| Literature DB >> 31624332 |
Annika Malmström1,2, Malgorzata Łysiak3, Lisa Åkesson3,4, Ingrid Jakobsen5, Munila Mudaisi6, Peter Milos7, Martin Hallbeck3,8, Victoria Fomichov9, Helle Broholm10, Kirsten Grunnet11, Hans Skovgaard Poulsen11,12, Charlotte Bratthäll13, Michael Strandeus14, Angeliki Papagiannopoulou3,8, Marie Stenmark-Askmalm15, Henrik Green5,16, Peter Söderkvist3.
Abstract
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.Entities:
Year: 2019 PMID: 31624332 DOI: 10.1038/s41397-019-0107-z
Source DB: PubMed Journal: Pharmacogenomics J ISSN: 1470-269X Impact factor: 3.550