首页> 外文期刊>Journal of Clinical Oncology >Phase II study of modified docetaxel, cisplatin, and fluorouracil with bevacizumab in patients with metastatic gastroesophageal adenocarcinoma.
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Phase II study of modified docetaxel, cisplatin, and fluorouracil with bevacizumab in patients with metastatic gastroesophageal adenocarcinoma.

机译:改良的多西他赛,顺铂和氟尿嘧啶与贝伐单抗在转移性胃食管腺癌患者中的II期研究。

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PURPOSE: To evaluate the safety and efficacy of a modified administration schedule of docetaxel, cisplatin, and fluorouracil (mDCF) with bevacizumab in patients with advanced gastroesophageal malignancies. PATIENTS AND METHODS: Previously untreated patients with metastatic gastroesophageal adenocarcinoma received bevacizumab 10 mg/kg, docetaxel 40 mg/m(2), fluorouracil 400 mg/m(2), leucovorin 400 mg/m(2) on day 1, fluorouracil 1,000 mg/m(2)/d x 2 days intravenous continuous infusion beginning on day 1, and cisplatin 40 mg/m(2) on day 3. The primary objective was to improve 6-month progression-free survival (PFS) from 43% (historical DCF control) to 63% with the addition of bevacizumab. The target accrual was 44 patients to have 10% type I and II error rates. RESULTS: In total, 44 eligible patients with cancer were enrolled from October 2006 to October 2008: 22 gastric, 20 gastroesophageal junction (GEJ), and two esophagus. In 39 patients with measurable disease, the confirmed response rate was 67% (95% CI, 50% to 81%). Six-month PFS was 79% (95% CI, 63% to 88%), and median PFS was 12 months (95% CI, 8.8 to 18.2 months). With 26-month follow-up, median overall survival (OS) was 16.8 months (95% CI, 12.1 to 26.1 months), and 2-year survival was 37%. Treatment-related grade 3 to 4 toxicity was as follows: neutropenia without fever (50%), fatigue (25%), venous thromboembolism (39%), and nausea, vomiting, mucositis, neuropathy, and febrile neutropenia less than 10% each. In subset analysis, diffuse gastric cancer had significantly worse PFS and OS, and the response rate in proximal/GEJ tumors was 85% (95% CI, 62% to 97%). CONCLUSION: mDCF with bevacizumab appears tolerable and has notable patient outcomes in patients with advanced gastroesophageal adenocarcinoma. Six-month PFS was 79%, surpassing our predefined efficacy end point, and median and 2-year OS were 16.8 months and 37%, respectively.
机译:目的:评估贝伐单抗联合多西他赛,顺铂和氟尿嘧啶(mDCF)改良给药方案对晚期胃食管恶性肿瘤患者的安全性和有效性。患者和方法:先前未经治疗的转移性胃食管腺癌患者在第1天接受贝伐单抗10 mg / kg,多西他赛40 mg / m(2),氟尿嘧啶400 mg / m(2),亚叶酸钙400 mg / m(2),氟尿嘧啶1,000 mg / m(2)/ dx从第1天开始连续2天静脉滴注,第3天开始顺铂40 mg / m(2)。主要目标是将6个月无进展生存期(PFS)从43%提高(使用DCF的历史对照)加上贝伐单抗即可达到63%。目标应计入数为44名患者,I型和II型错误率均为10%。结果:从2006年10月至2008年10月,共有44例符合条件的癌症患者入组:22例胃,20例胃食管连接(GEJ)和2例食道。在39例可测量疾病患者中,确诊的缓解率为67%(95%CI,50%至81%)。六个月的PFS为79%(95%CI,63%至88%),中位PFS为12个月(95%CI,8.8至18.2个月)。经过26个月的随访,中位总生存期(OS)为16.8个月(95%CI,12.1至26.1个月),2年生存期为37%。与治疗相关的3至4级毒性如下:无发热的中性粒细胞减少症(50%),疲倦(25%),静脉血栓栓塞(39%)以及恶心,呕吐,粘膜炎,神经病和发热性中性粒细胞减少症各少于10% 。在子集分析中,弥漫性胃癌的PFS和OS显着恶化,近端/ GEJ肿瘤的缓解率为85%(95%CI,62%至97%)。结论:mDCF与贝伐单抗在晚期胃食管腺癌患者中似乎可以耐受并且具有显着的患者预后。六个月的PFS为79%,超过了我们预定的疗效终点,中位OS​​和2年OS分别为16.8个月和37%。

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