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首页> 外文期刊>Journal of Clinical Oncology >Multicenter phase II study of irinotecan, cisplatin, and bevacizumab in patients with metastatic gastric or gastroesophageal junction adenocarcinoma.
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Multicenter phase II study of irinotecan, cisplatin, and bevacizumab in patients with metastatic gastric or gastroesophageal junction adenocarcinoma.

机译:伊立替康,顺铂和贝伐单抗在转移性胃或胃食管交界处腺癌患者中的多中心II期研究。

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PURPOSE: Bevacizumab improves survival in several solid tumor malignancies when combined with chemotherapy. We evaluated the efficacy and safety of the addition of bevacizumab to chemotherapy in the treatment of gastric and gastroesophageal junction (GEJ) adenocarcinoma. PATIENTS AND METHODS: Forty-seven patients with metastatic or unresectable gastric/GEJ adenocarcinoma were treated with bevacizumab 15 mg/kg on day 1, irinotecan 65 mg/m2, and cisplatin 30 mg/m2 on days 1 and 8, every 21 days. The primary end point was to demonstrate a 50% improvement in time to progression over historical values. Secondary end points included safety, response, and survival. RESULTS: Patient characteristics were as follows: median age 59 years (range, 25 to 75); Karnofsky performance status 90% (70% to 100%); male:female, 34:13; and gastric/GEJ, 24:23. With a median follow-up of 12.2 months, median time to progression was 8.3 months (95% CI, 5.5 to 9.9 months). In 34 patients with measurable disease, the overall response rate was 65% (95% CI, 46% to 80%). Median survival was 12.3 months (95% CI, 11.3 to 17.2 months). We observed no increase in chemotherapy related toxicity. Possible bevacizumab-related toxicity included a 28% incidence of grade 3 hypertension, two patients with a gastric perforation and one patient with a near perforation (6%), and one patient with a myocardial infarction (2%). Grade 3 to 4 thromboembolic events occurred in 25% of patients. Although the primary tumor was unresected in 40 patients, we observed only one patient with a significant upper gastrointestinal bleed. CONCLUSION: Bevacizumab can be safely given with chemotherapy even with primary gastric and GEJ tumors in place. The response rate, time to disease progression (TTP), and overall survival are encouraging, with TTP improved over historical controls by 75%. Further development of bevacizumab in gastric and GEJ cancers is warranted.
机译:目的:贝伐单抗联合化疗可提高几种实体瘤的生存率。我们评估了在化疗中添加贝伐单抗治疗胃和胃食管连接(GEJ)腺癌的有效性和安全性。患者与方法:47例转移性或不可切除的胃/ GEJ腺癌患者在第1天,第21天和第1天和第8天分别接受贝伐单抗15 mg / kg,伊立替康65 mg / m2和顺铂30 mg / m2的治疗。主要目的是证明进展时间比历史值缩短了50%。次要终点包括安全性,反应性和生存率。结果:患者特征如下:中位年龄59岁(范围25至75);卡诺夫斯基绩效状态90%(70%至100%);男:女,34:13;和胃/ GEJ,24:23。中位随访期为12.2个月,中位进展时间为8.3个月(95%CI,5.5至9.9个月)。在34例可测量疾病的患者中,总缓解率为65%(95%CI,46%至80%)。中位生存期为12.3个月(95%CI,11.3至17.2个月)。我们观察到与化疗相关的毒性没有增加。与贝伐单抗相关的可能毒性包括28%的3级高血压发生率,2例胃穿孔患者和1例近穿孔患者(6%)和1例心肌梗塞患者(2%)。 25%的患者发生3至4级血栓栓塞事件。尽管40例患者未切除原发肿瘤,但我们仅观察到1例患者有明显的上消化道出血。结论:即使原发性胃癌和GEJ肿瘤均已到位,贝伐单抗也可以安全地接受化学疗法治疗。响应率,疾病进展时间(TTP)和总体存活率令人鼓舞,与历史对照相比,TTP改善了75%。有必要进一步开发贝伐单抗治疗胃癌和GEJ癌症。

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