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Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer

Optimal selection of high‐risk patients with stage II colon cancer is crucial to ensure clinical benefit of adjuvant chemotherapy. Here, we investigated the prognostic value of genomic intratumor heterogeneity and aneuploidy for disease recurrence. We combined targeted sequencing, SNP arrays, fluore...

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Autores principales: Lahoz, Sara, Archilla, Ivan, Asensio, Elena, Hernández‐Illán, Eva, Ferrer, Queralt, López‐Prades, Sandra, Nadeu, Ferran, Del Rey, Javier, Sanz‐Pamplona, Rebeca, Lozano, Juan José, Castells, Antoni, Cuatrecasas, Miriam, Camps, Jordi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790656/
https://www.ncbi.nlm.nih.gov/pubmed/35066875
http://dx.doi.org/10.1002/path.5870
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author Lahoz, Sara
Archilla, Ivan
Asensio, Elena
Hernández‐Illán, Eva
Ferrer, Queralt
López‐Prades, Sandra
Nadeu, Ferran
Del Rey, Javier
Sanz‐Pamplona, Rebeca
Lozano, Juan José
Castells, Antoni
Cuatrecasas, Miriam
Camps, Jordi
author_facet Lahoz, Sara
Archilla, Ivan
Asensio, Elena
Hernández‐Illán, Eva
Ferrer, Queralt
López‐Prades, Sandra
Nadeu, Ferran
Del Rey, Javier
Sanz‐Pamplona, Rebeca
Lozano, Juan José
Castells, Antoni
Cuatrecasas, Miriam
Camps, Jordi
author_sort Lahoz, Sara
collection PubMed
description Optimal selection of high‐risk patients with stage II colon cancer is crucial to ensure clinical benefit of adjuvant chemotherapy. Here, we investigated the prognostic value of genomic intratumor heterogeneity and aneuploidy for disease recurrence. We combined targeted sequencing, SNP arrays, fluorescence in situ hybridization, and immunohistochemistry on a retrospective cohort of 84 untreated stage II colon cancer patients. We assessed the clonality of copy‐number alterations (CNAs) and mutations, CD8(+) lymphocyte infiltration, and their association with time to recurrence. Prognostic factors were included in machine learning analysis to evaluate their ability to predict individual relapse risk. Tumors from recurrent patients displayed a greater proportion of CNAs compared with non‐recurrent (mean 31.3% versus 23%, respectively; p = 0.014). Furthermore, patients with elevated tumor CNA load exhibited a higher risk of recurrence compared with those with low levels [p = 0.038; hazard ratio (HR) 2.46], which was confirmed in an independent cohort (p = 0.004; HR 3.82). Candidate chromosome‐specific aberrations frequently observed in recurrent cases included gain of the chromosome arm 13q (p = 0.02; HR 2.67) and loss of heterozygosity at 17q22–q24.3 (p = 0.05; HR 2.69). CNA load positively correlated with intratumor heterogeneity (R = 0.52; p < 0.0001). Consistently, incremental subclonal CNAs were associated with an elevated risk of relapse (p = 0.028; HR 2.20), which we did not observe for subclonal single‐nucleotide variants and small insertions and deletions. The clinico‐genomic model rated an area under the curve of 0.83, achieving a 10% incremental gain compared with clinicopathological markers (p = 0.047). In conclusion, tumor aneuploidy and copy‐number intratumor heterogeneity were predictive of poor outcome and improved discriminative performance in early‐stage colon cancer. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
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spelling pubmed-97906562022-12-28 Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer Lahoz, Sara Archilla, Ivan Asensio, Elena Hernández‐Illán, Eva Ferrer, Queralt López‐Prades, Sandra Nadeu, Ferran Del Rey, Javier Sanz‐Pamplona, Rebeca Lozano, Juan José Castells, Antoni Cuatrecasas, Miriam Camps, Jordi J Pathol Original Articles Optimal selection of high‐risk patients with stage II colon cancer is crucial to ensure clinical benefit of adjuvant chemotherapy. Here, we investigated the prognostic value of genomic intratumor heterogeneity and aneuploidy for disease recurrence. We combined targeted sequencing, SNP arrays, fluorescence in situ hybridization, and immunohistochemistry on a retrospective cohort of 84 untreated stage II colon cancer patients. We assessed the clonality of copy‐number alterations (CNAs) and mutations, CD8(+) lymphocyte infiltration, and their association with time to recurrence. Prognostic factors were included in machine learning analysis to evaluate their ability to predict individual relapse risk. Tumors from recurrent patients displayed a greater proportion of CNAs compared with non‐recurrent (mean 31.3% versus 23%, respectively; p = 0.014). Furthermore, patients with elevated tumor CNA load exhibited a higher risk of recurrence compared with those with low levels [p = 0.038; hazard ratio (HR) 2.46], which was confirmed in an independent cohort (p = 0.004; HR 3.82). Candidate chromosome‐specific aberrations frequently observed in recurrent cases included gain of the chromosome arm 13q (p = 0.02; HR 2.67) and loss of heterozygosity at 17q22–q24.3 (p = 0.05; HR 2.69). CNA load positively correlated with intratumor heterogeneity (R = 0.52; p < 0.0001). Consistently, incremental subclonal CNAs were associated with an elevated risk of relapse (p = 0.028; HR 2.20), which we did not observe for subclonal single‐nucleotide variants and small insertions and deletions. The clinico‐genomic model rated an area under the curve of 0.83, achieving a 10% incremental gain compared with clinicopathological markers (p = 0.047). In conclusion, tumor aneuploidy and copy‐number intratumor heterogeneity were predictive of poor outcome and improved discriminative performance in early‐stage colon cancer. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2022-04-06 2022-05 /pmc/articles/PMC9790656/ /pubmed/35066875 http://dx.doi.org/10.1002/path.5870 Text en © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Lahoz, Sara
Archilla, Ivan
Asensio, Elena
Hernández‐Illán, Eva
Ferrer, Queralt
López‐Prades, Sandra
Nadeu, Ferran
Del Rey, Javier
Sanz‐Pamplona, Rebeca
Lozano, Juan José
Castells, Antoni
Cuatrecasas, Miriam
Camps, Jordi
Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer
title Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer
title_full Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer
title_fullStr Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer
title_full_unstemmed Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer
title_short Copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage II colon cancer
title_sort copy‐number intratumor heterogeneity increases the risk of relapse in chemotherapy‐naive stage ii colon cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790656/
https://www.ncbi.nlm.nih.gov/pubmed/35066875
http://dx.doi.org/10.1002/path.5870
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