Pachmann Katharina, Camara Oumar, Kavallaris Andreas, Krauspe Sabine, Malarski Nele, Gajda Mieczyslaw, Kroll Torsten, Jörke Cornelia, Hammer Ulrike, Altendorf-Hofmann Annelore, Rabenstein Carola, Pachmann Ulrich, Runnebaum Ingo, Höffken Klaus
Department of Experimental Hematology and Oncology, Clinic for Internal Medicine II, Friedrich Schiller Universität Jena, Erlanger Allee 101, D-07747, Jena, Germany.
J Clin Oncol. 2008 Mar 10;26(8):1208-15. doi: 10.1200/JCO.2007.13.6523.
To demonstrate that it is possible to monitor the response to adjuvant therapy by repeated analysis of circulating epithelial tumor cells (CETCs) and to detect patients early who are at risk of relapse.
In 91 nonmetastatic primary breast cancer patients, CETCs were quantified using laser scanning cytometry of anti-epithelial cell adhesion molecule-stained epithelial cells from whole unseparated blood before and during adjuvant chemotherapy.
Numbers of CETCs were analyzed before therapy, before each new cycle, and at the end of chemotherapy. The following three typical patterns of response were observed: (1) decrease in cell numbers (> 10-fold); (2) marginal changes in cell numbers (< 10-fold); and (3) an (sometimes saw-toothed) increase or an initial decrease with subsequent reincrease (> 10-fold) in numbers of CETCs. Twenty relapses (22%) were observed within the accrual time of 40 months, including one of 28 patients from response group 1, five of 30 patients from response group 2, and 14 of 33 patients from response group 3. The difference in relapse-free survival was highly significant for CETC (hazard ratio = 4.407; 95% CI, 1.739 to 9.418; P < .001) between patients with decreasing cell numbers and those with marginal changes and between patients with marginal changes and those with an increase of more than 10-fold (linear Cox regression model).
These results show that peripherally circulating tumor cells are influenced by systemic chemotherapy and that an increase (even after initial response to therapy) of 10-fold or more at the end of therapy is a strong predictor of relapse and a surrogate marker for the aggressiveness of the tumor cells.
通过反复分析循环上皮肿瘤细胞(CETC)来证明监测辅助治疗反应以及早期发现有复发风险患者的可能性。
对91例非转移性原发性乳腺癌患者,在辅助化疗前及化疗期间,采用激光扫描细胞术对抗上皮细胞黏附分子染色的全血中未分离的上皮细胞进行CETC定量分析。
在治疗前、每个新周期前以及化疗结束时分析CETC数量。观察到以下三种典型的反应模式:(1)细胞数量减少(>10倍);(2)细胞数量有微小变化(<10倍);(3)CETC数量增加(有时呈锯齿状)或先减少后再增加(>10倍)。在40个月的观察期内观察到20例复发(22%),包括反应组1的28例患者中的1例、反应组2的30例患者中的5例以及反应组3的33例患者中的14例。细胞数量减少的患者与细胞数量有微小变化的患者之间以及细胞数量有微小变化的患者与细胞数量增加超过10倍的患者之间,无复发生存率差异具有高度统计学意义(风险比=4.407;95%可信区间,1.739至9.418;P<.001)(线性Cox回归模型)。
这些结果表明外周循环肿瘤细胞受全身化疗影响,治疗结束时细胞数量增加10倍或更多(即使在对治疗有初始反应之后)是复发的有力预测指标以及肿瘤细胞侵袭性的替代标志物。