Combinations of gemcitabine (Gemzar) with cisplatin (Platinol) are among th
e most active new chemotherapy regimens developed for advanced non-small-ce
ll lung cancer. Carboplatin (Paraplatin) is a platinum analog devoid of man
y of the nonhematologic toxicities associated with cisplatin. Although few
direct comparisons have been made, when administered by area under the conc
entration-time curve (AUC) dosing, carboplatin is probably equivalent to ci
splatin in advanced non-small-cell lung cancer and provides an improved the
rapeutic index. Based on its favorable toxicity profile, carboplatin has su
pplanted cisplatin for use in combination with paclitaxel in several differ
ent tumor types. Initial trials combining gemcitabine and carboplatin using
standard days 1, 8, and 15 dosing of gemcitabine suggested that thrombocyt
openia was problematic. More recently, 21-day schedules in which gemcitabin
e is administered only on days I and 8 have demonstrated both efficacy and
improved toxicity profiles. Here we review recent studies investigating gem
citabine plus carboplatin and preliminary data regarding combinations of ge
mcitabine with the new platinum analog oxaliplatin.