alexander Fleming Institution, Cramer 1180 caba, Buenos Aires CP 1426, Argentina.
Crit Rev Oncol Hematol. 2022 Dec;180:103847. doi: 10.1016/j.critrevonc.2022.103847. Epub 2022 Oct 17.
This article reviews the role of ALK tyrosine kinase inhibitors (TKIs) in the literature and provides expert commentary on local use in Argentina, Brazil, China, Russia, South Korea, and Turkey. We identified 56 articles involving patients with ALK-positive non-small cell lung cancer (NSCLC) and brain metastases (BM) treated with ALK TKIs published between January 2000 and June 2021. In first-line settings, central nervous system response rates in clinical trials with alectinib (86-94%), brigatinib (67-78%), and lorlatinib (42-82%) were generally higher than those reported with crizotinib (16-71%). Median progression-free survival in patients receiving crizotinib (5.6-7.4 months) was lower than alectinib (not reached), brigatinib (24.0 months), and ceritinib (10.7-25.2 months). Across these counties, next-generation TKIs are preferred for patients with progressing BM lesions. Although next-generation ALK TKIs demonstrate significant activity in these patients and following progression on crizotinib, access remains a challenge for personalized therapy.
本文综述了 ALK 酪氨酸激酶抑制剂(TKI)在文献中的作用,并就阿根廷、巴西、中国、俄罗斯、韩国和土耳其的局部应用提供了专家评论。我们确定了 56 篇涉及 2000 年 1 月至 2021 年 6 月期间接受 ALK TKI 治疗的 ALK 阳性非小细胞肺癌(NSCLC)和脑转移(BM)患者的文章。在一线治疗中,阿来替尼(86-94%)、布加替尼(67-78%)和劳拉替尼(42-82%)临床试验中中枢神经系统反应率通常高于克唑替尼(16-71%)。接受克唑替尼治疗的患者中位无进展生存期为 5.6-7.4 个月,低于阿来替尼(未达到)、布加替尼(24.0 个月)和塞瑞替尼(10.7-25.2 个月)。在这些国家,对于进展性 BM 病变的患者,优先选择下一代 TKI。尽管下一代 ALK TKI 在这些患者中以及在克唑替尼进展后显示出显著的活性,但获得个性化治疗仍然是一个挑战。