Cargando…
Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen
PURPOSE: To investigate the impact of CYP2D6 and CYP2C19 polymorphisms in predicting tamoxifen efficacy and clinical outcomes in Thai breast cancer patients. METHODS: Polymorphisms of CYP2D6 and CYP2C19 were genotyped by the AmpliChip™ CYP450 Test (Roche Molecular Diagnostics, Branchburg, NJ, USA) f...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681433/ https://www.ncbi.nlm.nih.gov/pubmed/23776391 http://dx.doi.org/10.2147/PGPM.S42330 |
_version_ | 1782273262421540864 |
---|---|
author | Chamnanphon, Montri Pechatanan, Khunthong Sirachainan, Ekapob Trachu, Narumol Chantratita, Wasun Pasomsub, Ekawat Noonpakdee, Wilai Sensorn, Insee Sukasem, Chonlaphat |
author_facet | Chamnanphon, Montri Pechatanan, Khunthong Sirachainan, Ekapob Trachu, Narumol Chantratita, Wasun Pasomsub, Ekawat Noonpakdee, Wilai Sensorn, Insee Sukasem, Chonlaphat |
author_sort | Chamnanphon, Montri |
collection | PubMed |
description | PURPOSE: To investigate the impact of CYP2D6 and CYP2C19 polymorphisms in predicting tamoxifen efficacy and clinical outcomes in Thai breast cancer patients. METHODS: Polymorphisms of CYP2D6 and CYP2C19 were genotyped by the AmpliChip™ CYP450 Test (Roche Molecular Diagnostics, Branchburg, NJ, USA) for 57 patients, who were matched as recurrent versus non-recurrent breast cancers (n = 33 versus n = 24, respectively, with a 5-year follow-up). RESULTS: Based on the genotype data, five CYP2D6 predicted phenotype groups were identified in this study including homozygous extensive metabolizer (13 of 57, 22.80%), extensive/intermediate metabolizer (23 of 57, 40.40%), extensive/poor metabolizer (3 of 57, 5.30%), homozygous intermediate metabolizer (14 of 57, 24.50%), and intermediate/poor metabolizer (4 of 57, 7.00%), and three CYP2C19 genotype groups including homozygous extensive metabolizer (27 of 57, 47.40%), extensive/intermediate metabolizer (27 of 57, 47.40%), and homozygous poor metabolizer (3 of 57, 5.30%). The CYP2D6 variant alleles were *10 (52 of 114, 45.60%), *5 (5 of 114, 4.40%), *41 (2 of 114, 1.80%), *4 (1 of 114, 0.90%), and *36 (1 of 114, 0.90%); the CYP2C19 variant alleles were *2 (27 of 114, 23.70%) and *3 (6 of 114, 5.30%). Kaplan–Meier estimates showed significantly shorter disease-free survival in patients with homozygous TT when compared to those with heterozygous CT or homozygous CC at nucleotides 100C>T and 1039C>T (CYP2D6*10) post-menopausal (log-rank test; P = 0.046). They also had increased risk of recurrence, but no statistically significant association was observed (hazard ratio 3.48; 95% confidence interval 0.86–14.07; P = 0.080). CONCLUSION: The CYP2D6 and CYP2C19 polymorphisms were not involved in tamoxifen efficacy. However, in the subgroup of post-menopausal women, the polymorphisms in CYP2D6 and CYP2C19 might be useful in predicting tamoxifen efficacy and clinical outcomes in breast cancer patients receiving adjuvant tamoxifen treatment. As the number of breast cancer patients was relatively small in this study, results should be confirmed in a larger group of prospective patients. |
format | Online Article Text |
id | pubmed-3681433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36814332013-06-17 Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen Chamnanphon, Montri Pechatanan, Khunthong Sirachainan, Ekapob Trachu, Narumol Chantratita, Wasun Pasomsub, Ekawat Noonpakdee, Wilai Sensorn, Insee Sukasem, Chonlaphat Pharmgenomics Pers Med Original Research PURPOSE: To investigate the impact of CYP2D6 and CYP2C19 polymorphisms in predicting tamoxifen efficacy and clinical outcomes in Thai breast cancer patients. METHODS: Polymorphisms of CYP2D6 and CYP2C19 were genotyped by the AmpliChip™ CYP450 Test (Roche Molecular Diagnostics, Branchburg, NJ, USA) for 57 patients, who were matched as recurrent versus non-recurrent breast cancers (n = 33 versus n = 24, respectively, with a 5-year follow-up). RESULTS: Based on the genotype data, five CYP2D6 predicted phenotype groups were identified in this study including homozygous extensive metabolizer (13 of 57, 22.80%), extensive/intermediate metabolizer (23 of 57, 40.40%), extensive/poor metabolizer (3 of 57, 5.30%), homozygous intermediate metabolizer (14 of 57, 24.50%), and intermediate/poor metabolizer (4 of 57, 7.00%), and three CYP2C19 genotype groups including homozygous extensive metabolizer (27 of 57, 47.40%), extensive/intermediate metabolizer (27 of 57, 47.40%), and homozygous poor metabolizer (3 of 57, 5.30%). The CYP2D6 variant alleles were *10 (52 of 114, 45.60%), *5 (5 of 114, 4.40%), *41 (2 of 114, 1.80%), *4 (1 of 114, 0.90%), and *36 (1 of 114, 0.90%); the CYP2C19 variant alleles were *2 (27 of 114, 23.70%) and *3 (6 of 114, 5.30%). Kaplan–Meier estimates showed significantly shorter disease-free survival in patients with homozygous TT when compared to those with heterozygous CT or homozygous CC at nucleotides 100C>T and 1039C>T (CYP2D6*10) post-menopausal (log-rank test; P = 0.046). They also had increased risk of recurrence, but no statistically significant association was observed (hazard ratio 3.48; 95% confidence interval 0.86–14.07; P = 0.080). CONCLUSION: The CYP2D6 and CYP2C19 polymorphisms were not involved in tamoxifen efficacy. However, in the subgroup of post-menopausal women, the polymorphisms in CYP2D6 and CYP2C19 might be useful in predicting tamoxifen efficacy and clinical outcomes in breast cancer patients receiving adjuvant tamoxifen treatment. As the number of breast cancer patients was relatively small in this study, results should be confirmed in a larger group of prospective patients. Dove Medical Press 2013-05-24 /pmc/articles/PMC3681433/ /pubmed/23776391 http://dx.doi.org/10.2147/PGPM.S42330 Text en © 2013 Chamnanphon et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Chamnanphon, Montri Pechatanan, Khunthong Sirachainan, Ekapob Trachu, Narumol Chantratita, Wasun Pasomsub, Ekawat Noonpakdee, Wilai Sensorn, Insee Sukasem, Chonlaphat Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
title | Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
title_full | Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
title_fullStr | Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
title_full_unstemmed | Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
title_short | Association of CYP2D6 and CYP2C19 polymorphisms and disease-free survival of Thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
title_sort | association of cyp2d6 and cyp2c19 polymorphisms and disease-free survival of thai post-menopausal breast cancer patients who received adjuvant tamoxifen |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681433/ https://www.ncbi.nlm.nih.gov/pubmed/23776391 http://dx.doi.org/10.2147/PGPM.S42330 |
work_keys_str_mv | AT chamnanphonmontri associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT pechatanankhunthong associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT sirachainanekapob associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT trachunarumol associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT chantratitawasun associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT pasomsubekawat associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT noonpakdeewilai associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT sensorninsee associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen AT sukasemchonlaphat associationofcyp2d6andcyp2c19polymorphismsanddiseasefreesurvivalofthaipostmenopausalbreastcancerpatientswhoreceivedadjuvanttamoxifen |