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ROS1 重排非小细胞肺癌患者的真实世界检测实践、特征和治疗模式(ROS1REAL 研究)。

Non-Small-Cell Lung Cancer Patients Harboring ROS1 Rearrangement: Real World Testing Practices, Characteristics and Treatment Patterns (ROS1REAL Study).

机构信息

Department of Medical Oncology, University Clinic Golnik, 4204 Golnik, Slovenia.

Medical Faculty Ljubliana, University of Ljubliana, 1000 Ljubljana, Slovenia.

出版信息

Curr Oncol. 2024 Jul 30;31(8):4369-4381. doi: 10.3390/curroncol31080326.

DOI:10.3390/curroncol31080326
PMID:39195309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11352911/
Abstract

ROS1 rearrangements are considered rare in non-small-cell lung cancer (NSCLC). This retrospective real-world study aimed to evaluate first-line treatment with crizotinib, a tyrosine kinase inhibitor (TKI) standard of care vs. new generation ROS1 anti-cancer agents. Forty-nine ROS1-expressing NSCLC patients, diagnosed with advanced metastatic disease, were included. Molecular profiling using either FISH/CISH or NGS was performed on tissue samples. Twenty-eight patients were treated with crizotinib, while fourteen patients were administered newer drugs (entrectinib, repotrectinib) and seven patients received platinum-doublet chemotherapy in a first-line setting. Overall response rate and disease control rate for the crizotinib and entrectinb/repotrectinib cohort were 68% and 82% vs. 86% and 93%, respectively. Median progression free survival was 1.6 years (95% CI 1.15-2.215) for the crizotinib treatment vs. 2.35 years for the entrectinib/repotrectinib cohort (95% CI 1.19-3.52). Central nervous system progression was noted in 20% and 25% of the crizotinib and entrectinib/repotrectinib cohorts, respectively. This multi-center study presents real-world treatment patterns of ROS1 NSCLC population, indicating that crizotinib exhibited comparable results to entrectinib/repotrectinib in a first-line setting, although both response rate and survival was numerically longer with treatment with newer agents.

摘要

ROS1 重排被认为在非小细胞肺癌(NSCLC)中较为罕见。本回顾性真实世界研究旨在评估克唑替尼(一种酪氨酸激酶抑制剂[TKI]标准治疗药物)与新一代 ROS1 抗癌药物作为一线治疗的效果。共纳入 49 例 ROS1 表达的 NSCLC 患者,均诊断为晚期转移性疾病。对组织样本进行了荧光原位杂交(FISH/CISH)或下一代测序(NGS)的分子谱分析。28 例患者接受了克唑替尼治疗,14 例患者接受了新一代药物(恩曲替尼、瑞波替尼)治疗,7 例患者在一线治疗中接受了铂类双重化疗。克唑替尼和恩曲替尼/瑞波替尼组的总缓解率和疾病控制率分别为 68%和 82%,86%和 93%。克唑替尼治疗组的中位无进展生存期为 1.6 年(95%CI:1.15-2.215),恩曲替尼/瑞波替尼组为 2.35 年(95%CI:1.19-3.52)。克唑替尼和恩曲替尼/瑞波替尼组分别有 20%和 25%的患者出现中枢神经系统进展。这项多中心研究展示了 ROS1 NSCLC 患者的真实世界治疗模式,表明克唑替尼在一线治疗中与恩曲替尼/瑞波替尼的疗效相当,尽管新一代药物治疗的反应率和生存率在数值上更长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bba/11352911/94c34364563e/curroncol-31-00326-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bba/11352911/8ebfa03a87e4/curroncol-31-00326-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bba/11352911/94c34364563e/curroncol-31-00326-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bba/11352911/8ebfa03a87e4/curroncol-31-00326-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bba/11352911/94c34364563e/curroncol-31-00326-g002.jpg

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Cancers (Basel). 2024 Jan 26;16(3):528. doi: 10.3390/cancers16030528.
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Repotrectinib: First Approval.Repotrectinib:首次获批。
Drugs. 2024 Feb;84(2):239-246. doi: 10.1007/s40265-023-01990-6.
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Repotrectinib effective in ROS1-fusion-positive NSCLC.瑞波替尼对ROS1融合阳性的非小细胞肺癌有效。
Nat Rev Clin Oncol. 2024 Mar;21(3):167. doi: 10.1038/s41571-024-00864-4.
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Repotrectinib in Fusion-Positive Non-Small-Cell Lung Cancer.Repotrectinib 治疗融合阳性非小细胞肺癌。
N Engl J Med. 2024 Jan 11;390(2):118-131. doi: 10.1056/NEJMoa2302299.
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Progress of non-small-cell lung cancer with rearrangement.伴有重排的非小细胞肺癌的进展
Front Mol Biosci. 2023 Dec 22;10:1238093. doi: 10.3389/fmolb.2023.1238093. eCollection 2023.
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