The objective of this paper is to describe our experience with a desensitiz
ation protocol to paclitaxel using the original paclitaxel solution in pati
ents following severe hypersensitivity reactions. A retrospective review of
75 consecutive patients with ovarian cancer who received intravenous pacli
taxel-based chemotherapy between January 1996 and May 1998 at the Gynecolog
ic Oncology Unit at Meir Hospital-Sapir Medical Center, Kfar-Saba, Israel.
All patients who developed a hypersensitivity reaction to paclitaxel were t
reated with a desensitization protocol. The protocol included serial 10-fol
d dilutions (up to 1:100,000) of the actual paclitaxel infusate, delivered
in successive volumes of 1, 2, 4, and 8 mi. These escalating doses of pacli
taxel were given intravenously at 15-min intervals for each dilution. Follo
wing administration of the last diluted dose, the patient received a 1-ml d
ose of the undiluted solution. If no side effects were recorded, the rest o
f the actual dose was delivered at a 3-h infusion rate. Vital signs were mo
nitored and recorded throughout the course of treatment. Six patients with
a previous paclitaxel-associated hypersensitivity reaction were successfull
y treated with the desensitization protocol.
In conclusion, we demonstrate that the desensitization protocol is feasible
and safe without compromising cytotoxic activity. Our results show that th
is strategy is a reasonable choice in this clinical setting and potentially
avoids paclitaxel-based regimen interruption.