Drugs & Aging

, Volume 22, Issue 9, pp 785–791

Effect of Creatinine Clearance on Patterns of Toxicity in Older Patients Receiving Adjuvant Chemotherapy for Breast Cancer


    • Memorial Sloan-Kettering Cancer Center
  • Anju Hurria
    • Memorial Sloan-Kettering Cancer Center
  • Kelly Brogan
    • Memorial Sloan-Kettering Cancer Center
  • Katherine S. Panageas
    • Memorial Sloan-Kettering Cancer Center
  • Carol Pearce
    • Memorial Sloan-Kettering Cancer Center
  • Larry Norton
    • Memorial Sloan-Kettering Cancer Center
  • Ann Jakubowski
    • Memorial Sloan-Kettering Cancer Center
  • Jane Howard
    • Memorial Sloan-Kettering Cancer Center
  • Clifford Hudis
    • Memorial Sloan-Kettering Cancer Center
Original Research Article

DOI: 10.2165/00002512-200522090-00007

Cite this article as:
Hurria, A., Hurria, A., Brogan, K. et al. Drugs Aging (2005) 22: 785. doi:10.2165/00002512-200522090-00007



A number of age-related physiological changes contribute to an increased risk of toxicity of cancer chemotherapy in the elderly. One of the most important of these changes is the progressive decline in renal function with aging. We sought to determine the association between calculated creatinine clearance (CLCR) and grade 3 or 4 toxicities during adjuvant chemotherapy in women ≥65 years of age with breast cancer.

Design and methods

We identified 1405 patients ≥65 years of age who had been treated for primary invasive breast cancer at Memorial Sloan-Kettering Cancer Center between January 1998 and December 2000. Patients were included in this analysis if they had stage I–III breast cancer and had received adjuvant chemotherapy. Patients were excluded if they had a prior history of breast cancer or chemotherapy, or had no baseline creatinine value available for review.


The 126 patients who met our criteria had received either cyclophos-phamide, methotrexate and fluorouracil (CMF) [n = 65, mean age 71, range 65–78] or an anthracycline-based regimen (n = 61, mean age 69, range 65–79). The majority of patients (97%) had a normal creatinine. CLCR, as calculated by the Cockcroft-Gault and Jeliffe formulas, decreased with increasing age (increased age associated with decreased Cockcroft-Gault [p = 0.02]; increased age associated with decreased Jeliffe [p < 0.01]). In multivariate analysis, after controlling for age and co-morbidity, a CLCR <50 mL/min by the Cockcroft-Gault formula was associated with an increased risk of fever and neutropenia (odds ratio [OR] 3.60; 95% CI 1.00, 12.94; p = 0.05) and a CLCR <50 mL/min by the Jeliffe formula was associated with a trend towards an increased risk of fever and neutropenia (OR 3.30; 95% CI 0.91, 12.33; p = 0.07), grade 3 or 4 haematological toxicity (OR 2.43; 95% CI 0.90, 6.55; p = 0.08), and need for erythropoietin (OR 4.15; 95% CI 0.81, 2.99; p = 0.09). An increase in creatinine (as a continuous variable) was associated with a trend towards an increased risk of grade 3 or 4 haematological toxicity (OR 5.81; 95% CI 0.96, 35.33; p = 0.06).


In this cohort of older breast cancer patients, a decreased CLCR and increased creatinine was associated with an increased risk of fever and neutropenia or haematological toxicity. CLCR should be considered when determining chemotherapy dosage in the elderly.

Copyright information

© Adis Data Information BV 2005