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首页> 外文期刊>Clinical & translational oncology : >Panitumumab and irinotecan every 3 weeks is an active and convenient regimen for second-line treatment of patients with wild-type K-RAS metastatic colorectal cancer
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Panitumumab and irinotecan every 3 weeks is an active and convenient regimen for second-line treatment of patients with wild-type K-RAS metastatic colorectal cancer

机译:每三周使用Panitumumab和irinotecan是一种有效且方便的方案,用于野生型K-RAS转移性结直肠癌患者的二线治疗

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Purpose: To evaluate the efficacy and safety profile of the combination of panitumumab and irinotecan every 3 weeks in a phase II trial as second-line treatment in patients with advanced wild-type (WT) K-RAS colorectal cancer (CRC). Methods: Fifty-three patients received 9 mg/kg of panitumumab followed by 350 mg/m2 of irinotecan every 21 days until disease progression, unacceptable toxicity or consent withdrawal. Results: Median age of patients included was 67 years. All patients had previously received 5-fluorouracil, 84 % oxaliplatin and 8 % irinotecan as first-line treatment. Patients received a median of five infusions of panitumumab and irinotecan. On an intention-to-treat analysis, 12 patients (23 %) achieved partial responses and 22 patients (41 %) achieved disease stabilization. Median progression-free survival and overall survival were 4.5 and 15.1 months, respectively. The most frequent treatment-related severe toxicities per patient were diarrhoea (35.8 %), followed by skin rash (32.1 %), asthenia (18.9 %) and neutropenia (13.2 %). A significant association between clinical response and incidence and grade of skin toxicity was observed (p = 0.0032). Conclusion: This study shows that the administration of panitumumab plus irinotecan every 3 weeks is safe, active and feasible as second-line treatment in patients with advanced WT K-RAS CRC.
机译:目的:在一项II期试验中评估帕尼单抗和伊立替康的组合每三周对晚期野生型(WT)K-RAS大肠癌(CRC)患者的疗效和安全性。方法:53名患者每21天接受9 mg / kg帕尼单抗治疗,然后接受350 mg / m2伊立替康治疗,直至疾病进展,不可接受的毒性或同意撤药。结果:患者的中位年龄为67岁。所有患者先前均接受过5-氟尿嘧啶,84%的奥沙利铂和8%的伊立替康作为一线治疗。患者接受了五次帕尼单抗和伊立替康的输注。在意向性治疗分析中,有12例患者(23%)获得了部分缓解,22例患者(41%)获得了疾病稳定。中位无进展生存期和总生存期分别为4.5和15.1个月。每位患者最常见的与治疗相关的严重毒性为腹泻(35.8%),其次是皮疹(32.1%),乏力(18.9%)和中性粒细胞减少症(13.2%)。观察到临床反应与发病率和皮肤毒性等级之间存在显着关联(p = 0.0032)。结论:这项研究表明,对于晚期WT K-RAS CRC患者,每三周给予帕尼单抗加伊立替康是安全,有效和可行的二线治疗。

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