The Excretion of Cisplatin after Hyperthermic Intrathoracic Chemotherapy.
Christopher LarischTill MarkowiakMichael RiedDennis NowakHans-Stefan HofmannStefan RaketePublished in: Cancers (2023)
Hyperthermic intrathoracic chemotherapy (HITOC) is an additional intraoperative treatment option within the multimodality therapy of pleural malignancies. A chemotherapy perfusion with high-dose cisplatin is performed over a period of 60 min after surgical cytoreduction to improve local tumour control through the eradication of residual tumour cells. Although HITOC is increasingly used, there is only little scientific evidence about the necessary safety measures after HITOC. Therefore, the objective of this study was an analysis of cisplatin excretion via various body fluids after HITOC, with the aim of providing recommendations on occupational health and safety. Five patients undergoing HITOC were included. Before and after the HITOC, as well as during the following days, serum, urine, and bronchial secretion, as well as pleural effusion, were sampled. The platinum levels in the samples were measured using ICP-MS (inductively coupled plasma-mass spectrometry). Immediately after the HITOC, the mean levels of cisplatin increased dramatically in the serum (from 0.79 to 1349 µg/L), urine (from 3.48 to 10,528 µg/g creatinine), and bronchial secretion (from 0.11 to 156 µg/L). Thereafter, the cisplatin levels dropped to 133 µg/L in the serum and 994 µg/g creatinine in the urine within nine days after the HITOC. The AUC ratio shows 59% of the cisplatin being excreted via the urine after 48 h. The sampling of pleural effusion started 24 h after the HITOC, and the cisplatin levels decreased from 618 to 93 µg/L within nine days. Although the cisplatin levels in the body fluids of HITOC patients are much lower compared to patients receiving intravenous chemotherapy, a significant amount of cisplatin is excreted via these body fluids. Consequently, safety precautions must be implemented in the post-HITOC care of patients to avoid occupational exposure to cisplatin.
Keyphrases
- mass spectrometry
- high dose
- patients undergoing
- healthcare
- end stage renal disease
- ejection fraction
- chronic kidney disease
- palliative care
- locally advanced
- mental health
- low dose
- prognostic factors
- multiple sclerosis
- squamous cell carcinoma
- magnetic resonance imaging
- liquid chromatography
- risk assessment
- cell death
- cell proliferation
- radiation therapy
- helicobacter pylori infection
- helicobacter pylori
- signaling pathway
- patient reported
- uric acid
- climate change
- capillary electrophoresis
- cell therapy
- solid phase extraction