Molecularly determined total tumour load in lymph nodes of stage I–II colon cancer patients correlates with high-risk factors. A multicentre prospective study

dc.contributor.author
Aldecoa, Iban
dc.contributor.author
Atares, Begoña
dc.contributor.author
Tarragona Foradada, Jordi
dc.contributor.author
Bernet, Laia
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Sardon, Jose Domingo
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Pereda, Teresa
dc.contributor.author
Villar, Carlos
dc.contributor.author
Mendez, M. Carmen
dc.contributor.author
Gonzalez-Obeso, Elvira
dc.contributor.author
Elorriaga, Kepa
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Lopez Alonso, Guadalupe
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Zamora, Javier
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Planell, Nuria
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Palacios, José
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Castells, Antoni
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Matias-Guiu, Xavier
dc.contributor.author
Cuatrecasas, Miriam
dc.date.accessioned
2024-12-05T21:58:25Z
dc.date.available
2024-12-05T21:58:25Z
dc.date.issued
2021-03-19T10:50:14Z
dc.date.issued
2021-03-19T10:50:14Z
dc.date.issued
2016
dc.identifier
https://doi.org/10.1007/s00428-016-1990-1
dc.identifier
0945-6317
dc.identifier
http://hdl.handle.net/10459.1/70811
dc.identifier.uri
http://hdl.handle.net/10459.1/70811
dc.description.abstract
Stage I–II (pN0) colorectal cancer patients are surgically treated although up to 25 % will eventually die from disease recurrence. Lymph node (LN) status is an independent prognostic factor in colorectal cancer (CRC), and molecular tumour detection in LN of early-stage CRC patients is associated with an increased risk of disease recurrence and poor survival. This prospective multicentre study aimed to determine the relationship between LN molecular tumour burden and conventional high-risk factors in stage I–II colon cancer patients. A total of 1940 LN from 149 pathologically assessed pN0 colon cancer patients were analysed for the amount of tumour cytokeratin 19 (CK19) messenger RNA (mRNA) with the quantitative reverse transcription loop-mediated isothermal amplification molecular assay One-Step Nucleic Acid Amplification. Patient’s total tumour load (TTL) resulted from the sum of all CK19 mRNA tumour copies/μL of each positive LN from the colectomy specimen. A median of 15 LN were procured per case (IQR 12;20). Molecular positivity correlated with high-grade (p < 0.01), mucinous/signet ring type (p = 0.017), male gender (p = 0.02), number of collected LN (p = 0.012) and total LN weight per case (p < 0.01). The TTL was related to pT stage (p = 0.01) and tumour size (p < 0.01) in low-grade tumours. Multivariate logistic regression showed independent correlation of molecular positivity with gender, tumour grade and number of fresh LN [AUC = 0.71 (95 % CI = 0.62–0.79)]. Our results show that lymph node CK19 mRNA detection correlates with classical high-risk factors in stage I–II colon cancer patients. Total tumour load is a quantitative and objective measure that may help to better stage early colon cancer patients.
dc.description.abstract
Work supported by the Banc de Tumors-Biobanc Hospital Clinic-IDIBAPS and Xarxa de Bancs de Tumors de Catalunya (XBTC), and by grants from the Fundación Científica de la Asociación Española Contra el Cáncer (GCB13131592CAST), Ministerio de Economía y Competitividad (SAF2014–54,453-R), Agència de Gestió d’Ajuts Universitaris i de Recerca (2014SGR135), and by Sysmex Coorp Spain (Sant Just Desvern, Spain). CIBERehd is funded by the Instituto de Salud Carlos III
dc.language
eng
dc.publisher
Springer
dc.relation
info:eu-repo/grantAgreement/MINECO//SAF2014-54453-R/ES/DETECCION DE MIRNA EN HECES COMO NUEVA ESTRATEGIA DE CRIBADO DEL CANCER COLORRECTAL: IDENTIFICACION Y VALIDACION EN POBLACION DE RIESGO MEDIO/
dc.relation
Reproducció del document publicat a https://doi.org/10.1007/s00428-016-1990-1
dc.relation
Virchows Archiv, 2016, vol. 469, p. 385-394
dc.rights
cc-by (c) Aldecoa et al., 2016
dc.rights
info:eu-repo/semantics/openAccess
dc.rights
http://creativecommons.org/licenses/by/4.0/
dc.subject
Colorectal neoplasms
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Neoplasm staging
dc.subject
Molecular pathology
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Lymph nodes
dc.subject
Cytokeratin 19
dc.title
Molecularly determined total tumour load in lymph nodes of stage I–II colon cancer patients correlates with high-risk factors. A multicentre prospective study
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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