Cytokeratin 20 positive circulating tumor cells are a marker for response after neoadjuvant chemoradiation but not for prognosis in patients with rectal cancer

被引:37
|
作者
Hinz, Sebastian [1 ]
Roeder, Christian [2 ]
Tepel, Juergen [3 ]
Hendricks, Alexander [1 ]
Schafmayer, Clemens [1 ]
Becker, Thomas [1 ]
Kalthoff, Holger [2 ]
机构
[1] Univ Hosp Schleswig Holstein, Dept Gen & Thorac Surg, D-24105 Kiel, Germany
[2] Univ Hosp Schleswig Holstein, Inst Expt Canc Res, Canc Ctr North, Div Mol Oncol, D-24105 Kiel, Germany
[3] Klinikum Osnabruck, Clin Gen Thorac & Visceral Surg, D-49076 Osnabruck, Germany
来源
BMC CANCER | 2015年 / 15卷
关键词
Rectal cancer therapy; Circulating tumor cells; CK20; RT-PCR; Response to chemoradiation; POSTOPERATIVE CHEMORADIOTHERAPY; BONE-MARROW; MUTATIONS; STAGE; BLOOD;
D O I
10.1186/s12885-015-1989-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Several studies have shown, that circulating tumor cells (CTC) have a negative prognostic value in colorectal cancer patients. Aim of this study was to evaluate the role of CTC in specifically rectal cancer patients regarding the influence on overall survival and to elucidate the impact of CTC in predicting response after chemoradiation (RCTX). Methods: In this prospective monocentric study 267 patients with rectal cancer were included. Patients with locally advanced tumors were treated with RCTX followed by surgery. The primary endpoints were: Evaluation of CTC at the time of surgery and correlation with main tumor characteristics, response to neoadjuvant RCTX and overall survival (OS). CTC were detected in the blood using CK20 RT-PCR. esults: Sixty-three patients were treated with neoadjuvant RCTX. In 46.8 % of the patients receiving neoadjuvant RCTX CTC were detected, which was significantly higher than in the group without RCTX (p = 0.002). Histopathologic regression after RCTX was evident in 27.8 % of the patients. In the subgroup of responders after RCTX we found CTC at a significantly lower rate than in non- responders (p = 0.03). No significant association was found between CTC detection and tumor characteristics and OS. The OS was significantly improved for responders compared to non- responders (p = 0.007). Conclusions: Responders after neoadjuvant RCTX had a lower incidence of CTC compared to non- responders, which might be a result of effective systemic and local treatment prior to surgery. Interestingly, detection of CTC did not correlate with tumor stage and OS, which is in contrast to previous reports of patients with colon cancer.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Distribution of Residual Cancer Cells in the Bowel Wall After Neoadjuvant Chemoradiation in Patients With Rectal Cancer
    Duldulao, Marjun P.
    Lee, Wendy
    Streja, Leanne
    Chu, Peiguo
    Li, Wenyan
    Chen, Zhenbin
    Kim, Joseph
    Garcia-Aguilar, Julio
    DISEASES OF THE COLON & RECTUM, 2013, 56 (02) : 142 - 149
  • [22] Cytokeratin 20 positive cells in blood of colorectal cancer patients as an unfavorable prognostic marker
    Kust, Davor
    Samija, Ivan
    Kirac, Iva
    Radic, Jasna
    Kovacevic, Dujo
    Kusic, Zvonko
    ACTA CLINICA BELGICA, 2016, 71 (04) : 235 - 243
  • [23] Tumor Volume Predicts for Pathologic Complete Response in Rectal Cancer Patients Treated With Neoadjuvant Chemoradiation
    Yang, Fan
    Hill, Jordan
    Abraham, Aswin
    Ghosh, Sunita
    Steed, Tanner
    Kurtz, Clay
    Joseph, Kurian
    Yun, Jihyun
    Warkentin, Brad
    Thai, JoAnn
    Nijjar, Tirath
    Severin, Diane
    Tankel, Keith
    Fairchild, Alysa
    Usmani, Nawaid
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2022, 45 (10): : 405 - 409
  • [24] Tumor Volume Predicts for Pathological Complete Response in Rectal Cancer Patients Treated With Neoadjuvant Chemoradiation
    Hill, J.
    Yang, F.
    Abraham, A.
    Ghosh, S.
    Steed, T. M.
    Kurtz, C.
    Joseph, K. J.
    Yun, J.
    Nijjar, T.
    Severin, D. M.
    Tankel, K.
    Fairchild, A. M.
    Usmani, N. H.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2021, 111 (03): : E44 - E44
  • [25] Nodal Disease in Rectal Cancer Patients With Complete Tumor Response After Neoadjuvant Chemoradiation: Danger Below Calm Waters
    Baucom, Rebeccah B.
    Maguire, Lillias H.
    Kavalukas, Sandra L.
    Geiger, Timothy M.
    Ford, Molly M.
    Muldoon, Roberta L.
    Hopkins, M. Benjamin
    Hawkins, Alexander T.
    DISEASES OF THE COLON & RECTUM, 2017, 60 (12) : 1260 - 1266
  • [26] Predictive factors of tumour response after neoadjuvant chemoradiation for rectal cancer
    Lopez Campos, F.
    Hervas, A.
    De la Pinta, C.
    Dominguez, J. A.
    Fernandez, E.
    Martin, M.
    RADIOTHERAPY AND ONCOLOGY, 2016, 119 : S604 - S604
  • [27] Complete Clinical Response after Neoadjuvant Chemoradiation for Distal Rectal Cancer
    Habr-Gama, Angelita
    Perez, Rodrigo
    Proscurshim, Igor
    Gama-Rodrigues, Joaquim
    SURGICAL ONCOLOGY CLINICS OF NORTH AMERICA, 2010, 19 (04) : 829 - +
  • [28] Microsatellite instability as a predictive marker for response to neoadjuvant chemoradiation in locally advanced rectal cancer
    Shulman, Rebecca Maria
    Avkshtol, Vladimir
    DeMora, Lyudmila
    Esnaola, Nestor F.
    Hall, Michael J.
    Handorf, Elizabeth
    Meyer, Joshua E.
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (04)
  • [29] Cytokeratin-20 as a Marker for Detection of Circulating Tumor Cells in Preoperative and Postoperative Blood Samples from Colorectal Cancer Patients
    Samija, I.
    Lukac, J.
    Koncar-Mubrin, M.
    Kirac, I.
    Kovacevic, D.
    Kusic, Z.
    EUROPEAN JOURNAL OF CANCER, 2012, 48 : S178 - S178
  • [30] Circulating cytokeratin-positive cells and tumor budding in colorectal cancer
    Maerkl, Bruno
    Wilhelms, Narjes
    Anthuber, Matthias
    Schenkirsch, Gerhard
    Schlimok, Guenter
    Oruzio, Daniel
    WORLD JOURNAL OF CLINICAL ONCOLOGY, 2016, 7 (06): : 433 - 440