Liquid biopsy has become a useful alternative in metastatic colorectal cancer (mCRC) patients when tissue biopsy of metastatic sites is not feasible. In this study we aimed to investigate the clinical utility of circulating exosomes DNA in the management of mCRC patients. Exosomes level and KRAS mutational status in exosomal DNA was assesed in 70 mCRC patients and 29 CRC primary tumor and were analysed at different disease steps evaluating serial blood samples (240 blood samples). There was a significant correlation between the extension of disease and exosomes level and the resection of primary localized tumor was correlated with a decrease of KRAS G12V/ D copies and fractional abundance in metastatic disease. CEA expression and liver metastasis correlated with a higher number of KRAS G12V/D copies/ml and a higher fractional abundance; in the subgroup of mCRC patients eligible for surgery, the size of tumor and the radiological response were related to exosomes level but only the size was related to the number of KRAS WT copies; both KRAS wild-type and mutated levels were identified as a prognostic factor related to OS. Finally, we found that 91% of mutated mCRC patients became wild type after the first line chemotherapy but this status reverted in mutated one at progression in 80% of cases. In a prospective cohort of mCRC patients, we show how longitudinal monitoring using exosome-based liquid biopsy provides clinical information relevant to therapeutic stratification.

Lucchetti, D., Zurlo, I. V., Colella, F., Ricciardi-Tenore, C., Di Salvatore, M., Tortora, G., De Maria, R., Giuliante, F., Cassano, A., Basso, M., Crucitti, A., Laurenzana, I., Artemi, G., Sgambato, A., Mutational status of plasma exosomal KRAS predicts outcome in patients with metastatic colorectal cancer, <<SCIENTIFIC REPORTS>>, 2021; 11 (1): 22686-N/A. [doi:10.1038/s41598-021-01668-7] [http://hdl.handle.net/10807/205535]

Mutational status of plasma exosomal KRAS predicts outcome in patients with metastatic colorectal cancer

Lucchetti, D.;Zurlo, I. V.;Colella, F.;Di Salvatore, M.;Tortora, G.;Giuliante, F.;Crucitti, A.;Artemi, G.;Sgambato, A.
2021

Abstract

Liquid biopsy has become a useful alternative in metastatic colorectal cancer (mCRC) patients when tissue biopsy of metastatic sites is not feasible. In this study we aimed to investigate the clinical utility of circulating exosomes DNA in the management of mCRC patients. Exosomes level and KRAS mutational status in exosomal DNA was assesed in 70 mCRC patients and 29 CRC primary tumor and were analysed at different disease steps evaluating serial blood samples (240 blood samples). There was a significant correlation between the extension of disease and exosomes level and the resection of primary localized tumor was correlated with a decrease of KRAS G12V/ D copies and fractional abundance in metastatic disease. CEA expression and liver metastasis correlated with a higher number of KRAS G12V/D copies/ml and a higher fractional abundance; in the subgroup of mCRC patients eligible for surgery, the size of tumor and the radiological response were related to exosomes level but only the size was related to the number of KRAS WT copies; both KRAS wild-type and mutated levels were identified as a prognostic factor related to OS. Finally, we found that 91% of mutated mCRC patients became wild type after the first line chemotherapy but this status reverted in mutated one at progression in 80% of cases. In a prospective cohort of mCRC patients, we show how longitudinal monitoring using exosome-based liquid biopsy provides clinical information relevant to therapeutic stratification.
Inglese
Lucchetti, D., Zurlo, I. V., Colella, F., Ricciardi-Tenore, C., Di Salvatore, M., Tortora, G., De Maria, R., Giuliante, F., Cassano, A., Basso, M., Crucitti, A., Laurenzana, I., Artemi, G., Sgambato, A., Mutational status of plasma exosomal KRAS predicts outcome in patients with metastatic colorectal cancer, <<SCIENTIFIC REPORTS>>, 2021; 11 (1): 22686-N/A. [doi:10.1038/s41598-021-01668-7] [http://hdl.handle.net/10807/205535]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/205535
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