The association of cisplatin pharmacokinetics and skeletal muscle mass in patients with head and neck cancer: The prospective PLATISMA study

被引:22
作者
Chargi, Najiba [1 ,2 ]
Molenaar-Kuijsten, Laura [3 ]
Huiskamp, Laura F. J. [1 ,2 ]
Devriese, Lot A. [2 ,4 ,5 ]
de Bree, Remco [1 ,2 ]
Huitema, Alwin D. R. [3 ,5 ,6 ,7 ]
机构
[1] Univ Med Ctr Utrecht, Div Imaging, Dept Head & Neck Surg Oncol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Oncol Ctr, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[3] Netherlands Canc Inst Antoni van Leeuwenhoek, Dept Pharm & Pharmacol, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[4] Univ Med Ctr Utrecht, Div Imaging, Dept Med Oncol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[5] Univ Utrecht, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[6] Univ Med Ctr Utrecht, Dept Clin Pharm, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[7] Princess Maxima Ctr Pediat Oncol, Dept Pharmacol, Heidelberglaan 25, NL-3584 CS Utrecht, Netherlands
关键词
Cisplatin pharmacokinetics; Skeletal muscle mass; Sarcopenia; Dose-limiting toxicity; Head and neck cancer; Chemoradiotherapy; PLATINUM; TISSUE; PREVALENCE;
D O I
10.1016/j.ejca.2021.10.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Locally advanced head and neck squamous cell carcinoma (HNSCC) is commonly treated with cisplatin-based chemoradiotherapy (CRT). Cisplatin is associated with severe toxicity, which negatively affects survival. In recent years, a relationship between low skeletal muscle mass (SMM) and increased toxicity has been described. This increased toxicity may be related to altered cisplatin distribution and binding in the fat-free body mass of which SMM is the largest contributor. This study aims to investigate the association between cisplatin pharmacokinetics and SMM in patients with HNSCC. Methods: We performed a prospective observational study in patients with HNSCC treated with CRT. Patients received standard-of-care chemotherapy with three cycles of cisplatin at a dose of 100 mg/m2 per cycle. Quantitative data on SMM, measured on computed tomography scans and cisplatin pharmacokinetics (total and ultrafilterable plasma concentrations) were collected, as well as data on toxicity. Results: A total of 45 evaluable patients were included in the study. A large proportion of the study population had a low SMM (46.7%). The majority of patients ( 57.8%) experienced cisplatin dose-limiting toxicities. Pharmacokinetic analysis showed a significant relationship between cisplatin pharmacokinetics and SMM, weight, fat-free mass and body surface area (p < 0.005). In a simulation, patients with a low SMM (< 25.8 kg) were predicted to reach higher-bound cisplatin concentrations. Conclusion: We found an association between cisplatin pharmacokinetics and SMM; however, this relationship was also seen between cisplatin pharmacokinetics and other body composition descriptors.(c) 2021 The Author(s). Published by Elsevier Ltd.
引用
收藏
页码:92 / 99
页数:8
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