Evans W K, Eisenhauer E, Hughes P, Maroun J A, Ayoub J, Shepherd F A, Feld R
Ottawa Regional Cancer Centre, Canada.
Br J Cancer. 1988 Oct;58(4):464-8. doi: 10.1038/bjc.1988.242.
Thirty-four previously untreated patients with extensive small cell lung cancer were treated with a combination of carboplatin 300 mg m-2 i.v. on day 1 and etoposide 100 mg m-2 i.v. on days 1, 2 and 3 every 28 days. Thirty-two patients were assessable for response. Eighteen patients (56%) achieved an objective response (95% confidence limits 38%-73%). Five (16%) had a complete response and 13 (41.0%) had a partial response. The median time to response was 7.8 weeks and the median duration of response was 23.1 weeks (range 6.2 to 54 weeks). The median survival of all 34 extensive disease patients was 34.7 weeks (range 1.3-59.3 weeks). Myelosuppression (leukopenia) was the main toxicity. There was one early death that may have been treatment-related. Biochemical renal dysfunction was noted in two patients. Paresthesiae and tinnitus/hearing loss were described by three and two patients respectively. Serious gastrointestinal toxicity was infrequent. This and other studies have shown this combination to be active and well tolerated in small cell lung cancer; however, it is not yet clear if it is as efficacious as the more commonly used VP-16-cisplatin regimen.
34例既往未接受过治疗的广泛期小细胞肺癌患者接受了如下联合治疗:第1天静脉注射卡铂300mg/m²,第1、2、3天静脉注射依托泊苷100mg/m²,每28天为一周期。32例患者可评估疗效。18例患者(56%)获得客观缓解(95%置信区间38%-73%)。5例(16%)完全缓解,13例(41.0%)部分缓解。缓解的中位时间为7.8周,缓解持续时间的中位值为23.1周(范围6.2至54周)。所有34例广泛期疾病患者的中位生存期为34.7周(范围1.3-59.3周)。骨髓抑制(白细胞减少)是主要毒性。有1例早期死亡,可能与治疗相关。2例患者出现生化性肾功能不全。分别有3例和2例患者描述有感觉异常和耳鸣/听力丧失。严重的胃肠道毒性不常见。本研究及其他研究表明,这种联合方案在小细胞肺癌中具有活性且耐受性良好;然而,它是否与更常用的VP-16-顺铂方案一样有效尚不清楚。