Kawaishi Makoto, Fujiwara Yutaka, Fukui Tomoya, Kato Terufumi, Yamada Kazuhiko, Ohe Yuichiro, Kunitoh Hideo, Sekine Ikuo, Yamamoto Noboru, Nokihara Hiroshi, Watabe Takeshi, Shimoda Yuji, Arao Tokuzo, Nishio Kazuto, Tamura Tomohide, Koizumi Fumiaki
Shien-Lab, National Cancer Center Hospital, Tokyo, Japan.
J Thorac Oncol. 2009 Feb;4(2):208-13. doi: 10.1097/JTO.0b013e318193030d.
Circulating endothelial cells (CECs) increase in cancer patients and play an important role in tumor neovascularization.
This study was designed to investigate the role of CEC as a marker for predicting the effectiveness of a carboplatin plus paclitaxel based first line chemotherapy in advanced non-small cell lung cancer (NSCLC).
The CEC count in 4 ml of peripheral blood before starting chemotherapy (baseline value) was significantly higher in NSCLC patients, ranging from 32 to 4501/4 ml (n = 31, mean +/- SD = 595 +/- 832), than in healthy volunteers (n = 53, 46.2 +/- 86.3). We did not detect a significant correlation between the CEC count and estimated tumor volume. CECs were significantly decreased by chemotherapy as compared with pretreatment values (175.6 +/- 24 and 173.0 +/- 24, day +8, +22, respectively). We investigated the correlation between baseline CEC and the clinical effectiveness of chemotherapy. CEC values are significantly higher in patients with clinical benefit (partial response and stable disease, 516 +/- 458, 870.8 +/- 1215, respectively) than in progressive disease patients (211 +/- 150). Furthermore, a statistically significant decrease in CECs, on day 22, was observed only in patients with partial response. Patients who had a baseline CEC count greater than 400/4 ml showed a longer progression-free survival (>400, 271 days [range: 181-361] versus <400, 34 [range: 81-186], p = 0.019).
CEC is suggested to be a promising predictive marker of the clinical efficacy of the CBDCA plus paclitaxel regimen in patients with NSCLC.
循环内皮细胞(CECs)在癌症患者中数量增加,并在肿瘤新生血管形成中发挥重要作用。
本研究旨在探讨CEC作为预测以卡铂加紫杉醇为基础的一线化疗对晚期非小细胞肺癌(NSCLC)疗效的标志物的作用。
NSCLC患者化疗开始前(基线值)4ml外周血中的CEC计数显著高于健康志愿者(n = 53,46.2±86.3),范围为32至4501/4ml(n = 31,平均±标准差 = 595±832)。我们未检测到CEC计数与估计肿瘤体积之间存在显著相关性。与治疗前值相比,化疗后CECs显著降低(分别在第8天和第22天为175.6±24和173.0±24)。我们研究了基线CEC与化疗临床疗效之间的相关性。有临床获益(部分缓解和疾病稳定,分别为516±458、870.8±1215)的患者的CEC值显著高于疾病进展患者(211±150)。此外,仅在部分缓解的患者中观察到第22天时CECs有统计学意义的下降。基线CEC计数大于400/4ml的患者无进展生存期更长(>400,271天[范围:181 - 361];<400,34天[范围:81 - 186],p = 0.019)。
CEC被认为是NSCLC患者中CBDCA加紫杉醇方案临床疗效的有前景的预测标志物。