Mackay H J, McInnes A, Paul J, Raby N, Lofts F J, McDonald A C, Soukop M, Fullarton G M, Harris A L, Garcia-Vargas J, Evans T R
CRC Department of Medical Oncology Beatson Oncology Centre, Western Infirmary, Glasgow, UK.
Ann Oncol. 2001 Oct;12(10):1407-10. doi: 10.1023/a:1012552823543.
The aim of this study was to evaluate the efficacy of the combination of epirubicin, cisplatin and ralitrexed (Tomudex). ECT, in patients with advanced oesophageal or gastric adenocarcinoma. Efficacy was assessed primarily as response rate and secondarily in terms of toxicity, time to progression and survival.
Twenty-one patients with histologically and/or cytologically proven unresectable (7) or metastatic (14) gastro-oesophageal adenocarcinoma, who had bi-dimensionally measurable disease, with ECOG performance status < or = 2. with adequate haematological, hepatic and renal function received first-line chemotherapy with epirubicin (50 mg/m2). cisplatin (60 mg/m2) and Tomudex (2.5 mg/m2), ECT, at three-weekly intervals. Treatment consisted of three cycles of chemotherapy, with a further three cycles if there was disease response or stabilisation.
ECT is an active regimen in the treatment of advanced gastro-oesophageal adenocarcinoma with an overall intention-to-treat response rate of 29% (95% confidence intervals (CI): 11%-52%). In addition, 4 (19%) patients had stable disease. Median time to progression was 19 weeks (95% CI: 7-31 weeks). Median overall survival was 18 weeks (95% CI: 11-24 weeks). Seventeen patients failed to complete the six cycles of treatment due to disease progression (5). toxicity (3), non-toxic death (1 pulmonary embolism, 1 cardiac), severe allergy to epirubicin (1), patient decision (1) and five patients after the study was discontinued early due to toxicity. There were three toxic deaths: two due to sepsis complicating neutropaenia and one due to cardiorespiratory failure following drug induced enteritis. Nine patients experienced grade 3 or 4 neutropaenia, two patients experienced grade 3 or 4 nausea and vomiting and one patient had grade 4 diarrhoea.
The combination of epirubicin, cisplatin and tomudex is active against advanced gastro-oesophageal adenocarcinoma but the toxicity suggests that further evaluation in a randomised comparison to ECF is not appropriate.
本研究旨在评估表柔比星、顺铂和雷替曲塞(拓优得)联合化疗方案(ECT)治疗晚期食管或胃腺癌的疗效。疗效主要评估指标为缓解率,次要指标为毒性、疾病进展时间和生存期。
21例经组织学和/或细胞学证实为不可切除(7例)或转移性(14例)胃食管腺癌患者,具有可二维测量的病灶,东部肿瘤协作组(ECOG)体能状态评分为≤2,血液学、肝肾功能良好,接受表柔比星(50mg/m²)、顺铂(60mg/m²)和拓优得(2.5mg/m²)联合化疗方案(ECT)一线治疗,每3周1次。治疗包括3个周期化疗,若疾病缓解或稳定则再进行3个周期化疗。
ECT方案治疗晚期胃食管腺癌具有活性,总体意向性治疗缓解率为29%(95%可信区间(CI):11%-52%)。此外,4例(19%)患者疾病稳定。疾病进展的中位时间为19周(95%CI:7-31周)。总生存期的中位时间为18周(95%CI:11-24周)。17例患者因疾病进展(5例)、毒性(3例)、非毒性死亡(1例肺栓塞、1例心脏疾病)、对表柔比星严重过敏(1例)、患者决定(1例)以及5例在研究因毒性提前终止后未能完成6个周期治疗。有3例毒性死亡:2例因脓毒症并发中性粒细胞减少,1例因药物性肠炎后心肺功能衰竭。9例患者发生≥3级中性粒细胞减少,2例患者发生≥3级恶心和呕吐,1例患者发生4级腹泻。
表柔比星、顺铂和拓优得联合方案对晚期胃食管腺癌有活性,但毒性提示与ECF方案进行随机对照进一步评估并不合适。