Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study
Platinum-based chemotherapy is the main type of I-line treatment of advanced and non-operative NSCLC patients without <em>EGFR</em> gene mutation. The excision repair cross-complementation group 1 (ERCC1) is an enzyme that executes the incision of the damaged DNA strand a...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Via Medica
2012-04-01
|
Series: | Folia Histochemica et Cytobiologica |
Subjects: | |
Online Access: | http://czasopisma.viamedica.pl/fhc/article/view/18700 |
id |
doaj-a214071a2d724f62845ce02a36765364 |
---|---|
record_format |
Article |
spelling |
doaj-a214071a2d724f62845ce02a367653642020-11-25T00:24:13ZengVia MedicaFolia Histochemica et Cytobiologica0239-85081897-56312012-04-01501808610.5603/18700Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot studyJanusz MilanowskiBeata BiernackaRadosław MlakTomasz KucharczykKamila Wojas-KrawczykPaweł KrawczykPlatinum-based chemotherapy is the main type of I-line treatment of advanced and non-operative NSCLC patients without <em>EGFR</em> gene mutation. The excision repair cross-complementation group 1 (ERCC1) is an enzyme that executes the incision of the damaged DNA strand and removes platinum-induced DNA adducts. We investigated whether <em>ERCC1</em> gene polymorphism has an effect on the response to chemotherapy and survival in 43 patients with NSCLC treated with platinum-based chemotherapy. <em>ERCC1</em> 19007 T&gt;C SNPs were assessed using a PCR-RFLP methods in DNA isolated from peripheral blood lymphocytes. Disease control occurred significantly (p = 0.045) more frequently in patients with CC or CT genotype compared to patients with TT genotype. Median PFS and OS for CC homozygous were 4 and 10.5 months, 4 and 12.5 months for CT heterozygous, but only 0.3 and 1.5 months for TT homozygous patients, respectively. The probability of PFS was significantly higher (HR = 0.438, 95% CI: 0.084–0.881, p = 0.03) and probability of OS was insignificantly<br />higher (HR = 0.503, 95% CI: 0.129–1.137, p = 0.084) in patients with CC or CT genotype than in patients with TT genotype. Uncommon TT genotype of <em>ERCC1</em> 19007 T&gt;C polymorphism could predict poor response and shortening of progression free survival in NSCLC patients treated with platinum-based I-line chemotherapy. The analysis of this polymorphism may serve as a promising tool in the qualification of advanced NSCLC patients for appropriate chemotherapy.http://czasopisma.viamedica.pl/fhc/article/view/18700ERCC1single-nucleotide polymorphismnon-small cell lung cancer stagingplatinum-based chemotherapy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Janusz Milanowski Beata Biernacka Radosław Mlak Tomasz Kucharczyk Kamila Wojas-Krawczyk Paweł Krawczyk |
spellingShingle |
Janusz Milanowski Beata Biernacka Radosław Mlak Tomasz Kucharczyk Kamila Wojas-Krawczyk Paweł Krawczyk Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study Folia Histochemica et Cytobiologica ERCC1 single-nucleotide polymorphism non-small cell lung cancer staging platinum-based chemotherapy |
author_facet |
Janusz Milanowski Beata Biernacka Radosław Mlak Tomasz Kucharczyk Kamila Wojas-Krawczyk Paweł Krawczyk |
author_sort |
Janusz Milanowski |
title |
Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study |
title_short |
Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study |
title_full |
Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study |
title_fullStr |
Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study |
title_full_unstemmed |
Predictive value of ERCC1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study |
title_sort |
predictive value of ercc1 single-nucleotide polymorphism in patients receiving platinum-based chemotherapy for locally-advanced and advanced non-small cell lung cancer — a pilot study |
publisher |
Via Medica |
series |
Folia Histochemica et Cytobiologica |
issn |
0239-8508 1897-5631 |
publishDate |
2012-04-01 |
description |
Platinum-based chemotherapy is the main type of I-line treatment of advanced and non-operative NSCLC patients without <em>EGFR</em> gene mutation. The excision repair cross-complementation group 1 (ERCC1) is an enzyme that executes the incision of the damaged DNA strand and removes platinum-induced DNA adducts. We investigated whether <em>ERCC1</em> gene polymorphism has an effect on the response to chemotherapy and survival in 43 patients with NSCLC treated with platinum-based chemotherapy. <em>ERCC1</em> 19007 T&gt;C SNPs were assessed using a PCR-RFLP methods in DNA isolated from peripheral blood lymphocytes. Disease control occurred significantly (p = 0.045) more frequently in patients with CC or CT genotype compared to patients with TT genotype. Median PFS and OS for CC homozygous were 4 and 10.5 months, 4 and 12.5 months for CT heterozygous, but only 0.3 and 1.5 months for TT homozygous patients, respectively. The probability of PFS was significantly higher (HR = 0.438, 95% CI: 0.084–0.881, p = 0.03) and probability of OS was insignificantly<br />higher (HR = 0.503, 95% CI: 0.129–1.137, p = 0.084) in patients with CC or CT genotype than in patients with TT genotype. Uncommon TT genotype of <em>ERCC1</em> 19007 T&gt;C polymorphism could predict poor response and shortening of progression free survival in NSCLC patients treated with platinum-based I-line chemotherapy. The analysis of this polymorphism may serve as a promising tool in the qualification of advanced NSCLC patients for appropriate chemotherapy. |
topic |
ERCC1 single-nucleotide polymorphism non-small cell lung cancer staging platinum-based chemotherapy |
url |
http://czasopisma.viamedica.pl/fhc/article/view/18700 |
work_keys_str_mv |
AT januszmilanowski predictivevalueofercc1singlenucleotidepolymorphisminpatientsreceivingplatinumbasedchemotherapyforlocallyadvancedandadvancednonsmallcelllungcancerapilotstudy AT beatabiernacka predictivevalueofercc1singlenucleotidepolymorphisminpatientsreceivingplatinumbasedchemotherapyforlocallyadvancedandadvancednonsmallcelllungcancerapilotstudy AT radosławmlak predictivevalueofercc1singlenucleotidepolymorphisminpatientsreceivingplatinumbasedchemotherapyforlocallyadvancedandadvancednonsmallcelllungcancerapilotstudy AT tomaszkucharczyk predictivevalueofercc1singlenucleotidepolymorphisminpatientsreceivingplatinumbasedchemotherapyforlocallyadvancedandadvancednonsmallcelllungcancerapilotstudy AT kamilawojaskrawczyk predictivevalueofercc1singlenucleotidepolymorphisminpatientsreceivingplatinumbasedchemotherapyforlocallyadvancedandadvancednonsmallcelllungcancerapilotstudy AT pawełkrawczyk predictivevalueofercc1singlenucleotidepolymorphisminpatientsreceivingplatinumbasedchemotherapyforlocallyadvancedandadvancednonsmallcelllungcancerapilotstudy |
_version_ |
1725353311404556288 |