CEA, CA19-9, circulating DNA and circulating tumour cell kinetics in patients treated for metastatic colorectal cancer (mCRC)

Background We previously reported that CEA kinetics are a marker of progressive disease (PD) in metastatic colorectal cancer (mCRC). This study was specifically designed to confirm CEA kinetics for predicting PD and to evaluate CA19-9, cell-free DNA (cfDNA), circulating tumour DNA (ctDNA) and circul...

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Veröffentlicht in:British journal of cancer 2021-08, Vol.125 (5), p.725-733
Hauptverfasser: Sefrioui, David, Beaussire, Ludivine, Gillibert, André, Blanchard, France, Toure, Emmanuel, Bazille, Céline, Perdrix, Anne, Ziegler, Frédéric, Gangloff, Alice, Hassine, Mélanie, Elie, Caroline, Bignon, Anne-Laure, Parzy, Aurélie, Gomez, Philippe, Thill, Caroline, Clatot, Florian, Sabourin, Jean-Christophe, Frebourg, Thierry, Benichou, Jacques, Bouhier-Leporrier, Karine, Gallais, Marie-Pierre, Sarafan-Vasseur, Nasrin, Michel, Pierre, Di Fiore, Frédéric
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Sprache:eng
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Zusammenfassung:Background We previously reported that CEA kinetics are a marker of progressive disease (PD) in metastatic colorectal cancer (mCRC). This study was specifically designed to confirm CEA kinetics for predicting PD and to evaluate CA19-9, cell-free DNA (cfDNA), circulating tumour DNA (ctDNA) and circulating tumour cell (CTC) kinetics. Methods Patients starting a chemotherapy (CT) with pre-treatment CEA > 5 ng/mL and/or CA19.9 > 30 UI/mL were prospectively included. Samples were collected from baseline to cycle 4 for CEA and CA19-9 and at baseline and the sixth week for other markers. CEA kinetics were calculated from the first to the third or fourth CT cycle. Results A total of 192 mCRC patients were included. CEA kinetics based on the previously identified >0.05 threshold was significantly associated with PD ( p  
ISSN:0007-0920
1532-1827
DOI:10.1038/s41416-021-01431-9