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与甲状腺癌和肝细胞癌患者接受仑伐替尼治疗的依从性相关的因素。

Factors associated with lenvatinib adherence in thyroid cancer and hepatocellular carcinoma.

机构信息

Department of Pharmacy, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Division of Drug Informatics, Keio University Faculty of Pharmacy, Tokyo, Japan.

出版信息

PLoS One. 2023 Nov 16;18(11):e0294320. doi: 10.1371/journal.pone.0294320. eCollection 2023.

Abstract

BACKGROUND

Lenvatinib is an oral anticancer medication used to treat radioiodine-refractory thyroid cancer and unresectable hepatocellular carcinoma. The purpose of this study is to evaluate lenvatinib adherence by patients and to identify factors associated with decreased lenvatinib adherence.

METHODS

Among 153 patients who started treatment with lenvatinib for unresectable thyroid cancer or unresectable hepatocellular carcinoma between May 1, 2015 and August 31 2021 at the Cancer Institute Hospital of the Japanese Foundation for Cancer Research, 102 were eligible for this study (55 thyroid cancer, 47 hepatocellular carcinoma). The lenvatinib adherence rate in a treatment cycle was defined as the number of times a patient took lenvatinib in a 28-day cycle divided by the prescribed 28 doses. The rate was determined by pill counting and self-reporting at the pharmaceutical outpatient clinic. Reasons for non-adherence were established by interview and analyzed.

RESULTS

The median adherence rate of lenvatinib in the first cycle was 90.1% (n = 55) in thyroid cancer and 94.9% (n = 47) in hepatocellular carcinoma. In thyroid cancer, there were 255 incidents of lenvatinib non-adherence. Non-adherence was mainly associated with bleeding events (18.6%), followed by hand-foot skin reactions (10.6%). In hepatocellular carcinoma, there were 97 incidents of non-adherence. Hypertension accounted for 20.6%, followed by hoarseness (18.6%) and diarrhea (17.5%).

CONCLUSION

The adherence rate for lenvatinib in Japanese patients with thyroid and hepatocellular carcinoma in real-world clinical practice was more than 90% in this study. Hypertension was a major reason for non-adherence, followed by hand-foot skin reactions and diarrhea.

摘要

背景

仑伐替尼是一种口服抗癌药物,用于治疗放射性碘难治性甲状腺癌和不可切除的肝细胞癌。本研究旨在评估患者对仑伐替尼的依从性,并确定与仑伐替尼依从性降低相关的因素。

方法

在日本癌症研究所癌症医院,2015 年 5 月 1 日至 2021 年 8 月 31 日期间,共有 153 名无法手术的甲状腺癌或无法手术的肝细胞癌患者开始接受仑伐替尼治疗,其中 102 名患者符合本研究条件(55 名甲状腺癌患者,47 名肝细胞癌患者)。一个治疗周期内的仑伐替尼依从率定义为患者在 28 天周期内服用仑伐替尼的次数除以规定的 28 剂。通过药剂门诊的药片计数和自我报告来确定依从率。通过访谈确定不依从的原因并进行分析。

结果

在甲状腺癌中,第一个周期仑伐替尼的依从率中位数为 90.1%(n=55),在肝细胞癌中为 94.9%(n=47)。在甲状腺癌中,有 255 例仑伐替尼不依从事件。不依从主要与出血事件有关(18.6%),其次是手足皮肤反应(10.6%)。在肝细胞癌中,有 97 例不依从事件。高血压占 20.6%,其次是声音嘶哑(18.6%)和腹泻(17.5%)。

结论

在这项真实世界的临床实践研究中,日本甲状腺癌和肝细胞癌患者对仑伐替尼的依从率超过 90%。高血压是不依从的主要原因,其次是手足皮肤反应和腹泻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ba/10653419/ff953ffe6762/pone.0294320.g001.jpg

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