TY - JOUR
T1 - Prognostic value of ALDH2 polymorphism for patients with oropharyngeal cancer in a Japanese population
AU - Shinomiya, Hirotaka
AU - Shinomiya, Hitomi
AU - Kubo, Mie
AU - Saito, Yuki
AU - Yoshida, Masafumi
AU - Ando, Mizuo
AU - Teshima, Masanori
AU - Otsuki, Naoki
AU - Kiyota, Naomi
AU - Sasaki, Ryohei
AU - Nibu, Ken ichi
N1 - Funding Information:
This work is partly supported by Grant-in-Aid for Scientific Research (26861379, H. S. & 16H0548, 16H05481 K.N) and Japan Agency for Medical Research and Development (16ck0106223h001, K.N.). We would like to express our special gratitude to Ms. Yoko Kurihara for her outstanding technical support for this project.
Publisher Copyright:
© 2017 Shinomiya et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2017/12
Y1 - 2017/12
N2 - Background: Half of Japanese possess a polymorphism of aldehyde dehydrogenase 2(ALDH2), while few white individuals possess this mutation. The purpose of this study was to investigate the possibility of ALDH2 polymorphism as a prognostic factor for oropharyngeal cancer (OPC) among Japanese population. Methods: We analyzed 82 Japanese patients with OPC treated between 2006 and 2011. The median observation period was 50 months. P16-staining and ALDH2 polymorphisms were investigated. To examine the frequencies of second primary pharyngeal and esophageal cancers (SPPEC),37 Japanese patients with OPC treated at Tokyo University Hospital were included for statistical analysis. Results: Statistically significant differences were noted in OS among sex, age, N classification, and p16 (p = 0.045, 0.024, 0.020, 0.007, respectively). In addition, OS and DSS rates of the patients with heterozygous ALDH2 tended to be worse than those of the patients with homozygous ALDH2 (p = 0.21, 0.086, respectively). Of note, OS and DSS of the patients with p16-negative OPC and heterozygous ALDH2 was significant poorer than those of the patients with p16-positive OPC (p = 0.002, 0.006, respectively), while there was no significant difference in OS and DSS between patients with p16-positive OPC and patients with p16-negative OPC and homozygous ALDH2. Conclusions: ALDH2 polymorphism might be a promising prognostic factor for Japanese patients with p16-negative OPC.
AB - Background: Half of Japanese possess a polymorphism of aldehyde dehydrogenase 2(ALDH2), while few white individuals possess this mutation. The purpose of this study was to investigate the possibility of ALDH2 polymorphism as a prognostic factor for oropharyngeal cancer (OPC) among Japanese population. Methods: We analyzed 82 Japanese patients with OPC treated between 2006 and 2011. The median observation period was 50 months. P16-staining and ALDH2 polymorphisms were investigated. To examine the frequencies of second primary pharyngeal and esophageal cancers (SPPEC),37 Japanese patients with OPC treated at Tokyo University Hospital were included for statistical analysis. Results: Statistically significant differences were noted in OS among sex, age, N classification, and p16 (p = 0.045, 0.024, 0.020, 0.007, respectively). In addition, OS and DSS rates of the patients with heterozygous ALDH2 tended to be worse than those of the patients with homozygous ALDH2 (p = 0.21, 0.086, respectively). Of note, OS and DSS of the patients with p16-negative OPC and heterozygous ALDH2 was significant poorer than those of the patients with p16-positive OPC (p = 0.002, 0.006, respectively), while there was no significant difference in OS and DSS between patients with p16-positive OPC and patients with p16-negative OPC and homozygous ALDH2. Conclusions: ALDH2 polymorphism might be a promising prognostic factor for Japanese patients with p16-negative OPC.
UR - http://www.scopus.com/inward/record.url?scp=85037041176&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85037041176&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0187992
DO - 10.1371/journal.pone.0187992
M3 - Article
C2 - 29206831
AN - SCOPUS:85037041176
SN - 1932-6203
VL - 12
JO - PLoS One
JF - PLoS One
IS - 12
M1 - e0187992
ER -