The discovery of cisplatin more than two decades ago was the most important
therapeutic advance in the treatment of ovarian cancer. Today, cisplatin o
r carboplatin in combination with paclitaxel is the most commonly used firs
t-line treatment for patients with advanced ovarian cancer.
Although platinum drugs remain a critical component of chemotherapy in this
type of cancer, cumulative toxicities can limit their use. These toxicitie
s include nephrotoxicity, neurotoxicity and ototoxicity with cisplatin and
myelosuppression with carboplatin. Although these adverse events can often
be managed, the interventions themselves can complicate and add to the cost
s of treatment. Importantly, acquired resistance to traditional platinum dr
ugs often develops in patients with ovarian cancer and can limit the useful
ness of these drugs.
Research into new platinum drugs has focused on identifying compounds with
improved tolerability profiles and, importantly, those which can circumvent
mechanisms of platinum resistance. New platinum drugs currently under deve
lopment that are showing promise in ovarian cancer include oxaliplatin, ned
aplatin, satraplatin, BBR3464 and ZD0473. If the encouraging in vitro activ
ity shown by new compounds, such as ZD0473 and BBR3464, translates into eff
icacy in the clinic, they may offer an extended spectrum of activity which
includes patients with ovarian cancer resistant to the classical platinum d
rugs.