Betticher D C, Anderson H, Ranson M, Meely K, Oster W, Thatcher N
CRC Department of Medical Oncology, Christie and Wythenshawe Hospitals, Manchester, UK.
Br J Cancer. 1995 Dec;72(6):1551-5. doi: 10.1038/bjc.1995.546.
Amifostine (WR-2721), a thiol compound, has been shown to protect normal tissue from alkylating agents and cisplatin-induced toxicity without loss of anti-tumour effects. To confirm this result, we conducted a phase II randomised trial to determine if the addition of amifostine reduces the toxicity of carboplatin without loss of anti-tumour activity in patients with inoperable non-small-cell lung cancer (NSCLC). After the first course of carboplatin (600 mg m-2 i.v. infusion), 21 patients were randomised to receive three cycles of carboplatin alone (C arm) or three infusions of amifostine at 910 mg m-2 (CA arm) at 28 day intervals. The amifostine was given 20 min before and at 2 and 4 h after carboplatin. Since the 910 mg m-2 amifostine infusion led to hypotension in six patients, the dosage was reduced by 25%, to 683 mg m-2 t.i.d., in the other four patients. Amifostine was well tolerated at this dose level. Five patients in the CA arm and three in the C arm had their planned treatment discontinued owing to progressive disease (n = 3), amifostine side-effects (hypotension, sneezing and sickness, n = 4), and carboplatin-induced thrombocytopenia (n = 1). Bone marrow and renal function at study entry and after the first course of carboplatin before randomisation were similar in both treatment arms. Twenty courses of carboplatin+amifostine have been compared with 25 courses of carboplatin alone. Although there was no statistically significant difference with respect to haematological values comparing both arms, the median time to platelet recovery (> 100 x 10(9) l-1) (13.5 days vs 21 days; P = 0.04) and the need for hospitalisation for i.v. antibiotic and other supportive treatment tended to be reduced in the CA arm (0/20 vs 6/25 patient courses; P = 0.06). Response rates and median survival (14 vs 9 months) were no different, excluding tumour protection activity by amifostine. These results with a small number of patients suggest that amifostine given with carboplatin may reduce the duration of thrombocytopenia and hospitalisation.
氨磷汀(WR-2721)是一种硫醇化合物,已被证明可保护正常组织免受烷化剂和顺铂诱导的毒性影响,同时不丧失抗肿瘤作用。为证实这一结果,我们进行了一项II期随机试验,以确定在无法手术的非小细胞肺癌(NSCLC)患者中,添加氨磷汀是否能降低卡铂的毒性,同时不丧失抗肿瘤活性。在首个疗程的卡铂(600mg/m²静脉输注)之后,21例患者被随机分为两组,一组接受三个疗程的单纯卡铂治疗(C组),另一组接受三个疗程的氨磷汀治疗,剂量为910mg/m²(CA组),每28天输注一次。氨磷汀在卡铂输注前20分钟、输注后2小时和4小时给药。由于910mg/m²的氨磷汀输注导致6例患者出现低血压,另外4例患者的剂量降低25%,至683mg/m²,每日三次。在此剂量水平下,氨磷汀耐受性良好。CA组有5例患者和C组有3例患者因疾病进展(n = 3)、氨磷汀副作用(低血压、打喷嚏和恶心,n = 4)以及卡铂诱导的血小板减少症(n = 1)而中断计划治疗。两个治疗组在研究入组时以及随机分组前首个疗程卡铂治疗后的骨髓和肾功能相似。已对20个疗程的卡铂+氨磷汀与25个疗程的单纯卡铂进行了比较。尽管两组在血液学值方面无统计学显著差异,但CA组血小板恢复至>100×10⁹/L的中位时间(13.5天对21天;P = 0.04)以及因静脉使用抗生素和其他支持治疗而住院的需求趋于减少(0/20对6/25患者疗程;P = 0.06)。排除氨磷汀的肿瘤保护活性后,缓解率和中位生存期(14个月对9个月)无差异。这些少量患者的结果表明,卡铂联合氨磷汀给药可能会缩短血小板减少症的持续时间和住院时间。