Management of anaemia and iron deficiency in patients with cancer: ESMO Clinical Practice Guidelines

M. Aapro, Y. Beguin, C. Bokemeyer, M. Dicato, P. Gascón, J. Glaspy, A. Hofmann, H. Link, T. Littlewood, H. Ludwig, A. Österborg, P. Pronzato, V. Santini, D. Schrijvers, R. Stauder, K. Jordan, J. Herrstedt

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Abstract

Ann Oncol 2018; 29: iv96-iv110 (doi:10.1093/annonc/mdx758) The following corrections have been made: In "Table 2. Managing anaemia in patients with MDS" In the last sentence, the word: patient has been replaced with: patients In "Table 4. Approved ESAs and i.v. iron compounds and their approved dosing in patients with solid tumours and haematological malignanciesa,b" For iron isomaltoside, maximum infusion dose, a new footnote 'e' has been added: eThe authors suggest a dose up to 1000 mg, while drug labels might allow more. For iron isomaltoside, minimum infusion time: 60 min Has been replaced with: 15 minf For iron isomaltoside, minimum infusion time, a new footnote 'f' has been added: fIf dose is up to 1000 mg; if dose exceeds 1000 mg iron, more than 30 min is recommended, as per label. In Figure 2: "Management of chemotherapy-induced anaemia in patients with very low to intermediate-risk MDS" The title has been replaced with: Management of anaemia in patients with very low to intermediate-risk MDS Under the section "Conclusions" MDS patients with low to intermediate-1 risk (IPSS) or very low to intermediate risk (revised; IPSS-R) disease and symptomatic anaemia should be considered for ESA therapy, despite the fact that ESAs are currently not EMA-approved for use in patients withMDS [I, A]. Has been replaced with: MDS patients with low to intermediate-1 risk (IPSS) or very low to intermediate risk (revised; IPSS-R) disease and symptomatic anaemia should be considered for ESA therapy, despite the fact that not all ESAs are currentlyEMA-approved for use in patients withMDS [I, A].

OriginalsprogEngelsk
Sider (fra-til)iv271
TidsskriftAnnals of Oncology
Vol/bind29
DOI
StatusUdgivet - 1 okt. 2018

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