Adenis A
Département de médecine, centre Oscar-Lambret, Lille.
Bull Cancer. 1994 Apr;81(4):331-3.
This study was aimed to confirm the therapeutic activity of the combination of etoposide, doxorubicin and cisplatin which has shown some clinical efficiency as first line therapy in advanced gastric cancer. Seventeen patients with metastatic gastric cancer were treated with etoposide (120 mg/m2, i.v., on day 5, 6 and 7), epirubicin (20 mg/m2, i.v., on day 1 and 7) and cisplatin (40 mg/m2, i.v., on day 2 and 8), q 4 weeks. In 16 patients evaluable for response, three (19%) obtained a partial response lasting from 93 to 360 days. Fifteen patients were evaluable for toxicity. Main toxicities > grade 2 included anemia (2/15), neutropenia (5/15), alopecia (8/15), fatigue (3/15), diarrhea (2/15), vomiting (2/15). Twenty nine per cent of severe toxic events were documented all along 52 cycles. Therefore we failed to confirm that this regimen could be of clinical efficiency in advanced gastric cancer as regards the benefits/toxicity ratio.
本研究旨在证实依托泊苷、阿霉素和顺铂联合使用的治疗活性,该联合用药作为晚期胃癌的一线治疗已显示出一定的临床疗效。17例转移性胃癌患者接受依托泊苷(120mg/m²,静脉注射,第5、6和7天)、表柔比星(20mg/m²,静脉注射,第1和7天)和顺铂(40mg/m²,静脉注射,第2和8天)治疗,每4周重复一次。在16例可评估疗效的患者中,3例(19%)获得部分缓解,持续时间为93至360天。15例患者可评估毒性。主要的2级以上毒性包括贫血(2/15)、中性粒细胞减少(5/15)、脱发(8/15)、疲劳(3/15)、腹泻(2/15)、呕吐(2/15)。在52个周期中,29%的患者出现严重毒性事件。因此,就获益/毒性比而言,我们未能证实该方案对晚期胃癌具有临床疗效。