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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Cetuximab plus cisplatin-5-fluorouracil versus cisplatin-5-fluorouracil alone in first-line metastatic squamous cell carcinoma of the esophagus: a randomized phase II study of the Arbeitsgemeinschaft Internistische Onkologie.
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Cetuximab plus cisplatin-5-fluorouracil versus cisplatin-5-fluorouracil alone in first-line metastatic squamous cell carcinoma of the esophagus: a randomized phase II study of the Arbeitsgemeinschaft Internistische Onkologie.

机译:食管一线转移性鳞状细胞癌中西妥昔单抗加顺铂5-氟尿嘧啶与单独的顺铂5-氟尿嘧啶:Arbeitsgemeinschaft Internistische Onkologie的随机II期研究。

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BACKGROUND: This study assessed the activity of the mAb cetuximab in combination with cisplatin and 5-fluorouracil (5-FU) in advanced esophageal squamous cell carcinoma. PATIENTS AND METHODS: For a maximum of six 29-day cycles, patients received cisplatin 100 mg/m(2), day 1, plus 5-FU 1000 mg/m(2), days 1-5 (CF), either alone or in combination with cetuximab (CET-CF; 400 mg/m(2) initial dose followed by 250 mg/m(2) weekly thereafter). The primary end point was tumor response. Tumor material was obtained for analysis of KRAS mutation status. RESULTS: Sixty-two eligible patients were included, 32 receiving CET-CF and 30 CF. Cetuximab did not exacerbate grade 3/4 toxicity, except for rash (6% versus 0%) and diarrhea (16% versus 0%). The overall response rate according to RECIST criteria was 19% and 13% and the disease control rate 75% and 57% for the CET-CF and CF arms, respectively. With a median follow-up of 21.5 months, the median progression-free survival was 5.9 and 3.6 months and median overall survival 9.5 and 5.5 months for CET-CF and CF, respectively. No KRAS codon 12/13 tumor mutations were identified in 37 evaluated samples. CONCLUSION: Cetuximab can be safely combined with CF chemotherapy and may increase the efficacy of standard CF chemotherapy.
机译:背景:这项研究评估了单克隆抗体西妥昔单抗联合顺铂和5-氟尿嘧啶(5-FU)在晚期食管鳞状细胞癌中的活性。患者和方法:在最多六个29天的周期中,患者单独接受顺铂100 mg / m(2),第1天,加上5-FU 1000 mg / m(2),第1-5天(CF),单独服用或与西妥昔单抗联用(CET-CF;初始剂量为400 mg / m(2),随后每周一次为250 mg / m(2))。主要终点是肿瘤反应。获得肿瘤材料用于分析KRAS突变状态。结果:纳入了62例合格患者,其中32例接受了CET-CF,30例接受了CF。西妥昔单抗除皮疹(6%对0%)和腹泻(16%对0%)外,并未加剧3/4级毒性。根据RECIST标准,CET-CF和CF组的总缓解率分别为19%和13%,疾病控制率分别为75%和57%。 CET-CF和CF的中位随访时间为21.5个月,中位无进展生存期分别为5.9和3.6个月,中位总体生存期为9.5和5.5个月。在37个评估样品中未鉴定出KRAS密码子12/13肿瘤突变。结论:西妥昔单抗可以安全地与CF化疗联合使用,并可以提高标准CF化疗的疗效。

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