Literature DB >> 657154

Acute renal failure after cis-dichlorodiammineplatinum(II) and gentamicin-cephalothin therapies.

J C Gonzalez-Vitale, D M Hayes, E Cvitkovic, S S Sternberg.   

Abstract

Combined gentamicin-cephalothin therapy in four patients after treatment with cis-dichlorodiammineplatinum(II) (CPDD) for advanced solid tumors was complicated by severe acute renal failure. The total dose of gentamicin varied from 240 to 945 mg and that of cephalothin varied from 28 to 48 g. Low-dose (0.5 mg/kg x 8) CPDD was given to one patient, high-dose (3 mg/kg) CPDD was given to two patients, and very high-dose (5 mg/kg) CPDD was given to one patient. The high and very high doses of CPDD were given with concomitant mannitol diuresis. CPDD therapy was complicated by mild transient azotemia in three patients and by severe acute renal failure in one. In the latter, the azotemia began to improve on Day 7 after CPDD treatment. Following gentamicin-cephalothin therapy, all patients developed severe acute renal failure which persisted until death. At autopsy, all patients had extensive renal tubular necrosis at various stages. These findings indicate that gentamicin-cephalothin therapy after treatment with CPDD can be severely nephrotoxic, and that this antibiotic combination should be given with great caution, if at all, to patients receiving CPDD treatment for malignancy.

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Year:  1978        PMID: 657154

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  12 in total

1.  Pharmacokinetics of cisplatin in patients receiving interleukin-2-containing treatment regimens.

Authors:  D R Gandara; E A Perez; A Denham; V J Wiebe; M W DeGregorio
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

2.  Increased tissue deposition and decreased excretion of platinum following administration of cisplatin to cisplatin-pretreated animals.

Authors:  C L Litterst; V G Schweitzer
Journal:  Cancer Chemother Pharmacol       Date:  1984       Impact factor: 3.333

3.  [Pharmacokinetic of platin in plasma and urine of man under 1-, 8-, and 24 h-infusion with cis-dichlorodiamine-platin (II) (cis-DDP) (author's transl)].

Authors:  H W von Heyden; H Henkel; G A Nagel; N Weinstock
Journal:  Klin Wochenschr       Date:  1982-03-01

Review 4.  [Cis-diamminedichloroplatinum(II). A new antineoplastic agent derived from the group of heavy metal complexes (author's transl)].

Authors:  R Osieka; C G Schmidt
Journal:  Klin Wochenschr       Date:  1979-12-03

5.  Potentiated nephrotoxicity of cisplatin when combined with amikacin comparing young and adult rats.

Authors:  H T Jongejan; A P Provoost; J C Molenaar
Journal:  Pediatr Nephrol       Date:  1989-07       Impact factor: 3.714

6.  Comparative nephrotoxicity of carboplatin and cisplatin in combination with tobramycin.

Authors:  C L Bregman; P D Williams
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

Review 7.  Cisplatin: a review of clinical applications and renal toxicity.

Authors:  D T Sleijfer; S Meijer; N H Mulder
Journal:  Pharm Weekbl Sci       Date:  1985-12-13

Review 8.  Comparative adverse effect profiles of platinum drugs.

Authors:  M J McKeage
Journal:  Drug Saf       Date:  1995-10       Impact factor: 5.606

9.  Potentiation of cis-diamminedichloroplatinum nephrotoxicity by amikacin in rats.

Authors:  H T Jongejan; A P Provoost; J C Molenaar
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

10.  Absence of relation between nutritional parameters and renal function in non-seminomatous testicular cancer patients.

Authors:  J A Gietema; E G de Vries; S Meijer; J J Offerman; P O Mulder; D T Sleijfer
Journal:  J Cancer Res Clin Oncol       Date:  1988       Impact factor: 4.553

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