S. Retsas, STRATEGIES FOR IMPROVING SURVIVAL IN MALIGNANT-MELANOMA - FOCUS ON VINDESINE, Journal of drug development and clinical practice, 7(3), 1995, pp. 159-171
This paper summarises the systemic treatments used for metastatic mela
noma in the Melanoma Unit at Charing Cross Hospital, UK, and offers an
appraisal of adjuvant therapy with special emphasis on recent reports
in the literature. Since 1977, patients presenting to this service wi
th metastatic disease have been treated with protocols based primarily
on vindesine as a single agent or in combinations with dacarbazine, p
latinum derivatives and fotemustine. Observed response rates ranged be
tween 20% and 30% with the median duration of response not exceeding o
ne year. Although the response rates ore not much higher with combinat
ion regimens than monotherapy, large tumour volumes involving multiple
organ sites ore more likely to regress with polychemotherapy than sin
gle-agent treatment. Among 240 patients with widespread metastatic dis
ease treated by these different vindesine-containing chemotherapy prot
ocols and evaluated for survival, 36 (15%) survived longer than two ye
ars from onset of treatment Included among these long-term survivors w
ere Patients with hepatic and cerebral metastases. Encouraging though
they may be, these results emphasise the need for adjuvant treatment i
n critical stages in the evolution of malignant melanoma. In the setti
ng of clinical and histological metastases in the regional lymph nodes
, adjuvant vindesine has been shown to result in a survival advantage.
This and other studies are reviewed.