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      Prevalence of iron deficiency across different tumors and its association with poor performance status, disease status and anemia

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          Abstract

          Background

          Only limited data on the prevalence of iron deficiency (ID) and its correlation with clinical parameters are available in cancer. ID frequently contributes to the pathogenesis of anemia in patients with cancer and may lead to several symptoms such as impaired physical function, weakness and fatigue.

          Patients and methods

          Parameters of iron status and clinical parameters were evaluated in 1528 patients with cancer who presented consecutively within a four-month period at our center. One thousand fifty-three patients had solid tumors and 475 hematological malignancies.

          Results

          ID [transferrin saturation (TSAT) < 20%] was noted in 645 (42.6%) of the 1513 patients with TSAT tests available and 500 (33.0%) were anemic. ID rates were highest in pancreatic (63.2%), colorectal (51.9%) and lung cancers (50.7%). Of the 409 iron-deficient patients in whom serum ferritin levels were available additionally to TSAT, 335 (81.9%) presented with functional ID (FID) (TSAT < 20%, serum ferritin ≥30 ng/ml) and 74 (18.1%) with absolute ID. In patients with solid tumors, prevalence of ID correlated with cancer stage at diagnosis ( P = 0.001), disease status ( P = 0.001) and ECOG performance status ( P = 0.005).

          Conclusions

          ID was frequently noted in cancer and was associated with advanced disease, close proximity to cancer therapy, and poor performance status in patients with solid tumors.

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          Most cited references17

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          Assessing iron status: beyond serum ferritin and transferrin saturation.

          The increasing prevalence of multiple comorbidities among anemic patients with chronic kidney disease has made the use of serum ferritin and transferrin saturation more challenging in diagnosing iron deficiency. Because serum ferritin is an acute-phase reactant and because the inflammatory state may inhibit the mobilization of iron from reticuloendothelial stores, the scenario of patients with serum ferritin >800 ng/ml, suggesting iron overload, and transferrin saturation <20%, suggesting iron deficiency, has become more common. This article revisits the basis for the Kidney Disease Outcomes Quality Initiative recommendations regarding the use of serum ferritin and transferrin saturation in guiding iron therapy, then explores some of the newer alternative markers for iron status that may be useful when serum ferritin and transferrin saturation are insufficient. These newer tests include reticulocyte hemoglobin content, percentage of hypochromic red cells, and soluble transferrin receptor, all of which have shown some promise in limited studies. Finally, the role of hepcidin, a hepatic polypeptide, in the pathophysiology of iron mobilization is reviewed briefly.
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            Randomised study of cognitive effects of iron supplementation in non-anaemic iron-deficient adolescent girls.

            Up to 25% of adolescent girls in the USA are iron deficient. This double-blind, placebo-controlled clinical trial assessed the effects of iron supplementation on cognitive function in adolescent girls with non-anaemic iron deficiency. 716 girls who enrolled at four Baltimore high schools were screened for non-anaemic iron deficiency (serum ferritin < or = 12 micrograms/L with normal haemoglobin). 98 (13.7%) girls had non-anaemic iron deficiency of whom 81 were enrolled in the trial. Participants were randomly assigned oral ferrous sulphate (650 mg twice daily) or placebo for 8 weeks. The effect of iron treatment was assessed by questionnaires and haematological and cognitive tests, which were done before treatment started and repeated after the intervention. We used four tests of attention and memory to measure cognitive functioning. Intention-to-treat and per-protocol analyses were done. Of the 81 enrolled girls with non-anaemic iron deficiency, 78 (96%) completed the study (39 in each group). Five girls (three control, two treatment) developed anaemia during the intervention and were excluded from the analyses. Thus, 73 girls were included in the per-protocol analysis. Ethnic distribution, mean age, serum ferritin concentrations, haemoglobin concentrations, and cognitive test scores of the groups did not differ significantly at baseline. Postintervention haematological measures of iron status were significantly improved in the treatment group (serum ferritin 27.3 vs 12.1 micrograms/L, p < 0.001). Regression analysis showed that girls who received iron performed better on a test of verbal learning and memory than girls in the control group (p < 0.02). In this urban population of non-anaemic iron-deficient adolescent girls, iron supplementation improved verbal learning and memory.
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              Iron supplementation for unexplained fatigue in non-anaemic women: double blind randomised placebo controlled trial.

              F Verdon (2003)
              To determine the subjective response to iron therapy in non-anaemic women with unexplained fatigue. Double blind randomised placebo controlled trial. Academic primary care centre and eight general practices in western Switzerland. 144 women aged 18 to 55, assigned to either oral ferrous sulphate (80 mg/day of elemental iron daily; n=75) or placebo (n=69) for four weeks. Level of fatigue, measured by a 10 point visual analogue scale. 136 (94%) women completed the study. Most had a low serum ferritin concentration;
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                Author and article information

                Journal
                Ann Oncol
                Ann. Oncol
                annonc
                annonc
                Annals of Oncology
                Oxford University Press
                0923-7534
                1569-8041
                July 2013
                7 April 2013
                7 April 2013
                : 24
                : 7
                : 1886-1892
                Affiliations
                [1 ]Department of Medicine I, Center for Oncology, Haematology and Palliative Care, Wilhelminenspital , Vienna
                [2 ]Central Laboratory, Wilhelminenspital , Vienna, Austria
                Author notes
                [* ] Correspondence to: Prof. H. Ludwig, Department of Medicine I, Center for Oncology, Hematology and Palliative Care, Wilhelminenspital, Montleartstrasse. 37, 1160 Vienna, Austria. Tel: +43-1-49150-2101; Fax: +43-1-49150-2109; E-mail: heinz.ludwig@ 123456wienkav.at
                Article
                mdt118
                10.1093/annonc/mdt118
                3690908
                23567147
                430053ff-b29a-4659-a60a-b6a3790f95ed
                © The Author 2013. Published by Oxford University Press on behalf of the European Society for Medical Oncology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.

                History
                : 6 December 2012
                : 7 February 2013
                : 8 February 2013
                Categories
                Original Articles
                Quality of Life and Supportive Care

                Oncology & Radiotherapy
                iron deficiency,absolute iron deficiency,cancer-related anemia,chemotherapy-induced anemia,functional iron deficiency,iron deficiency anemia

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