Everolimus in acute kidney injury in a patient with breast cancer: A case report

被引:7
作者
Donders F. [1 ]
Kuypers D. [2 ]
Wolter P. [3 ]
Neven P. [1 ]
机构
[1] Department of Obstetrics and Gynecology - Gyn. Oncol., University Hospitals Leuven, KU Leuven-University of Leuven, Herestraat 49, Leuven
[2] Department of Nephrology, University Hospitals Leuven, KU Leuven-University of Leuven, Herestraat 49, Leuven
[3] Department of General Medical Oncology, University Hospitals Leuven, KU Leuven-University of Leuven, Herestraat 49, Leuven
关键词
Acute renal injury; Breast cancer; Everolimus; Metastatic;
D O I
10.1186/1752-1947-8-386
中图分类号
学科分类号
摘要
Introduction: Everolimus, a mammalian target of Rapamycin inhibitor, has recently been approved for the treatment of metastatic estrogen receptor-positive breast cancer, in combination with exemestane at a daily dose of 10mg. In the literature, few cases of acute kidney injury have been reported related to everolimus use, but none of them in a patient with breast cancer as we report here. Our case report of acute kidney injury demonstrates the potential nephrotoxic effects of everolimus therapy, necessitating close monitoring of renal function prior to, during and after discontinuation of the drug. Case presentation: We report the first published case of acute kidney injury shortly after initiation of exemestane and everolimus for metastatic breast cancer resistant to letrozole in a 69-year-old Caucasian woman, initially treated for a stage IIB estrogen receptor-positive breast cancer in 1997. Within 2 weeks of therapy, she developed grade 1 to 2 diarrhea, lower extremity edema, lethargy, and anorexia. After 4 weeks of therapy, her blood pressure was 85/59mmHg and she lost 4kg bodyweight. Her serum creatinine was 3.34mg/dL. Everolimus was stopped, and she was hospitalized for rehydration. Her serum creatinine levels peaked at 8.85mg/dL 8 days after treatment discontinuation, with a calculated creatinine clearance of 7mL/minute. Dialysis was not required. A month later, her serum creatinine levels slowly dropped to 2.26mg/dL but did not return to baseline. No re-challenge of everolimus was attempted. Conclusions: Extreme vigilance should be used when prescribing everolimus for metastatic breast cancer. Although the exact cause of acute kidney injury in our case is unknown, dehydration must be avoided and renal function closely monitored after initiating therapy. Spontaneous recovery after drug discontinuation is possible. © 2014 Donders et al.; licensee BioMed Central Ltd.
引用
收藏
相关论文
共 11 条
[1]  
Choueiri T.K., Je Y., Sonpavde G., Richards C.J., Galsky M.D., Nguyen P.L., Schutz F., Heng D.Y., Kaymakcalan M.D., Incidence and risk of treatment-related mortality in cancer patients treated with the mammalian target of rapamycin inhibitors, Ann Oncol, 24, pp. 2092-2097, (2013)
[2]  
Izzedine H., Escudier B., Rouvier P., Gueutin V., Varga A., Bahleda R., Soria J.C., Acute tubular necrosis associated with mTOR inhibitor therapy: A real entity biopsy-proven, Ann Oncol, 24, pp. 2421-2425, (2013)
[3]  
Baselga J., Campone Campone M., Piccart M., Burris H.A., Rugo H.S., Sahmoud T., Noguchi S., Gnant M., Pritchard K.I., Lebrun F., Beck J.T., Ito Y., Yardley D., Deleu I., Perez A., Bachelot T., Vittori L., Xu Z., Mukhopadhyay P., Lebwohl D., Hortobagyi G.N., Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer, N Engl J Med, 366, pp. 520-529, (2012)
[4]  
Nakagawa S., Nishihara K., Inui K., Masuda S., Involvement of autophagy in the pharmacological effects of the mTOR inhibitor everolimus in acute kidney injury, Eur J Pharmacol, 696, pp. 143-154, (2012)
[5]  
Kamdem L.K., Flockhart D.A., Desta Z., In vitro cytochrome P450-mediated metabolism of exemestane, Drug Metab Dispos, 39, pp. 98-105, (2011)
[6]  
Ravaud A., Urva S.R., Grosch K., Cheung W.K., Anak O., Sellami D.B., Relationship between everolimus exposure and safety and efficacy: Meta-analysis of clinical trials in oncology, Eur J Cancer, 50, pp. 486-495, (2014)
[7]  
Podder H., Stepkowski S.M., Napoli K.L., Clark J., Verani R.R., Chou T.C., Kahan B.D., Pharmacokinetic interactions augment toxicities of sirolimus/cyclosporine combinations, J Am Soc Nephrol, 12, pp. 1059-1071, (2001)
[8]  
Huober J., Fasching P.A., Hanusch C., Rezai M., Eidtmann H., Kittel K., Hilfrich J., Schwedler K., Blohmer J.U., Tesch H., Gerber B., Hoss C., Kummel S., Mau C., Jackisch C., Khandan F., Costa S.D., Krabisch P., Loibl S., Nekljudova V., Untch M., Minckwitz G., Neoadjuvant chemotherapy with paclitaxel and everolimus in breast cancer patients with non-responsive tumours to epirubicin/cyclophosphamide (EC) +/- bevacizumab - Results of the randomised GeparQuinto study (GBG 44), Eur J Cancer, 49, pp
[9]  
Eisen H.J., Tuzcu E.M., Dorent R., Kobashigawa J., Mancini D., Valantine-von Kaeppler H.A., Starling R.C., Sorensen K., Hummel M., Lind J.M., Abeywickrama K.H., Bernhardt P., Everolimus for the prevention of allograft rejection and vasculopathy in cardiac-transplant recipients, N Engl J Med, 349, pp. 847-858, (2003)
[10]  
Pritchard K.I., Burris H.A., Ito Y., Rugo H.S., Dakhil S., Hortobagyi G.N., Campone M., Csoszi T., Baselga J., Puttawibul P., Piccart M., Heng D., Noguchi S., Srimuninnimit V., Bourgeois H., Gonzalez Martin A., Osborne K., Panneerselvam A., Taran T., Sahmoud T., Gnant M., Safety and efficacy of everolimus with exemestane vs. Exemestane alone in elderly patients with HER2-negative, hormone receptor-positive breast cancer in BOLERO-2, Clin Breast Cancer, 13, pp. 421-432, (2013)