Ferric Carboxymaltose in the treatment of chemotherapy-induced anaemia: an effective, safe and cost- sparing alternative to blood transfusion.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
31 12 2019
31 12 2019
Historique:
received:
22
01
2019
accepted:
11
12
2019
entrez:
2
1
2020
pubmed:
2
1
2020
medline:
11
11
2020
Statut:
epublish
Résumé
Anaemia is highly prevalent in cancer patients, adversely affects quality of life and impacts survival. The pathogenesis is multifactorial, with iron deficiency being a major and potentially treatable contributor. This study aimed to assess the effectiveness and economic impact of ferric carboxymaltose in chemotherapy-induced anaemia. This prospective cohort study between 2015-2016 of chemotherapy-treated patients for solid tumours, grade ≥2 anaemia and iron deficiency evaluated hematopoietic response four weeks after ferric carboxymaltose treatment. Transfusion rate of all cancer patients treated at our ambulatory unit during the two-year study period (2015-2016) was compared to a retrospective cohort (2013-2014) who received blood transfusion only. Between 2015-2016, 99 patients were included and treated with ferric carboxymaltose, the majority of whom (n = 81) had relative iron deficiency. Mean haemoglobin concentrations improved from 9.2 [6.7-10.8] g/dL to 10.6 [7.8-14.2] g/dL four weeks after treatment. A 26% reduction in the transfusion rate was observed from control retrospective to the prospective study group including ferric carboxymaltose treated patients [relative risk 0.74 (95% CI:0.66-0.83)]. The cost analysis showed a benefit for the use of ferric carboxymaltose in chemotherapy-induced anaemia. This study shows that ferric carboxymaltose is an effective, cost-saving support treatment, reducing the need for allogeneic transfusions saving blood units which are a limited resource.
Identifiants
pubmed: 31892732
doi: 10.1038/s41598-019-56999-3
pii: 10.1038/s41598-019-56999-3
pmc: PMC6938480
doi:
Substances chimiques
Antineoplastic Agents
0
Ferric Compounds
0
ferric carboxymaltose
6897GXD6OE
Maltose
69-79-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
20410Références
Med Oncol. 2014 Dec;31(12):302
pubmed: 25373320
Ther Adv Hematol. 2014 Apr;5(2):48-60
pubmed: 24688754
Cochrane Database Syst Rev. 2012 Dec 12;12:CD003407
pubmed: 23235597
Clin Epidemiol. 2016 Apr 18;8:61-71
pubmed: 27186078
Eur J Cancer. 2004 Oct;40(15):2293-306
pubmed: 15454256
JCI Insight. 2018 Dec 6;3(23):
pubmed: 30518682
Pharmaceuticals (Basel). 2018 Sep 30;11(4):
pubmed: 30274354
Ann Oncol. 2013 Feb;24(2):475-482
pubmed: 23071262
PLoS One. 2012;7(9):e45604
pubmed: 23029129
Support Care Cancer. 2017 Jul;25(7):2313-2319
pubmed: 28386789
Ann Oncol. 2004 Jun;15(6):979-86
pubmed: 15151958
Clin Drug Investig. 2016 Mar;36(3):177-94
pubmed: 26692005
Ann Oncol. 2018 Oct 1;29(Suppl 4):iv96-iv110
pubmed: 29471514
Ann Oncol. 2010 Oct;21 Suppl 7:vii167-72
pubmed: 20943610
Ann Oncol. 2013 Jul;24(7):1886-1892
pubmed: 23567147
Haematologica. 2015 Jan;100(1):124-32
pubmed: 25239265
Support Care Cancer. 2016 Jan;24(1):67-75
pubmed: 25921449
Transfusion. 2014 Feb;54(2):306-15
pubmed: 23772856
Nephrol Dial Transplant. 2014 Apr;29(4):833-42
pubmed: 23963731
Br J Cancer. 2010 Jan 19;102(2):301-15
pubmed: 20051958
Acta Haematol. 2019;142(1):13-20
pubmed: 30970366
Clin Transl Oncol. 2014 Sep;16(9):823-8
pubmed: 24458881
Vasc Med. 2011 Apr;16(2):119-30
pubmed: 21112902
Mol Pharm. 2013 Nov 4;10(11):4055-62
pubmed: 24044612
J Intern Med. 2019 Feb;285(2):205-214
pubmed: 30141278
Hemodial Int. 2017 Jun;21 Suppl 1:S83-S92
pubmed: 28371203
Rev Bras Hematol Hemoter. 2016 Oct - Dec;38(4):325-330
pubmed: 27863761
Clin Ther. 2009;31 Pt 2:2416-32
pubmed: 20110050
Technol Health Care. 2016;24(1):111-20
pubmed: 26409561