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卡培他滨用于老年晚期结直肠癌患者的常规一线治疗——一项非干预性观察研究的结果

Capecitabine in the routine first-line treatment of elderly patients with advanced colorectal cancer--results from a non-interventional observation study.

作者信息

Stein Alexander, Quidde Julia, Schröder Jan Klaus, Göhler Thomas, Tschechne Barbara, Valdix Annette-Rosel, Höffkes Heinz-Gert, Schirrmacher-Memmel Silke, Wohlfarth Tim, Hinke Axel, Engelen Andreas, Arnold Dirk

机构信息

Department of Oncology, Hematology, BMT with section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Schwerpunktpraxis für Hämatologie und Onkologie, Mühlheim an der Ruhr, Germany.

出版信息

BMC Cancer. 2016 Feb 10;16:82. doi: 10.1186/s12885-016-2113-8.

Abstract

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 compared to patients >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, p<0.0001) was decreased in elderly patients.

CONCLUSION

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.

摘要

背景

本观察性研究旨在评估卡培他滨在转移性结直肠癌患者一线常规治疗中的可行性、疗效结果及毒性观察情况,尤其关注老年患者(>75岁)。

方法

将接受卡培他滨作为一线治疗一部分的结直肠癌患者记录在标准化评估表上,直至疾病进展或最多12个周期。在两个随访时间点获取有关长期结局、无进展生存期和总生存期的额外信息。根据年龄≤75岁和>75岁对获得的数据进行分析。由于研究的非干预性质,对患者选择和治疗实施没有特定要求。

结果

德国共纳入1249例可评估患者。研究人群的中位年龄为74岁(范围:21 - 99岁)。总体人群中56%的患者接受了以卡培他滨为基础的联合治疗。中位治疗持续时间约为5个月。严重毒性反应很少发生,各年龄组之间无差异。最常见的血液学毒性是贫血。胃肠道副作用和手足综合征(HFS)是最常见的非血液学毒性。年龄≤75岁的患者组总体缓解率(ORR)显著高于>75岁的患者(38%对32%,p = 0.019)。老年患者的中位无进展生存期(PFS 9.7个月对8.2个月,p = 0.00021)和总生存期(OS 31.0个月对22.6个月,p < 0.0001)降低。

结论

随机研究已证实的卡培他滨单药或各种联合方案治疗的疗效和耐受性,在临床常规环境中得到了证实。75岁以上的患者可能从以卡培他滨为基础的一线治疗中获得显著益处,且耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06de/4750193/d9810f72d22c/12885_2016_2113_Fig1_HTML.jpg

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