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Endobronchial Ultrasound-guided Intratumoral Injection of Cisplatin for the Treatment of Isolated Mediastinal Recurrence of Lung Cancer
Published on: February 12, 2017
Individualized Estimated Glomerular Filtration Rate-based Renal Function Association With Cisplatin Treatment
Naoto Hoshino1,2, Kensuke Yoshida1, Yoshitomi Kanemitsu2
1Department of Drug Safety and Risk Management, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
Background/Aim:
Toxicity-related discontinuation remains problematic in cisplatin-based cervical cancer treatment. This study aimed to evaluate the association between renal function assessed using individualized estimated glomerular filtration rate (eGFR) and the completion rate of cisplatin-based concurrent chemoradiotherapy (CCRT) in patients with cervical cancer.
Patients And Methods:
This retrospective study included patients with cervical cancer who received CCRT with cisplatin (40 mg/m2/week, six cycles) at our institution between April 2015 and March 2024. Exclusion criteria included a Cockcroft-Gault-estimated creatinine clearance rate (CGCCr) <60 ml/min, prior chemotherapy or radiotherapy, initial cisplatin dose reduction, and Eastern Cooperative Oncology Group Performance Status ≥2. The primary endpoint was the cisplatin treatment completion rate. Renal function was assessed using individualized eGFR, and a comparative analysis was performed between the completion and non-completion groups.
Results:
A total of 80 patients were included, of whom 68 (85%) completed the planned cisplatin regimen. Although all patients had CGCCr ≥60 ml/min, individualized eGFR assessment revealed that 19% of patients had eGFR <60 ml/min. The proportion of patients with an eGFR <60 ml/min was significantly higher in the non-completion group (58% vs. 12%, p=0.001). Logistic regression analysis showed that patients with individualized eGFR <60 ml/min had a significantly higher risk of cisplatin treatment non-completion (adjusted odds ratio=8.69; 95% confidence interval=2.14-35.3, p=0.0025).
Conclusion:
Patients with an individualized eGFR <60 ml/min showed significantly higher cisplatin non-completion rates even when their CGCCr was ≥60 ml/min. These findings suggest that individualized eGFR assessment, in addition to CGCCr, should be considered for optimizing cisplatin dosing in cervical cancer CCRT.
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