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Prognostic and Predictive Value of Tumor Budding in Colorectal Cancer.
Mitrovic, Bojana; Handley, Kelly; Assarzadegan, Naziheh; Chang, Hector Li; Dawson, Heather A E; Grin, Andrea; Hutchins, Gordon G A; Magill, Laura; Quirke, Philip; Riddell, Robert H; Gray, Richard G; Kirsch, Richard.
Afiliação
  • Mitrovic B; Department of Pathology and Laboratory Medicine, Health Sciences North, Sudbury, ON, Canada; University of Toronto, Toronto, Canada. Electronic address: bojana.mitrovic@utoronto.ca.
  • Handley K; Birmingham Clinical Trials Unit, Birmingham, United Kingdom.
  • Assarzadegan N; University of Toronto, Toronto, Canada.
  • Chang HL; University of Toronto, Toronto, Canada.
  • Dawson HAE; University of Toronto, Toronto, Canada.
  • Grin A; University of Toronto, Toronto, Canada.
  • Hutchins GGA; Section of Pathology and Tumour Biology, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
  • Magill L; Birmingham Clinical Trials Unit, Birmingham, United Kingdom.
  • Quirke P; Section of Pathology and Tumour Biology, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
  • Riddell RH; University of Toronto, Toronto, Canada; Mount Sinai Hospital, Toronto, ON, Canada.
  • Gray RG; Clinical Trial Service Unit & Epidemiological Studies, University of Oxford, United Kingdom.
  • Kirsch R; University of Toronto, Toronto, Canada; Mount Sinai Hospital, Toronto, ON, Canada.
Clin Colorectal Cancer ; 20(3): 256-264, 2021 09.
Article em En | MEDLINE | ID: mdl-34099382
BACKGROUND: Tumor budding (TB) is an adverse prognostic factor in colorectal cancer (CRC). International consensus on a standardized assessment method has led to its wider reporting. However, uncertainty regarding its clinical value persists. This study aimed to (1) confirm the prognostic significance of TB, particularly in stage II CRC; (2) to determine optimum thresholds for TB risk grouping; and (3) to determine whether TB influences responsiveness to chemotherapy. METHODS: TB was assessed in CRC sections from 1575 QUASAR trial patients randomized between adjuvant chemotherapy and observation. Optimal risk group cutoffs were determined by maximum likelihood methods, with their influence on recurrence and mortality investigated in stratified log-rank analyses on exploratory (n = 504), hypothesis-testing (n = 478), and final (n = 593) data sets. RESULTS: The optimal threshold for high-grade TB (HGTB) was ≥ 10 buds per 1.23 mm2. High-grade TB tumors had significantly worse outcomes than those with lower TB: 10-year recurrence 36% versus 22% (risk ratio, 2.00 [95% CI, 1.62-2.45]; 2P < .0001) and 10-year mortality 50% vs. 37% (risk ratio, 1.53 [95% CI, 1.34-1.76]; 2P < .0001). The prognostic significance remained equally strong after allowance for other pathological risk factors, including stage, grade, lymphovascular invasion, and mismatch repair status. There was a nonsignificant trend toward increasing chemotherapy efficacy with increasing bud counts. CONCLUSIONS: TB is a strong independent predictor of recurrence. Chemotherapy efficacy is comparable in patients with higher and lower TB; hence, absolute reductions in recurrence and death with chemotherapy should be about twice as large in patients with ≥ 10 than < 10 TB counts.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article