TY - JOUR
T1 - Circulating tumour cell analysis as an early marker for relapse in stage II and III colorectal cancer patients
T2 - A pilot study
AU - Garrigós, Noemi
AU - Gallego, Javier
AU - Guillén-Ponce, Carmen
AU - Guaraz, Patricia
AU - García-Bautista, Miriam
AU - Castillejo, Adela
AU - Gómez-Martínez, Ángeles
AU - Carrato, Alfredo
AU - Rodríguez-Lescure, Álvaro
AU - Soto, José L.
N1 - Funding Information:
Acknowledgements We are indebted to the patients for their co-operation. This work was supported by grants from the Instituto de Salud Carlos III (FIS: PI021118) and Generalitat Valenciana (CTDIB/2002/128 and SP0026/2005). Dr. Soto was granted a fellowship from the Fundación Científica, Asociación Española contra el Cáncer (AECC). The authors thank Diego Torres for his helpful advice on statistics.
PY - 2010/2
Y1 - 2010/2
N2 - Introduction Recent studies have identified both the prognostic and predictive utility of determining the number of circulating tumour cells (CTC) in patients with solid cancers. Material and methods In the present pilot study we evaluated the ability of two different methods to isolate CTC in combination with two strategies to enumerate CTC from patients with stages II and III surgically treated colorectal cancer (CRC). First, we used two systems for tumour cell enrichment (differential centrifugation and immunomagnetic beads), combined with two methods to enumerate CTC (real-time PCR and flow cytometry), to determine the most efficient combination. These experiments were performed in a model system using serial dilutions of HT29 tumour cell lines with lymphocytes. Then, CTC analysis using the technical approach selected before was performed in 109 blood samples from 16 stage II and III CRC patients during chemotherapy treatment and follow-up. Results Immunomagnetic beads followed by flow cytometry was the most efficient combination (ED=60.53; p=0.5). Two cases out of 16 patients analysed had clinical tumour relapse. In both, we detected a significant increase of CTC five and six months, respectively, before the relapse was clinically evidenced. An increase of CTC was also observed in another case without clinical evidence of relapse. The remaining cases (13) had very few or no detectable CTC and no clinical evidence of relapse (p=0.029). Conclusions Changes in CTC numbers during follow-up might predict tumour relapse. Further evaluation of CTC prognostic and predictive value in patients with early CRC is warranted.
AB - Introduction Recent studies have identified both the prognostic and predictive utility of determining the number of circulating tumour cells (CTC) in patients with solid cancers. Material and methods In the present pilot study we evaluated the ability of two different methods to isolate CTC in combination with two strategies to enumerate CTC from patients with stages II and III surgically treated colorectal cancer (CRC). First, we used two systems for tumour cell enrichment (differential centrifugation and immunomagnetic beads), combined with two methods to enumerate CTC (real-time PCR and flow cytometry), to determine the most efficient combination. These experiments were performed in a model system using serial dilutions of HT29 tumour cell lines with lymphocytes. Then, CTC analysis using the technical approach selected before was performed in 109 blood samples from 16 stage II and III CRC patients during chemotherapy treatment and follow-up. Results Immunomagnetic beads followed by flow cytometry was the most efficient combination (ED=60.53; p=0.5). Two cases out of 16 patients analysed had clinical tumour relapse. In both, we detected a significant increase of CTC five and six months, respectively, before the relapse was clinically evidenced. An increase of CTC was also observed in another case without clinical evidence of relapse. The remaining cases (13) had very few or no detectable CTC and no clinical evidence of relapse (p=0.029). Conclusions Changes in CTC numbers during follow-up might predict tumour relapse. Further evaluation of CTC prognostic and predictive value in patients with early CRC is warranted.
KW - Circulating tumour cells
KW - Early colorectal cancer
KW - Prognostic markers
UR - http://www.scopus.com/inward/record.url?scp=77951641767&partnerID=8YFLogxK
U2 - 10.1007/S12094-010-0479-7
DO - 10.1007/S12094-010-0479-7
M3 - Artículo
C2 - 20156783
AN - SCOPUS:77951641767
SN - 1699-048X
VL - 12
SP - 142
EP - 147
JO - Clinical and Translational Oncology
JF - Clinical and Translational Oncology
IS - 2
ER -