TY - JOUR
T1 - Cribriform colon cancer
T2 - A morphological growth pattern associated with extramural venous invasion, nodal metastases and microsatellite stability
AU - Taylor, Alexander S.
AU - Liu, Natalia
AU - Fang, Jiayun M.
AU - Panarelli, Nicole
AU - Zhao, Lili
AU - Cheng, Jerome
AU - Gopal, Purva
AU - Hammer, Suntrea
AU - Sun, Jing
AU - Appelman, Henry
AU - Westerhoff, Maria
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2021
Y1 - 2021
N2 - Background: Cribriform comedo-type adenocarcinoma was a colon cancer subtype recognised in the previous WHO classification of tumours that is no longer included in the recent edition. Previous reports have described colon cancers with cribriform growth as having worse overall survival and being associated with microsatellite stability. We sought to validate whether cribriform carcinoma (CC) is a distinct morphological subtype with clinical relevance in the context of modern colon cancer diagnosis. Methods: Consecutive cases of non-neoadjuvantly treated colon cancer resections were identified (n=177) and reviewed to evaluate for CC and other histopathological and clinical features. CC was defined as solid nests of cancer with round, € punched out' spaces and intraluminal bridges, reminiscent of ductal carcinoma in situ of the breast. Results: CC was present in 18.6% of the consecutive case cohort. Compared with all other cases, CC was associated with positive lymph nodes, increased depth of invasion, extramural venous involvement (EMVI), and microsatellite stability, and was less likely to have tumour infiltrating lymphocytes (p<0.05). In contrast to previous reports, we did not find significantly worse overall, disease-specific or recurrence-free survival for CC. Morphological features mimicking CC occurred in 33.3% of all other colon cancer cases. Conclusion: Identifying CC may be useful due to its association with worse stage at presentation and EMVI, but given that cribriform-like appearance may be found in many colon cancer cases and that we did not find a survival difference for CC, CC may not necessitate its own subtype classification.
AB - Background: Cribriform comedo-type adenocarcinoma was a colon cancer subtype recognised in the previous WHO classification of tumours that is no longer included in the recent edition. Previous reports have described colon cancers with cribriform growth as having worse overall survival and being associated with microsatellite stability. We sought to validate whether cribriform carcinoma (CC) is a distinct morphological subtype with clinical relevance in the context of modern colon cancer diagnosis. Methods: Consecutive cases of non-neoadjuvantly treated colon cancer resections were identified (n=177) and reviewed to evaluate for CC and other histopathological and clinical features. CC was defined as solid nests of cancer with round, € punched out' spaces and intraluminal bridges, reminiscent of ductal carcinoma in situ of the breast. Results: CC was present in 18.6% of the consecutive case cohort. Compared with all other cases, CC was associated with positive lymph nodes, increased depth of invasion, extramural venous involvement (EMVI), and microsatellite stability, and was less likely to have tumour infiltrating lymphocytes (p<0.05). In contrast to previous reports, we did not find significantly worse overall, disease-specific or recurrence-free survival for CC. Morphological features mimicking CC occurred in 33.3% of all other colon cancer cases. Conclusion: Identifying CC may be useful due to its association with worse stage at presentation and EMVI, but given that cribriform-like appearance may be found in many colon cancer cases and that we did not find a survival difference for CC, CC may not necessitate its own subtype classification.
KW - colon
KW - colorectal neoplasms
KW - gastrointestinal neoplasms
KW - molecular
KW - pathology
KW - pathology
KW - surgical
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U2 - 10.1136/jclinpath-2021-207485
DO - 10.1136/jclinpath-2021-207485
M3 - Article
C2 - 33782192
AN - SCOPUS:85103501424
SN - 0021-9746
JO - Molecular pathology : MP
JF - Molecular pathology : MP
M1 - 207485
ER -