Acute Kidney Injury in Patients Receiving Systemic Treatment for Cancer: A Population-Based Cohort Study

Author:

Kitchlu Abhijat12,McArthur Eric3,Amir Eitan4,Booth Christopher M35,Sutradhar Rinku36,Majeed Habeeb4,Nash Danielle M3,Silver Samuel A7,Garg Amit X38,Chan Christopher T2,Kim S Joseph23,Wald Ron2

Affiliation:

1. Department of Medicine

2. Division of Nephrology, University of Toronto, Toronto, ON, Canada

3. Institute for Clinical Evaluative Sciences, London, ON, Canada

4. Department of Medical Oncology, Princess Margaret Cancer Centre, Toronto, ON, Canada

5. Department of Oncology, Queen's University, Kingston, ON, Canada

6. Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada

7. Division of Nephrology, Queen's University, Kingston, ON, Canada

8. Division of Nephrology, Western University, London, ON, Canada (AXG)

Abstract

Abstract Background Patients undergoing treatment for cancer are at increased risk of acute kidney injury (AKI). There are few data on AKI incidence and risk factors in the current era of cancer treatment. Methods We conducted a population-based study of all patients initiating systemic therapy (chemotherapy or targeted agents) for a new cancer diagnosis in Ontario, Canada (2007–2014). The primary outcome was hospitalization with AKI or acute dialysis. We estimated the cumulative incidence of AKI and fitted Fine and Gray models, adjusting for demographics, cancer characteristics, comorbidities, and coprescriptions. We modeled exposure to systemic therapy (the 90-day period following treatments) as a time-varying covariate. We also assessed temporal trends in annual AKI incidence. Results We identified 163 071 patients initiating systemic therapy of whom 10 880 experienced AKI. The rate of AKI was 27 per 1000 person-years, with overall cumulative incidence of 9.3% (95% CI = 9.1% to 9.6%). Malignancies with the highest 5-year AKI incidence were myeloma (26.0%, 95% CI = 24.4% to 27.7%), bladder (19.0%, 95% CI = 17.6% to 20.5%), and leukemia (15.4%, 95% CI = 14.3% to 16.5%). Advanced cancer stage, chronic kidney disease, and diabetes were associated with increased risk of AKI (adjusted hazard ratios [aHR] = 1.41, 95% CI = 1.28 to 1.54; 1.80, 95% CI = 1.67 to 1.93; and 1.43, 95% CI = 1.37 to 1.50, respectively). In patients aged 66 years or older with universal drug benefits, diuretic, and angiotensin-converting enzyme inhibitor/angiotensin receptor blocker coprescription was associated with higher AKI risk (aHR = 1.20, 95% CI = 1.14 to 1.28; 1.30, 95% CI = 1.23 to 1.38). AKI risk was further accentuated during the 90-day period following systemic therapy (aHR = 2.34, 95% CI = 2.24 to 2.45). The annual incidence of AKI increased from 18 to 52 per 1000 person-years between 2007 and 2014. Conclusion Cancer-related AKI is common and associated with advanced stage, chronic kidney disease, diabetes, and concomitant receipt of diuretics or angiotensin-converting enzyme inhibitors/angiotensin receptor blockers. Risk is heightened in the 90 days after systemic therapy. Preventive strategies are needed to address the increasing burden of AKI in this population.

Funder

Institute for Clinical Evaluative Sciences

Ontario Ministry of Health and Long-Term Care

Academic Medical Organization of Southwestern Ontario

Schulich School of Medicine and Dentistry

Western University, and the Lawson Health Research Institute

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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