Microsatellite instability (MSI) is intrinsic to most colorectal carcinomas (CRC) from patients with hereditary nonpolyposis colorectal cancer (HNPCC), reflecting germline mutations in the mismatch-repair (MMR) genes. Its occurrence and chronological sequence of development in sporadic CRC appears l
Antipyrine metabolism in patients with liver metastases from colorectal cancer
β Scribed by Antonio Grieco; Carlo Barone; Paola Coletta; Rosario Castellano; Enzo Ragazzoni; Alessandra Cassano; Antonio Astone; Gino Gambassi
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 490 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
β¦ Synopsis
Background:
The influence of cancer on antipyrine metabolism is under debate.
Methods:
To assess the functional activity of a liver with solid metastases from primary colorectal cancer, antipyrine metabolism was studied after the drug was administered orally (18 mg/kg body weight) to 55 healthy volunteers, 62 patients with well-compensated cirrhosis, and 42 patients with small (class a) or massive (class b) metastatic liver involvement.
Results:
In patients with cancer, antipyrine clearance (0.472 +/- 0.177 ml/min/kg) was similar to that in healthy volunteers (0.456 +/- 0.198 ml/min/kg) and significantly higher than in those with cirrhosis (0.259 +/- 0.17 ml/min/kg, p less than 0.001). there was no difference in antipyrine pharmacokinetics between class a and b involvement. in the entire population, antipyrine clearance was correlated with serum albumin levels (r = 0.294, p = 0.0002) and prothrombin activity (r = 0.416, p = 0.001). this positive correlation was not present when only the neoplastic group was considered. no correlation was found between antipyrine clearance and alkaline phosphatase levels. in patients with cancer, no relationship was found between antipyrine clearance and carcinoembryonic antigen and lactic dehydrogenase levels.
Conclusions:
These results show that patients with livers largely replaced by solid metastases are able to metabolize antipyrine to the same extent as healthy subjects.
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