Literature DB >> 27196764

Clinical Significance of TLR1 I602S Polymorphism for Patients with Metastatic Colorectal Cancer Treated with FOLFIRI plus Bevacizumab.

Satoshi Okazaki1, Fotios Loupakis2, Sebastian Stintzing3, Shu Cao4, Wu Zhang1, Dongyun Yang4, Yan Ning1, Yu Sunakawa1, Stefan Stremitzer1, Satoshi Matsusaka1, Martin D Berger1, Anish Parekh1, Jordan D West1, Yuji Miyamoto1, Mitsukuni Suenaga1, Marta Schirripa1, Chiara Cremolini2, Alfredo Falcone2, Volker Heinemann3, R William DePaolo5, Heinz-Josef Lenz6.   

Abstract

The purpose of this study was to evaluate the clinical significance of single-nucleotide polymorphisms in TLR1, TLR2, TLR6, and TAK1 in patients with metastatic colorectal cancer (mCRC). We genotyped 9 SNPs of TLR1, TLR2, TLR6, and TAK1 in mCRC patients treated with first-line FOLFIRI (combination therapy of irinotecan, 5-fluorouracil, and folinic acid) plus bevacizumab, using a discovery cohort (TRIBE trial, n = 228) and a validation cohort (FIRE-3 trial, n = 297), and analyzed for the association with response rate (RR), progression-free survival (PFS), and overall survival (OS). There was a significant association of TLR1 rs5743618 (T1805G) with the clinical outcome. In the TRIBE cohort, a homozygous wild-type genotype (T/T) associated with a significantly lower RR compared with variant T/G and G/G genotypes (43% vs. 62%, P = 0.025), and this observation was validated in the FIRE-3 cohort (46% vs. 65%, P = 0.021). In addition, those patients with the T/T genotype had significantly worse PFS (median, 8.2 vs. 10.5 months; HR, 1.57; 95% CI, 1.09-2.28, P = 0.014) and OS (median: 19.9 vs. 27.9 months; HR, 1.63; 95% CI, 1.14-2.35, P = 0.007), compared with those with other genotypes in the TRIBE cohort. These differences remained statistically significant in multivariate analysis. Our data suggest that TLR1 rs5743618 could serve as a predictor of clinical response to FOLFIRI plus bevacizumab in patients with mCRC. Mol Cancer Ther; 15(7); 1740-5. ©2016 AACR. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27196764      PMCID: PMC4936942          DOI: 10.1158/1535-7163.MCT-15-0931

Source DB:  PubMed          Journal:  Mol Cancer Ther        ISSN: 1535-7163            Impact factor:   6.261


  28 in total

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4.  Phase II trial of infusional fluorouracil, irinotecan, and bevacizumab for metastatic colorectal cancer: efficacy and circulating angiogenic biomarkers associated with therapeutic resistance.

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9.  Th17-type cytokines, IL-6 and TNF-α synergistically activate STAT3 and NF-kB to promote colorectal cancer cell growth.

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Journal:  Oncogene       Date:  2014-09-01       Impact factor: 9.867

10.  TLR1-induced chemokine production is critical for mucosal immunity against Yersinia enterocolitica.

Authors:  Y Sugiura; K Kamdar; S Khakpour; G Young; W J Karpus; R William DePaolo
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2.  Genetic Variants of ANGPT1, CD39, FGF2 and MMP9 Linked to Clinical Outcome of Bevacizumab Plus Chemotherapy for Metastatic Colorectal Cancer.

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