Cumulative pemetrexed dose increases the risk of nephrotoxicity

被引:25
作者
de Rouw, N. [1 ,2 ]
Boosman, R. J. [3 ]
van de Bruinhorst, H. [4 ]
Biesma, B. [5 ]
van den Heuvel, M. M. [6 ]
Burger, D. M. [1 ]
Hilbrands, L. B. [7 ]
ter Heine, R. [1 ]
Derijks, H. J. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Radboud Inst Hlth Sci, Med Ctr, Dept Pharm, Nijmegen, Netherlands
[2] Jeroen Bosch Hosp, Dept Pharm, sHertogenbosch, Netherlands
[3] Antoni van Leeuwenhoek Netherlands Canc Inst, Dept Pharm & Pharmacol, Amsterdam, Netherlands
[4] Univ Utrecht, Sch Pharm, Utrecht, Netherlands
[5] Jeroen Bosch Hosp, Dept Pulmonol, sHertogenbosch, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Dept Pulmonol, Nijmegen, Netherlands
[7] Radboud Univ Nijmegen, Med Ctr, Dept Nephrol, Nijmegen, Netherlands
关键词
Pemetrexed; Nephrotoxicity; Non-small cell lung cancer; ACUTE KIDNEY INJURY; INDUCTION TREATMENT; CANCER-PATIENTS; PLUS CISPLATIN; PHASE-III; CREATININE; SECRETION; TOXICITY; MODEL;
D O I
10.1016/j.lungcan.2020.05.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Pemetrexed is a pharmacotherapeutic cornerstone in the treatment of non-small cell lung cancer. As it is primarily eliminated by renal excretion, adequate renal function is essential to prevent toxic exposure. There is growing evidence for the nephrotoxic potential of pemetrexed, which even becomes a greater issue now combined immuno-chemotherapy prolongs survival. Therefore, the aim of this study was to describe the incidence of nephrotoxicity and related treatment consequences during pemetrexed-based treatment. Methods: A retrospective cohort study was conducted in the Jeroen Bosch Hospital, Den Bosch, the Netherlands. All patients that received at least 1 cycle of pemetrexed based therapy were included in the dataset. The primary outcome was defined as a >= 25 % reduction in eGFR. Additionally, the treatment consequences of decreased renal function were assessed. Logistic regression was used to identify risk factors for nephrotoxicity during treatment with pemetrexed. Results: Of the 359 patients included in this analysis, 21 % patients had a clinically relevant decline in renal function after treatment and 8.1 % of patients discontinued treatment due to nephrotoxicity. Cumulative dose (>= 10 cycles of pemetrexed based therapy) was identified as a risk factor for the primary outcome measure (adjusted OR 5.66 (CI 1.73-18.54)). Conclusion: This study shows that patients on pemetrexed-based treatment are at risk of developing renal impairment. Risk significantly increases with prolonged treatment. Renal impairment is expected to become an even greater issue now that pemetrexed-based immuno-chemotherapy results in longer survival and thus longer treatment duration.
引用
收藏
页码:30 / 35
页数:6
相关论文
共 44 条
[1]   Effect of renal function on pemetrexed-induced haematotoxicity [J].
Ando, Yosuke ;
Hayashi, Takahiro ;
Ujita, Moeko ;
Murai, Sumie ;
Ohta, Hideki ;
Ito, Kaori ;
Yamaguchi, Teppei ;
Funatsu, Minori ;
Ikeda, Yoshiaki ;
Imaizumi, Kazuyoshi ;
Kawada, Kenji ;
Yasuda, Kimio ;
Yamada, Shigeki .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2016, 78 (01) :183-189
[2]   Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed [J].
Assayag, Maureen ;
Rouvier, Philippe ;
Gauthier, Marion ;
Costel, Ghania ;
Cluzel, Philippe ;
Mercadal, Lucile ;
Deray, Gilbert ;
Bagnis, Corinne Isnard .
BMC CANCER, 2017, 17
[3]   Pemetrexed A Review of its Use in the Management of Advanced Non-Squamous Non-Small Cell Lung Cancer [J].
Baldwin, Claudine M. ;
Perry, Caroline M. .
DRUGS, 2009, 69 (16) :2279-2302
[4]   Pemetrexed-induced acute kidney injury leading to chronic kidney disease [J].
Chauvet, Sophie ;
Courbebaisse, Marie ;
Ronco, Pierre ;
Plaisier, Emmanuelle .
CLINICAL NEPHROLOGY, 2014, 82 (06) :402-406
[5]   Incidence of acute kidney injury in cancer patients: A Danish population-based cohort study [J].
Christiansen, Christian Fynbo ;
Johansen, Martin Berg ;
Langeberg, Wendy J. ;
Fryzek, Jon P. ;
Sorensen, Henrik Toft .
EUROPEAN JOURNAL OF INTERNAL MEDICINE, 2011, 22 (04) :399-406
[6]   Proximal Tubular Secretion of Creatinine by Organic Cation Transporter OCT2 in Cancer Patients [J].
Ciarimboli, Giuliano ;
Lancaster, Cynthia S. ;
Schlatter, Eberhard ;
Franke, Ryan M. ;
Sprowl, Jason A. ;
Pavenstadt, Hermann ;
Massmann, Vivian ;
Guckel, Denise ;
Mathijssen, Ron H. J. ;
Yang, Wenjian ;
Pui, Ching-Hon ;
Relling, Mary V. ;
Herrmann, Edwin ;
Sparreboom, Alex .
CLINICAL CANCER RESEARCH, 2012, 18 (04) :1101-1108
[7]   Clinicopathological features of acute kidney injury associated with immune checkpoint inhibitors [J].
Cortazar, Frank B. ;
Marrone, Kristen A. ;
Troxell, Megan L. ;
Ralto, Kenneth M. ;
Hoenig, Melanie P. ;
Brahmer, Julie R. ;
Le, Dung T. ;
Lipson, Evan J. ;
Glezerman, Ilya G. ;
Wolchok, Jedd ;
Cornell, Lynn D. ;
Feldman, Paul ;
Stokes, Michael B. ;
Zapata, Sarah A. ;
Hodi, F. Stephen ;
Ott, Patrick A. ;
Yamashita, Michifumi ;
Leaf, David E. .
KIDNEY INTERNATIONAL, 2016, 90 (03) :638-647
[8]  
Du Bois D, 1989, Nutrition, V5, P303
[9]   Foreword [J].
Eckardt, Kai-Uwe ;
Kasiske, Bertram L. .
KIDNEY INTERNATIONAL SUPPLEMENTS, 2012, 2 (01) :7-7
[10]  
European Medicine Agency (EMA), 2017, ALIMTA EPAR PROD INF