Abstract
Among 242 Japanese pancreatic cancer patients, three patients (1.2%) encountered life-threatening toxicities, including myelosuppression, after gemcitabine-based chemotherapies. Two of them carried homozygous CDA*3 (CDA208G>A[Ala70Thr]), and showed extremely low plasma cytidine deaminase activity and gemcitabine clearance. Our results suggest that homozygous *3 is a major factor causing gemcitabine-mediated severe adverse reactions among the Japanese population.
| Original language | English |
|---|---|
| Pages (from-to) | 870-873 |
| Number of pages | 4 |
| Journal | British Journal of Cancer |
| Volume | 100 |
| Issue number | 6 |
| DOIs | |
| State | Published - 24 Mar 2009 |
| Externally published | Yes |
Keywords
- CDA208G>A
- Gemcitabine
- Pharmacogenomics
- Polymorphism
- Toxicity
- pancreatic cancer