Hajdenberg Julio, Grote Thomas, Yee Lorrin, Arevalo-Araujo Roberto, Latimer Laurie A
M. D. Anderson Cancer Center Orlando, 1400 S. Orange Ave., Orlando, Florida 32806, USA.
J Support Oncol. 2006 Oct;4(9):467-71.
Serotonin (5-HT3) receptor antagonists are the foundation of standard antiemetic care for cancer patients receiving emetogenic chemotherapy. To enhance the efficacy of these supportive care agents, dexamethasone is routinely admixed with the 5-HT3 receptor antagonist, which is administered by intravenous infusion before chemotherapy begins. This phase II study evaluated the safety and efficacy of intravenous palonosetron admixed with dexamethasone to prevent chemotherapy-induced nausea and vomiting (CINV) in patients receiving moderately emetogenic chemotherapy. Cancer patients received palonosetron 0.25 mg plus dexamethasone 8 mg admixed in 50 mL of infusion solution before receiving at least one qualifying chemotherapeutic agent (cyclophosphamide < or = 1,500 mg/m2, doxorubicin > or = 20 mg/m2, carboplatin, or oxaliplatin). Patients used diaries to record nausea and emesis experienced and rescue medications used. Of 32 participants, 27 (84%) had a complete response (no emesis and no rescue medication) during the acute (0-24 hours) interval posttherapy, 19 (59%) had a complete response during the delayed (> 24-120 hours) posttherapeutic interval, and 19 (59%) had a complete response during the overall (0-120 hours) posttreatment interval. A total of 23 patients (72%) had no emetic episodes, 16 (50%) had no nausea, and 21 (66%) used no rescue medication throughout the overall 5-day interval. The combination was well tolerated. Palonosetron plus dexamethasone given as a pretreatment infusion is effective and safe in preventing acute and delayed CINV in patients receiving moderately emetogenic chemotherapy.
5-羟色胺(5-HT3)受体拮抗剂是接受致吐性化疗的癌症患者标准止吐治疗的基础。为提高这些支持性治疗药物的疗效,地塞米松通常与5-HT3受体拮抗剂混合使用,并在化疗开始前通过静脉输注给药。这项II期研究评估了静脉注射帕洛诺司琼与地塞米松混合使用对接受中度致吐性化疗的患者预防化疗引起的恶心和呕吐(CINV)的安全性和有效性。癌症患者在接受至少一种符合条件的化疗药物(环磷酰胺≤1500mg/m²、多柔比星≥20mg/m²、卡铂或奥沙利铂)之前,先接受在50mL输液溶液中混合的0.25mg帕洛诺司琼加8mg地塞米松。患者使用日记记录经历的恶心和呕吐情况以及使用的解救药物。在32名参与者中,27名(84%)在治疗后急性(0-24小时)期间有完全缓解(无呕吐且未使用解救药物),19名(59%)在治疗后延迟(>24-120小时)期间有完全缓解,19名(59%)在治疗后总体(0-120小时)期间有完全缓解。在整个5天期间,共有23名患者(72%)没有呕吐发作,16名(50%)没有恶心,21名(66%)未使用解救药物。该联合用药耐受性良好。作为预处理输注给予的帕洛诺司琼加地塞米松在预防接受中度致吐性化疗的患者的急性和延迟性CINV方面有效且安全。