The identification of new chemotherapeutic agents for the treatment of
non-small cell lung cancer should proceed in a structured, logical fa
shion, Agents should be evaluated on the basis of multiple objective a
nd subjective end points. A 15% or greater major objective response ra
te, demonstrated in multiple single-agent phase II trials, is consider
ed the lower limit for an agent to be deemed clinically active in this
disease. A number of drugs previously have been identified in this ca
tegory, including cisplatin, ifosfamide, mitomycin, paclitaxel, and th
e vinca alkaloids vinblastine and vindesine. Most of these conventiona
l agents have been explored alone, in a variety of doses and schedules
, and in combination. In the last several years clinical development h
as produced new agents, including chloroquinoxaline sulfonamide, docet
axel, edatrexate, gemcitabine, irinotecan, topotecan, and vinorelbine,
which hold promise for more successful treatment of this lethal disea
se.