Ikegawa Kiwako, Suzuki Shinya, Nomura Hisanaga, Enokida Tomohiro, Yamazaki Tomoko, Okano Susumu, Endo Kazushi, Saito Shinichiro, Yamaguchi Masakazu, Tahara Makoto
1 Department of Pharmacy, National Cancer Center Hospital East, National Research and Development Agency, Kashiwa, Japan.
2 Department of Head and Neck Medical Oncology, National Research and Development Agency, Kashiwa, Japan.
J Int Med Res. 2017 Aug;45(4):1378-1385. doi: 10.1177/0300060517713531. Epub 2017 Jun 12.
Objectives We evaluated infusion-related reactions associated with cetuximab combination chemotherapy comprising an H1-receptor antagonist plus dexamethasone as anti-allergy premedications for patients with head and neck cancer. Methods We retrospectively evaluated 248 patients who received a cetuximab combination regimen between December 2012 and August 2015. All patients received 5 mg intravenous dichlorpheniramine (H1-receptor antagonist), and dexamethasone (DEX) was adjusted from 6.6 mg to 13.2 mg according to the emetogenic risk. Results We identified 248 subjects, including 13 (5.2%) with infusion-related reactions (grade 1 in five [2.0%], grade 2 in seven [2.8%], and grade 4 in one [0.4%]). The incidence of these reactions in cetuximab combination regimens, each employing an H1-receptor antagonist, using a higher dose of dexamethasone (13.2 mg) was not significantly lower compared with those using 6.6 mg DEX (2.4% vs 8.3%, respectively; p = 0.43). Twelve patients experienced infusion-related reactions associated with the first cetuximab administration, and one reaction occurred after the third administration. Conclusions The incidence of infusion-related reactions was lower compared with those of previous studies. Dexamethasone combined with an H1-receptor antagonist was useful for preventing allergic responses. The incidence of infusion-related reactions was not lower with 13.2 mg dexamethasone, and 6.6 mg DEX prevented infusion-related reactions.
目的 我们评估了与西妥昔单抗联合化疗相关的输注相关反应,该联合化疗方案包含一种H1受体拮抗剂加地塞米松,作为头颈癌患者的抗过敏预处理药物。方法 我们回顾性评估了2012年12月至2015年8月期间接受西妥昔单抗联合方案治疗的248例患者。所有患者均接受5mg静脉注射氯苯那敏(H1受体拮抗剂),并根据致吐风险将地塞米松(DEX)的剂量从6.6mg调整至13.2mg。结果 我们确定了248名受试者,其中13名(5.2%)出现输注相关反应(1级5名[2.0%],2级7名[2.8%],4级1名[0.4%])。在每种使用H1受体拮抗剂的西妥昔单抗联合方案中,使用较高剂量地塞米松(13.2mg)的这些反应的发生率与使用6.6mg DEX的方案相比,并无显著降低(分别为2.4%和8.3%;p = 0.43)。12名患者在首次使用西妥昔单抗时出现输注相关反应,1例反应发生在第三次给药后。结论 与先前研究相比,输注相关反应的发生率较低。地塞米松联合H1受体拮抗剂可有效预防过敏反应。13.2mg地塞米松并未降低输注相关反应的发生率,而6.6mg DEX可预防输注相关反应。