Osteoradionecrosis in Head-and-Neck Cancer Has a Distinct Genotype-Dependent Cause
| Autor: | Dawn Howell, N. Slevin, Clara Chan, Siobhan Crichton, Richard Shaw, G. Rinck, Janet M. Risk, Andrew Lyons, Catharine M L West |
|---|---|
| Rok vydání: | 2012 |
| Předmět: |
Adult
Male Cancer Research medicine.medical_specialty Genotype Osteoradionecrosis medicine.medical_treatment Gastroenterology Transforming Growth Factor beta1 RC0254 Internal medicine medicine Humans Radiology Nuclear Medicine and imaging Allele Alleles Aged Retrospective Studies Gynecology Radiation business.industry Head and neck cancer Cancer Heterozygote advantage Variant allele Middle Aged medicine.disease Radiation therapy Oncology Head and Neck Neoplasms Case-Control Studies Female business |
| Zdroj: | INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS |
| ISSN: | 0360-3016 |
| DOI: | 10.1016/j.ijrobp.2011.05.016 |
| Popis: | Purpose We performed a case-control study to establish whether the development of osteoradionecrosis (ORN) was related to a variant allele substituting T for C at -509 of the transforming growth factor-β1 gene (TGF-β1). Patients and Methods A total of 140 patients, 39 with and 101 without ORN, who underwent radiotherapy for head-and-neck cancer with a minimum of 2 years follow-up, were studied. None of the patients had clinical evidence of recurrence at this time. DNA extracted from blood was genotyped for the -509 C-T variant allele of the TGF-β1 gene. Results There were no significant differences in patient, cancer treatment, or tumor characteristics between the two groups. Of the 39 patients who developed ORN, 9 were homozygous for the common CC allele, 19 were heterozygous, and 11 were homozygous for the rare TT genotype. Of the 101 patients without ORN, the distribution was 56 (CC), 33 (CT), and 12 (TT). The difference in distribution was significant, giving an increased risk of ORN of 5.7 (95% CI, 1.7–19.2) for homozygote TT patients (p = 0.001) and 3.6 (95% CI, 1.3–10.0) for heterozygotes (p = 0.004) when compared with patients with the CC genotype. Postradiotherapy dentoalveolar surgery preceding the development of ORN was associated with the CC genotype (p = 0.02). Conclusions Our findings support the postulate that the development of ORN is related to the presence of the T variant allele at -509 within the TGF-β1 gene. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|