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首页> 外文期刊>Medical oncology >Clinical outcomes of Chinese patients with metastatic colorectal cancer receiving first-line bevacizumab-containing treatment
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Clinical outcomes of Chinese patients with metastatic colorectal cancer receiving first-line bevacizumab-containing treatment

机译:接受贝伐单抗一线治疗的中国转移性结直肠癌患者的临床结局

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摘要

After the approval of bevacizumab for the first-line treatment of metastatic colorectal cancer (mCRC) in China, published information was still limited. This observational cohort study enrolled 175 mCRC patients who initiated bevacizumab-containing first-line chemotherapies at Sun Yet-sen University Cancer Center. Backbone chemotherapies included FOLFIRI (45.6 %), FOLFOX (34.9 %), and XELOX(19.5 %). Effectiveness data, safety profiles, and treatment patterns were collected and compared between oxaliplatin-and irinotecan-based groups. The median treatment durations of bevacizumab in first-line and total were equivalent between oxaliplatin-and irinotecan-based group (5.0 vs. 4.8 and 6.0 vs. 5.9 months, respectively). Median progression-free survival (PFS) was 10.6 months, and median overall survival (OS) was 24.2 months in entire population. No significant difference was found between irinotecan-and oxaliplatin-based groups in PFS (10.8 vs. 10.1 months, p = 0.21) or in OS (27.5 vs. 23.7 months, p = 0.68). Overall response rate in entire population was 38.3 %, and the disease control rate was 86.3 %. Bevacizumab-associated serious adverse events included hypertension (4.2 %), bleeding (3.6 %), proteinuria (3.0 %), venous thromboembolism (0.6 %), and wound-healing complications (0.6 %). Curative-intent surgery after conversion chemotherapy was carried out in 23 patients (13.7 %). Multivariate analyses showed that maintenance therapy (p = 0.001), resection of metastatic sites (p = 0.002), and disease-free interval (p = 0.003) were independent prognostic factors for OS survival. In spite of small discrepancies in treatment patterns, irinotecan-and oxaliplatin-based chemotherapeutic regimens are equally compatible partners for bevacizumab in first-line Chinese mCRC treatment.
机译:在贝伐单抗被批准用于中国转移性结直肠癌(mCRC)的一线治疗后,发表的信息仍然有限。这项观察性队列研究招募了175例mCRC患者,他们在中山大学附属大学癌症中心发起了含贝伐单抗一线化疗的研究。骨干化学疗法包括FOLFIRI(45.6%),FOLFOX(34.9%)和XELOX(19.5%)。收集有效性数据,安全性概况和治疗模式,并在基于奥沙利铂和伊立替康的组之间进行比较。在基于奥沙利铂和伊立替康的治疗组中,贝伐单抗的一线治疗和持续治疗的中位时间相等(分别为5.0 vs. 4.8和6.0 vs. 5.9个月)。中值无进展生存期(PFS)为10.6个月,中值总体生存期(OS)在整个人群中为24.2个月。在PFS(10.8 vs. 10.1个月,p = 0.21)或OS(27.5 vs. 23.7个月,p = 0.68)中,基于伊立替康和奥沙利铂的组之间无显着差异。整个人群的总缓解率为38.3%,疾病控制率为86.3%。贝伐单抗相关的严重不良事件包括高血压(4.2%),出血(3.6%),蛋白尿(3.0%),静脉血栓栓塞(0.6%)和伤口愈合并发症(0.6%)。转换化疗后进行的有针对性的手术治疗了23例患者(13.7%)。多因素分析表明,维持治疗(p = 0.001),切除转移部位(p = 0.002)和无病间隔(p = 0.003)是OS生存的独立预后因素。尽管治疗方式上的差异很小,但基于伊立替康和奥沙利铂的化疗方案是贝伐单抗在中国一线mCRC治疗中的同等相容性伴侣。

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