DNA Topoisomerase I Gene Copy Number and mRNA Expression Assessed as Predictive Biomarkers for Adjuvant Irinotecan in Stage II/III Colon Cancer
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
26542057
DOI
10.1158/1078-0432.ccr-15-0561
PII: 1078-0432.CCR-15-0561
Knihovny.cz E-zdroje
- MeSH
- adjuvantní chemoterapie MeSH
- biologické markery MeSH
- DNA-topoisomerasy I genetika MeSH
- exprese genu * MeSH
- fytogenní protinádorové látky terapeutické užití MeSH
- genová dávka * MeSH
- hybridizace in situ fluorescenční MeSH
- inhibitory topoisomerasy I terapeutické užití MeSH
- irinotekan MeSH
- kamptothecin analogy a deriváty terapeutické užití MeSH
- Kaplanův-Meierův odhad MeSH
- lidé MeSH
- messenger RNA genetika MeSH
- nádory tračníku diagnóza farmakoterapie genetika mortalita MeSH
- prognóza MeSH
- staging nádorů MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- biologické markery MeSH
- DNA-topoisomerasy I MeSH
- fytogenní protinádorové látky MeSH
- inhibitory topoisomerasy I MeSH
- irinotekan MeSH
- kamptothecin MeSH
- messenger RNA 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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