Received: February 5, 2019
Accepted: March 21, 2019
Mediterr J Hematol Infect Dis 2019, 11(1): e2019030 DOI 10.4084/MJHID.2019.030
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issue of iron overload in hemopoietic cell transplantation has been
first discussed in the field of transplantation for thalassemia.
Thalassemia major is characterized by ineffective erythropoiesis and
hemolysis leading to severe anemia. Patients require regular blood
transfusion therefore they develop iron overload causing organ damage
and hematopoietic cell transplantation (HCT) is a consolidated
reliably curative option.
More than 30 years have passed since the first successful Hematopoietic Cell Transplantation (HCT) in thalassemia. Since then, more than 3000 transplants have been performed worldwide with outstanding results. Gene therapy has been now finally developed and promises to be a further improvement in thalassemia cure option.
Firstly in this category of patients iron overload toxicity has emerged as an important issue for transplant outcome. Clinical results revealed how iron exceeded before HCT affects the outcome in TDT. Subsequently the role of iron overload / toxicity have been investigated in others transfusion dependent diseases including myelodysplastic syndromes (MDS). It is well known that iron overload is deleterious for organs such as liver, heart and endocrine glands and, it has been postulated could also increases the risk of infections and Graft versus Host Disease (GvHD) early after HCT. High baseline Ferritin levels before HCT have been shown to negatively influence clinical outcome in diseases different from TDT.[4-6]
If solid clinical evidence has established the negative impact of high iron burden and related tissue damage on the outcome of HCT for TDT, recent preclinical data has shown how increased production of reactive oxygen species (ROS) resulting under iron overload condition, could impair the hemopoietic niche and therefore the stem cells clonality capacity, proliferation and maturation independently from baseline disease. Also, microenvironment cells could be affected through this mechanism. Moving from this hypothesis, in-vitro and animal model experimental studies started to understand if iron toxicity could be an issue also in the HCT engraftment period.
The aim of this review is to update consolidated knowledge about the role of iron overload/iron toxicity in the HCT setting introducing the concept of exposition of free toxic iron forms and related cellular damage.
Recently Understood Mechanisms Support Iron Toxicity and Cell Damage
Iron in Phisiological and Pathological Conditions
|Table 1. Free iron forms types and property.|
The exceed iron, is deposited in the stable ferritin form. Excess LCI can enter the mitochondria and take part to increase the cellular ROS production through the Fenton’s reaction. Usually the cell holds physiological adaptation mechanisms against the ROS level increases, mainly mediated by the activation of nuclear factor erythroid 2-related factor (Nrf2). Oxidative stress, normally produced in the cell, activates the Nrf2 pathway that is able to enter the nucleus and up-regulate the expression of antioxidant enzymes. Although Nrf2 can protect normal cells from oxidative stress, when the LCI level increases this mechanism becomes inadequate to control the ROS surplus and an oxidative stress state is established in the cell. Maintaining ROS at an appropriate level plays an important role in biological phenomena; increasing ROS or damage of the antioxidant system could lead to oxidative stress reactions and finally to cell damage (Figure 1).
Nowadays, ferritin is considered a steady and not biological active form of iron, while LPI is considered the main trigger of cell damage more representative of the dynamic tissue damage. The scientific community is moving the iron disease from a “Bulky” disease, such as classically in thalassemia (based on quantitative iron parameters as ferritin, red blood cell transfusion number, MRI) to a “toxic” disease (based on active and dynamic biological markers as NTBI/LPI).
The mechanisms leading to iron dependent tissue / cells toxicity have been recently summarized by the following equation:
Iron toxicity tissue = Σ Tissue reactive iron x Genetics x Environmental Factors x Time
This formula proposes that tissue toxicity arises from both the quantity of toxic iron species (i.e., tissue reactive species = NTBI/LPI). The detrimental effects are further modulated by the host genetic characteristics, by the individual anti‐oxidant mechanisms and by environmental factors.
Free Iron Toxicity before Transplant
Recently Angelucci et al revisited the Pesaro TDT score system based on the above-mentioned new concept of iron toxicity. It is evident that all the three risk factors were not quantitative direct markers of iron overload “per se”, but indirect measures of intensity and extent of tissue exposure to toxic iron. Authors concluded that “adequacy of chelation” clearly means consistent and sufficient suppression of tissue reactive iron species (NTBI/LPI) over time. “Liver fibrosis” is definitely a marker of toxic iron exposure and environmental factors (i.e., viral infections) in the liver and “Hepatomegaly” reflects the extent of iron deposition and the time throughout exposure to NTBI and toxic reactive iron.
At this time in all the published studies outside TDT, only the correlation between direct or indirect estimates of iron overload (mainly serum ferritin, transfusion burden and MRI values) and outcome parameters has been explored, while the duration of exposure to toxic iron species has not been taken into account.[4,5,13-16]
The first study that explored the LPI role in relationship with outcome was published by Wermke and colleagues in malignancies. They investigated the predictive value of both stored (MRI-derived liver iron content) and non-transferrin-bound-iron, defined as enhanced labile plasma iron (eLPI) (see table 1) on post-transplantation outcomes in patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) . Their prospective, observational ALLIVE study recruited 112 patients transplanted in three years and showed that patients who had raised eLPI concentration at baseline, also had significantly increased incidence of non-relapse mortality at day 100 (33%) compared with those who had normal eLPI at baseline (7%) (P= 0.00034).They concluded that peri-transplantation eLPI-scavenging strategies could be explored in prospective international clinical trials for patients with systemic iron overload.
Free Iron Toxicity During the Engraftment Period
Firstly in patients who underwent HCT for several hematologic malignancies, it has been demonstrated how LPI levels, although normal at baseline measurements, increased substantially 48h after the start of conditioning with a peak around day 0, and remained increased until engraftment when it returned to baseline levels.
The fast and substantial increase in LPI levels on Day 0 reflects a disruption of iron homeostasis by conditioning due to massive iron release by myeloablation and the temporary lack of iron uptake by the ablated erythroid system. In addition, it can be speculated that the conditioning-induced ablation of erythropoiesis could reduce the synthesis of erythroferrone, an erythroid hormone that suppresses hepcidin, favoring increased hepcidin levels that block the cellular iron efflux.
Subsequently, reutilization of iron by restored erythropoiesis by engraftment leads to a substantial drop in LPI levels, but not in hepcidin levels, probably modulated also by inflammation. The interesting information is that ferritin levels that were already increased at baseline did not change throughout the engraftment period; so that cytotoxic chemotherapy and subsequent engraftment in HCT patients leads to changes in LPI but not in ferritin. For this reason LPI represents the marker that better reflects the modifications in iron status and could serve as a target of a possible chelation therapy in the early period of HCT.
Similar results are shown by Duca et al regarding NTBI levels in thalassemic and leukemic patients. NTBI levels were constantly higher at baseline in the thalassemia group but the relative increase compared to baseline was higher in leukemia patients (between 2.2- and 3-fold) than in thalassemia patients (between 1.6- and 2.5-fold). Early after transplant, concomitant with erythropoietic recovery, NTBI returned to respective baseline values. The marked increase of NTBI in serum after myeloablative chemotherapy was originally attributed to suppression of erythropoietic activity. Other possible sources of extracellular iron after myeloablative conditioning include lysis of erythroid bone marrow cells by cytotoxic injury. Also, this study confirms reduction of the iron uptake by erythroid precursors during and immediately after chemotherapy. Furthermore, in this case, NTBI decrement in all the patients after HCT could be explained by high iron requirement during allogeneic erythroid marrow rebuilding. High levels of iron overload, in the absence of chelation, are responsible for the persistence of NTBI high levels even after marrow reconstitution in thalassemia patients.
A growing body of evidence describes how iron induced oxidative stress and increased ROS levels can modulate several signaling pathways (such as Protein kinase B, Tumor protein p53 and Wnt protein family,) which promote cell survival, avoid apoptosis, allow escape from growth arrest, and facilitate cancer transformation. Actually, ROS are involved in a complicated web of signaling networks where their generation is regulated by multiple pathways. Conversely, ROS act as signaling molecules for other signaling pathways such as PTEN, PTP1B, MAPK and NF-κB involved in different ways with the HSCs fate.[23,24]
In 2013, Chai and colleagues established an iron overloaded mouse model to investigate the effects of iron overload on hematopoietic stem and progenitor cells (HSPCs). Results show that iron overload markedly decreased the ratio of immature hematopoietic cells and reduced HSPCs clonogenic capacity. Iron overload increased ROS levels of HSPCs through the NOX4/ROS/P38 MAPK signaling pathway.
Similar results were found using bone marrow mesenchymal cells (BM-MSCs) in a similar murine model suggesting that iron can impair not only the HSPCs clonogenic capacity but similarly the quantity and quality of BM-MSCs and the bone marrow microenvironment as well.[26,27]
The effect of oxidative stress on hemopoiesis has been investigated in a murine transplant setting. A murine model was used to investigate the possible relationship between iron overload and engraftment post-allogeneic hematopoietic cell transplant. Donor bone marrow mononuclear cells (BM-MNCs) from iron overloaded mice and normal mice were transplanted into recipient mice. Flow cytometry analysis of peripheral blood cells from the recipient mice demonstrated that recipient mice of iron- overloaded donor had, after transplant, lower levels of myeloid B and T-lymphocytic lineage engraftments compared to the recipient mice of normal donor.
A different conclusion was described by Okabe and colleagues, who showed in an iron overloaded mouse recipient that oxidative stress could affect the engraftment of hematopoietic cells from a normal donor by modifying microenvironment and remarkably reducing expression of CXCL12, VCAM-1, Kit-ligand, erythropoietin and thrombopoietin. They concluded that iron overload can damage bone marrow stromal and other key organs (liver, kidney) and therefore, indirectly, hematopoiesis.
Interestingly, in almost all the above murine models, hematopoietic insufficiency improved by treating recipient mice with iron chelator or with the powerful antioxidant N-acetyl-cysteine (NAC), conveying that iron overload may be closely related to high oxidative stress.
It is important to note that these experimental observations have not yet led to an operative approach. Little literature is available addressing the issue of peri-transplant chelation in thalassemia. These studies were designed with different objectives from the principles described above, but demonstrated the safety (no significant severe side effects) of iron chelation during the peri-transplant phase. Fritsch et al utilized Deferasirox during the administration of conditioning regimens and it was found to be safe and reduced the appearance of LPI shortly after allo-HSCT in this preliminary study.
The basic idea today would be to suppress, by adequate (not necessarily intensive) peri-transplant chelation, the NTBI/LPI increment occurring during transplant. Obviously, this rationale should be applied, at the moment, only in the context of a well-designed controlled clinical trial.
Free Iron Toxicity During the Early Transplant Phase (Before a Sustained Engraftment is Achieved)
This model could also be applied after a sustained engraftment, not requiring blood transfusion, has been achieved. In fact, hematopoietic cell transplantation does not eliminate the iron excess acquired during previous years of thalassemia. Serum ferritin and the transferrin saturation slowly return to normal levels and only in patients with a very low iron burden before transplantation. 
Accordingly, with these observations, excess iron removing is essential after HCT. This recommendation is based on the evidence that progression of liver disease to cirrhosis has been documented in some patients in the years after transplantation. Data demonstrated a synergistic deleterious effect of Hepatitis C Virus (HCV) infection with iron overload with a multiplicative fibrogenic effect.[5,32] Recently a basic research paper has been published demonstrating a novel and intricate mechanism by which HCV interferes with the crosstalk between the Nrf2/ARE-signaling, elevated ROS levels and autophagy. Basically HCV impairing Nrf2/ARE-signaling through the ROS increase create an amplified and deleterious hepatotoxic effect, favoring the HCV autophagy and its release and spread, worsening the preexistent hepatic failure. Others synergisms with others damage factors (for example alcohol abuse) are likely.
Because a condition of iron overload leads to the release of reactive oxygen species, even in absence of ongoing transfusion need, defining iron overload post-transplant is essential and the gold standard for iron detection remain the liver iron concentration (LIC) because serum ferritin is particularly unreliable in this setting.
Recently the importance of LIC measurement by magnetic resonance imaging (MRI) has grown since it is non-invasive, rapid, and widely available. Today MRI techniques T2* and R2 are reported to have sensitivity and specificity of 89% and 80% in determination of LIC, respectively.
Few studies examine the alterations of hepatic and myocardial T2* MRI values in TDT patients after HCT just before starting chelation therapy. The main study included fifty-two TDT patients with mean age of 7.6 years. Hepatic and myocardial T2* values before and 6 months after HCT were measured and analyzed. Results showed that there was not a statistically significant increase in myocardial T2* values after HCT, instead Hepatic T2* values significantly decreased after HCT showing an increase of the liver iron.
Serum ferritin levels appeared to have a poor correlation with LIC in thalassemic patients after HCT. Ferritin can be a good screening test but a poor predictor of tissue iron overload.
The above reported ALLIVE study in malignancies has been shown that only eLPI correlated with LIC (not ferritin neither hepcidin values) and patients with elevated eLPI baseline values had a worsening outcome due to an increased non -transplant related mortality.
The hypothesis is that LPI/ NTBI might be used to assess the iron exposition status of organs after transplant, deciding initiation and duration of iron chelation and monitoring efficacy with the goals to protect organs from ROS exposition suppressing LPI and NTBI.
It is important to note that, in the current state of knowledge, it must be assumed that a normal transferrin saturation (i.e. 20-30%) excludes the presence of toxic iron forms of in the circulation and consequent progressing tissue damage; for this reason, it can be used as surrogate of normal ROS level.
Iron Chelation Therapy after Transplant in TDT
In transplanted patients undergoing phlebotomy, iron can be completely removed (final target: normal transferrin saturation, serum ferritin concentration <100 μg/L), and after this achievement, patients are free from iron overload and no maintenance therapy is required. Duration of treatment is strictly related to the magnitude of the iron overload, and it ranges from a few months to several years.
Two oral iron chelators have been tested in ß-TM (Deferiprone and Deferasirox, but only Deferasirox has been tested after transplantation. Reported cases of deferiprone-induced neutropenia in medically treated thalassemia patients raise concern for its use in the post-transplant setting.
The oral iron chelator Deferasirox has recently been tested in this setting on patients in prospective trials. Firstly, data from a prospective phase IV trials conducted by Vallejo et al showed that Deferasirox is efficient and safe in the post-transplant period in hematologic malignancies. Patients at least six months post-transplanted were treated with deferasirox dispersible tablets (DT) at a starting dose of 10 mg/kg/day for 52 weeks or until serum ferritin was less than 400 ng/mL on two consecutive occasions. A significant reduction from baseline in median serum ferritin and in liver iron concentration at 52 weeks was observed in the overall population. There were no drug-related serious adverse events.
Similar results are recently described in the Thalassemic population. A prospective, phase II, multicenter, single-arm study evaluates the efficacy and safety of deferasirox-DT in patients age >2 to <18 years with TDT who had undergone HCT and had evidence of iron overload (serum ferritin >1000 µg/L; cardiac MRI T2* <20 ms, or liver iron concentration ≥5 mg/g). Patients received deferasirox at an initial dose of 10 mg/kg/day, with up-titration to a maximum of 20 mg/kg/day. There was a continuous decrease in median serum ferritin level from 1718.0 µg/L at baseline to 845.3 µg/L following 52 weeks of therapy (P < .001). There was also a significant decrease in median LIC and an increase in median cardiac T2* from baseline to week 52. A manageable safety profile was observed.
A prospective randomized 1 year phase II trial comparing efficacy and safety of Deferasirox-DT versus the standard of care phlebotomy has been recently published in the population of transplanted thalassemia patients. Deferasirox-DT starting dose was 10 mg/Kg/day increased till 20 mg/Kg/day during the trials. They showed that Deferasirox is efficient and safe post-transplant; no differences were reported in reducing serum ferritin ability in both arms.
The advantage of Deferasirox is that it is administrated orally. The disadvantages regard the possible renal and hepatic toxicity considering that such patients are receiving in this period cyclosporine and other drugs as well as its noticeable cost. In 2016 Jaekel et al showed that Deferasirox is efficient and safe, even in patients receiving cyclosporine. Deferasirox was initiated at a median of 168 days after HCT, with 84% of patients still on immunosuppression. The incidence of AEs appeared to be dose related, with 7.5 mg/kg/day of deferasirox-DT being the best-tolerated dose. They concluded that low-dose deferasirox is an effective chelation therapy after allogeneic HCT, with a manageable safety profile, even in patients receiving cyclosporine. The recently released film coated tablets (FCT) formulation promises to further increase tolerability.
Reasons to select phlebotomies or deferasirox have been published.
It is important to note that all transplanted patients after successful HCT face a normal life expectancy and therefore their target iron level must be a “normal “iron burden with normal ferritin and, mostly, normal transferrin saturation.
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