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Eculizumab in the management of paroxysmal nocturnal hemoglobinuria: patient selection and special considerations

Authors Al-Ani F, Chin-Yee I, Lazo-Langner A

Received 17 May 2016

Accepted for publication 9 July 2016

Published 1 August 2016 Volume 2016:12 Pages 1161—1170


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 4

Editor who approved publication: Professor Garry Walsh

Fatimah Al-Ani,1 Ian Chin-Yee,1 Alejandro Lazo-Langner1,2

1Department of Medicine, Division of Hematology, 2Department of Epidemiology and Biostatistics, Western University, London, ON, Canada

Abstract: Paroxysmal nocturnal hemoglobinuria (PNH) is a nonmalignant clonal disorder resulting from somatic mutation in the PIG-A gene leading to a deficiency of the membrane-anchoring molecule glycosylphosphatidylinositol. The lack of expression of two glycosylphosphatidylinositol-anchored proteins involved in the regulation of the complement system renders PNH erythrocytes susceptible to complement-mediated lysis. Clinical manifestations include thromboembolic disease, chronic kidney injury, pulmonary hypertension, smooth muscle dysfunction, and chronic hemolysis. Until recently, treatment was mainly supportive with most patients suffering from significant morbidity and shortened survival compared to age-matched controls. The development of eculizumab, a humanized monoclonal antibody directed against the terminal complement protein C5, has resulted in dramatic improvements of survival and reduction in complications. In this paper, we review some special considerations pertaining to the use of eculizumab for PNH.

Keywords: somatic mutation, GPI, survival, hemolysis, MDS, anemia

Overview of paroxysmal nocturnal hemoglobinuria

Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired hemolytic anemia resulting from a somatic mutation in the PIG-A gene in the hematopoietic stem cells.1 This mutation leads to a deficiency of glycosylphosphatidylinositol (GPI) membrane-anchoring proteins on the surface of PNH cells. Two of these anchoring proteins, CD55 and CD59, are complement inhibitors, and the deficiency of such proteins will render PNH erythrocytes susceptible to complement-mediated lysis.2 Recently, new evidence on PNH pathogenesis supports the notion that the expansion of the PNH clone results from escape from T-cell-mediated autoimmune damage to hematopoietic stem cells, with the GPI molecule as a target. This might further consolidate the observed association between PNH and aplastic anemia (AA).3 PNH is a very rare disease with a prevalence of ~16 per million people,4 and it can present at any age but mainly occurs in young adults, with the usual age at diagnosis being early 30s.46

Despite being rare, PNH is “the most vicious acquired thrombophilic state known”, yet the mechanism of this virulent thrombotic behavior is still elusive.3,7 Thromboembolic (TE) events occur in ~50% of PNH patients, and it is the main cause of death in approximately one-third of patients with PNH.8 The intravascular hemolysis in PNH is a critical factor in triggering thrombosis. The release of hemoglobin (Hb) into the blood stream results in massive nitric oxide scavenging leading to vasospasm and to increase in platelets’ reactivity and aggregation.9,10 Therefore, the process of nitric oxide depletion by the free Hb will not only predispose patients to developing thromboembolism but also lead to vascular constriction (manifested as pulmonary hypertension, renal dysfunction, and erectile dysfunction) and smooth muscle dystonia of the gastrointestinal tract (manifested as abdominal pain, dysphagia, and esophageal spasm).2,9,11 Additionally, renal dysfunction is also caused by chronic hemolysis-induced hemosiderin deposition in the proximal renal tubules, in addition to alterations in renal blood flow caused by nitric oxide depletion.9,10

Until a decade ago, the treatment options for PNH were mainly supportive including blood transfusion, erythropoiesis-stimulating agents, corticosteroids, anabolic steroids, iron therapy, thrombosis prophylaxis, and sometimes thrombolytic therapy or allogenic bone marrow transplantation.2,3 Eculizumab was first introduced in 2004 in a preliminary pilot study of eleven participants.12 It was found to dramatically reduce intravascular hemolysis and blood transfusion requirements. Despite the open-label design, the potential risk of bias was minimal as all the reported outcomes were objectively measurable. However, other issues including the small sample size, short-term follow-up, and the potential risk of selection bias (only transfusion-dependent patients were included) should be considered when interpreting the results of this study. Subsequently, two Phase III trials – the TRIUMPH and SHEPHERD studies – proved that eculizumab therapy for PNH is effective, safe, and well tolerated in a standardized setting with predefined outcome criteria.11,13 A total of 87 and 97 patients were enrolled in these studies, respectively, overcoming the small sample size issue of the pilot study. However, issues such as selection of only transfusion-dependent patients and failure to report on TE rates as most patients were receiving concomitant anticoagulants remained. Eculizumab was finally approved for the treatment of patients with PNH in 2007 by the US Food and Drug Administration and by the European Medicines Agency.2,8

In this review, we focus on the up-to-date established positive impacts of eculizumab on PNH and its potential adverse events, highlighting certain issues that need to be addressed with eculizumab use.


Eculizumab is a humanized monoclonal antibody directed against the terminal complement protein C5, which blocks the formation of the membrane attack complex (C5–9), thus protecting PNH red blood cells from complement-mediated intravascular hemolysis.3,14 Its effectiveness has been evidenced by reduction or elimination of the need for blood transfusion, decrease in the incidence of thrombosis, improvement in anemia and quality of life (QoL), and prolongation of overall survival (OS).1,8,11 Furthermore, due to its use, stem cell transplantation is only considered for cases of severe marrow failure.3,15

Pharmacodynamics and pharmacokinetics

An inhibition of C5 sufficient to prevent hemolysis occurs at eculizumab plasma concentrations in excess of 35 g/mL.2 At therapeutic doses, maximum plasma concentrations of eculizumab are achieved within 1 hour of infusion.2 Eculizumab reduces hemolysis in ~1 week, and its half-life elimination is ~11 days (range: 8–15 days). The clearance for a typical PNH patient weighing 70 kg is ~22 mL/h, and the volume of distribution is ~7.7 L.16

Dose and schedule

For PNH, eculizumab is administered as a weekly dose of 600 mg by intravenous infusion for 35 minutes from week 1 to week 4, followed by infusion of 900 mg at week 5, and then 900 mg every 14 days for an indefinite period.1,2

Eculizumab and PNH – clinical efficacy

The effect of eculizumab on PNH patients has dramatically changed the clinicians’ management and patients’ perspective toward this disease.

Reducing blood transfusion requirement and stabilizing Hb level

Symptoms of PNH are often disproportionate to the degree of anemia.11 However, achieving sustained stability of Hb and transfusion independence were the main outcomes measured with eculizumab therapy in PNH studies.1113 Those two outcomes were chosen because both are measurable, and can be easily compared with pre- or no-eculizumab treatment end points to assess its response. Studies assessing the transfusion requirement and transfusion independence rates with eculizumab are illustrated in Table 1.

Table 1 Studies assessing hematological response and transfusion requirement in PNH patients treated with eculizumab
Abbreviations: PNH, paroxysmal nocturnal hemoglobinuria; Hb, hemoglobin; PRBC, packed red blood cell.

In the TRIUMPH study, 43 patients on eculizumab were compared with 44 patients on placebo in a double-blind randomized controlled trial, with the outcomes being the stabilization of Hb and transfusion independence.11 Hb stabilization occurred in 49% in the eculizumab group compared to 0% in the placebo group (P<0.001). Furthermore, there was a significant reduction in the median number of units transfused in eculizumab group as compared to the placebo group. Similar findings were also reported in the SHEPHERD study.13

Kelly et al evaluated 79 consecutive PNH patients over 8 years, and compared them with 30 matched historical controls from the pre-eculizumab era.8 The 12-month mean transfusion requirement was significantly reduced in patients receiving eculizumab compared to controls. Although this study was non-randomized, the inclusion of consecutive patients might reduce the risk of bias.

Long-term safety and efficacy data of eculizumab have been reported in two studies: the study by Hillmen et al and AEGIS study.17,18 The first study included a total of 195 patients from three Phase III trials with a maximum duration of 66 months, and reported a total transfusion independence in 82% of patients.17 The AEGIS trial was an open-label, noncomparative, multicenter Phase II study of 29 Japanese PNH patients, followed by a further 2-year extension study.18 Only 27 patients were included in the extension study with a total transfusion independence of 96%.17,18 The importance of the AEGIS extension study lies in the fact that it is the first study reporting long-term data of eculizumab in a trial setting among Asian PNH patients, a population in which PNH seems to be more frequent than in the Western population.19

In patients in whom transfusion independence was not reached, the TRIUMPH trial11 and the studies by Kelly et al8 and Hillmen et al17 reported similar findings of reduction in the number of red cell units transfused after starting eculizumab as compared to before eculizumab treatment.

Finally, a recent retrospective study included 123 PNH patients treated with eculizumab and 191 historical controls from the French registry. Although the transfusion requirements were not reported in the study, the authors did suggest that anemia could persist in some patients.1

Improving QoL

QoL is affected in the majority of patients with PNH with 96% complaining of fatigue and >40% having symptoms of smooth muscle spasm often of sufficient severity to require narcotic analgesics.20 Fatigue is multifactorial and is not simply the result of anemia, as 60% of these patients are transfusion independent.20 The fluctuation in Hb and the inconvenience of the frequent blood transfusions may also contribute to the impaired QoL. Nevertheless, eculizumab has impacted favorably on the QoL in both transfusion-dependent and transfusion-independent patients.3,9,11,21,22

In the TRIUMPH study, QoL assessments were performed with the use of two instruments: the Functional Assessment of Chronic Illness Therapy – Fatigue (FACIT-F) scale and the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire. Patients in the eculizumab group had a mean increase (improvement) in scores on the FACIT-F of 6.4±1.2 points from baseline to week 26, compared to the placebo group in which the mean score decreased by 4.0±1.7 points during this period (P<0.001).11 Importantly, only transfusion-dependent patients were included, and QoL was assessed prior to transfusion and after eculizumab, without posttransfusion assessments. Therefore, it is not possible to fully determine whether differences are a result of eculizumab or the anemia correction.2 However, improvement in the FACIT-F score was also noted independent of improvement in Hb level in patients receiving eculizumab as compared to placebo, supporting the positive impact of eculizumab on QoL regardless of Hb level.

With respect to the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire, the eculizumab group had overall significant improvements in scores of functional status, fatigue, pain, dyspnea, loss of appetite, and insomnia, compared to placebo.11 Similarly, improvements were demonstrated in several QoL parameters including physical, emotional, and cognitive functioning, global health, fatigue, dyspnea, and insomnia.12 Similarly, the AEGIS study also showed a consistent improvement in QoL in the majority of patients with sustained reductions in fatigue and dyspnea.18

Of note, ~25% of PNH patients treated with eculizumab still need recurrent blood transfusions; however, even these patients report improved QoL.3 Improvements in symptoms including abdominal pain, dysphagia, and erectile dysfunction have been reported during eculizumab therapy despite the observation that total Hb levels were unchanged or not completely corrected.11,12,21 This supports the notion that intravascular hemolysis plays an important role in diminishing QoL in PNH patients.11

Reducing intravascular hemolysis

As previously mentioned, intravascular hemolysis results in symptoms of smooth muscle dystonia, including abdominal pain, dysphagia, and erectile dysfunction.3,11 Eculizumab therapy results in a reduction of hemolysis and a new steady-state Hb level, due to balance of the underlying bone marrow dysfunction, the increased half-life of PNH erythrocytes, and the new level of transfusions (if any) required.11 High percentages of PNH-type red blood cells have been observed after eculizumab treatment, indicating that these cells have not undergone hemolytic destruction.10,18

Lactate dehydrogenase (LDH), a biochemical marker of hemolysis, is used frequently to assess intravascular hemolytic activity. In the pre-eculizumab era, PNH patients with hemolysis (LDH ≥1.5× upper limit of normal) had a 4.8-fold increase in mortality compared to the general population.23 The TRIUMPH study showed a rapid, significant, and sustained reduction in the LDH to normal or near-normal levels in patients on eculizumab.11 Other studies have reported similar findings that last beyond 8 years of eculizumab therapy, reflecting inhibition of chronic hemolysis.8,17,18

Preventing thrombosis

Thromboembolism occurs in 50% of patients, and represents the major cause of death in PNH.6,24,25 Once an initial thrombosis occurs, the risk of further thrombotic events increases, with a five- to ten-fold increase in mortality.8 Interestingly, TE events in PNH are not restricted to the venous system.4,6,22 Eculizumab was able to show a substantial impact in lowering the risk of thrombosis in PNH as summarized in Table 2.

Table 2 Studies assessing thromboembolism rates with eculizumab
Notes: aPercentage, not rate. bIncidence rate calculated from information available in the study.
Abbreviations: TE, thromboembolic; PYs, person-years.

It has been shown that patients on eculizumab have a significant and sustained decrease in activation of both the plasmatic hemostatic system and the endothelium.26 Compared to pretreatment values, patients on eculizumab were found to have lower levels of coagulation factors such as von Willebrand factor, of by-products of coagulation such as D-dimer, and also of endothelial cell molecules such as vascular cell adhesion molecule 1.26 These changes might be due to the blocking effect of eculizumab on C5, thus reducing platelet and endothelial activation, intravascular hemolysis, and release of thromboplastin-like substances.7,27

Initial studies were not designed to establish the effect of eculizumab on thrombosis as most trial patients were receiving concomitant anticoagulants.2,12,13 However, in later studies, eculizumab has consistently shown a protective effect against thrombosis.8,17,22,26 In a prespecified analysis, data from three combined studies1113 showed that TE rate in patients receiving exclusively anticoagulants was reduced from 11.54 events per 100 patient-years before eculizumab treatment to 0.72 events per 100 patient-years during eculizumab treatment (P<0.001), with a relative risk reduction of 94%.22 Despite heterogeneity in the individual pre-study TE event rates, eculizumab treatment consistently resulted in a marked reduction in thromboembolism (Table 2). Other studies have also reported dramatic reductions in thrombosis after initiating eculizumab therapy (0.8 vs 5.6 events per 100 patient-years; P<0.001) even after accounting for the shorter duration of follow-up since starting eculizumab.8 Of note, in the latter study, 50% of the pre-eculizumab thrombosis events occurred on anticoagulants, which supports the notion that in PNH patients with a previous history of thrombosis, anticoagulation alone may not be sufficient in preventing thromboses. On the other hand, after eculizumab treatment, primary prophylaxis with warfarin was stopped, whereas anticoagulation for secondary prophylaxis was not routinely stopped. Thus, cessation of anticoagulation in patients on eculizumab with no prior history of thrombosis is the current recommended practice in some centers.8 Similar TE reductions have been reported in other studies.17,18 TE events decreased by 81.8%, with 96.4% of patients remaining free of TE events.17 In the AEGIS study, no TE events were reported during the 2-year extension period.18

A recent study from the French registry also provided evidence for significantly lower TE rates in patients on eculizumab compared to historical controls (4% vs 29%). However, the study showed that thromboembolism remains a major issue in PNH, even in the eculizumab era, as highlighted by the negative impact of a previous thromboembolism on OS in adjusted analysis (hazard ratio [HR] 4.48, 95% confidence interval [CI] 2.46–8.16; P<0.001).1

Improving renal function

Renal dysfunction has been well reported in PNH,11,18 and patients with PNH have a sixfold greater risk of chronic kidney disease (CKD) compared to the general population.9,11,18 More importantly, CKD is associated with an elevated risk of premature mortality contributing to 8%–18% of PNH-related deaths.6,17 Renal impairment in PNH is multifactorial and involves a direct effect of nitric oxide depletion, induced by cell-free Hb, on the glomerular filtration rate and on renal plasma flow, and the repetitive exposure to cell-free Hb leading to chronic hemosiderin deposition in the proximal renal tubules.9,10 Supportive care measures do not prevent the occurrence or the progression of CKD. However, by inhibiting terminal complement activation and intravascular hemolysis, treatment with eculizumab significantly improves renal function. Several studies have shown consistently that eculizumab has a protective role leading to improvement in, or less progression of, renal disease.9,10,17

Hillmen et al provided evidence that sustained long-term therapy with eculizumab can reverse early-stage renal damage sustained prior to treatment initiation, particularly when administered early and prior to advanced renal impairment.17 In this study, CKD stages28 were assessed following each 6-month eculizumab treatment period. Continued time-dependent improvement in CKD was observed with sustained eculizumab treatment, with 24.4% of patients showing improvement in CKD after only 6 months of treatment and 45% of patients showing improvement after 36 months. Overall, patients were significantly more likely to experience an improvement than a worsening in renal function (P=0.015).17

Similar findings have been reported in the AEGIS study. Sustained administration of eculizumab in patients with CKD at baseline was associated with improved renal function in 71%, whereas 29% had their renal function stabilized. Eculizumab also improved renal function, particularly if administered early in the course of disease and before the kidney is more severely impaired. Improvements in renal function were observed in 88% of patients with stage 1 CKD, 67% of patients with stage 2 CKD, and 33% of patients with stages 3–4 CKD.18

A large cohort of 195 PNH patients from parent eculizumab clinical trials was also assessed for their kidney function by Hillmen et al.9 In this study, improvement in renal function was more commonly seen in patients with baseline CKD stages 1–2 (67.1% improvement), although improvement was also observed in patients with CKD stages 3–4. Overall, 40 (21%) of 195 patients who demonstrated renal dysfunction or damage at baseline were no longer classified as such after 18 months of treatment.9

Improving OS

Historical studies have shown the median survival in PNH patients to be between 10 and 15 years from the time of diagnosis.4 More recently, data from a French series of patients in the pre-eculizumab era showed an improvement in median survival to 22 years, which is probably the result of improvements in supportive care and in the management of disease complications.25 With the use of eculizumab, the OS of PNH patients has consistently shown a remarkable improvement, approaching that of the general population.1,8,17 The survival rate of PNH patients in eculizumab studies was 97.6% at 3 years,17 95.5% at 5 years (P<0.03 as compared to eculizumab-untreated patients),8 and 92% at 6 years (P=0.037 as compared with controls).1,8,17 Furthermore, Kelly et al reported no significant difference in OS between the PNH patients treated with eculizumab compared with sex- and age-matched controls from the UK population.8 Another study suggested that the two factors statistically associated with a worse OS were the absence of treatment with eculizumab (HR 6.26, 95% CI 2.72–14.43; P<0.001) and a previous history of TE events (HR 4.48, 95% CI 2.46–8.16; P<0.001).1

Absent or inadequate response to eculizumab in PNH

It has been reported that, with eculizumab, up to two-thirds of PNH patients who are transfusion dependent become transfusion independent.3 However, ~25% of them still need recurrent albeit less frequent blood transfusion.3 The authors suggested that these heterogeneous hematological responses may be related to factors including underlying AA,13 C3-mediated extravascular hemolysis,3,15,29 breakthrough hemolysis,30 or the presence of a specific mutation in the C5 gene which prevents eculizumab from binding to C5 protein.6

The association of PNH with AA

In some patients, a poor or suboptimal response to eculizumab may indicate that the extent to which bone marrow failure was contributing to anemia had been underestimated.3 There is a close relationship between AA and PNH, and a history of severe AA is present in at least one-half of all newly diagnosed PNH cases,31 whereas PNH clones are found in up to 70% of patients with AA.2,31 Recently, new evidence on PNH pathogenesis supports the notion that expansion of the PNH clone results from escape from T-cell-mediated autoimmune damage to normal hematopoietic stem cells, with the GPI molecule as target, consolidating further the observed association between PNH and AA. Indeed, GPI-specific CD8+ T cells – which have been identified in PNH patients – would spare selectively GPI-negative stem cells, thus enabling them to repopulate the marrow of a patient who would otherwise have AA.3

In the AEGIS trial, the effect of eculizumab was assessed in patients with PNH plus AA/myelodysplastic syndrome (MDS) and those with PNH alone, and no significant differences were found between the two groups in the end points assessed, namely hemolysis and blood transfusion. This finding suggests that patients with PNH and AA/MDS experience similar hemolysis-associated complications and can benefit from treatment with eculizumab.18

Another interesting observation has been reported by a case report of a PNH patient who was initially diagnosed with AA and treated subsequently with eculizumab.32 Erythropoiesis improved, and the patient became transfusion independent shortly after initiation of iron chelation with deferasirox.32 Similarly, the same finding has also been seen in MDS patients after starting deferasirox.33,34 The significance of this management modality needs to be addressed in future studies.

It is too early to draw robust conclusions on the effect of eculizumab on patients with PNH plus AA, yet the evidence of the association between the two suggests that an inadequate marrow response to anemia may be a contributing factor to the observed persistent anemia in PNH patients receiving eculizumab. More importantly as many as 25% of patients with a previous diagnosis of AA treated with immunosuppression may progress on to develop hemolytic PNH requiring therapy.35

Extravascular hemolysis with eculizumab

Two studies have described the development of “iatrogenic” extravascular hemolysis with eculizumab.15,29 Risitano et al have suggested that binding of C3 by PNH red blood cells may constitute an additional disease mechanism, strongly enhanced by eculizumab treatment and producing a variable degree of extravascular hemolysis.15 Eculizumab affects only the distal complement pathway, thus neutralizing the deficiency of CD59 on PNH red blood cells by inhibition of C5 cleavage, but since these are also deficient in CD55, upstream complement activation may lead to C3 opsonization leading to a gradual accumulation of C3 fragments on their surface. These C3-opsonized red blood cells will be susceptible to phagocytosis by macrophages in the reticuloendothelial system, resulting in extravascular hemolysis.3,7 This phenomenon may explain the residual low-level hemolysis occurring in some eculizumab-treated patients,29 indicated by a positive Coombs test (classically negative in untreated PNH).3,7,29

More importantly, researchers have suggested that this process may play a role in limiting anemia improvement because it develops at the same time that intravascular hemolysis ceases.3,7 However, fortunately in many cases, it seems to have little or no clinical relevance.7 This conclusion has also been supported by studies in which a dramatic reduction in transfusion requirements was observed, indicating that the phenomenon of extravascular hemolysis is of limited clinical importance for most patients.8,17 In the next decade, researchers may quest for a way to control extravascular hemolysis.7 It has been recommended that selective splenic artery embolization can be used to treat severe extravascular hemolysis, as an alternative to splenectomy.3 Of note, selective splenic artery embolization has also been used to reduce spleen size and alleviate cytopenias in splenomegaly with hypersplenism in PNH patients.3

Breakthrough hemolysis

According to Nakayama et al, eculizumab-dosing intervals >17 days may be associated with an increased risk of developing breakthrough hemolysis in patients with PNH (odds ratio 1.6, 95% CI 1.3–2.0; P<0.01).30 The recommended schedule is thus to maintain eculizumab administration every 14 days, although this needs to be further confirmed.1,2 Other factors may also account for breakthrough hemolysis such as pregnancy (detailed in the “Eculizumab in pregnancy” section).

C5 gene mutation

C5 gene mutation has been detected among Japanese patients with PNH, identified as having poor response to eculizumab.6 A poor response was defined as markedly high levels of LDH during treatment, indicating that intravascular hemolysis remained unaffected, regardless of the persistence or improvement in other laboratory findings or clinical symptoms. This mutation prevents binding and blockade by eculizumab while retaining the functional capacity of the mutant C5 to cause hemolysis. The prevalence of this mutation among the patients with PNH (3.2%) was similar to that among healthy Japanese persons (3.5%).

Special considerations

Meningococcal meningitis and other infections

Complement inhibition by eculizumab leads to impairment in neutrophil and monocyte function, consequently affecting their ability to clear infections by encapsulated organisms, such as Neisseria meningitidis.2,8 Patients who are to be treated with eculizumab must be vaccinated against N. meningitidis at least 2 weeks prior to starting treatment.2

The tetravalent meningococcal vaccine is available against subgroups A, C, W, and Y but not for serogroup B, which is the most common serotype isolated in meningococcal sepsis in areas such as the UK.8,9 This explains the reported rates of meningococcal infections in some studies despite all patients being vaccinated appropriately.8,9 Hillmen et al and Kelly et al reported a rate of 1% and 2.5%, respectively, for meningococcal meningitis on eculizumab.8,9 Therefore, in January 2010, the UK policy changed to include antibiotic prophylaxis for all patients (penicillin V 500 mg twice a day or erythromycin 500 mg twice a day for patients intolerant to penicillin), in addition to the tetravalent meningococcal vaccination.8 In 2013, Bexsero® became the first broad-coverage vaccine to be licensed for active immunization against serotype B meningococcal disease.36 Bexsero is now licensed in >35 countries worldwide for varying age groups, including the European Union, Australia, Brazil, Canada, Chile, Uruguay, and the USA, and it is usually combined with the tetravalent vaccine in PNH patients planned for eculizumab for full coverage of the five serotypes.36 However, in daily practice, clinicians may still prefer to continue on penicillin or amoxicillin prophylaxis while awaiting the vaccines to kick in, and some would still choose to continue penicillin even after vaccinated because other subtypes may not be covered.

Other infections have also been reported in eculizumab studies. The AEGIS study reported a total of 159 treatment-emergent infections, of which the majority were mild in severity (87.4%). Only seven of the 159 infections (4%) were considered probably related to eculizumab, of which three (one case each of pneumonia, cellulitis, and sepsis) were severe. There were no meningococcal infections reported.18 Hillmen et al also reported an overall infection rate of 12.8%.9

Overall, studies indicate that eculizumab is well tolerated over the long term, and its profile is consistently safe across studies. However, further precautions might be considered in immune-compromised categories such as elderly or neutropenic patients.

Eculizumab in pregnancy

The median age at diagnosis of PNH is 34 years, so affected females are often in the reproductive age group.37 Although PNH is not known to adversely affect female fertility, several fetal–maternal complications have been reported in pregnant PNH patients related to exacerbated intravascular hemolysis, including spontaneous miscarriages (45%), premature births, increased blood transfusion requirements, thrombocytopenia, thromboembolism, and accelerated preeclampsia.3739 In PNH, maternal mortality has been reported to range between 8% and 21%, mostly occurring in the postpartum period, and thromboembolism being the primary cause. On the other hand, fetal mortality has been reported to range between 4% and 9%, mostly associated with premature births.38,40,41 Close monitoring of all pregnant patients with PNH is thus recommended.

Pregnancy activates the complement cascade, with increased terminal complex formation in the third trimester.14,42 Therefore, PNH has been considered a relative contraindication for pregnancy, and patients were usually discouraged from conceiving.37,39 Because of the risk of life-threatening thrombotic complications, pregnant women with PNH in the pre-eculizumab era were to receive full anticoagulation during pregnancy and for at least 4–6 weeks postpartum.38

Several studies and case reports have described the use of eculizumab in pregnant PNH patients.32,37,39,4345 It has been noted that the dose of eculizumab required to block complement during the later stages of pregnancy is greater than that required in the nonpregnant state.44 The increased activity of lysosomal enzyme, as well as the physiologic changes that occur during pregnancy, such as the physiologic expansion of intravascular volume, may account for the higher doses required.32,39

In pregnant patients, the eculizumab schedule has been modified by reducing the interval between eculizumab dose administration to ~7–12 days,4345 by administering higher doses of eculizumab (1,200 mg every 2 weeks during the third trimester),37 or by using both modalities together,32,39 according to physician discretion in order to control hemolysis as pregnancy progresses.32,37,39,4345

The largest PNH study in pregnancy so far has been reported by Kelly et al in 2015.39 Data were reported on 75 pregnancies in 61 women with PNH from the International PNH Interest Group and the International PNH Registry.39 In 54% of pregnancies that progressed past the first trimester, the dose or the frequency of use of eculizumab had to be increased. Requirements for transfusion of red blood cells increased during pregnancy, from a mean of 0.14 units per month in the 6 months before pregnancy to 0.92 units per month during pregnancy, and platelet transfusions were required in 21% of pregnancies, mostly administered at the time of delivery.39 Furthermore, premature birth rate of 29% was reported. Two TE events were documented, and both occurred during the postpartum period, despite that thromboprophylaxis with low-molecular weight heparin was used in the majority of patients (88%). One of the thrombotic events occurred after a plasma infusion was administered to treat a postpartum hemorrhage. Plasma contains high levels of complement and can overcome the effects of eculizumab and thereby render the patient susceptible to complications of PNH. The use of plasma should probably be avoided if possible.

Initially, it was thought that eculizumab would cross the placenta and appear in breast milk.2 However, subsequent studies reported that eculizumab does not appear to cross the placenta nor it is excreted in breast milk.37,4345 However, in a study on 21 cord-blood samples, eculizumab was detected in seven of the samples, whereas the drug was not detected in any of the ten breast milk samples tested.39 Recently, two studies suggested that if eculizumab crosses the placenta, the level is not high enough to affect complement activation.39,46

Overall, studies highlighted the significance of regular and frequent monitoring of hemolytic parameters in PNH patients during pregnancy to detect early disease activity. In the end, there are no adequate and well-controlled studies of eculizumab in pregnant women, and a firm conclusion is difficult to be drawn. Nevertheless, all studies available suggested that eculizumab provided benefit for women with PNH during pregnancy, as evidenced by a high rate of fetal survival, a low rate of fetomaternal complications, and a reduced rate of blood transfusion, compared to pregnant PNH patients not treated with eculizumab.37,39,4345 It also appears that eculizumab can be safely used throughout pregnancy.

In summary, the recommended practice in pregnant women with PNH receiving eculizumab includes dose escalation and/or reduction in dose interval to control hemolysis, avoidance of the use of plasma if possible, and thromboprophylaxis with low-molecular weight heparin throughout the pregnancy up to 6 weeks following delivery, even with the use of eculizumab. However, whether combining thromboprophylaxis with eculizumab (specifically during the postpartum period) would be sufficient for preventing thromboembolism, or whether dose escalation is needed in high-risk patients, such as those having a prior history of thromboembolism or requiring C-section, still remain as questions.

Eculizumab in elderly

The median age at diagnosis of PNH is in the early 30s, and thus, patients aged >80 years were rarely enrolled, yet PNH can still present at any age.5,6,37 In view of the known age-associated reduction in immune function and the effect of eculizumab on the suppression of the terminal complement pathway, one concern is that treatment with eculizumab may elevate the risk of infection in elderly patients.10 In the TRIUMPH and SHEPHERD trials, there were no apparent age-related differences observed in patients aged 65 years or older treated with eculizumab. However, the number of those patients was only 15, and clearly, this number would not be sufficient to determine whether they respond differently than younger patients.2

A case report by Ooe and Nagai in Japan has described the use of eculizumab in an 86-year-old PNH patient.10 Despite that poor prognosis was considered in this patient due to PNH-induced chronic renal failure and concomitant underlying myelodysplasia, eculizumab use was associated with rapid suppression of hemolysis, and significant improvement in both blood transfusion requirement and renal function from CKD stage 4 to stage 3 with no infections reported.

Although findings from available studies suggest that eculizumab can be used safely in elderly PNH patients with proved efficacy, the overall experience of eculizumab in geriatric population is still very limited, and decisions should be made on a case-by-case basis.

Risk of MDS/acute leukemia with eculizumab

An important concern with eculizumab is the possibility of clonal evolutions arising from a prolonged complement blockade. One study reported no significant difference regarding clonal evolution to MDS or acute myeloid leukemia in both eculizumab and control cohorts.1 However, no conclusions can be drawn, since a longer follow-up will be necessary as the median time to clonal evolution is 10 years.1 Furthermore, the rate of clonal myeloid evolution into MDS or acute leukemia was reported to be ~4% in PNH patients receiving eculizumab in another study,8 which is a similar rate reported in PNH patients before eculizumab therapy.6,25,26 Interestingly, in the study by Kelly et al, MDS and/or acute leukemia occurred within the GPI-negative clone of cells, indicating that the majority of hematopoiesis in these patients was derived from PNH stem cells.8 Long-term administration of eculizumab to Japanese patients with PNH showed that the burden of PNH disease and baseline characteristics were similar in patients with and without a history of bone marrow dysfunction such as AA or MDS.18 No cases of clonal evolution were reported by Hillmen et al.17

In fact, the effect of eculizumab on the development of clonal diseases is still unclear, and long-term data are definitely required.

Paucity of long-term “real-world” data

In view of the rarity of PNH, and the relatively recent introduction and approval of eculizumab, long-term data are scarce. Perhaps, the best standardized long-term safety and efficacy data of eculizumab were presented by Hillmen et al.17 They investigated 195 patients with PNH who had participated in one of three prospective parent trials: the Phase II pilot study and its extensions – TRIUMPH and SHEPHERD trials.1113 The median eculizumab treatment duration was 30.3 months, with a maximum duration of 66 months. Overall, long-term treatment with eculizumab resulted in sustained improvement in patient outcomes by rapidly reducing hemolysis and improving patient survival due to significant reduction in the frequency of severe and life-threatening morbidities, such as TE events and CKD with a favorable safety profile. However, “real-world” data with long-term follow-up are still lacking. The International PNH Registry ( is providing further opportunities to continue studying and understanding the long-term benefits of eculizumab in patients with PNH outside the clinical trial setting.17


The advent of eculizumab has resulted in a dramatic improvement of the natural history of PNH patients with improvement in virtually every aspect of these patients’ lives. This is supported by the available data about which some limitations should be noted. First, the size of available studies is relatively small but dictated by the rarity of the disease. Second, most (if not all) research is funded by the pharmaceutical industry, which conveys an inherent risk of bias. Third, availability of randomized data is scarce, and many studies use historical controls, also risking the introduction of bias. Fourth, the treatment is very costly limiting access to it. In spite of these limitations, the data available so far are strong enough (and differences quite striking in some cases) to support the use of this therapy, although independent confirmatory data are sorely needed. Fifth, notwithstanding the available evidence, many questions remain unanswered, in particular regarding long-term safety (eg, infections, clonal evolution), optimal management of special populations (eg, pregnant, elderly), role of eculizumab in PNH/AA, and need/utility of clinical and laboratory monitoring, among others. Finally, since the main deterrent to a wide adoption of this therapy is mainly of an economic nature and many patients who might benefit from it are unable to access this treatment, patient support programs and access to public funding as well as novel and more accessible agents are highly desirable.


ALL and ICY have received research funding from Alexion Pharmaceuticals in the past but none at the time of the preparation of this manuscript. ICY is a member of the Canadian PNH Network which is sponsored in part by Alexion Pharma Canada. No professional writing services were employed. Alexion Pharma (or its employees) was (were) not involved at any point in any aspect of the manuscript, from conception to submission. FAA reports no conflicts of interest in this work.



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