Raghavan D, Gianoutsos P, Bishop J, Lee J, Young I, Corte P, Bye P, McCaughan B
Department of Clinical Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.
J Clin Oncol. 1990 Jan;8(1):151-4. doi: 10.1200/JCO.1990.8.1.151.
Thirty-one patients with advanced malignant mesothelioma, previously untreated or having received only one prior cytotoxic regimen, were treated in a prospective, single-arm phase II trial with carboplatin (NSC 241240) at a dose of 150 mg/m2 per day intravenously (IV) for 3 days (450 mg/m2/course). One complete remission and four partial remissions were achieved, yielding an overall objective response rate of 16% (95% confidence interval [CI], 5.4% to 34%). The median duration of remission was 8 months (range, 5 to 17). Nonhematological toxicity was mild (only 12% with World Health Organization [WHO] grade 3 vomiting); 16% suffered WHO grade 3 to 4 hematological toxicity, but there were no life-threatening episodes and no treatment-related deaths. Carboplatin has modest activity against malignant mesothelioma and, because of its low toxicity, has a role in the management of this disease.
31例晚期恶性间皮瘤患者,既往未接受过治疗或仅接受过一种细胞毒性治疗方案,在一项前瞻性单臂II期试验中接受卡铂(NSC 241240)治疗,剂量为每日150mg/m²静脉注射,共3天(450mg/m²/疗程)。1例完全缓解,4例部分缓解,总客观缓解率为16%(95%置信区间[CI],5.4%至34%)。缓解的中位持续时间为8个月(范围,5至17个月)。非血液学毒性较轻(世界卫生组织[WHO]3级呕吐仅12%);16%的患者出现WHO 3至4级血液学毒性,但无危及生命的事件,也无治疗相关死亡。卡铂对恶性间皮瘤有一定活性,且因其毒性低,在该疾病的治疗中具有一定作用。