Hager Avery, Kondle Shreya, Agarwal Amulya, Chintapenta Monica, Horadam Rochelle, Sadeghi Navid, Syed Samira
University of Texas Southwestern Medical School, Dallas, TX, USA.
Department of Internal Medicine, Texas Health Dallas Presbyterian Hospital, Dallas, TX, USA.
J Oncol Pharm Pract. 2025 Mar;31(2):236-244. doi: 10.1177/10781552241232692. Epub 2024 Feb 29.
IntroductionDocetaxel can cause fluid retention reactions (FRRs) and hypersensitivity reactions (HSRs). The manufacturer recommends a multi-day oral dexamethasone premedication to prevent these toxicities, but steroid related side effects and regimen compliance remain a concern. This study aimed to determine if modified dexamethasone premedication regimens resulted in differences in HSRs or FRRs to docetaxel. We also examined side effects of dexamethasone and delays in chemotherapy.MethodsA retrospective chart review was conducted on 82 early breast cancer patients treated with docetaxel. Three steroid regimens were examined: IV 20 mg single-dose dexamethasone, or IV 12 mg dexamethasone with either dexamethasone 8 mg BID for three days starting the day before chemotherapy or dexamethasone 4 mg BID for three days following chemotherapy. Adverse effects, delays in chemotherapy, and reasons for delays in chemotherapy were recorded.ResultsThe incidence and severity of FRRs and HSRs was low, with less than 10% incidence of HSRs or FRRs in any group. Delays were most common in the group receiving dexamethasone 8 mg BID for 3 days starting the day before chemotherapy (63.3%) ( < 0.05) and were most commonly due to patient noncompliance (26%).ConclusionA single dose of intravenous dexamethasone alone or followed by lower doses of oral dexamethasone may improve patient compliance and avoid delays in chemotherapy, without an increase in docetaxel toxicity.
引言
多西他赛可引起液体潴留反应(FRR)和超敏反应(HSR)。制造商建议采用多日口服地塞米松进行预处理以预防这些毒性反应,但类固醇相关的副作用和方案依从性仍是一个问题。本研究旨在确定改良的地塞米松预处理方案是否会导致多西他赛的HSR或FRR出现差异。我们还研究了地塞米松的副作用和化疗延迟情况。
方法
对82例接受多西他赛治疗的早期乳腺癌患者进行回顾性病历审查。研究了三种类固醇方案:静脉注射20mg单剂量地塞米松,或静脉注射12mg地塞米松,同时在化疗前一天开始给予8mg地塞米松每日两次,共三天,或在化疗后给予4mg地塞米松每日两次,共三天。记录不良反应、化疗延迟情况以及化疗延迟的原因。
结果
FRR和HSR的发生率和严重程度较低,任何组中HSR或FRR的发生率均低于10%。延迟最常见于化疗前一天开始给予8mg地塞米松每日两次,共3天的组(63.3%)(P<0.05),最常见的原因是患者不依从(26%)。
结论
单独静脉注射单剂量地塞米松或随后给予较低剂量的口服地塞米松可能会提高患者依从性并避免化疗延迟,而不会增加多西他赛的毒性。