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治疗前血清血管内皮生长因子(VEGF)水平较高与小细胞肺癌的不良预后相关。

High pre-treatment serum level of vascular endothelial growth factor (VEGF) is associated with poor outcome in small-cell lung cancer.

作者信息

Salven P, Ruotsalainen T, Mattson K, Joensuu H

机构信息

Department of Oncology, Helsinki University Central Hospital, Finland.

出版信息

Int J Cancer. 1998 Apr 17;79(2):144-6. doi: 10.1002/(sici)1097-0215(19980417)79:2<144::aid-ijc8>3.0.co;2-t.

DOI:10.1002/(sici)1097-0215(19980417)79:2<144::aid-ijc8>3.0.co;2-t
PMID:9583728
Abstract

Vascular endothelial growth factor (VEGF) is an important regulator of angiogenesis and vascular permeability. Increased serum VEGF concentrations (S-VEGF) have been found in patients with various types of human cancer, including cancer of the lung. However, the clinical and prognostic significance of S-VEGF in cancer is unknown. We measured S-VEGF, using enzyme-linked immunosorbent assay, in sera taken from 68 untreated patients with small-cell lung cancer (SCLC) at the time of diagnosis. The patients were treated with 6 cycles of cisplatin and etoposide, and were randomly assigned to receive recombinant interferon, leukocyte interferon or neither. S-VEGF ranged from 70 to 1738 pg/ml (mean, 527 pg/ml). The patients who achieved partial or complete response to treatment had lower pre-treatment S-VEGF than the non-responding patients (p = 0.0083, Mann-Whitney test). High (>527 pg/ml) S-VEGF was associated with poor survival (p = 0.012, Log Rank Test), and all 3-year survivors had lower than mean pre-treatment S-VEGF. In a multivariate analysis, S-VEGF and stage were the only independent prognostic factors, and the estimated 3-year survival of the patients with limited stage disease and low pretreatment S-VEGF (n = 17, 25% of all patients) was 41% (p = 0.0055, log rank test). These data show that high pretreatment S-VEGF is associated with poor response to treatment and unfavourable survival in patients with SCLC treated with combination chemotherapy with or without interferon.

摘要

血管内皮生长因子(VEGF)是血管生成和血管通透性的重要调节因子。在包括肺癌在内的各类人类癌症患者中,均发现血清VEGF浓度(S-VEGF)升高。然而,S-VEGF在癌症中的临床和预后意义尚不清楚。我们采用酶联免疫吸附测定法,对68例未经治疗的小细胞肺癌(SCLC)患者诊断时采集的血清进行了S-VEGF检测。患者接受了6个周期的顺铂和依托泊苷治疗,并被随机分配接受重组干扰素、白细胞干扰素治疗或不接受任何治疗。S-VEGF范围为70至1738 pg/ml(均值为527 pg/ml)。治疗取得部分或完全缓解的患者,其治疗前S-VEGF低于未缓解患者(曼-惠特尼检验,p = 0.0083)。高S-VEGF(>527 pg/ml)与生存率低相关(对数秩检验,p = 0.012),所有3年幸存者的治疗前S-VEGF均低于均值。多因素分析显示,S-VEGF和分期是仅有的独立预后因素,局限期疾病且治疗前S-VEGF低的患者(n = 17,占所有患者的25%)的估计3年生存率为41%(对数秩检验,p = 0.0055)。这些数据表明,对于接受联合化疗(无论是否使用干扰素)治疗的SCLC患者,治疗前高S-VEGF与治疗反应差和生存不良相关。

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