Literature DB >> 1865503

Measures of renal function in patients with cisplatin-related chronic renal disease.

E Reed1, J Jacob, O Brawley.   

Abstract

Twenty-seven patients with advanced stage refractory ovarian cancer were studied to determine if chronic stable cisplatin-related renal dysfunction was present. Medical histories were examined to determine the types of therapy previously received as well as the total previous platinum doses received that ranged from 200 to 2,100 mg/m2. Standard assessments of renal function were made prior to administering current chemotherapy or immunotherapy to the patient, which included 24-hour creatinine clearance, serum creatinine, and blood urea nitrogen (BUN). For patients with a 24-hour creatinine clearance of less than 60 mL/minute, serum creatinine was highly variable (range: 0.9 to 2.0 mg/dL) and was not related to the degree of diminution in the 24-hour creatinine clearance value. Conversely, for patients with a serum creatinine of less than 1.5, the 24-hour creatinine clearance values varied by almost three-fold, ranging between 46 and 120 mL/minute. Two patients with serum creatinines of less than 1 had creatinine clearances of less than 50 mL per minute. Similarly, BUN measurements did not correlate with 24-hour creatinine clearance values, and the 24-hour creatinine clearance value was not related to the total cumulative platinum dose. We conclude that patients who receive substantive doses of cisplatin may experience chronic stable cisplatin-related renal dysfunction and that serum creatinine cannot be relied on to assess the degree of renal compromise. In such patients, we recommended that the 24-hour creatinine clearance value should be used when medical management is influenced by renal function.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1865503      PMCID: PMC2571487     

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  6 in total

1.  Some effects of combination chemotherapy with cis-platinum on renal function in patients with nonseminomatous testicular carcinoma.

Authors:  S Meijer; D T Sleijfer; N H Mulder; W J Sluiter; J Marrink; H S Koops; T M Brouwers; J Oldhoff; G K van der Hem; E Mandema
Journal:  Cancer       Date:  1983-06-01       Impact factor: 6.860

2.  Successful continuation of cisplatin therapy after partial recovery from acute renal failure.

Authors:  D C Wong; A B Deisseroth
Journal:  Cancer Treat Rep       Date:  1985-06

3.  Platinum-DNA adducts in leukocyte DNA correlate with disease response in ovarian cancer patients receiving platinum-based chemotherapy.

Authors:  E Reed; R F Ozols; R Tarone; S H Yuspa; M C Poirier
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

4.  Cisplatin nephrotoxicity in rats: defect in papillary hypertonicity.

Authors:  R Safirstein; P Miller; S Dikman; N Lyman; C Shapiro
Journal:  Am J Physiol       Date:  1981-08

5.  The measurement of cisplatin-DNA adduct levels in testicular cancer patients.

Authors:  E Reed; R F Ozols; R Tarone; S H Yuspa; M C Poirier
Journal:  Carcinogenesis       Date:  1988-10       Impact factor: 4.944

6.  The application of dose intensity to problems in chemotherapy of ovarian and endometrial cancer.

Authors:  L Levin; W Hryniuk
Journal:  Semin Oncol       Date:  1987-12       Impact factor: 4.929

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.