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血管生成拟态是肺腺癌无进展生存期的负向指标,与一线治疗和表皮生长因子受体突变状态无关。

Vasculogenic mimicry, a negative indicator for progression free survival of lung adenocarcinoma irrespective of first line treatment and epithelial growth factor receptor mutation status.

机构信息

Oncology Department, the Second People's Hospital of Taizhou affiliated to Medical College of Yangzhou University, No. 27, Jiangyan District, Taizhou, 225500, China.

Orthopaedic Department, the Second People's Hospital of Taizhou Affiliated to Medical College of Yangzhou University, Taizhou, China.

出版信息

BMC Cancer. 2021 Feb 6;21(1):132. doi: 10.1186/s12885-021-07863-z.


DOI:10.1186/s12885-021-07863-z
PMID:33549061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7866877/
Abstract

BACKGROUND: Vascular mimicry (VM) was associated with the prognosis of cancers. The aim of the study was to explore the association between VM and anticancer therapy response in patients with lung adenocarcinoma. METHODS: This was a single-center retrospective study of patients with lung adenocarcinoma between March 1st, 2013, to April 1st, 2019, at the Second People's Hospital of Taizhou City. All included patients were divided into the VM and no-VM groups according to whether VM was observed or not in the specimen. Vessels with positive PAS and negative CD34 staining were confirmed as VM. The main outcome was progression-free survival (PFS). RESULTS: Sixty-six (50.4%) patients were male. Eighty-one patients received chemotherapy as the first-line treatment, and 50 patients received TKIs. Forty-five (34.4%) patients were confirmed with VM. There was no difference regarding the first-line treatment between the VM and no-VM groups (P = 0.285). The 86 patients without VM had a median PFS of 279 (range, 90-1095) days, and 45 patients with VM had a median PFS of 167 (range, 90-369) days (P < 0.001). T stage (hazard ratio (HR) = 1.37, 95% confidence interval (CI): 1.10-1.71), N stage (HR = 1.43, 95%CI: 1.09-1.86), M stage (HR = 2.85, 95%CI: 1.76-4.61), differentiation (HR = 1.85, 95%CI: 1.29-2.65), therapy (HR = 0.32, 95%CI: 0.21-0.49), VM (HR = 2.12, 95%CI: 1.33-3.37), and ECOG (HR = 1.41, 95%CI: 1.09-1.84) were independently associated with PFS. CONCLUSION: The benefits of first-line TKIs for NSCLC with EGFR mutation are possibly better than those of platinum-based regimens in patients without VM, but there is no difference in the benefit of chemotherapy or target therapy for VM-positive NSCLC harboring EGFR mutations.

摘要

背景:血管拟态(VM)与癌症的预后有关。本研究旨在探讨肺腺癌患者中 VM 与抗癌治疗反应之间的关系。

方法:这是一项单中心回顾性研究,纳入了 2013 年 3 月 1 日至 2019 年 4 月 1 日期间在泰州市第二人民医院就诊的肺腺癌患者。所有纳入的患者根据标本中是否观察到 VM 将其分为 VM 组和非 VM 组。阳性 PAS 和阴性 CD34 染色的血管被确认为 VM。主要结局是无进展生存期(PFS)。

结果:66(50.4%)名患者为男性。81 名患者接受化疗作为一线治疗,50 名患者接受 TKI 治疗。45(34.4%)名患者被证实存在 VM。VM 组和非 VM 组的一线治疗无差异(P=0.285)。86 名无 VM 的患者的中位 PFS 为 279(范围,90-1095)天,45 名有 VM 的患者的中位 PFS 为 167(范围,90-369)天(P<0.001)。T 分期(危险比(HR)=1.37,95%置信区间(CI):1.10-1.71)、N 分期(HR=1.43,95%CI:1.09-1.86)、M 分期(HR=2.85,95%CI:1.76-4.61)、分化程度(HR=1.85,95%CI:1.29-2.65)、治疗方式(HR=0.32,95%CI:0.21-0.49)、VM(HR=2.12,95%CI:1.33-3.37)和 ECOG(HR=1.41,95%CI:1.09-1.84)与 PFS 独立相关。

结论:在无 VM 的患者中,EGFR 突变的非小细胞肺癌一线 TKI 治疗的获益可能优于铂类方案,而在 EGFR 突变的 VM 阳性 NSCLC 患者中,化疗或靶向治疗的获益无差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/1ac69fb54632/12885_2021_7863_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/ebc6f0292505/12885_2021_7863_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/7b774029fa33/12885_2021_7863_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/45dec6a30f9a/12885_2021_7863_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/b31bf13b8c27/12885_2021_7863_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/1ac69fb54632/12885_2021_7863_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/ebc6f0292505/12885_2021_7863_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/7b774029fa33/12885_2021_7863_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/45dec6a30f9a/12885_2021_7863_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/b31bf13b8c27/12885_2021_7863_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/7866877/1ac69fb54632/12885_2021_7863_Fig5_HTML.jpg

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引用本文的文献

[1]
Vasculogenic mimicry in non-small cell lung cancer: a systematic review.

Front Oncol. 2025-7-25

[2]
A novel vasculogenic mimicry-related nomogram predicts prognosis in hepatocellular carcinoma.

Front Genet. 2025-7-7

[3]
Engineered in vivo and in vitro tumor model recapitulates vasculogenic mimicry signatures in melanoma.

Bioeng Transl Med. 2024-1-27

[4]
Acidosis promotes the metastatic colonization of lung cancer via remodeling of the extracellular matrix and vasculogenic mimicry.

Int J Oncol. 2023-12

[5]
Relationship between the expression of ARHGAP25 and RhoA in non-small cell lung cancer and vasculogenic mimicry.

BMC Pulm Med. 2022-10-7

[6]
Recent Progress in Second Near-Infrared (NIR-II) Fluorescence Imaging in Cancer.

Biomolecules. 2022-7-28

本文引用的文献

[1]
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BMC Cancer. 2020-9-14

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BMB Rep. 2020-6

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Front Oncol. 2019-10-11

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