R24, a mouse monodonal antibody against GD(3) ganglioside, is potent a
t mediating in vitro effector functions such as human complement-media
ted cytotoxicity and antibody-dependent cellular cytotoxicity, and can
block melanoma tumor growth in animal models. Because of these proper
ties and the fact that GD(3) is abundantly expressed on virtually all
melanomas but is found on few normal tissues, R24 has been tested in a
series of clinical trials in patients with metastatic melanoma. As a
single agent, R24 can induce responses in patients treated with metast
atic melanoma. Overall, there have been 10 responders out of 103 patie
nts reported; two responses have been complete responses, Responses ha
ve largely occurred in patients treated with intermediate doses of R24
and have included complete responses. Combining R24 with either cytot
oxic drugs or cytokines has not increased this response rate, although
one trial with R24 and interleukin-2 resulted in a 43% response rate
and merits further investigation, Local-regional treatments R24 (intra
tumor injections, regional limb perfusion, intrathecal administration)
have also been attempted in a small number of patients and responses
have been described. Taken together, multiple centers have reported re
sponses in patients with metastatic melanoma treated with R24.