TREATMENT OF OCULAR MELANOMA METASTATIC TO THE LIVER BY HEPATIC ARTERIAL CHEMOTHERAPY

Citation
S. Leyvraz et al., TREATMENT OF OCULAR MELANOMA METASTATIC TO THE LIVER BY HEPATIC ARTERIAL CHEMOTHERAPY, Journal of clinical oncology, 15(7), 1997, pp. 2589-2595
Citations number
20
Categorie Soggetti
Oncology
ISSN journal
0732183X
Volume
15
Issue
7
Year of publication
1997
Pages
2589 - 2595
Database
ISI
SICI code
0732-183X(1997)15:7<2589:TOOMMT>2.0.ZU;2-9
Abstract
Purpose: Ocular melanoma is characterized by a high rate of liver meta stases and is associated with a median survival time less than 5 month s. There is no standard treatment available. Treatment strategies have , without success, relied on the experience with metastatic cutaneous melanoma. The only effective treatment is chemoembolization using cisp latin and polyvinyl sponge, which has never become accepted on a large scale. The objective of the study was to establish prospectively the efficacy and toxicity of hepatic intraarterial fotemustine, a third-ge neration nitrosourea, in patients with liver metastases from ocular me lanoma. Patients and Methods: Thirty-one patients were subjected to la parotomy to place a totally implantable catheter into the hepatic arte ry and received fotemustine 100 mg/m(2) as a 4-hour infusion, first on ce a week for four times and then, after a 5-week rest period, every 3 weeks until progression or toxicity, Cox regression models were used to assess the prognostic role of patient survival characteristics. Res ults: Objective responses were observed in 12 of 30 assessable patient s (40%; 95% confidence interval, 22% to 59%), The median duration of r esponse was 11 months and the median overall survival time, 14 months. Lactate dehydrogenase (LDH) appeared to be the strongest prognostic f actor for survival. Toxicity was minimal and treatment could be admini stered on an outpatient basis. Conclusion: The results of hepatic arte rial chemotherapy with fotemustine produced a high response rate and s urvival similar to chemoembolization therapy. It involves no major tox icity and preserves the quality of life. To assess further its effecti veness, a randomized study to compare hepatic intraarterial versus int ravenous chemotherapy is being planned. (C) 1997 by American Society o f Clinical Oncology.