Bajetta E, Di Bartolomeo M, Carnaghi C, Buzzoni R, Mariani L, Gebbia V, Comella G, Pinotti G, Ianniello G, Schieppati G, Bochicchio A M, Maiorino L
ITMO, c/o Division of Medical Oncology B of Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
Br J Cancer. 1998 Apr;77(7):1149-54. doi: 10.1038/bjc.1998.191.
The new regimens developed over the last few years have led to an improvement in the treatment of advanced gastric cancer, and our previous experience confirmed the fact that the combination of etoposide, doxorubicin and cisplatin (EAP regimen) is an active treatment that leads to interesting complete remission rates. The primary end point of the present multicentre, randomized, parallel-group phase II study was to determine the activity of the simplified 2-day EAP schedule in patients with locally advanced or metastatic gastric cancer, and to verify whether the addition of low doses of granulocyte-macrophage colony-stimulating factor (GM-CSF) made it possible to increase dose intensity. Of the 62 enrolled patients, 30 were randomized to receive epirubicin 35 mg m(-2), etoposide 120 mg m(-2) and cisplatin 45 mg m(-2) (FEP) on days 1 and 2 every 28 days and 32 to receive the same schedule plus subcutaneous GM-CSF (molgramostin) 150 microg day(-1) on days 5-14 every 21 days. The patients were stratified by age and the number of disease sites. The characteristics of the patients were well balanced between the two groups. The objective response rate of the patients as a whole was 34% (21 out of 62; 95% confidence interval 22-46), with only one complete remission. The median response duration was 4.5 months (range 1-24 months). The median time to treatment failure was 5 months (range 1-14 months), without any difference between the two groups. The median survival of the patients as a whole was 9 months. Full doses were administered in 92% and 94% of the cycles in the control and GM-CSF arms respectively. The average dose intensity calculated for all drugs was 0.96% in the control and 1.27% in the GM-CSF group. CTC-NCI grade 3-4 neutropenia was reported in 39% vs 45% of patients, thrombocytopenia in 11% vs 35% (P = 0.020) and anaemia in 7% vs 35% (P = 0.014). The FEP combination is as active (OR: 34%) in the treatment of patients with advanced gastric cancer as the EAP regimen, although it leads to fewer complete remissions. The patients randomized to receive low-dose GM-CSF achieved a significantly higher dose intensity than controls (P = 0.0001).
过去几年研发的新方案已使晚期胃癌的治疗有所改善,我们之前的经验证实,依托泊苷、阿霉素和顺铂联合方案(EAP方案)是一种有效的治疗方法,可带来可观的完全缓解率。本多中心、随机、平行组II期研究的主要终点是确定简化的2天EAP方案对局部晚期或转移性胃癌患者的有效性,并验证添加低剂量粒细胞-巨噬细胞集落刺激因子(GM-CSF)是否能提高剂量强度。在62例入组患者中,30例被随机分配接受表柔比星35mg/m²、依托泊苷120mg/m²和顺铂45mg/m²(FEP方案),每28天的第1天和第2天给药;32例接受相同方案,外加每21天的第5 - 14天皮下注射GM-CSF(莫拉司亭)150μg/天。患者按年龄和疾病部位数量分层。两组患者的特征均衡良好。总体患者的客观缓解率为34%(62例中的21例;95%置信区间22 - 46),仅有1例完全缓解。中位缓解持续时间为4.5个月(范围1 - 24个月)。中位治疗失败时间为5个月(范围1 - 14个月),两组之间无差异。总体患者的中位生存期为9个月。对照组和GM-CSF组分别有92%和94%的周期给予了全剂量。所有药物计算得出的平均剂量强度在对照组为0.96%,在GM-CSF组为1.27%。报告的美国国立癌症研究所(NCI)CTC 3 - 4级中性粒细胞减少症患者比例分别为39%和45%,血小板减少症分别为11%和35%(P = 0.020),贫血分别为7%和35%(P = 0.014)。FEP联合方案在晚期胃癌患者治疗中的有效性(OR:34%)与EAP方案相当,尽管完全缓解的病例较少。随机接受低剂量GM-CSF的患者剂量强度显著高于对照组(P = 0.0001)。