Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer

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Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer. / Palshof, Jesper Andreas; Hogdall, Estrid Vilma Solyom; Poulsen, Tim Svenstrup; Linnemann, Dorte; Jensen, Benny Vittrup; Pfeiffer, Per; Tarpgaard, Line Schmidt; Brunner, Nils; Stenvang, Jan; Yilmaz, Mette; Nielsen, Dorte Lisbet.

In: BMC Cancer, Vol. 17, 48, 11.01.2017.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Palshof, JA, Hogdall, EVS, Poulsen, TS, Linnemann, D, Jensen, BV, Pfeiffer, P, Tarpgaard, LS, Brunner, N, Stenvang, J, Yilmaz, M & Nielsen, DL 2017, 'Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer', BMC Cancer, vol. 17, 48. https://doi.org/10.1186/s12885-016-3001-y

APA

Palshof, J. A., Hogdall, E. V. S., Poulsen, T. S., Linnemann, D., Jensen, B. V., Pfeiffer, P., Tarpgaard, L. S., Brunner, N., Stenvang, J., Yilmaz, M., & Nielsen, D. L. (2017). Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer. BMC Cancer, 17, [48]. https://doi.org/10.1186/s12885-016-3001-y

Vancouver

Palshof JA, Hogdall EVS, Poulsen TS, Linnemann D, Jensen BV, Pfeiffer P et al. Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer. BMC Cancer. 2017 Jan 11;17. 48. https://doi.org/10.1186/s12885-016-3001-y

Author

Palshof, Jesper Andreas ; Hogdall, Estrid Vilma Solyom ; Poulsen, Tim Svenstrup ; Linnemann, Dorte ; Jensen, Benny Vittrup ; Pfeiffer, Per ; Tarpgaard, Line Schmidt ; Brunner, Nils ; Stenvang, Jan ; Yilmaz, Mette ; Nielsen, Dorte Lisbet. / Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer. In: BMC Cancer. 2017 ; Vol. 17.

Bibtex

@article{c22e10c8b3024b4e92063b6495f6349f,
title = "Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer",
abstract = "BackgroundNo biomarker exists to guide the optimal choice of chemotherapy for patients with metastatic colorectal cancer. We examined the copy numbers (CN) of topoisomerase I (TOP1) as well as the ratios of TOP1/CEN-20 and TOP1/CEN-2 as biomarkers for irinotecan efficacy in patients with metastatic colorectal cancer.MethodsFrom a national cohort, we identified 163 patients treated every third week with irinotecan 350 mg/m2 as second-line therapy. Among these 108 were eligible for analyses and thus entered the study. Primary tumors samples were collected and tissue microarray (TMA) blocks were produced. FISH analysis was performed using two probe-mixes: TOP1/CEN-20 and TOP1/CEN-2. Only samples harboring all three signals (TOP1, CEN-20 and CEN-2) using FISH were included in the analyses.ResultsIn the TOP1/CEN-20 probe-mix the median TOP1- and CEN-20 CN were 4.46 (range: 1.5–9.5) and 2.00 (range: 0.55–4.55), respectively. The median TOP1- and CEN-2 CN in the TOP1/CEN-2 probe-mix, were 4.57 (range: 1.82–10.43) and 1.98 (range: 1.22–6.14), respectively. The median TOP1/CEN-20 ratio and TOP1/CEN-2 ratio were 1.25 (range: 0.92–2.90) and 2.05 (range: 1.00–6.00), respectively. None of the markers TOP1 CN, TOP1/CEN-20-ratio or TOP1/CEN-2-ratio were associated with progression free survival, overall survival or baseline characteristics. Yet, we observed a borderline association for a stepwise increase of the TOP1 CN in relation to objective response as hazard ratio were 1.35 (95% CI 0.96–1.90; p = 0.081).ConclusionsWe verified a borderline significant association between increasing TOP1 CN and objective response as previously reported. Applying the probes representing CEN-20 and CEN-2, in order to investigate the ratios of TOP1/CEN-20 and TOP1/CEN-2 provided no further information in search of a biomarker driven patient stratification. Other biomarkers to be paired with TOP1 CN are therefore highly warranted.",
keywords = "Biomarker, Colorectal cancer, FISH, Gene copy number, Irinotecan, Topoisomerase I",
author = "Palshof, {Jesper Andreas} and Hogdall, {Estrid Vilma Solyom} and Poulsen, {Tim Svenstrup} and Dorte Linnemann and Jensen, {Benny Vittrup} and Per Pfeiffer and Tarpgaard, {Line Schmidt} and Nils Brunner and Jan Stenvang and Mette Yilmaz and Nielsen, {Dorte Lisbet}",
year = "2017",
month = jan,
day = "11",
doi = "10.1186/s12885-016-3001-y",
language = "English",
volume = "17",
journal = "B M C Cancer",
issn = "1471-2407",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Topoisomerase I copy number alterations as biomarker for irinotecan efficacy in metastatic colorectal cancer

AU - Palshof, Jesper Andreas

AU - Hogdall, Estrid Vilma Solyom

AU - Poulsen, Tim Svenstrup

AU - Linnemann, Dorte

AU - Jensen, Benny Vittrup

AU - Pfeiffer, Per

AU - Tarpgaard, Line Schmidt

AU - Brunner, Nils

AU - Stenvang, Jan

AU - Yilmaz, Mette

AU - Nielsen, Dorte Lisbet

PY - 2017/1/11

Y1 - 2017/1/11

N2 - BackgroundNo biomarker exists to guide the optimal choice of chemotherapy for patients with metastatic colorectal cancer. We examined the copy numbers (CN) of topoisomerase I (TOP1) as well as the ratios of TOP1/CEN-20 and TOP1/CEN-2 as biomarkers for irinotecan efficacy in patients with metastatic colorectal cancer.MethodsFrom a national cohort, we identified 163 patients treated every third week with irinotecan 350 mg/m2 as second-line therapy. Among these 108 were eligible for analyses and thus entered the study. Primary tumors samples were collected and tissue microarray (TMA) blocks were produced. FISH analysis was performed using two probe-mixes: TOP1/CEN-20 and TOP1/CEN-2. Only samples harboring all three signals (TOP1, CEN-20 and CEN-2) using FISH were included in the analyses.ResultsIn the TOP1/CEN-20 probe-mix the median TOP1- and CEN-20 CN were 4.46 (range: 1.5–9.5) and 2.00 (range: 0.55–4.55), respectively. The median TOP1- and CEN-2 CN in the TOP1/CEN-2 probe-mix, were 4.57 (range: 1.82–10.43) and 1.98 (range: 1.22–6.14), respectively. The median TOP1/CEN-20 ratio and TOP1/CEN-2 ratio were 1.25 (range: 0.92–2.90) and 2.05 (range: 1.00–6.00), respectively. None of the markers TOP1 CN, TOP1/CEN-20-ratio or TOP1/CEN-2-ratio were associated with progression free survival, overall survival or baseline characteristics. Yet, we observed a borderline association for a stepwise increase of the TOP1 CN in relation to objective response as hazard ratio were 1.35 (95% CI 0.96–1.90; p = 0.081).ConclusionsWe verified a borderline significant association between increasing TOP1 CN and objective response as previously reported. Applying the probes representing CEN-20 and CEN-2, in order to investigate the ratios of TOP1/CEN-20 and TOP1/CEN-2 provided no further information in search of a biomarker driven patient stratification. Other biomarkers to be paired with TOP1 CN are therefore highly warranted.

AB - BackgroundNo biomarker exists to guide the optimal choice of chemotherapy for patients with metastatic colorectal cancer. We examined the copy numbers (CN) of topoisomerase I (TOP1) as well as the ratios of TOP1/CEN-20 and TOP1/CEN-2 as biomarkers for irinotecan efficacy in patients with metastatic colorectal cancer.MethodsFrom a national cohort, we identified 163 patients treated every third week with irinotecan 350 mg/m2 as second-line therapy. Among these 108 were eligible for analyses and thus entered the study. Primary tumors samples were collected and tissue microarray (TMA) blocks were produced. FISH analysis was performed using two probe-mixes: TOP1/CEN-20 and TOP1/CEN-2. Only samples harboring all three signals (TOP1, CEN-20 and CEN-2) using FISH were included in the analyses.ResultsIn the TOP1/CEN-20 probe-mix the median TOP1- and CEN-20 CN were 4.46 (range: 1.5–9.5) and 2.00 (range: 0.55–4.55), respectively. The median TOP1- and CEN-2 CN in the TOP1/CEN-2 probe-mix, were 4.57 (range: 1.82–10.43) and 1.98 (range: 1.22–6.14), respectively. The median TOP1/CEN-20 ratio and TOP1/CEN-2 ratio were 1.25 (range: 0.92–2.90) and 2.05 (range: 1.00–6.00), respectively. None of the markers TOP1 CN, TOP1/CEN-20-ratio or TOP1/CEN-2-ratio were associated with progression free survival, overall survival or baseline characteristics. Yet, we observed a borderline association for a stepwise increase of the TOP1 CN in relation to objective response as hazard ratio were 1.35 (95% CI 0.96–1.90; p = 0.081).ConclusionsWe verified a borderline significant association between increasing TOP1 CN and objective response as previously reported. Applying the probes representing CEN-20 and CEN-2, in order to investigate the ratios of TOP1/CEN-20 and TOP1/CEN-2 provided no further information in search of a biomarker driven patient stratification. Other biomarkers to be paired with TOP1 CN are therefore highly warranted.

KW - Biomarker

KW - Colorectal cancer

KW - FISH

KW - Gene copy number

KW - Irinotecan

KW - Topoisomerase I

U2 - 10.1186/s12885-016-3001-y

DO - 10.1186/s12885-016-3001-y

M3 - Journal article

C2 - 28077117

VL - 17

JO - B M C Cancer

JF - B M C Cancer

SN - 1471-2407

M1 - 48

ER -

ID: 173508051