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首页> 外文期刊>BMC Cancer >Capecitabine in the routine first-line treatment of elderly patients with advanced colorectal cancer - results from a non-interventional observation study
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Capecitabine in the routine first-line treatment of elderly patients with advanced colorectal cancer - results from a non-interventional observation study

机译:卡培他滨在老年晚期结直肠癌患者的常规一线治疗中-非干预性观察研究的结果

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Background The purpose of this observational study was to evaluate feasibility, efficacy results and toxicity observations of capecitabine in routine first line treatment of patients with metastatic colorectal cancer, with particular regard of elderly patients (>75?years of age). Methods Patients with colorectal cancer receiving capecitabine as part of their first-line treatment were recorded until detection of disease progression or up to a maximum of 12?cycles on standardized evaluation forms. Additional information on long-term outcomes, progression-free survival, and overall survival were retrieved at two follow-up time points. Obtained data were analyzed with regard to age up to 75 and >75?years of age. There were no specific requirements for patient selection and conduct of therapy, corresponding to the non-interventional nature of the study. Results In total, 1249 evaluable patients were enrolled in Germany. The median age of the study population was 74?years (range: 21–99). Capecitabine-based combination was administered in 56?% of patients in the overall population. The median treatment duration was about 5?months. Severe toxicities occurred rarely without any difference regarding age groups. The most common hematological toxicity was anemia. Gastrointestinal side effects and hand-food-syndrome (HFS) were the most frequent non-hematologic toxicities. Overall response rate (ORR) was significantly higher in the patient group 75 years of age (38 vs. 32 %, p=0.019). Median progression free survival (PFS 9.7 vs. 8.2 months, p=0.00021) and overall survival (OS 31.0 vs. 22.6 months, pConclusion Efficacy and tolerability of capecitabine treatment either as single drug or in various combination regimens, as proven in randomized studies, could be confirmed in a clinical routine setting. Patients older than 75?years may derive a relevant benefit by first line capecitabine-based treatment with good tolerability.
机译:背景技术这项观察性研究的目的是评估卡培他滨在转移性结直肠癌患者常规一线治疗中的可行性,疗效结果和毒性观察,尤其是对老年患者(> 75岁)。方法记录接受卡培他滨作为一线治疗一部分的结直肠癌患者,直到在标准评估表上检测到疾病进展或最多12个周期为止。在两个随访时间点检索了有关长期结局,无进展生存期和总体生存期的其他信息。对获得的数据进行了分析,分析年龄不超过75岁且年龄大于75岁。对患者的选择和治疗没有特殊要求,这与研究的非介入性质相对应。结果在德国共有1249名可评估患者入组。研究人群的中位年龄为74岁(范围:21–99)。以卡培他滨为基础的联合治疗在总人群中占56%。中位治疗时间约为5个月。严重毒性反应很少发生,并且在年龄组之间没有任何差异。最常见的血液学毒性是贫血。胃肠道副作用和手食综合征(HFS)是最常见的非血液学毒性。 75岁患者组的总缓解率(ORR)明显更高(38%vs. 32%,p = 0.019)。中位数无进展生存期(PFS 9.7对8.2个月,p = 0.00021)和总体生存期(OS 31.0对22.6个月,p结论卡培他滨单药或多种联合用药的疗效和耐受性,在随机研究中得到证实,年龄大于75岁的患者通过以卡培他滨为基础的一线治疗具有良好的耐受性,可以从中获益。

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