A. Polyzos et al., Hypersensitivity reactions to carboplatin administration are common but not always severe: A 10-year experience, ONCOL-BASEL, 61(2), 2001, pp. 129-133
We have retrospectively evaluated and characterized the hypersensitivity re
actions associated with carboplatin administration in ovarian cancer patien
ts treated mainly on an outpatient basis at the Laikon Hospital from 1988 t
o 1998. A total of 240 patients, who had never been exposed to platinum com
pounds previously, received carboplatin plus cyclophosphamide (n = 58) or p
aclitaxel (n = 136) intravenously, and intraperitoneal carboplatin plus int
ravenous cyclophosphamide (n = 46). The median number of carboplatin course
s was 6 (range 3-12) and 5 (range 4-6) for the intravenous and intraperiton
eal treatment regimens, respectively. Thirty-two of 194 patients (16%) who
were on intravenous carboplatin treatment developed symptoms compatible wit
h a hypersensitivity reaction to carboplatin, that was always verified by m
anifestation of at least similar symptoms on rechallenging. In contrast, in
the group of 46 patients on intraperitoneal carboplatin treatment, no hype
rsensitivity reaction was ever noticed. Hypersensitivity reactions always o
ccurred after administration of the first 4 intravenous courses of carbopla
tin; 4, 19, 4, and 5 reactions occurred at the 5th, 6th, 7th, and 8th cours
es, respectively. These reactions could be distinguished in: (a) mild hyper
sensitivity reactions in 20 of 194 patients, which manifested as itching (2
0 patients) and small area erythema plus erythema of the palms and soles (1
2 patients), occurring either during intravenous injection when most of the
drug scheduled had been administered, or within 3 days, and (b) in severe
reactions in 12 of 194 patients, which manifested acutely as itching, diffu
se erythroderma, rigor, facial swelling, throat and chest tightness, tachyc
ardia (12 patients) and bronchospasm (2 patients), and hypertension or hypo
tension in 8 and 4 patients, respectively. With appropriate symptomatic man
agement, discontinuation of carboplatin treatment was not required in patie
nts with mild hypersensitivity reactions, but none of the 12 patients with
severe reactions was able to receive a full subsequent dose of carboplatin
on rechallenging. However, in 4 of these 12 patients carboplatin was replac
ed by cisplatin, which was given for 4-6 courses without side effects. Thes
e findings indicate that although hypersensitivity reactions are common in
general, occurring in almost 1 of every 6 patients treated intravenously wi
th carboplatin, their clinical picture is variable, leading to discontinuat
ion of treatment in only 6% of patients. This is not the case when the intr
aperitoneal route of carboplatin administration is used when indicated. Cop
yright (C) 2001 S. Karger AG, Basel.