Ilson D H, Sirott M, Saltz L, Heelan R, Huang Y, Keresztes R, Kelsen D P
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Cancer. 1995 May 1;75(9):2197-202. doi: 10.1002/1097-0142(19950501)75:9<2197::aid-cncr2820750902>3.0.co;2-s.
The combination of 5-fluorouracil (5-FU) and cisplatin has moderate antitumor activity in the treatment of metastatic epidermoid carcinoma of the esophagus. The authors have recently shown activity for the combination of 5-FU and interferon-alpha 2a (IFN-alpha) in both esophageal epidermoid and adenocarcinoma. A Phase II trial, therefore, was undertaken to evaluate the antitumor activity of the three-drug combination of IFN-alpha, 5-FU, and cisplatin in unresectable or metastatic esophageal carcinoma.
Twenty-seven patients with locally advanced or metastatic carcinoma of the esophagus were treated. No prior chemotherapy was allowed. Twelve patients had epidermoid carcinoma (44%) and 15 patients had adenocarcinoma (56%). Patients received IFN-alpha at a dose of 3 x 10(6) units/day given daily by subcutaneous injection on days 1 to 28, 5-FU at a dose of 750 mg/m2/day for 5 days by continuous intravenous infusion on days 1 to 5, and cisplatin at a dose of 100 mg/m2 on day 1. Treatment was recycled every 28 days, and after the first three cycles, cisplatin was administered only on alternate cycles. Twenty-seven patients completed a median of 4 cycles (range, 1-13 cycles), and 26 patients were evaluable for response.
Major responses were observed in 13 patients (50%, 95% confidence intervals, 31-69%), including two complete responses (8%). The response proportion in epidermoid carcinoma (8 of 11 patients, 73%) was higher than the response proportion in adenocarcinoma (5 of 15 patients, 33%). The median duration of response was 29 weeks (range, 11-74 weeks), similar in epidermoid carcinoma and adenocarcinoma. Toxicity was moderately severe but manageable with dose attenuations. Grade 3/4 hematologic toxicity was observed in 41% of patients and grade 3/4 nonhematologic toxicity was observed in 26% of patients. IFN-alpha was reduced to either a 3- or 5-day a week schedule because of fatigue and/or myelosuppression in 12 patients (44%). There were two treatment-related deaths (7%).
In this Phase II trial, the combination of IFN-alpha, 5-FU, and cisplatin had substantial antitumor activity in esophageal carcinoma with apparently greater antitumor activity in epidermoid carcinoma than adenocarcinoma. A larger confirmatory trial comparing this treatment to conventional 5-FU and cisplatin is warranted for epidermoid carcinoma. In future chemotherapy trials, the response assessment for epidermoid and adenocarcinoma should continue to be stratified.
5-氟尿嘧啶(5-FU)和顺铂联合用药在治疗转移性食管表皮样癌方面具有中等抗肿瘤活性。作者最近发现5-FU与α-2a干扰素(IFN-α)联合用药对食管表皮样癌和腺癌均有活性。因此,进行了一项II期试验,以评估IFN-α、5-FU和顺铂三药联合方案对不可切除或转移性食管癌的抗肿瘤活性。
27例局部晚期或转移性食管癌患者接受了治疗。不允许之前接受过化疗。12例患者为表皮样癌(44%),15例患者为腺癌(56%)。患者在第1至28天每天皮下注射剂量为3×10⁶单位/天的IFN-α,在第1至5天通过持续静脉输注给予剂量为750mg/m²/天的5-FU,共5天,在第1天给予剂量为100mg/m²的顺铂。治疗每28天循环一次,在前三个周期后,顺铂仅在交替周期给药。27例患者完成的中位周期数为4个周期(范围1-13个周期),26例患者可评估疗效。
13例患者(50%,95%置信区间,31%-69%)观察到主要缓解,包括2例完全缓解(8%)。表皮样癌的缓解比例(11例患者中的8例,73%)高于腺癌的缓解比例(15例患者中的5例,33%)。缓解的中位持续时间为29周(范围11-74周),在表皮样癌和腺癌中相似。毒性为中度严重,但通过剂量调整可控制。41%的患者观察到3/4级血液学毒性,26%的患者观察到3/4级非血液学毒性。12例患者(44%)因疲劳和/或骨髓抑制将IFN-α减至每周3天或5天的给药方案。有2例与治疗相关的死亡(7%)。
在这项II期试验中,IFN-α、5-FU和顺铂联合用药在食管癌中具有显著的抗肿瘤活性,在表皮样癌中的抗肿瘤活性明显高于腺癌。对于表皮样癌,有必要进行一项更大规模的验证性试验,将该治疗方案与传统的5-FU和顺铂方案进行比较。在未来的化疗试验中,表皮样癌和腺癌的疗效评估应继续进行分层。