Abstract
OBJECTIVE:
The
objective of this study is to evaluate the impact of
premedications
given as an adjunct to carboplatin on the incidence of hypersensitivity
reactions in women with ovarian cancer. Medications of interest include a
histamine
1 (H
1 ) and histamine
2 (H
2 ) blocker
in addition to dexamethasone.
METHODS:
This was a retrospective chart review evaluating the addition of an H
1 and H
2
blocker in addition to dexamethasone as standard premedications on the
incidence of carboplatin hypersensitivity reactions (CHR) in women with
ovarian cancer.
MAIN RESULTS:
The
odds ratio for premedication use was 0.46 with a 95% confidence
interval (0.17-1.27), suggesting that patients with premedication use
had approximately one-half of the risk of CHR compared to patients
without premedication. The overall incidence of CHR decreased from 7.9%
at baseline to 3.2% after the addition of premedications. The incidence
of CHR was
5.2% in patients with recurrent or progressive disease (N=58)
compared to
2.1% in the newly diagnosed patients (N=96).
Lifetime dose
greater than 3377 milligrams, number of cycles greater than six, and
progressive or recurrent disease were predictive factors of CHR in women
with ovarian cancer.
PRINCIPAL CONCLUSIONS:
Total
lifetime exposure to
carboplatin remains the greatest predictive factor
of CHR in women with ovarian cancer. While data analysis indicates the
addition of premedications for all ovarian cancer patients receiving
carboplatin did not result in a statistically significant reduction in
CHR, a patient benefit in CHR reduction was observed. A prospective
study is needed to confirm these findings.
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