ABCB1 single-nucleotide variants and survival in patients with glioblastoma treated with radiotherapy concomitant with temozolomide

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作者
Annika Malmström
Malgorzata Łysiak
Lisa Åkesson
Ingrid Jakobsen
Munila Mudaisi
Peter Milos
Martin Hallbeck
Victoria Fomichov
Helle Broholm
Kirsten Grunnet
Hans Skovgaard Poulsen
Charlotte Bratthäll
Michael Strandeus
Angeliki Papagiannopoulou
Marie Stenmark-Askmalm
Henrik Green
Peter Söderkvist
机构
[1] Linköping University,Department of Advanced Home Care
[2] Linköping University,Department of Clinical and Experimental Medicine
[3] Region Östergötland,Regional Cancer Center South East
[4] Linköping University,Division of Drug Research, Department of Medical and Health Sciences
[5] Linköping University,Department of Oncology
[6] Linköping University,Department of Neurosurgery
[7] Linköping University,Department of Clinical Pathology
[8] Linköping University,Centre for Organizational Support and Development, Region Östergötland
[9] Copenhagen University Hospital,Department of Pathology
[10] Copenhagen University Hospital,Department of Radiation Biology
[11] Copenhagen University Hospital,Section for Neuro
[12] County Hospital,Oncology
[13] Ryhov Hospital,Department of Oncology
[14] University and Regional Laboratories,Department of Oncology
[15] Skåne University Hospital,Department of Clinical Genetics
[16] Lund University,Department of Forensic Genetics and Forensic Toxicology
[17] National Board of Forensic Medicine,undefined
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Standard treatment for glioblastoma (GBM) patients is surgery and radiochemotherapy (RCT) with temozolomide (TMZ). TMZ is a substrate for ABCB1, a transmembrane drug transporter. It has been suggested that survival for GBM patients receiving TMZ is influenced by different single-nucleotide variants (SNV) of ABCB1. We therefore examined SNV:s of ABCB1, namely 1199G>A, 1236C>T, 2677G>T/A, and 3435C>T and correlated to survival for GBM patients receiving RCT. In a pilot cohort (97 patients) a significant correlation to survival was found for SNV 1199G>A, with median OS for variant G/G patients being 18.2 months versus 11.5 months for A/G (p = 0.012). We found no correlation to survival for the other SNV:s. We then expanded the cohort to 179 patients (expanded cohort) and also included a confirmatory cohort (49 patients) focusing on SNV 1199G>A. Median OS for G/G versus A/G plus A/A was 15.7 and 11.5 months, respectively (p = 0.085) for the expanded cohort and 13.8 versus 16.8 months (p = 0.19) for the confirmatory. In conclusion, in patients with GBM receiving RCT with TMZ, no correlation with survival was found for the SNV:s 1236C>T, 2677G>T/A, and 3435C>T of ABCB1. Although the SNV 1199G>A might have some impact, a clinically significant role could not be confirmed.
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页码:213 / 219
页数:6
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