Retrospective Evaluation of Heptaplatin Toxicities in Patients with Advanced Gastric Cancer

말기 암환자에 투여한 Heptaplatin의 신독성에 대한 후향적 평가

  • Park, Mi-Sook (Department of Pharmacy, Chungnam National Hospital) ;
  • Kang, Min-Hee (College of Pharmacy, Chungbuk National University) ;
  • Lim, Sung-Cil (College of Pharmacy, Chungbuk National University) ;
  • Choi, Soon-Ok (Department of Pharmacy, Chungnam National Hospital) ;
  • Lee, Byung-Koo (Department of Pharmacy, Seoul National University Bundang Hospital) ;
  • Lee, Myung-Koo (College of Pharmacy, Chungbuk National University)
  • Published : 2006.12.30

Abstract

Heptaplatin, a new platinum derivative, has several contradicting reports on the nephrotoxicity. Therefore, the aim of this study is to compare the toxicities of heptaplatin-containing regimens in the chemotherapy. This study was performed retrospectively on seventy-seven patients with advanced gastric cancer who did not receive chemotherapy within the last 1 months before taking of heptaplatin- or cisplatin-containing chemotherapy. The 38 patients among total patients was received heptaplatin-containing regimens (26 with SEF regimens: heptaplatin/epirubicin/5-FU, 12 with SF regimens: heptaplatin/5-FU) and the rest 39 patients was received cisplatin-containg regimens (11 with CEF regimens: cisplatin/epirubicin/5-FU, 28 with ELF regimens: epirubicin/leucovorin/5-FU). Before and after the chemotherapy serum creatinine (Scr) and proteinuria were measured by urine stick test in all patient groups. Also Scr was measured a day before the second cycle and did not vary significantly between groups. However Scr on cycle 3 were significantly higher in SEF and SF groups. In case of proteinuria, it was more frequent on cycle 1 in heptaplatin/5-FU group. Proteinuria before and after on cycle 2 was not different between the two cisplatin -containing groups, but was more frequent in heptaplatin-containing groups. The reason why the Scr measured was not so different could be because we excluded the patients who received only one cycle of heptaplatin and changed the regimen due to signs of nephrotoxcity. As the results nephrotoxicity such as protienuria was appeared to be more frequent with heptaplatin-treated patients. It suggests that the clinical consequences of the toxicity need to further evaluation and also the modalities to prevent or minimize nephrotoxicity of heptaplatin should be studied for future utilization of the drug.

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