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Systematic review of tumour budding and association with common mutations in patients with colorectal cancer
[Display omitted] •Meta-analysis evaluated relationship between mutated KRAS/BRAF or MSI tumour and tumour budding in colorectal cancer patients.•17 potential studies were included in this review.•Mutated KRAS and MSS/pMMR tumour significantly associated with high-grade budding phenotype. Despite a...
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Published in: | Critical reviews in oncology/hematology 2021-11, Vol.167, p.103490-103490, Article 103490 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Meta-analysis evaluated relationship between mutated KRAS/BRAF or MSI tumour and tumour budding in colorectal cancer patients.•17 potential studies were included in this review.•Mutated KRAS and MSS/pMMR tumour significantly associated with high-grade budding phenotype.
Despite a well-known prognostic role in colorectal cancer, the genomic profiling of tumour budding remains to be elucidated. We aim to review the association of common mutations with tumour budding.
A systematic review of studies relating to tumour budding and genetic mutation in CRC was performed. The relationship between mutational status and tumour budding was evaluated using meta-analysis.
A total of 6153 patients from 17 articles were included. According to the meta-analysis, high-grade tumour budding was significantly associated with KRAS mutation (OR = 1.52, 95 %CI: 1.13–2.02, P = 0.005) and MSS/pMMR (OR = 2.06, 95 %CI: 1.42–2.97, P = 0.0001).
The significant association between high-grade tumour budding and mutated KRAS or MSS/pMMR may suggest a role of these mutations in the development of the tumour budding phenotype and be useful for stratifying patient outcome in CRC. |
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ISSN: | 1040-8428 1879-0461 |
DOI: | 10.1016/j.critrevonc.2021.103490 |