Detection of circulating tumor cells in patients with locally advanced rectal cancer undergoing neoadjuvant therapy followed by curative surgery

被引:41
|
作者
Magni, Elena [1 ]
Botteri, Edoardo [2 ]
Ravenda, Paola S. [1 ]
Cassatella, Maria C. [4 ]
Bertani, Emilio [3 ]
Chiappa, Antonio [3 ]
Luca, Fabrizio [3 ]
Zorzino, Laura [4 ]
Bianchi, Paolo Pietro [3 ]
Adamoli, Laura [5 ]
Sandri, Maria T. [4 ]
Zampino, Maria G. [1 ]
机构
[1] European Inst Oncol, Gastrointestinal & Neuroendocrine Tumors Unit, I-20141 Milan, Italy
[2] European Inst Oncol, Epidemiol & Biostat Dept, I-20141 Milan, Italy
[3] European Inst Oncol, Dept Surg, I-20141 Milan, Italy
[4] European Inst Oncol, Lab Unit, I-20141 Milan, Italy
[5] European Inst Oncol, Data Management Off, I-20141 Milan, Italy
关键词
Locally advanced rectal cancer; Circulating tumor cells; Prognostic factors; Neoadjuvant chemoradiotherapy; RESISTANT PROSTATE-CANCER; SURVIVAL; PROGRESSION;
D O I
10.1007/s00384-014-1958-z
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Circulating tumor cells (CTCs) represent an independent prognostic factor in metastatic colorectal cancer, while their significance in early stages is still an open issue. The aim of the study is to investigate the role of CTCs in rectal cancer patients undergoing neoadjuvant chemoradiotherapy (CT-RT). In this prospective single institutional study, cT3-4 and/or N+ rectal cancer was treated with neoadjuvant CT-RT. The primary endpoints were as follows: evaluation of CTCs at baseline (t0), after CT-RT (t1), within 7 days after surgery (t2), and at 6 months from surgery (t3) and correlation with main patient/tumor characteristics, CEA, response to neoadjuvant therapy, and disease-free survival (DFS). CTCs were enumerated with the CellSearch System in 22.5 ml peripheral blood. A repeated measure analysis for binary outcome was used to evaluate over time changes in the percentage of CTCs detectable in blood samples. Of the 90 patients enrolled in this study, 85 were eligible consisting of 52 males and 33 females. Median age was 63 years and median follow-up was 38 months. CTCs were available for all patients at t0, for 67 at t1, for 68 at t2, and for 62 at t3. CTCs > 0 were reported on 16 (19 %) at t0, on 5 (7.5 %) at t1, on 6 (9 %) at t2, and on 3 (5 %) at t3 (P value for trend 0.039). Only for CT-RT responders, CTCs reduced from t0 to t1. No statistically significant association was found between CTCs and main patient/tumor characteristics and DFS. Sixteen patients (19 %) had CTCs a parts per thousand yen1 at t0 with reduction in CTC number in case of objective remissions. The proportion of patients with CTCs a parts per thousand yen1 decreased over the time as the therapeutic course proceeded. Much effort should be oriented toward increasing CTC detection rate by enhancing technical tests and achieving better patient characterization.
引用
收藏
页码:1053 / 1059
页数:7
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