Literature DB >> 17701006

Preliminary experience with a modified premedication protocol that included intravenous diphenhydramine and calcium bromide for the prophylaxis of paclitaxel-related hypersensitivity reactions.

Shinji Sasada1, Tomonori Hirashima, Yukiko Nakamura, Takayuki Takimoto, Mitsugi Furukawa, Masashi Kobayashi, Takashi Nitta, Kaoru Matsui, Ichiro Kawase.   

Abstract

BACKGROUND: Paclitaxel often causes severe hypersensitivity reactions (HSRs) rapidly after infusion, even in patients given prophylactic therapy. The purpose of this study was to analyze the incidence of paclitaxel-related HSRs in patients with non-small cell lung cancer (NSCLC) retrospectively, and to assess the feasibility of a modified premedication protocol.
METHODS: One hundred and seven patients who were pretreated with either a conventional premedication regimen (two doses of dexamethasone) or a short premedication regimen (single dose of dexamethasone with oral diphenhydramine and intravenous ranitidine), prior to paclitaxel infusion were retrospectively analyzed. A modified premedication regimen, consisting of 12.5 ml of Rescalmin (intravenous diphenhydramine 50 mg and calcium bromide 437.5 mg), intravenous ranitidine 100 mg, and intravenous dexamethasone 20 mg, was given 30 min prior to paclitaxel, with oral dexamethasone 8 mg given on the night before the paclitaxel. Patients received paclitaxel intravenously at 175 mg/m(2) over 3 h, followed by carboplatin, AUC 5, over 1 h on day 1 every 3 weeks.
RESULTS: In the conventional premedication group, 21 patients had HSRs (32.3%); in 1 of these patients the HSR was considered to be severe (1.5%). In the short premedication group, 19 patients had HSRs (45.2%); in 6 of these patients the HSRs were considered to be severe (14.3%). The incidence of severe HSRs was significantly higher in the short premedication group than in the conventional premedication group (P = 0.027). In the modified premedication protocol study, HSR events were recorded in 14 patients (63.6%); 14 showed flushing, 2 had skin rash, and 1 had tachycardia. No severe HSRs were seen.
CONCLUSIONS: The incidence of HSRs in the short premedication group tended to be higher than that in the conventional premedication group. The modified premedication protocol was found to be feasible for preventing paclitaxel-related HSR, but case accumulation is needed.

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Year:  2007        PMID: 17701006     DOI: 10.1007/s10147-007-0675-9

Source DB:  PubMed          Journal:  Int J Clin Oncol        ISSN: 1341-9625            Impact factor:   3.402


  17 in total

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Authors:  M Markman; A Kennedy; K Webster; B Kulp; G Peterson; J Belinson
Journal:  J Clin Oncol       Date:  2000-01       Impact factor: 44.544

2.  Multicenter phase I/II study of cetuximab with paclitaxel and carboplatin in untreated patients with stage IV non-small-cell lung cancer.

Authors:  Christiane D Thienelt; Paul A Bunn; Nasser Hanna; Arthur Rosenberg; Michael N Needle; Michael E Long; Daniel L Gustafson; Karen Kelly
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Journal:  N Engl J Med       Date:  1995-04-13       Impact factor: 91.245

9.  Phase I trial of taxol given as a 3-hour infusion every 21 days.

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10.  Fatal outcome of a hypersensitivity reaction to paclitaxel: a critical review of premedication regimens.

Authors:  J S Kloover; M A den Bakker; H Gelderblom; J P van Meerbeeck
Journal:  Br J Cancer       Date:  2004-01-26       Impact factor: 7.640

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  1 in total

1.  Pre-medication protocols for the prevention of paclitaxel-induced infusion related reactions: a systematic review and meta-analysis.

Authors:  Samuel Dubinsky; Deep Patel; Xiang Wang; Amirrtha Srikanthan; Terry L Ng; Corey Tsang
Journal:  Support Care Cancer       Date:  2022-02-12       Impact factor: 3.603

  1 in total

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