González García Jonathan, Gutiérrez Nicolás Fernando, Nazco Casariego Gloria Julia, Batista López José Norberto, Ceballos Lenza Isaac, Ramos Díaz Ruth, Llabrés Martínez Matías
1 Complejo Hospitalario Universitario de Canarias (Santa Cruz de Tenerife), La Laguna, Spain.
2 Fundación Canaria para la Investigación Sanitaria (FUNCANIS), Santa Cruz de Tenerife, La Laguna, Canarias, Spain.
Ann Pharmacother. 2017 Nov;51(11):976-980. doi: 10.1177/1060028017715727. Epub 2017 Jun 23.
Plasma concentrations of trastuzumab <20 µg/mL in patients with gastric cancer are associated with reduced progression-free and overall survival. In breast cancer treatment, this relationship has not yet been studied, but a suboptimal pharmacodynamic exposure to trastuzumab could be a reason for therapeutic failure of treatment of HER2-positive breast cancer.
The objective of the present study was to determine the proportion of nonmetastatic HER2-positive breast cancers that do not reach a minimum plasma concentration ( C) of 20 µg/mL after first drug administration, established as therapeutically effective in clinical trials. The secondary objective was to identify the physiological and anthropometric characteristics that determine interindividual pharmacokinetic variability.
Serum concentrations of trastuzumab were assessed by ELISA on day 1 of the second cycle before administration of the second dose ( C).
Of 19 patients included, 9 (47.4%) had a mean C of 19.0 µg/mL (±12.1) after the first administration. Body mass index (BMI) and weight was the main variable that determined the achievement of therapeutic levels after the first administration. Thus, the proportion of patients reaching the target concentration was 89% when BMI was ≤30 kg/m but only 11% when BMI was >30 kg/m ( P < 0.01).
The standard dose of 600 mg subcutaneous trastuzumab did not ensure adequate pharmacodynamic exposure from the first administration in 52% of patients, with weight and BMI being related to the plasma levels obtained.
在胃癌患者中,曲妥珠单抗血浆浓度<20μg/mL与无进展生存期和总生存期缩短相关。在乳腺癌治疗中,尚未对这种关系进行研究,但曲妥珠单抗的药效学暴露不足可能是HER2阳性乳腺癌治疗失败的一个原因。
本研究的目的是确定首次给药后未达到20μg/mL最低血浆浓度(C)的非转移性HER2阳性乳腺癌患者的比例,该浓度在临床试验中被确定为治疗有效。次要目的是确定决定个体间药代动力学变异性的生理和人体测量特征。
在第二次给药前的第二个周期第1天通过ELISA评估曲妥珠单抗的血清浓度(C)。
纳入的19例患者中,9例(47.4%)首次给药后的平均C为19.0μg/mL(±12.1)。体重指数(BMI)和体重是决定首次给药后达到治疗水平的主要变量。因此,BMI≤30kg/m²时达到目标浓度的患者比例为89%,而BMI>30kg/m²时仅为11%(P<0.01)。
600mg皮下注射曲妥珠单抗的标准剂量在52%的患者中不能确保首次给药后有足够的药效学暴露,体重和BMI与所获得的血浆水平相关。