Department of Medical Oncology, Cancer Institute (WIA), Adyar, Chennai, Tamil Nadu, 600036, India.
Department of Radiation Oncology, Cancer Institute (WIA), Adyar, Chennai, Tamil Nadu, 600036, India.
Int J Clin Pharm. 2020 Apr;42(2):662-666. doi: 10.1007/s11096-020-00997-3. Epub 2020 Mar 9.
Background There is limited data on specific antiemetic protocols for control of chemotherapy-induced nausea/vomiting (CINV) caused by weekly cisplatin regimens. Olanzapine is an active agent against CINV and may offer better control of nausea compared to aprepitant/fosaprepitant-based regimens. The usual antiemetic dose of olanzapine (10 mg for four days) causes problems with drowsiness. A lower dose may be as effective with lesser side effects in patients receiving weekly cisplatin. Objective To assess the control of nausea, vomiting, and occurrence of side effects with a modified olanzapine-based antiemetic regimen among patients with carcinoma of the cervix receiving concurrent cisplatin with pelvic radiotherapy. Setting Tertiary cancer hospital in Southern India. Methods We used a modified regimen "mini-OPD", oral olanzapine (5 mg) days 1 and 2, intravenous palonosetron (0.25 mg) and dexamethasone (12 mg) on day 1 of cisplatin administration in patients with carcinoma of the cervix receiving concurrent chemoradiotherapy with weekly cisplatin (40 mg/m/week). At our centre, these patients remained inpatients throughout chemoradiotherapy. CINV-related outcomes were captured in the patients' records by the treating physician in the subsequent week (up to 6 times per patient depending on the number of cycles). We audited these records to calculate the complete response (CR defined as no emetic episodes and no use of rescue medication) rate. Main outcome measure Grades of nausea, vomiting, and drowsiness as per CTCAE v4.0. Results Data of 65 patients (median age: 48 years) who received mini-OPD regimen (median doses of cisplatin/patient: 4) was available. The CR rate was 55%. Considering all cycles together (217 weekly assessment points), "no nausea" target was attained in 125 (58%) assessments and "no vomiting" in 168 (77%). There were no significant side effects. Conclusions The mini-OPD regimen is an inexpensive, non-toxic and effective regimen for the prevention of CINV in patients receiving weekly cisplatin concurrent with pelvic radiotherapy.
对于每周顺铂方案引起的化疗所致恶心/呕吐(CINV),目前针对特定止吐方案的数据有限。奥氮平是一种针对 CINV 的有效药物,与阿瑞匹坦/福沙匹坦为基础的方案相比,可能能更好地控制恶心。奥氮平的常规止吐剂量(连用 4 天 10mg)会引起嗜睡问题。对于接受每周顺铂治疗的患者,较低剂量可能同样有效,且副作用更少。目的:评估改良奥氮平为基础的止吐方案在接受顺铂联合盆腔放疗的宫颈癌患者中对恶心、呕吐和不良反应发生的控制效果。地点:印度南部的一所三级癌症医院。方法:我们使用改良方案“迷你 OPD”,宫颈癌患者接受每周顺铂(40mg/m/周)同期放化疗时,在顺铂给药的第 1 天,给予奥氮平(5mg)口服 1 天和 2 天,帕洛诺司琼(0.25mg)和地塞米松(12mg)静脉注射。在我们中心,这些患者在整个放化疗期间均为住院患者。治疗医生会在接下来的一周内(根据患者周期数,每位患者最多记录 6 次)在患者病历中记录 CINV 相关结局。我们对这些记录进行审核,以计算完全缓解(CR,定义为无呕吐发作且无使用解救药物)率。主要观察指标:根据 CTCAE v4.0 评估恶心、呕吐和嗜睡的程度。结果:共 65 例患者(中位年龄:48 岁)接受迷你 OPD 方案治疗,方案中位剂量(每位患者)为 4 个周期。CR 率为 55%。考虑所有周期,217 次每周评估中有 125 次(58%)达到“无恶心”目标,168 次(77%)达到“无呕吐”目标。没有明显的副作用。结论:迷你 OPD 方案是一种经济实惠、无毒且有效的方案,可预防接受每周顺铂联合盆腔放疗的患者发生 CINV。