Abstract
AIM:
To
assess the efficacy and safety of the combination of pegylated
liposomal doxorubicin (PLD) and carboplatin in patients with recurrent
epithelial ovarian carcinoma (ROC), following disease progression on single agent PLD.
METHODS:
An
analysis of the medical records of 10 patients with ROC, treated in our
institution with a combination of PLD and carboplatin following
progression on single-agent PLD therapy was performed. The median age
was 59.1 years (range, 45 to 77 years). All diagnoses were
histological-proven. Eight of the 10 patients were platinum-resistant.
Following disease progression on single-agent PLD treatment, carboplatin
area under the curve (AUC)-5 was added to PLD in all 10 patients. In
order to assess disease status, Ca-125 was assessed before each
PLD/carboplatin treatment. Relative changes in Ca-125 values were
calculated, and response defined as a greater than 50% reduction in
Ca-125 from baseline. Radiographic studies were re-evaluated and
responses to therapy based on computer tomography (CT) scans carried out
on a regular basis every 2-3 mo in each patient. Statistical analysis
was performed using SPSS (V19).
RESULTS:
A median of 10
cycles (range, 2-26) of the carboplatin-PLD combination was given. Of
the 10 treated patients, 6 had > 50% reduction in Ca-125 levels from
baseline, 4 of these had a partial response according to Response
Evaluation Criteria in Solid Tumors (RECIST) criteria, and the other 2
patients had no measurable disease. In a further 2 patients with a best
response of disease stabilization and < 50% reduction of Ca-125
levels, one had progression of disease after 26 cycles, and the second
progressed with brain metastases following 12 cycles. Seven of the eight
patients who were platinum-resistant showed evidence of clinical
benefit on carboplatin-PLD combination therapy; 5 of these had > 50%
reduction in Ca-125 level, 4 also showed a partial response on CT scan.
The treatment was generally well-tolerated by the patients.
CONCLUSION:
Addition
of carboplatin to PLD, after disease progression on single-agent PLD
therapy, is both effective and safe in patients with ROC, even in those
with Platinum-resistant disease.
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