Division of Pharmacotherapy, Kinki University School of Pharmacy, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan.
Int J Clin Oncol. 2011 Jun;16(3):244-9. doi: 10.1007/s10147-010-0170-6. Epub 2011 Jan 18.
Oxaliplatin is a third-generation platinum compound and a key agent for the management of colorectal cancer. Patients treated with oxaliplatin are at risk for hypersensitivity reactions. We designed a modified premedication regimen to prevent oxaliplatin-related hypersensitivity reactions and assessed if this approach is effective.
A retrospective cohort study of patients with advanced colorectal cancer who received modified FOLFOX6 (mFOLFOX6) was performed. Patients received routine premedication with dexamethasone 8 mg and granisetron 3 mg for the first five cycles of mFOLFOX6. From the sixth cycle onward, cohort 1 received the same premedication, and cohort 2 received modified premedication (diphenhydramine 50 mg orally, followed by dexamethasone 20 mg, granisetron 3 mg, and famotidine 20 mg). We compared the incidence of hypersensitivity reactions, duration of treatment, and reasons for treatment withdrawal between the two cohorts.
A total of 181 patients were studied (cohort 1, 81; cohort 2, 100). Hypersensitivity reactions developed in 16 patients (20%) in cohort 1 and 7 (7.0%) in cohort 2 (P = 0.0153). The median number of cycles increased from 9 in cohort 1 to 12 in cohort 2. Apart from progressive disease, neurotoxicity was the reason for discontinuing treatment in 20% of the patients in cohort 1, as compared with 53% in cohort 2.
Increased doses of dexamethasone and antihistamine significantly reduced oxaliplatin-related hypersensitivity reactions. This effective approach should be considered for all patients who receive FOLFOX, allowing treatment to be completed as planned.
奥沙利铂是第三代铂类化合物,也是治疗结直肠癌的关键药物。接受奥沙利铂治疗的患者有发生过敏反应的风险。我们设计了一种改良的预处理方案来预防奥沙利铂相关的过敏反应,并评估这种方法是否有效。
对接受改良 FOLFOX6(mFOLFOX6)治疗的晚期结直肠癌患者进行了回顾性队列研究。前 5 个周期的 mFOLFOX6 治疗中,患者接受常规预处理,即地塞米松 8 mg 和格拉司琼 3 mg。从第 6 个周期开始,队列 1 接受相同的预处理,队列 2 接受改良的预处理(口服苯海拉明 50 mg,然后给予地塞米松 20 mg、格拉司琼 3 mg 和法莫替丁 20 mg)。我们比较了两组患者过敏反应的发生率、治疗持续时间和治疗终止的原因。
共纳入 181 例患者(队列 1,81 例;队列 2,100 例)。队列 1 中有 16 例(20%)患者发生过敏反应,队列 2 中有 7 例(7.0%)患者发生过敏反应(P = 0.0153)。队列 1 的中位治疗周期数从 9 个增加到 12 个,而队列 2 的中位治疗周期数从 9 个增加到 12 个。除了疾病进展外,神经毒性是导致队列 1 中 20%的患者停止治疗的原因,而队列 2 中则有 53%的患者停止治疗。
增加地塞米松和抗组胺药的剂量可显著降低奥沙利铂相关的过敏反应。对于所有接受 FOLFOX 治疗的患者,这种有效的方法都应被考虑,以确保治疗能按计划完成。