Serum phosphate level and its kinetic as an early marker of acute kidney injury in tumor lysis syndrome.


Journal

Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268

Informations de publication

Date de publication:
07 2022
Historique:
received: 13 08 2021
accepted: 07 12 2021
pubmed: 3 2 2022
medline: 23 7 2022
entrez: 2 2 2022
Statut: ppublish

Résumé

Acute kidney injury (AKI) is a major cause of mortality in tumor lysis syndrome. The biochemical parameters and kinetics of tumor lysis syndrome remain poorly described. Particularly, whether blood serum phosphate variations may help in the identification and management of patients who will eventually develop AKI remains to be studied. In this retrospective study, we included patients with tumor lysis syndrome episodes without AKI at diagnosis, and analyzed serum phosphate kinetic, clinical and tumor lysis syndrome biochemical variables to identify factors associated with AKI onset, and determine threshold values of phosphatemia associated with AKI development. One hundred thirty tumor lysis syndrome episodes occurred in 120 patients during an 11-year period at the University Hospital of Angers. AKI developed in 56 tumor lysis syndrome episodes. In multivariable analysis, among the analyzed factors, only an increase in serum phosphate levels (before AKI diagnosis), exposure to platinum salts and an increase in LDH levels were associated with AKI development. Before AKI onset, a serum phosphate cut-off of 2.1 mmol/L was not effective in predicting AKI development (sensitivity 48%, specificity 84%, area under the receiver operating characteristic curve (AUC) 0.63 [0.52-0.74]). No other biochemical parameters were effective to better predict AKI occurrence. This work suggests that increases in serum phosphate and LDH appear to be early and reliable biomarkers of AKI in tumor lysis syndrome. No valuable threshold value of serum phosphate was found to effectively predict AKI. This work is the basis for further prospective controlled studies on phosphate monitoring and phosphate lowering therapies to prevent AKI during tumor lysis syndrome.

Identifiants

pubmed: 35107777
doi: 10.1007/s40620-022-01263-7
pii: 10.1007/s40620-022-01263-7
doi:

Substances chimiques

Biomarkers 0
Phosphates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1627-1636

Informations de copyright

© 2022. The Author(s) under exclusive licence to Italian Society of Nephrology.

Références

Cairo MS, Bishop M (2004) Tumour lysis syndrome: new therapeutic strategies and classification. Br J Haematol 127(1):3–11. https://doi.org/10.1111/j.1365-2141.2004.05094.x
doi: 10.1111/j.1365-2141.2004.05094.x pubmed: 15384972
Mato AR, Riccio BE, Qin L, Heitjan DF, Carroll M, Loren A et al (2006) A predictive model for the detection of tumor lysis syndrome during AML induction therapy. Leuk Lymphoma 47(5):877–883. https://doi.org/10.1080/10428190500404662
doi: 10.1080/10428190500404662 pubmed: 16753873
Lopez-Olivo MA, Pratt G, Palla SL, Salahudeen A (2013) Rasburicase in tumor lysis syndrome of the adult: a systematic review and meta-analysis. Am J Kidney Dis 62(3):481–492. https://doi.org/10.1053/j.ajkd.2013.02.378
doi: 10.1053/j.ajkd.2013.02.378 pubmed: 23684124
Wössmann W, Schrappe M, Meyer U, Zimmermann M, Reiter A (2003) Incidence of tumor lysis syndrome in children with advanced stage Burkitt’s lymphoma/leukemia before and after introduction of prophylactic use of urate oxidase. Ann Hematol 82(3):160–165. https://doi.org/10.1007/s00277-003-0608-2
doi: 10.1007/s00277-003-0608-2 pubmed: 12634948
Darmon M, Vincent F, Camous L, Canet E, Bonmati C, Braun T et al (2013) Tumour lysis syndrome and acute kidney injury in high-risk haematology patients in the rasburicase era. A prospective multicentre study from the Groupe de Recherche en Réanimation Respiratoire et Onco-Hématologique. Br J Haematol 162(4):489–497. https://doi.org/10.1111/bjh.12415
doi: 10.1111/bjh.12415 pubmed: 23772757
Jones GL, Will A, Jackson GH, Webb NJA, Rule S, British Committee for Standards in Haematology (2015) Guidelines for the management of tumour lysis syndrome in adults and children with haematological malignancies on behalf of the British Committee for Standards in Haematology. Br J Haematol 169(5):661–671. https://doi.org/10.1111/bjh.13403
doi: 10.1111/bjh.13403 pubmed: 25876990
Canet E, Cheminant M, Zafrani L, Thieblemont C, Galicier L, Lengline E et al (2014) Plasma uric acid response to rasburicase: early marker for acute kidney injury in tumor lysis syndrome? Leuk Lymphoma 55(10):2362–2367. https://doi.org/10.3109/10428194.2013.874010
doi: 10.3109/10428194.2013.874010 pubmed: 24325633
Ad-hoc working group of ERBP, Fliser D, Laville M, Covic A, Fouque D, Vanholder R et al (2012) A European Renal Best Practice (ERBP) position statement on the Kidney Disease Improving Global Outcomes (KDIGO) clinical practice guidelines on acute kidney injury: part 1: definitions, conservative management and contrast-induced nephropathy. Nephrol Dial Transplant 27(12):4263–4272. https://doi.org/10.1093/ndt/gfs375
doi: 10.1093/ndt/gfs375
McBride A, Trifilio S, Baxter N, Gregory TK, Howard SC (2017) Managing tumor lysis syndrome in the era of novel cancer therapies. J Adv Pract Oncol 8(7):705–720
pubmed: 30333933 pmcid: 6188097
Leaf DE, Christov M (2019) Dysregulated mineral metabolism in AKI. Semin Nephrol 39(1):41–56. https://doi.org/10.1016/j.semnephrol.2018.10.004
doi: 10.1016/j.semnephrol.2018.10.004 pubmed: 30606407
van den Berg H, Reintsema AM (2004) Renal tubular damage in rasburicase: risks of alkalinisation. Ann Oncol 15(1):175–176. https://doi.org/10.1093/annonc/mdh029
doi: 10.1093/annonc/mdh029 pubmed: 14679140
Treuting PM, Albertson TM, Preston BD (2010) Case series: acute tumor lysis syndrome in mutator mice with disseminated lymphoblastic lymphoma. Toxicol Pathol 38(3):476–485. https://doi.org/10.1177/0192623310362249
doi: 10.1177/0192623310362249 pubmed: 20190201
Soares M, Feres GA, Salluh JIF (2009) Systemic inflammatory response syndrome and multiple organ dysfunction in patients with acute tumor lysis syndrome. Clinics (Sao Paulo) 64(5):479–481. https://doi.org/10.1590/s1807-59322009000500016
doi: 10.1590/s1807-59322009000500016
Gaudry S, Hajage D, Schortgen F, Martin-Lefevre L, Pons B, Boulet E et al (2016) Initiation strategies for renal-replacement therapy in the intensive care unit. N Engl J Med 375(2):122–133. https://doi.org/10.1056/NEJMoa1603017
doi: 10.1056/NEJMoa1603017 pubmed: 27181456

Auteurs

Marie Lemerle (M)

Service de Néphrologie, Dialyse, Transplantation, CHU Angers, Angers, France.

Aline Schmidt (A)

Service des Maladies du sang, CHU Angers, Angers, France.
Fédération Hospitalo-Universitaire Grand-Ouest Acute Leukemia, FHU-GOAL, Angers, France.
CRCINA, INSERM U1232, Université de Nantes, Université d'Angers, Angers, France.

Valérie Thepot-Seegers (V)

Service de Biométrie, Institut de Cancérologie de l'Ouest, Centre Paul Papin, Angers, France.

Achille Kouatchet (A)

Service de Médecine Intensive Réanimation, Médecine Hyperbare, CHU Angers, Angers, France.

Valérie Moal (V)

Département de Biochimie, CHU Angers, Angers, France.

Melina Raimbault (M)

Département de Pharmacie, CHU Angers, Angers, France.

Corentin Orvain (C)

Service des Maladies du sang, CHU Angers, Angers, France.
Fédération Hospitalo-Universitaire Grand-Ouest Acute Leukemia, FHU-GOAL, Angers, France.
CRCINA, INSERM U1232, Université de Nantes, Université d'Angers, Angers, France.

Jean-François Augusto (JF)

Service de Néphrologie, Dialyse, Transplantation, CHU Angers, Angers, France.

Julien Demiselle (J)

Service de Médecine Intensive Réanimation, Nouvel Hôpital Civil, CHU Strasbourg, 1 place de l'hôpital, 67 091, Strasbourg Cedex, France. julien.demiselle@chru-strasbourg.fr.
INSERM UMR 1260, Regenerative Nanomedecine (RNM), FMTS, Strasbourg, France. julien.demiselle@chru-strasbourg.fr.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH