Geh J I, Glynne-Jones R, Kwok Q S, Banerji U, Livingstone J I, Townsend E R, Harrison R A, Mitchell I C
Mount Vernon Hospital, Northwood, UK.
Clin Oncol (R Coll Radiol). 2000;12(3):182-7. doi: 10.1053/clon.2000.9147.
Epirubicin, cisplatin and continuous 5-fluorouracil (5-FU) infusion (ECF) has been reported to result in high clinical response rates in advanced gastro-oesophageal adenocarcinoma and is currently the 'gold standard' chemotherapy regimen for this tumour site. Despite this, its role as preoperative (neoadjuvant) treatment is unproven and therefore remains under investigation. We report our experience using ECF (intravenous epirubicin 50 mg/m2 and cisplatin 60 mg/m2 every 3 weeks, with continuous infusion of 5-FU 200 mg/m2 per day) as preoperative treatment in locally advanced adenocarcinoma of the lower oesophagus, gastro-oesophageal junction and stomach. Of the 23 patients treated (median age 54 years), 19 had potentially resectable disease, four were unresectable and seven had radiological evidence of lymph node involvement. A median of four cycles of ECF was delivered (range 1-6). Ten of 12 patients (83%) with dysphagia reported improvement of symptoms. Clinical disease progression occurred in six patients (26%) during chemotherapy. WHO grade 3 or 4 toxicity occurred in six patients (26%): four haematological, one mucositis, one vomiting. Seventeen patients (74%) proceeded to surgery; 14 (61%) were resected and three were unresectable. There were two (12%) postoperative deaths from respiratory failure. Major pathological response was seen in three patients (13%): one pathological complete response, two microscopic residual disease. Two patients had Stage II (T2N(0-1)) disease and nine were Stage III (T(3-4)N(0-1)). None of the patients with initially unresectable disease was rendered resectable. After a median follow-up interval of 33 months (range 26-53), the overall median survival was 12 months and 2-year survival was 30%. All patients who were initially unresectable or had radiological evidence of lymph node involvement have died. Therefore, despite good symptomatic response rates, ECF chemotherapy given in the preoperative setting did not appear to improve the outcome of patients with unresectable or radiologically lymph node-positive gastro-oesophageal adenocarcinoma. The role of ECF chemotherapy in resectable tumours is unclear and is currently under investigation in the randomized MRC Adjuvant Gastric Infusional Chemotherapy (MAGIC) study.
表柔比星、顺铂和持续输注5-氟尿嘧啶(5-FU)(ECF方案)已被报道在晚期胃食管腺癌中可产生较高的临床缓解率,目前是该肿瘤部位的“金标准”化疗方案。尽管如此,其作为术前(新辅助)治疗的作用尚未得到证实,因此仍在研究中。我们报告了我们使用ECF方案(静脉注射表柔比星50mg/m²和顺铂60mg/m²,每3周一次,同时持续输注5-FU 200mg/m²/天)作为食管下段、胃食管交界和胃局部晚期腺癌术前治疗的经验。在接受治疗的23例患者(中位年龄54岁)中,19例有潜在可切除疾病,4例不可切除,7例有淋巴结受累的影像学证据。ECF方案的中位疗程数为4个周期(范围1 - 6个周期)。12例吞咽困难患者中有10例(83%)报告症状改善。化疗期间6例患者(26%)出现临床疾病进展。6例患者(26%)发生世界卫生组织3级或4级毒性反应:4例血液学毒性,1例黏膜炎,1例呕吐。17例患者(74%)接受了手术;14例(61%)切除成功,3例不可切除。有2例(12%)患者术后死于呼吸衰竭。3例患者(13%)出现主要病理缓解:1例病理完全缓解,2例镜下有残留病灶。2例患者为Ⅱ期(T2N(0 - 1))疾病,9例为Ⅲ期(T(3 - 4)N(0 - 1))。最初不可切除的患者中无一例变为可切除。中位随访间隔33个月(范围26 - 53个月)后,总体中位生存期为12个月,2年生存率为30%。所有最初不可切除或有淋巴结受累影像学证据的患者均已死亡。因此,尽管症状缓解率良好,但术前给予ECF化疗似乎并未改善不可切除或影像学淋巴结阳性的胃食管腺癌患者的预后。ECF化疗在可切除肿瘤中的作用尚不清楚,目前正在随机MRC辅助胃灌注化疗(MAGIC)研究中进行调查。