Iron deficiency in gastrointestinal oncology
University Hospitals Leuve
Digestive Oncology, University Hospitals Leuven and Department of Oncology, KU Leuven, Belgium
Introduction
Anemia is a common finding in cancer patients, both at time of diagnosis and during antineoplastic treatment [1]. It is multifactorial and can be patient-, disease- or treatment-related (Table 1).
Table 1
Causes of anemia in cancer patients
Specific attention for anemia in cancer patients is important, as it is linked to a poorer prognosis [2], physical symptoms [3], and a poorer quality of life (QoL) [4,5]. Anemia can be corrected in different ways depending on the clinical setting, including transfusions, erythropoiesis stimulating agents (ESA) and iron supplementation. Still, anemia in cancer patients is undertreated with a treatment rate of 38.9% (ESA 17.4%, transfusions 14.9% and iron substitution 6.5%) and mean hemoglobin (Hb) to initiate treatment of 9.7 g/dL [1]. A recent European observational study showed that, despite growing evidence, the recognition and therapy of anemia and iron deficiency (ID) is still not optimal with a substantial variation across Europe [6].
In patients with anemia, the main goal is to improve QoL (especially fatigue) with limited toxicity and a good pharmaco-economic profile. However, treatment of anemia solely for fatigue is not sufficient, suggesting that chemotherapy-induced fatigue is multifactorial and management should be multidisciplinary [4].
As red blood cell (RBC) transfusions are expensive (300-500 € per transfused unit) and can be complicated by procedural problems, such as iron overload, viral and bacterial infections, and immune injury, other methods for anemia correction were needed [7]. ESA are effective in correcting chemotherapy-induced anemia and reducing the need for transfusions [8]. Following international guidelines, ESA could be started in symptomatic anemic (i.e. Hb <10.0 g/dL) cancer patients receiving chemotherapy with a palliative intention [9-11].
A recent Cochrane review [12] concluded that ESA significantly reduces the need for RBC transfusion (RR 0.65), the amount of transfusions needed (on average 0.98 unit less per patient) and induces a hematological response in a greater portion of patients (RR 3.93) in combination with a better QoL. However, ESA possibly increase mortality during the study period (HR 1.17), and there is some evidence that there is a decrease in overall survival (HR 1.05). There was also a higher risk for thromboembolic events (RR 1.52), hypertension (RR 1.3), thrombocytopenia/hemorrhage (RR 1.21), and no evidence to support an effect of ESA on tumor response (RR 1.02).
As the cost per quality-adjusted life-year is estimated to be 208,000 €, ESA therapy should be seen as an expensive therapy that profoundly increases healthcare costs [13]. Depending on the studies, the target Hb was only reached in 25-73% of patients treated with ESA [14-18].
The most important reason for ESA-refractory anemia is ID [19]. ID in cancer patients is very common. A recent prospective trial reported an ID rate of 42.6% in cancer patients, most common in patients with pancreatic, colorectal and lung cancer (63.2%, 52.2% and 51.3% respectively). ID was correlated with grade of anemia, tumor stage, time of last anticancer treatment (<12 weeks before), persistent and progressive disease status and Eastern Cooperative Oncology Group status 2-4 [20].
In this review, we will discuss the pathogenesis of ID, as well as the approach to treating it, since there are currently no clear guidelines available.
Iron homeostasis
Normal iron homeostasis
In a healthy person, iron metabolism is strictly regulated to meet the needs of the body and the bone marrow in particular, about 20-30 mg/day. The total body iron is about 50 mg/kg with iron distributed within RBC Hb (65%), in enzymes and cytochromes in myoglobin and other tissues (10%). The remainder is stored in the liver (5%), reticuloendothelial system (15%) and bone marrow (5%). The total body iron in premenopausal women is around 250-300 mg lower than in men. A normal Western diet contains 15-25 mg iron, of which only 1-2 mg/day is absorbed. Iron is lost from the human body via sloughed enterocytes, menstruation and other blood loss.
There is no substantial physiologic mechanism to regulate the iron loss. Accordingly, iron homeostasis is dependent on regulatory feedback between body iron needs and intestinal iron absorption. Iron absorption depends on the body’s iron stores, the level of erythropoietic activity in bone marrow, the blood Hb concentration, the blood oxygen content, and the presence or absence of inflammatory cytokines [21-23].
Iron homeostasis in cancer patients
In cancer patients, the iron metabolism is influenced by high levels of hepcidin (Fig. 1). Hepcidin is a 25 amino-acid peptide, produced by the liver and is the major regulator of iron homeostasis by inhibiting iron transport across the gut mucosa thereby maintaining normal iron levels within the body. It also inhibits iron transport out of macrophages. The production of hepcidin is upregulated by inflammation (IL-6), and down regulated by ID and erythropoietic activity (by mechanisms that are not well understood). Cytokine-induced synthesis of hepcidin plays a critical role in macrophage iron retention which underlies anemia of chronic disease; however little evidence is available about the relation of hepcidin levels and iron metabolism in chronically ill patients.
Figure 1
Overview of iron homeostasis in cancer patients. Cytokine-induced hepcidin production results in inhibition of iron uptake and promotion of iron sequestration. Inflammatory cytokines also directly inhibit erythropoietic activity and cause low blood hemoglobin concentration (by hemodilution) thus further worsening anemia in cancer patients
IL, interleukin; TNF, tumor necrosis factorHepcidin affects ferroportin, a major iron exporter located on the enterocytes, hepatocytes and macrophages, in two ways. First, by its direct binding to ferroportin, hepcidin forces its internalization and degradation [24]. Furthermore, hepcidin formation is inversely correlated with the expression of ferroportin [25].
ID in cancer patients
ID is generally divided in 3 groups: Absolute ID (AID), functional ID (FID), and iron sequestration (Fig. 2). AID is the most common group. AID is the absence of storage iron because of nutritional deficiencies, malabsorption or blood loss. Its therapy is focused on repletion of iron stores. FID occurs when the bone marrow needs are higher than the possible iron supply. It can be seen during intense stimulation of the bone marrow by endogenous erythropoietin or treatment with ESA. FID can occur in the presence of storage iron and/or oral iron supplementation. This is demonstrated by the 50% reduction of serum ferritin and transferrin saturation (TSAT) in individuals under ESA. Finally, iron sequestration is the immobilization of the available storage pools [26].
Figure 2
Types of iron deficiency (ID) in cancer patients
ESA, erythropoiesis stimulating agentsDiagnostic tools in ID
It is important to differentiate which mechanism is the most important in the particular patient to guide treatment, as FID, AID, and iron sequestration can be present in cancer patients [26].
Serum ferritin is commonly assessed as the reflection of the iron stores status, while transferrin saturation <20%, percentage of hypochromic red cells >5%, and Hb content of reticulocytes (CHr) <26 pg reflect the availability of iron in the body. Furthermore, serum ferritin is an acute-phase protein and can be elevated in inflammatory states (e.g. cancer) and liver injury. Hence, normal or elevated ferritin levels in patients with a chronic disease such as cancer do not necessarily indicate sufficient iron stores [27].
Soluble transferrin receptor levels, suggested to differentiate patients needing therapy with iron, ESA or the combination, rather reflects the erythropoietic activity than the iron status and cannot be assessed as iron status parameter when erythropoiesis is stimulated, as with ESA [28].
Recently, a diagnostic plot was suggested for the differentiation between the different mechanisms to guide therapy, based on iron stores (reflected as the ratio of soluble transferrin receptor to log ferritin) and iron demand (reflected as the Hb content of the reticulocytes) [28] (Fig. 3). As the ratio of soluble transferring receptor to log ferritin and CHr are not routinely measured, the plot is difficult to use in a day-to-day clinical practice. In routine clinical practice, serum ferritin levels below 100 ng/mL probably indicate insufficient iron stores in patients with cancer, and the combination of low TSAT (<20%) and normal or even elevated serum ferritin may indicate FID.
Figure 3
Diagnostic plot in anemia (in patients with CRP >5 mg/L, the cut-off for STFR/LOG FERR is 2.0).
CHr, Hemoglobin concentration in reticulocytes; sTfR/log ferritin, Ratio of soluble transferrin receptor to log ferritin [28]Iron therapy in cancer patients
Oral iron therapy
Theoretically, oral iron could be used in cancer patients with AID, who are not receiving ESA and do not have inflammation. But we believe that, although still commonly prescribed [6], there is no place for oral iron supplementation in cancer patients as they are highly susceptible for low iron intake, low iron absorption, and higher portion of blood loss. Even in addition to ESA, oral iron has no role in anemia treatment [14,15].
Formulations of intravenous (IV) iron
There are 4 formulations of IV iron available: low molecular weight iron dextran, iron gluconate, iron sucrose and iron ferric carboxymaltose (FCM). They all have an iron-oxyhydroxide core (FeOOH) and a carbohydrate coat, resembling ferritin which protects the organism against the toxicity of unbound inorganic ferric iron (Fe3+). Although they have the same basic structure, each formulation differs in core size, shell and global particle size. Due to these biochemical differences, serum clearance rate differs, with plasma half-lives from 30-60 h for iron dextran, 5.3 h for iron sucrose, 1 h for iron gluconate, and 7-12 h depending on dose for FCM [29].
Historically, there is some concern about the possible side effects of IV iron anaphylactic reactions, chronic iron overload, and possible stimulation of cancer cells. To our knowledge, in more than 50 years of IV iron use, no manifestations of chronic iron overload have been described when the agents were used at recommended doses and indications under frequent monitoring. Furthermore, although it is mostly seen in high molecular weight iron dextran [30], the most feared complication of parenteral iron still remains anaphylactic reactions. Fletes et al [31] showed a low overall risk for serious adverse events related to iron dextran infusion in clinical practice; globally in 20 cases per 100,000 doses admitted and mostly related to high molecular weight iron dextran. There are no clinical prospective data available about the oncogenic risk. Human data and animal models do show that chronic iron overload does increase cancer risk and promote tumor growth. However, epidemiological and non-clinical studies often show conflicting data and in absence of long-term safety studies, extrapolation to a clinical setting remains difficult [32].
IV iron in combination with ESA
According to the current evidence, it is recommended to optimize the available iron stores with IV iron before or during therapy with ESA [14-19] (Table 2).
Table 2
Overview of the available studies with IV iron in combination with ESA. Hematopoietic response was defined as Hb increase ≥2 g/dL, Hb ≥11g/dL, Hb ≥12 g/dL or Hb ≥13 g/dL in the different studies
In contrast to studies mentioned in Table 2, Steensma et al [33] did not find any difference in hematopoietic response rate, ESA dose requirements, transfusion needs, and QoL in 502 patients receiving darbepoetin every 3 weeks randomized to the combination with oral placebo, oral ferrous sulfate 325 mg per day and ferric gluconate 187.5 mg every 3 weeks. The negative results might be explained by the low dose of ferric gluconate, which was about 50% of the recommended single dose.
Overall, the available studies are heterogeneous in study design (different oncologic profiles, different iron formulations, different prevalence in ID and different endpoints), which makes the generalization of the results complicated. In general, there is compelling evidence that the response to ESA is better when IV iron is added.
IV iron as monotherapy
A body of evidence shows that IV administration of iron routinely in absence of ESA is favorable. Kim et al [34] showed in cervical cancer patients treated with chemoradiotherapy that giving iron sucrose every chemotherapy cycle reduces the need for transfusion (40% vs. 64% of the patients, and fewer units needed: 1.87 vs. 3.58 units). Dangsuwan [35] showed a significant reduction in transfusion need in the next chemotherapy cycle by giving iron sucrose in comparison to oral iron (22.7% vs. 63.6%).
A large German prospective, non-interventional 12-week study [36] showed that patients with baseline Hb up to 11.0 g/dL and serum ferritin up to 500 ng/mL benefited from FCM treatment (stable Hb ≥11.0 g/dL). Also patients with ferritin >500 ng/mL but low transferrin saturation benefited from FCM treatment. FCM was well tolerated, 2.3% of patients reported putative drug-related adverse events.
Concluding remarks
Anemia and ID in cancer patients are a major cause of cancer morbidity. Nevertheless, it still remains an underestimated problem and sensitization of physicians caring for cancer patients is necessary. It is important to differentiate between FID and AID as it implies the potential response on ESA and the possible need for iron supplements in patients receiving ESA. In general, most studies showed benefit from IV iron versus oral iron or no iron supplements with a good tolerance. However, these studies are very heterogeneous in their design (observational vs. per protocol; transfusion threshold; IV iron formulations and dosage regimen; and length of study) and study population, so it is difficult to estimate the expected effect on a particular patient with a particular IV iron formulation.
Iron overload can be prevented by strict follow up of the iron parameters during therapy, although there are no good clinical endpoints available so far. There are no good data available about the oncologic risk when IV iron is properly used, but there are some data suggesting an increased risk in chronic iron overload. Since ID has a negative impact on the outcome and QoL, aiming for a normal iron status with a TSAT target ranging from 20-50% seems to be reasonable in cancer patients.
As mentioned before, there are no specific studies or guidelines available for gastrointestinal cancer patients. But in general, based on the studies in general oncology patients (with heterogeneous study populations), we advise to be vigilant about ID in cancer patients in order to prevent anemia, anemia-related symptoms, and treatment with expensive ESA and transfusion. IV and not oral iron should be started when ferritin levels are <100 ng/mL and/or transferrin saturation is below 20%, independently from Hb level. Good clinical endpoints are lacking, but targeting TSAT between 20 and 50%, Hb levels above 10 g/dL, and absence of fatigue in combination with good QoL seem reasonably achievable. However, we need new prospective trials to investigate the optimal tailored iron therapies in the future in cancer patients, both in curative and palliative settings.
References
1. Ludwig H, Van Belle S, Barrett-Lee P, et al. The European Cancer Anemia Survey (ECAS):a large, multinational, prospective survey defining the prevalence, incidence, and treatment of anemia in cancer patients. Eur J Cancer 2004;40: 2293-2306.
2. Clarke H, Pallister CJ. The impact of anaemia on outcome in cancer. Clin Lab Haematol 2005;27:1-13.
3. Ludwig H, Strasser K. Symptomatology of anemia. Semin Oncol 2001;28: 7-14.
4. Holzner B, Kemmler G, Greil R, et al. The impact of hemoglobin levels on fatigue and quality of life in cancer patients. Ann Oncol 2002;13: 965-973.
5. Lind M, Vernon C, Cruickshank D, et al. The level of haemoglobin in anaemic cancer patients correlates positively with quality of life. Br J Cancer 2002;86: 1243-1249.
6. Ludwig H, Aapro M, Bokemeyer C, et al. A European patient record study on diagnosis and treatment of chemotherapy-induced anaemia . Support Care Cancer 2014;22: 2197-2206.
7. Schrijvers D. Management of Anemia in cancer patients:transfusions. Oncologist 2011;16: 12-18.
8. Bohlius J, Weingart O, Treele S, Engert A. Cancer-related anemia and recombinant human erythropoietin –an updated overview. Nat Clin Pract Oncol 2006;3: 152-164.
9. Rodgers GM 3rd, Becker PS, Blinder M, et al. Cancer- and chemotherapy-induced anemia. J Natl Compr Canc Netw 2012;10: 628-653.
10. Rizzo JD, Brouwers M, Hurley P, et al.American Society of Hematology and the American Society of Clinical Oncology Practice Guideline Update Committee. American Society of Hematology/American Society of Clinical Oncology clinical practice guideline update on the use of epoetin and darbepoetin in adult patients with cancer. Blood 2010;116: 4045-4059.
11. Schrijvers D, De Samblanx H, Roila F;ESMO Guidelines Working Group. Erythropoiesis-stimulating agents in the treatment of anaemia in cancer patients:ESMO Clinical Practice Guidelines for use. Ann Oncol 2010; 21(Suppl 5):v244-v247.
12. Tonia T, Mettler A, Robert N, et al. Erythropoietin or darbepoetin for patients with cancer. Cochrane Database of Syst Rev 2012;12:CD003407.
13. Wilson J, Yao GL, Raftery J, et al. A systematic review and economic evaluation of epoetin alpha, epoetin beta and darbepoetin alpha in anaemia associated with cancer, especially that attributable to cancer treatment . Health Technol Assess 2007;11: 1-202.
14. Auerbach M, Ballard H, Trout JR, et al. Intravenous iron optimizes the response to recombinant human erythropoietin in cancer patients witch chemotherapy-related anemia:a multicenter, open-label, randomized trial. J Clin Oncol 2004;22: 1301-1307.
15. Henry DH, Dahl NV, Auerbach M, Tchekmedyian S, Laufman LR. Intravenous ferric gluconate significantly improves response to epoetin alfa versus oral iron or no iron in anemic patiensts with cancer receiving chemotherapy. Oncologist 2007;12: 231-242.
16. Hedenus M, Birgegard G, Nasman P, et al. Addition of intravenous iron to epoetin beta increases hemoglobin response and decreases epoetin dose requirement in anemic patients witch lymphoproliferative malignancies:a randomized multicenter study. Leukemia 2007;21: 627-632.
17. Bastit L, Vandebroek A, Altintas S, et al. Randomized, multicenter, controlled trial comparing the efficacy and sefety of darbepoetin alpha administered every 3 weeks with or without intravenous iron in patients with chemotherapy-induced anemia. J Clin Oncol 2008;26: 1611-1618.
18. Pedrazzolli P, Farris A, Del Prete S, et al. Randomized trial of intravenous iron supplementation in patients with chemotherapy-related anemia without iron deficiency treated with darbepoetin alpha. J Clin Oncol 2008;26: 16919- 1625.
19. Goodnough LT. Erythropoietin and iron-restricted erythropoiesis. Exp Hematol 2007;35: 167-172.
20. Ludwig H, Müldür E, Endler G, Hübl W. Prevalence of iron deficiency across different tumors and its association with poor performance status, disease status and anemia. Ann Oncol 2013;24: 1886-1892.
21. Muñoz M, Villar I, García-Erce JA. An update on iron physiology. World J Gastroenterol 2009;15: 4617-4626.
22. Andrews NC. Disorders of iron metabolism. N Engl J Med 1999;341: 1986-1995.
23. Fleming RE, Bacon BR. Orchestration of iron homeostasis. N Eng J Med 2005;352: 1741-1744.
24. Ganz T, Nemeth E. Hepcidin and iron homeostasis. Biochim Biophys Act 2012; 1823: 1434-1443.
25. Theurl I, Aigner E, Theurl M, et al. Regulation of iron homeostasis in anemia of chronic disease and iron deficiency anemia:diagnostic and therapeutic implications. Blood 2009;113: 5277-5286.
26. Goodnough LT. Iron deficiency syndromes and iron-restricted erythropoiesis. Transfusion 2012;52: 1584-1592.
27. Wish JB. Assessing iron status:beyond serum ferritin and transferrin saturation. Clin J Am Soc Nephrol 2006;1:S4-S8.
28. Steinmetz HT, Tsamaloukas A, Schmitz S , et al. A new concept for the differential diagnosis and therapy of anaemia in cancer patients. Support Care Cancer 2010;19: 261-269.
29. Danielson BG. Structure, chemistry, and pharmacokinetics of intravenous iron agents. J Am Soc Nephrol 2004;15:S93-S98.
30. Chertow GM, Mason PD, Vaage-Nilsen O, Ahlmen J. Update on adverse drug events associated with parenteral iron. Nephrol Dial Transplant 2006: 21: 378-382.
31. Fletes R, Lazarus JM, Gage J, Chertow GM. Suspected iron dextran-related adverse drug events in hemodialysis patients . Am J Kidney Dis 2001;37: 743-749.
32. Beguin Y, Aapro M, Ludwig H, Mizzen L, Osterborg A. Epidemiological and nonclinical studies investigating effects of iron carcinogenesis –a critical review. Crit Rev Oncol Hematol 2014;89: 1-15.
33. Steensma DP, Sloan JA, Dakhill SR, et al. Phase III, randomized study of the effects of parenteral iron, oral iron, or no iron supplementation on the erythropoetic response to darbepoetin alfa for patients with chemotherapy-associated anemia. J Clin Oncol 2010;29: 97-105.
34. Kim YT, Kim SW, Yoon BS, et al. Effect of intravenously iron sucrose on the prevention of anemia in the cervical cancer patients treated with concurrent chemoradiotherapy. Gynecol Oncol 2007;105:199 204.
35. Dangsuwan P, Manchana T. Blood transfusion reduction with intravenous iron in gynecologic cancer patient receiving chemotherapy. Gynecol Oncol 2010;116: 522-525.
36. Steinmetz T, Tschechne B, Harlin O, et al. Clinical experience with ferric carboxymaltose in the treatment of cancer- and chemotherapy-associated anaemia . Ann Oncol 2013;24: 475-482. n, Belgium