DNA Topoisomerase I Gene Copy Number and mRNA Expression Assessed as Predictive Biomarkers for Adjuvant Irinotecan in Stage II/III Colon Cancer
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
26542057
DOI
10.1158/1078-0432.ccr-15-0561
PII: 1078-0432.CCR-15-0561
Knihovny.cz E-resources
- MeSH
- Chemotherapy, Adjuvant MeSH
- Biomarkers MeSH
- DNA Topoisomerases, Type I genetics MeSH
- Gene Expression * MeSH
- Antineoplastic Agents, Phytogenic therapeutic use MeSH
- Gene Dosage * MeSH
- In Situ Hybridization, Fluorescence MeSH
- Topoisomerase I Inhibitors therapeutic use MeSH
- Irinotecan MeSH
- Camptothecin analogs & derivatives therapeutic use MeSH
- Kaplan-Meier Estimate MeSH
- Humans MeSH
- RNA, Messenger genetics MeSH
- Colonic Neoplasms diagnosis drug therapy genetics mortality MeSH
- Prognosis MeSH
- Neoplasm Staging MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- DNA Topoisomerases, Type I MeSH
- Antineoplastic Agents, Phytogenic MeSH
- Topoisomerase I Inhibitors MeSH
- Irinotecan MeSH
- Camptothecin MeSH
- RNA, Messenger MeSH
PURPOSE: Prospective-retrospective assessment of the TOP1 gene copy number and TOP1 mRNA expression as predictive biomarkers for adjuvant irinotecan in stage II/III colon cancer. EXPERIMENTAL DESIGN: Formalin-fixed, paraffin-embedded tissue microarrays were obtained from an adjuvant colon cancer trial (PETACC3) where patients were randomized to 5-fluorouracil/folinic acid with or without additional irinotecan. TOP1 copy number status was analyzed by fluorescence in situ hybridization (FISH) using a TOP1/CEN20 dual-probe combination. TOP1 mRNA data were available from previous analyses. RESULTS: TOP1 FISH and follow-up data were obtained from 534 patients. TOP1 gain was identified in 27% using a single-probe enumeration strategy (≥4 TOP1 signals per cell) and in 31% when defined by a TOP1/CEN20 ratio ≥ 1.5. The effect of additional irinotecan was not dependent on TOP1 FISH status.TOP1 mRNA data were available from 580 patients with stage III disease. Benefit of irinotecan was restricted to patients characterized by TOP1 mRNA expression ≥ third quartile (RFS: HRadjusted, 0.59;P= 0.09; OS: HRadjusted, 0.44;P= 0.03). The treatment by TOP1 mRNA interaction was not statistically significant, but in exploratory multivariable fractional polynomial interaction analysis, increasing TOP1 mRNA values appeared to be associated with increasing benefit of irinotecan. CONCLUSIONS: In contrast to the TOP1 copy number, a trend was demonstrated for a predictive property of TOP1 mRNA expression. On the basis of TOP1 mRNA, it might be possible to identify a subgroup of patients where an irinotecan doublet is a clinically relevant option in the adjuvant setting of colon cancer.
Department of Pathology Rigshospitalet Copenhagen University Hospital Copenhagen Denmark
Digestive Oncology Unit University Hospital Gasthuisberg Leuven Belgium
Masaryk University Institute of Biostatistics and Analyses Brno Czech Republic
Oncosurgery Unit University Hospital of Geneva Geneva Switzerland
University of Copenhagen Faculty of Health and Medical Sciences Copenhagen Denmark
University of Lausanne University Institute of Pathology Lausanne Switzerland
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