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Hypokalemia secondary to capecitabine: a hidden toxicity?

BACKGROUND: Hyopkalemia is a listed toxicity in the capecitabine (Xeloda®; Roche, Nutley, NJ) package insert. However, the incidence and severity of this toxicity is not known. METHODS: We performed a retrospective evaluation of hypokalemia in 77 patients, who received capecitabine for gastrointesti...

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Autores principales: Saif, Muhammad Wasif, Fekrazad, Mohammad Houman, Ledbetter, Leslie, Diasio, Robert B
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1936298/
https://www.ncbi.nlm.nih.gov/pubmed/18360625
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author Saif, Muhammad Wasif
Fekrazad, Mohammad Houman
Ledbetter, Leslie
Diasio, Robert B
author_facet Saif, Muhammad Wasif
Fekrazad, Mohammad Houman
Ledbetter, Leslie
Diasio, Robert B
author_sort Saif, Muhammad Wasif
collection PubMed
description BACKGROUND: Hyopkalemia is a listed toxicity in the capecitabine (Xeloda®; Roche, Nutley, NJ) package insert. However, the incidence and severity of this toxicity is not known. METHODS: We performed a retrospective evaluation of hypokalemia in 77 patients, who received capecitabine for gastrointestinal malignancies between April 2002 and November 2004. Hypokalemia was defined as K(+) level <3.2 mEq/L. Patients with documented ≥grade 2 vomiting or diarrhea, diuretics, hypomagnesemia, hypokalemia, renal insufficiency, endocrine dysfunction (thyroid, adrenal, diabetic) were excluded. Hypokalemic patients were graded as: mild (grade 1: 3.0–3.2 mEq/L), moderate (grade 3: 2.5–2.9 mEq/L) and severe (grade 4: <2.5 mEq/L). We also reviewed the literature. RESULTS: Fifty-four patients met the above criteria. The most common cause of exclusion was ≥ grade 2 diarrhea (23 patients; 30%). Overall, hypokalemia was encountered in 11 patients (20.4%). Among hypokalemic patients, 8 patients (73%) presented with mild/grade 1 hypokalemia (3.0–3.2 mEq/L), 2 patients (18.18%) with moderate/grade 3 hypokalemia (2.5–2.9 mEq/L) and 1 patient (9.09%) with severe/grade 4 hypokalemia (<2.5 mEq/L) 8 (73%). Dose of capecitabine ranged between 1000–2000 mg/m(2). Hypokalemia occurred after an average of 83.7 days of capecitabine administration. No cardiac or neuromuscular complications were noticed. Replacement of K(+) was required in 6 patients (2 intravenous and 4 oral), while 2 patients (3.7%) required oral supplements >4 weeks. No patient had to stop capecitabine due to hypokalemia. One patient had persistent hypokalemia even after stopping capecitabine. Normalization of K(+) levels was achieved in 91% of patients. Four patients were on K(+) sparing diuretics for ascites and never presented with hypokalemia. Mean urine K(+) was 28 mEq/L. Only 5.5% patients had ≥grade 3 hypokalemia in our study compared with 2% and 14% in two other studies. CONCLUSIONS: Although diarrhea being the most common cause of hypokalemia in patients on capecitabine, we postulate that hypokalemia may also be related to the effect of capecitabine on renal tubules suggested by the urine K(+) in some patients. Due to potential complications, hypokalemia in patients on capecitabine deserves special diagnostic and therapeutic attention.
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spelling pubmed-19362982008-03-21 Hypokalemia secondary to capecitabine: a hidden toxicity? Saif, Muhammad Wasif Fekrazad, Mohammad Houman Ledbetter, Leslie Diasio, Robert B Ther Clin Risk Manag Original Research BACKGROUND: Hyopkalemia is a listed toxicity in the capecitabine (Xeloda®; Roche, Nutley, NJ) package insert. However, the incidence and severity of this toxicity is not known. METHODS: We performed a retrospective evaluation of hypokalemia in 77 patients, who received capecitabine for gastrointestinal malignancies between April 2002 and November 2004. Hypokalemia was defined as K(+) level <3.2 mEq/L. Patients with documented ≥grade 2 vomiting or diarrhea, diuretics, hypomagnesemia, hypokalemia, renal insufficiency, endocrine dysfunction (thyroid, adrenal, diabetic) were excluded. Hypokalemic patients were graded as: mild (grade 1: 3.0–3.2 mEq/L), moderate (grade 3: 2.5–2.9 mEq/L) and severe (grade 4: <2.5 mEq/L). We also reviewed the literature. RESULTS: Fifty-four patients met the above criteria. The most common cause of exclusion was ≥ grade 2 diarrhea (23 patients; 30%). Overall, hypokalemia was encountered in 11 patients (20.4%). Among hypokalemic patients, 8 patients (73%) presented with mild/grade 1 hypokalemia (3.0–3.2 mEq/L), 2 patients (18.18%) with moderate/grade 3 hypokalemia (2.5–2.9 mEq/L) and 1 patient (9.09%) with severe/grade 4 hypokalemia (<2.5 mEq/L) 8 (73%). Dose of capecitabine ranged between 1000–2000 mg/m(2). Hypokalemia occurred after an average of 83.7 days of capecitabine administration. No cardiac or neuromuscular complications were noticed. Replacement of K(+) was required in 6 patients (2 intravenous and 4 oral), while 2 patients (3.7%) required oral supplements >4 weeks. No patient had to stop capecitabine due to hypokalemia. One patient had persistent hypokalemia even after stopping capecitabine. Normalization of K(+) levels was achieved in 91% of patients. Four patients were on K(+) sparing diuretics for ascites and never presented with hypokalemia. Mean urine K(+) was 28 mEq/L. Only 5.5% patients had ≥grade 3 hypokalemia in our study compared with 2% and 14% in two other studies. CONCLUSIONS: Although diarrhea being the most common cause of hypokalemia in patients on capecitabine, we postulate that hypokalemia may also be related to the effect of capecitabine on renal tubules suggested by the urine K(+) in some patients. Due to potential complications, hypokalemia in patients on capecitabine deserves special diagnostic and therapeutic attention. Dove Medical Press 2007-03 2007-03 /pmc/articles/PMC1936298/ /pubmed/18360625 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Original Research
Saif, Muhammad Wasif
Fekrazad, Mohammad Houman
Ledbetter, Leslie
Diasio, Robert B
Hypokalemia secondary to capecitabine: a hidden toxicity?
title Hypokalemia secondary to capecitabine: a hidden toxicity?
title_full Hypokalemia secondary to capecitabine: a hidden toxicity?
title_fullStr Hypokalemia secondary to capecitabine: a hidden toxicity?
title_full_unstemmed Hypokalemia secondary to capecitabine: a hidden toxicity?
title_short Hypokalemia secondary to capecitabine: a hidden toxicity?
title_sort hypokalemia secondary to capecitabine: a hidden toxicity?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1936298/
https://www.ncbi.nlm.nih.gov/pubmed/18360625
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