Key result
Single agent doxorubicin was associated with a higher likelihood of an increase in serum creatinine ≥0.3 mg/dL compared to CHOP-based chemotherapy protocols in cats (OR 20.0; 95% CI 2.9-100).
Why the study?
Azotemia occurs in cats administered doxorubicin, but risk factors have not been explored.
What are the incidence and risk factors for progressive increases in serum creatinine concentrations in cats with cancer receiving doxorubicin?
Observational (n=70)
What are the incidence and risk factors for progressive increases in serum creatinine concentrations in cats with cancer receiving doxorubicin?
Progressive increases in serum creatinine are common in cats receiving doxorubicin, with single-agent therapy posing a higher risk than CHOP-based protocols.
May warrant closer renal monitoring with single-agent doxorubicin in cats; hypothesis-generating and leaves optimal protocols open.
BACKGROUND: Azotemia occurs in cats administered doxorubicin, but risk factors have not been explored. OBJECTIVE: To determine incidence of progressive increases in serum creatinine concentration in cats with cancer receiving doxorubicin in single or multiagent chemotherapy protocols and associated risk factors. ANIMALS: Seventy cats with cancer receiving doxorubicin. METHODS: A retrospective study (2007-2017) of cats with indices of kidney function recorded before and after doxorubicin administration was reviewed. Cats diagnosed with kidney injury because of known etiologies other than possible doxorubicin toxicosis were excluded. Variables were compared to identify risk factors. RESULTS: Mean age (±SD) was 10.9 years (±3.2). Cancer types included lymphoma (n = 36), sarcoma (n = 19) and carcinoma (n = 14). Chronic kidney disease was present in 29/70 (41%) cats before receiving doxorubicin. Of 70 cats, 24 (34%) developed an increase in serum creatinine concentration ≥0.3 mg/dL and 10 (14%) had an increase ≥50% from baseline. Mean time to increases in serum creatinine concentration ≥0.3 mg/dL from first administration of doxorubicin was 119.3 days (±89.7), with mean 2.8 (±1.2) doses administered. Neutropenia or anemia during chemotherapy and number of radiation therapy treatments under general anesthesia were risk factors for increases in serum creatinine concentration (P < .05). Cats receiving single agent doxorubicin had a higher likelihood of an increase in serum creatinine concentration ≥0.3 mg/dL from baseline than cats receiving CHOP-based chemotherapy protocols (OR 20.0, 95% CI 2.9-100). CONCLUSIONS AND CLINICAL IMPORTANCE: Progressive increases in serum creatinine concentration from baseline were common in cats receiving doxorubicin and associated risk factors were identified.
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Kopecny et al. (2020) conducted an observational in Cancer in cats (n=70). Single agent doxorubicin vs. CHOP-based chemotherapy protocols was evaluated on Increase in serum creatinine concentration ≥0.3 mg/dL from baseline (OR 20.0, 95% CI 2.9-100). Single agent doxorubicin was associated with a higher likelihood of an increase in serum creatinine ≥0.3 mg/dL compared to CHOP-based chemotherapy protocols in cats (OR 20.0; 95% CI 2.9-100).
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