Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Oncologist. 2020 Sep;25(9):e1286-e1291. doi: 10.1634/theoncologist.2020-0044. Epub 2020 Feb 14.
Administration of lapatinib with food significantly increased its plasma concentration in Chinese patients with metastatic breast cancer. There were no serious adverse events during the study and no significant differences in lapatinib-related adverse events between the fasted and fed states.
Lapatinib, a small molecular reversible dual tyrosine kinase inhibitor of epidermal growth factor receptor (EGFR) and human epidermal growth receptor 2 (HER2), was approved for use in combination with capecitabine to treat metastatic HER2-positive breast cancer. Administration of lapatinib in the fasted state was recommended; however, our preliminary phase II trial data showed that administration of lapatinib with food increased its concentration.
This study was a single-center, open-label, and prospective self-controlled clinical study. Ten Chinese patients with metastatic breast cancer were enrolled from June 2017 to April 2018. They were required to receive lapatinib plus physician's choice of chemotherapy. Patients were required to take lapatinib orally on an empty stomach continually for 10 days, and then take lapatinib with food continually for the next 10 days. Plasma concentration was measured by liquid chromatography on the 9th and 10th day of each state.
Area under the concentration-time curve (AUC) of the fasted state and the fed state was 21.23 ± 8.91 mgh/L (coefficient of variation (CV)% 42%) and 60.60 ± 16.64 mgh/L (CV% 27%), respectively. The mean plasma concentration in the fasted state was 0.88 ± 0.39 mg/L (CV% 45%), and that in the fed state was 2.53 ± 0.77 mg/L (CV% 30%). Compared with taking lapatinib on an empty stomach, receiving lapatinib with food significantly increased the plasma concentration of lapatinib (Wilcoxon match-paired test, p = .005). In addition, there were no serious adverse events during the study or significant difference in lapatinib-related adverse events between the two states.
Our study shows that receiving lapatinib with food can increase its plasma concentration with no significantly increased drug-related toxicity. We suggest that a larger-sample-size clinical trial is needed to fully understand the effect of administration of lapatinib with food.
在转移性乳腺癌中国患者中,与空腹状态相比,给予拉帕替尼时进食可显著增加其血药浓度。研究期间无严重不良事件发生,且空腹与进食状态下与拉帕替尼相关的不良事件无显著差异。
拉帕替尼是一种小分子可逆的表皮生长因子受体(EGFR)和人表皮生长因子受体 2(HER2)双重酪氨酸激酶抑制剂,获批与卡培他滨联合用于治疗转移性 HER2 阳性乳腺癌。推荐空腹给予拉帕替尼,但我们的初步 II 期试验数据显示,进食时给予拉帕替尼可增加其浓度。
这是一项单中心、开放标签、前瞻性自身对照临床研究。2017 年 6 月至 2018 年 4 月期间,招募了 10 例转移性乳腺癌中国患者,要求他们接受拉帕替尼联合医生选择的化疗。患者需连续 10 天空腹口服拉帕替尼,然后连续 10 天进食时口服拉帕替尼。于每个周期的第 9 天和第 10 天测量血药浓度。
空腹和进食状态下的药时曲线下面积(AUC)分别为 21.23±8.91 mgh/L(变异系数(CV)%42%)和 60.60±16.64 mgh/L(CV%27%)。空腹状态下的平均血药浓度为 0.88±0.39 mg/L(CV%45%),进食状态下为 2.53±0.77 mg/L(CV%30%)。与空腹服用拉帕替尼相比,进食时服用拉帕替尼可显著增加拉帕替尼的血药浓度(Wilcoxon 匹配对检验,p=0.005)。此外,研究期间无严重不良事件发生,且两种状态下与拉帕替尼相关的不良事件无显著差异。
本研究表明,进食时服用拉帕替尼可增加其血药浓度,且药物相关毒性无显著增加。我们建议进行更大样本量的临床试验,以充分了解进食时给予拉帕替尼的效果。