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abstract
Introduction: Oxaliplatin
is an important drug in treatment of several solid tumors. Ovarian
cancer (OC) is sensitive to chemotherapy and the overall response rate
with primary therapy is about 75%. Unfortunately, 60 – 70% of patients
experience recurrence requiring additional treatments and finally die of
progressive disease within 5 years of the initial diagnosis. Currently,
a platinum-based combination therapy is recommended in
platinum-sensitive disease while a non-platinum single-agent therapy is
preferred in platinum-resistant disease that is characterized by a low
response rate.
Expert opinion:
Platinum emerged as the mainstay of OC treatment in frontline therapy,
and platinum compounds remain a critical component of chemotherapy also
in relapsed disease. Unfortunately, increasing exposure to
carboplatin/cisplatin raises the risk of resistance or hypersensitivity
to platinum. Several studies have demonstrated the safety and
effectiveness of oxaliplatin, both alone and in combination regimens, in
relapsed OC, demonstrating a good tolerability profile. Moreover, the
therapeutic spectrum of oxaliplatin might be extended to OC patients who
experienced hypersensitivity to carboplatin because of its favorable
toxicity profile and at least equal efficacy.
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