The epidemic of lipid disorders in Poland and its consequences
Hypercholesterolemia is the most common cardiovascular (CV) risk factor in Poland,
affecting as many as 21 million people [1, 2]. Unfortunately, most of those affected
are not aware of this, and many still ignore the risk associated with elevated cholesterol.
Of the remaining patients, many are not treated optimally, and only about a quarter
reach low-density lipoprotein cholesterol (LDL-C) targets, including only 17% of patients
at very high CV risk [3, 4].
An equally important challenge, and an even larger unmet need, is associated with
dyslipidemia related rare diseases, including familial hypercholesterolemia (FH).
The prevalence of heterozygous FH (HeFH) in the Polish population is estimated to
be 1 : 250, which corresponds to 150 thousand HeFH patients, of which only a small
proportion have been diagnosed (~5%) and even fewer receive appropriate treatment
[5, 6]. Early diagnosis and optimal therapy are critically important for these patients,
as they might be at even 100-fold higher risk of occurrence of atherosclerotic cardiovascular
disease (ASCVD) and have a 3–5 higher risk of death [7].
Cardiovascular disease is still the leading cause of mortality worldwide, and as many
as 75% of all deaths may be attributable to ASCVD [1]. According to the 2020 Health
Needs Maps (data for 2019) in Poland, ischemic heart disease (IHD) is diagnosed each
year in 85,753 people (223.1 per 100,000 people), and the morbidity is 1,491,616 (3,880.9
per 100,000 people) [8]. The number of IHD deaths in 2019 was 97,188 (252.9 per 100
thousand people). Ischemic strokes were diagnosed in 74,455 people (193.7 per 100,000
people), with the prevalence 623,986 (117.4 per 100,000 people), and the number of
deaths in 2019 was 45,104 (117.4 per 100 thousand people). Finally, the incidence
of peripheral arterial disease (PAD) in the same investigated period was 85,157 people
(221.6 per 100,000 people), the incidence was 938,059 (2,440.7 per 100,000 people),
and the number of PAD-related deaths was 1,141 (3.0 per 100 thousand people) [8].
It needs to be emphasized that during the coronavirus pandemic, the above numbers
have essentially worsened, creating a large health debt, what was associated with
lack of (or late) diagnosis, insufficient disease monitoring, and lack of suitable
pharmacotherapy and delayed cardiovascular interventions (including angioplasty) [9].
Therefore, an urgent call for action is now necessary, including ensuring the widespread
availability of innovative therapies to mitigate this health debt and prevent further
needless deaths.
Inclisiran – a new effective therapeutic option in the treatment of hyperlipidemia
Inclisiran is a first-in-class cholesterol-lowering double-stranded small interfering
ribonucleic acid (siRNA) conjugated on the coding strand to N-acetylgalactosamine
(GalNAc) to facilitate its uptake by hepatocytes [10]. It binds to the asialoglycoprotein
receptors (ASGPRs) there, which are highly expressed only in hepatocytes, a fact which
explains the very good safety profile of this drug. Inclisiran uses the mechanism
of RNA interference and directs the catalytic breakdown of PCSK9 mRNA [10, 11]. This
increases the recycling and expression of LDL-C receptors on the surface of hepatocytes,
which enhances LDL-C uptake and effectively reduces circulating LDL-C levels [10,
11].
Several phase I–III studies with inclisiran have already been completed, while other
phase III studies are still ongoing under the ORION and VICTORION clinical development
programs (the details are available elsewhere [12]). The available results (mainly
based on the pooled analysis of ORION 9–11 studies) clearly show that inclisiran very
effectively reduces LDL-C by about 52–55% (and about 44-48% in patients with FH),
enabling LDL-C targets to be achieved in 76% and 58% of investigated patients in high
and very high-risk patients, respectively [12–14]. The analyses also showed that inclisiran
effectively reduced non-HDL-C, apolipoprotein B, and lipoprotein(a) (Lp(a)) by 42.8,
40.2, and 20%, respectively, thereby demonstrating good efficacy in the management
of residual risk [12–14]. This is especially important now, as in the recent Polish
guidelines, non-HDL is considered as an equal important lipid parameter to LDL-C,
and strong recommendations were also suggested for Lp(a) measurement (for all ASCVD
and FH patients with IIbC level of recommendations), which is still assessed very
rarely in Poland (mostly in patients at borderline CVD risk and in those with premature
myocardial infarction) [15].
There are still no data on the effect of inclisiran and cardiovascular outcomes, and
the ORION-4 cardiovascular outcomes trial (CVOT) is estimated to be completed in 2026
(based on the information from ClinicalTrial.gov) [16]. However, in our opinion these
results are not necessary to start reimbursing inclisiran within the drug program,
in light of an overwhelming body of data indicating a strong link between LDL-C reduction
and effective prevention of CVD events and death [17]. Moreover, the first meta-analyses
based on the available data (ORION 9–11 studies) showed that we might expect a reduction
of major adverse cardiac events (MACE) by as much as 24–30% [18, 19]. If we compare
this with the 15% reduction of the primary endpoint observed in the FOURIER trial
with evolocumab and ODYSSEY OUTCOMES with alirocumab, with the predictions that had
been at the same level as currently for inclisiran (also bearing in mind that the
population in the PCSK9 inhibitor CVOT were at higher CVD risk – acute coronary syndrome
(ACS) patients), the 15–20% reduction of the main endpoint with inclisiran (MACE defined
as time to first occurrence of coronary heart disease (CHD) death or myocardial infarction
or fatal or non-fatal ischemic stroke or urgent coronary revascularization procedure)
would represent a very important clinical success [16, 20].
It is also worth emphasizing that, considering the design of the ORION program, inclisiran
has also demonstrated effectiveness and safety in primary prevention (HeFH patients
were included in ORION-9, and ASCVD risk equivalent ones with HeFH, diabetes, those
at high CVD risk (10-year risk of a CV event of ≥ 20% as assessed by the Framingham
Risk Score) in the ORION-11 trial) [13, 14]. Also, patients with chronic kidney disease
(CKD) stage 4 (with eGFR within 15–29 ml/min/1.73 m2), based on the data from the
ORION-7 study, might benefit from inclisiran [21]. This is a group which is one of
the greatest challenges for cardiologists and lipidologists in the effective management
of lipid disorders, as there is currently no indicated lipid-lowering therapy [15,
22].
We have already emphasized the unique safety profile of inclisiran [11–14]. The only
adverse reactions related to inclisiran were injection site adverse reactions (8.2%);
however, the vast majority of these symptoms were mild, transient and did not require
discontinuation of treatment [11–14].
Inclisiran was approved by the European Medicines Agency (EMA) on 9 December 2020
[23] and a year later (22 December 2021) by the US Food and Drug Administration (FDA)
[24, 25]. The indications for inclisiran administration based on different agencies
and recommendations are presented in Table I.
Table I
Summary of available recommendations/approvals for inclisiran administration in lipid
disorder patients
Institution/Society (date of public release)
European Medicines Agency (EMA) (Dec. 9th 2020) [23]
PoLA/CFPiP/PCS/PSLD/PSD/PSH guidelines on diagnosis and therapy of lipid disorders
in Poland 2021 (Sept. 4th 2021) [15]
The National Institute for Health and Care Excellence (NICE) (Oct. 6th 2021) [25]
US Food and Drug Administration (FDA) (Dec. 22nd 2021) [24]
Indications for inclisiran administration in patients with lipid disorders
Inclisiran is indicated in adults with primary hypercholesterolemia (heterozygous
familial and non-familial) or mixed dyslipidemia, as an adjunct to diet:
In combination with a statin or statin with other lipid-lowering therapies in patients
unable to reach LDL-C goals with the maximum tolerated dose of a statin, or
Alone or in combination with other lipid-lowering therapies in patients who are statin-intolerant,
or for whom a statin is contraindicated
Recommendations on the use of inclisiran:
In patients with ASCVD and/or FH who do not achieve the target at the maximum tolerated
dose of a statin and ezetimibe, initiation of inclisiran may be considered (IIbB)
If a statin-based regimen is not tolerated at any dose (even after rechallenge), treatment
with inclisiran may be considered (IIbC)
In primary or secondary prevention in very high-risk patients who are non-adherent
to lipid-lowering therapy or who are not willing to use statin therapy, treatment
with inclisiran may be considered (IIbC)
Inclisiran is recommended as an option for treating primary hypercholesterolemia (heterozygous
familial and non-familial) or mixed dyslipidemia as an adjunct to diet in adults.
It is recommended only if:
There is a history of any of the following cardiovascular events:
– Acute coronary syndrome (such as myocardial infarction or unstable angina needing
hospitalization)
– Coronary or other arterial revascularization procedures
– Coronary heart disease
– Ischemic stroke or
– Peripheral arterial disease
AND
Low-density lipoprotein cholesterol (LDL-C) concentrations are persistently 2.6 mmol/l
or more, despite maximum tolerated lipid-lowering therapy, that is:
– Maximum tolerated statins with or without other lipid-lowering therapies or
– Other lipid-lowering therapies when statins are not tolerated or are contraindicated
Inclisiran injection was approved as a treatment to be used along with diet and maximally
tolerated statin therapy for adults with heterozygous familial hypercholesterolemia
(HeFH) or clinical atherosclerotic cardiovascular disease (ASCVD) who require additional
lowering of low-density lipoprotein cholesterol (LDL-C)
Key points for reimbursement of inclisiran in Poland
Based on all of the data above, we strongly believe that inclisiran should be immediately
available for very high-risk patients in Poland, as only 1/6 of these patients (17%)
currently reach their LDL-C target [3]. We think that the available data from the
ORION program on the high efficacy and unique safety (despite the indirect data on
cardiovascular outcomes) are enough to add inclisiran to the existing drug program
B-101 for PCSK9 inhibitors. There are several reasons to justify such an approach:
Despite the fact that the drugs act through different mechanisms to inhibit the PCSK9
protein, the target is the same, and in the scientific literature both classes are
referred to as ‘PCSK9 targeted approaches’ [26];
Despite some differences in the PROFICIO, ODYSSEY and (VICT)ORION programs, for the
most part, we observe similarities, especially in the group of patients being investigated
(FH, ASCVD, special populations) [11, 15, 20];
The effect on the lipid profile (not only on LDL-C but also on non-HDL, apoB, and
Lp(a)) also seems to be similar with a slightly (a few %), clinically irrelevant,
greater efficacy of PCSK9 inhibitors in the reduction of LDL-C, but with better safety
of inclisiran (also in respect of the response to therapy, which is 100% for this
drug) [11–15, 20];
Having three drugs in the drug program would also mean greater availability of innovative,
very effective therapy for the patients with the largest unmet needs in Poland – those
with HeFH and after ACS.
In our opinion, such an approach is not only effective (especially if the National
Health Fund finally announces competition procedures for new centers – mainly interventional
cardiology ones – which include patients with early ACS), but also the fastest approach
(the alternative is a new drug program, for which the approval process would be much
longer and probably less effective). Taking this into account, we would also like
to apply for some necessary amendments to the existing drug program for PCSK9 inhibitors
(B-101), to ease the process of patients’ qualification and increase their number
in both arms (as of March 2022 in both arms there are only about 350 patients included,
mostly in the FH arm). Therefore, we would like to recommend the following amendments
to the existing drug program, considering its possible extension for inclisiran:
– There is a great need to have a clear definition of statin intolerance based on
existing recommendations, including the most recent guidelines of six Polish scientific
societies [15] and recent recommendations of the International Lipid Expert Panel
(ILEP) [27]. We, therefore, recommend using the practical definition of statin intolerance
as ‘documented intolerance to at least two statins, including the second statin with
the lowest dose recorded, for a period of at least 3 months’;
– In the current version of the drug program the early (epidemiologically) acute coronary
syndrome was defined based on the data from the ODYSSEY OUTCOMES trial (within 12
months) [20], but there are also strong data available on both the very high risk
of recurrent CVD events and the effectiveness of PCSK9 targeted therapy for early
ACS defined as within 24 months (in the ORION program no such time limits are applied)
[20, 28, 29]. This may be of particular importance in Poland, as many patients after
ACS are automatically included in the comprehensive coordinated care after myocardial
infarction (KOS-Zawał) for only 12 months after an event [30]. So, the possibility
of also including these patients at very high and extremely high risk for over 12
months after an event would be expected to be of benefit for them;
– Finally, with respect to the existing program, we would like to recommend supplementing
the ‘Criteria for exclusion in the program’ with the possibility of inclusion of patients
with chronic kidney disease and eGFR 15–29 ml/min/1.73 m2, who might be treated with
inclisiran [21]. This might be indeed a great benefit for patients with kidney impairment,
which is common in ASCVD patients [15] (the updated version of the B-101 program with
the above changes is presented in Table II).
Future perspectives
We would like to emphasize that the above suggestions are only a kind of compromise
between the existing data, needs, and healthcare system and payer possibilities, in
order to enable inclisiran to be reimbursed as soon as possible for patients at a
very high CVD risk. We are aware, however, that this is merely the first step towards
establishing the final population of patients that should be treated with these innovative
PCSK9 targeted therapies. We should also do our best to improve the effectiveness
of the commonly available and cheap therapies, including high intensity statin therapy,
and especially the combination therapy of statins and ezetimibe (including as an upfront
therapy), which is severely underused in Poland [3, 7, 15, 31].
Table II
Experts’ suggestions on the extension of the existing therapeutic program B-101 (with
inclisiran inclusion): PCSK9 inhibition in patients with lipid disorders (ICD-10 E78.01,
I21, I22, I25)
Scope of guaranteed benefit
Beneficiaries
Dosing regimen in the program
Diagnostic tests performed as a part of the program
I. Eligibility criteriaI A. Treatment of patients with familial hypercholesterolemiaMeeting
of the following cumulative conditions:
Age 18 years and over
Definite diagnosis of heterozygous familial hypercholesterolemia, i.e., the Dutch
Lipid Clinic Network score > 8
LDL-C > 100 mg/dl (2.5 mmol/dl) despite dietary intake, and:
Intensive statin treatment at maximum doses, i.e., atorvastatin 80 mg or rosuvastatin
40 mg, followed by atorvastatin 40–80 mg or rosuvastatin 20–40 mg in combination with
ezetimibe 10 mg; used for a total of 3 months, including combination therapy with
ezetimibe for at least 1 month
or
Intensive statin treatment at maximum tolerated doses followed by a statin in combination
with ezetimibe 10 mg; used for a total of 3 months, including combination therapy
for at least 1 month
or
In patients who are completely statin intolerant, defined as a documented intolerance
to at least 2 statins, the latter with the lowest dose recorded, for a period of at
least 3 months
I B. Treatment of patients at very high cardiovascular riskMeeting of the following
cumulative conditions:
Age 18 years and over
LDL-C > 100 mg/dl (2.5 mmol/l) despite diet and intensive statin treatment at maximum
tolerated doses followed by statins at maximum tolerated doses with ezetimibe. A total
treatment period of at least 3 months is required, including at least 1 month of combination
therapy (a statin at maximum tolerated doses + ezetimibe). In patients with suspected
statin-related rhabdomyolysis, treatment duration is determined by the treating physician
according to ESC/EAS guidelines, but not less than 3 months
A history of myocardial infarction diagnosed using invasive methods within 24 months
prior to inclusion in the therapeutic program and
Additional history of myocardial infarction and multivessel coronary disease, defined
by at least 50% stenosis in at least 2 vessels
or
With atherosclerotic disease of non-coronary arteries, defined as:
Peripheral arterial disease (PAD), i.e., intermittent claudication with an ankle-arm
index (ABI) < 0.85 or a history of peripheral arterial revascularization or limb amputation
due to atherosclerotic disease
or
cerebrovascular disease, i.e., prior ischemic stroke or transient ischemic attack
(TIA)
I C. In addition, patients currently receiving evolocumab, alirocumab or inclisiran
may be eligible for the therapeutic program to ensure continuous therapy, provided
that they met the program’s eligibility criteria at the beginning of treatment with
evolocumab or alirocumab and did not meet the criteria described in section 3II. Determination
of treatment duration in the programThe treatment should be continued until the physician
decides to exclude a patient from the program in accordance with the criteria for
termination of the patient’s participation in the program presented in section 3III.
Criteria for termination of participation in the program
Severe allergic reaction following treatment administration
Lack of efficacy after 3 months of therapy, defined as reduction of LDL-C concentration
by < 30% from the baseline value determined:
At the time of inclusion in the program, in patients not treated previously with LDL
apheresis (including those enrolled in the program according to section 1.1 and 1.2)
At the time of treatment initiation, in patients enrolled in the program according
to section 1.3
IV. Criteria preventing inclusion in the program
Secondary hyperlipidemia
Homozygous familial hypercholesterolemia
Severe renal impairment (eGFR < 30 ml/min/1.73 m2 for PCSK9 inhibitors and eGFR <
15 ml/min/1.73 m2 for inclisiran)
Severe hepatic impairment (Child-Pugh class C)
Pegnancy
Breast feeding
Hypersensitivity to evolocumab, alirocumab or inclisiran, or to any of the excipients
Alirocumab
150 mg of alirocumab administered every 2 weeks
Evolocumab
140 mg of evolocumab administered every 2 weeks
Inclisiran
The recommended dose is 284 mg of inclisiran as a single subcutaneous injection: first
dose, again after 3 months, and then every 6 months
I. List of tests for qualification for treatment
Lipid profile
Alanine aminotransferase (ALT)
Creatinine/eGFR
Creatine kinase (CK)
II. Treatment monitoring
Lipid profile – after 3 months, then every 12 months
Monitoring of treatment safety at every visit
III. Monitoring of the program
Collection of data on treatment monitoring in the patient’s medical records and their
presentation at each request of the National Health Fund
Input of data as required by the registry (SMPT) available through a web application
provided by the Provincial Branch of the NHF, at the frequency consistent with the
program and at the end of treatment
Provision of reporting and accounting information to the NHF: the information is sent
to the NHF in a paper form or in an electronic form, in accordance with the requirements
published by the National Health Fund
We have, therefore, already completed the first part of the report on the group of
patients that might benefit the most (with the detailed calculation of the group sizes
and budget impact), based on the available data but also the characteristics of the
Polish healthcare system [32]. This might be the next step to be considered in the
extension of the group of patients on these innovative therapies. This includes, among
others: (1) reduction of the required level of LDL-C from 100 (2.5 mmol/l) to at least
70 mg/dl (1.8 mmol/l) for ACS patients and without the level limit (LDL-C ≥ 55 mg/dl/1.4
mmol/l) for those with two myocardial infarctions (MIs), (2) separation of the group
of patients after two MIs and multivessel coronary artery disease (MVCAD) into subjects
with two MIs and those with ACS and MVCAD, who are already identified as having extremely
high cardiovascular risk (it seems to be a mistake in the drug program from the beginning)
[15, 33, 34], (3) inclusion in the drug program of patients with premature myocardial
infarction (men ≤ 55 and women ≤ 60 years of age). In our opinion, future changes
should also consider patients with a high level of lipoprotein(a) (especially in light
of the first Polish epidemiological data on the number of patients with elevated Lp(a)
levels), as well as those in primary prevention at high CVD risk (we have such data
in the (VICT)ORION program), especially as this is in line with the recommendations
for therapy with PCSK9 inhibitors in primary prevention in the European and Polish
guidelines [15, 35].
Conflict of interest
Maciej Banach: speakers bureau: Amgen, Herbapol, Kogen, KRKA, Polpharma, Mylan/Viatris,
Novartis, Novo-Nordisk, Sanofi-Aventis, Teva, Zentiva; consultant to Amgen, Daichii
Sankyo, Esperion, Freia Pharmaceuticals, Novartis, Novo-Nordisk, Polfarmex, Sanofi-Aventis;
Grants from Amgen, Mylan/Viatris, Sanofi and Valeant; CMO at Nomi Biotech Corporation
Ltd; Jarosław Kaźmierczak: lecture fees and Advisory Boards: Amgen, Novartis, Sanofi;
Przemysław Mitkowski: speaking fees: Novartis, Pfizer, Servier, consultant fees: Novartis,
Sanofi-Aventis; Marlena Broncel: speaking fees: Amgen, Mylan/Viatris, Novartis, Novo-Nordisk,
Polpharma, Sanofi-Aventis, Servier, Teva, Zentiva; Mariusz Gąsior: lecture fees and
Advisory Boards: Amgen, Novartis, Sanofi-Aventis. Marek Gierlotka: speakers bureau:
Novartis, Bayer, Sanofi, Orion Pharma, Astra Zeneca, Boehringer Ingelheim; Robert
Gil: speakers bureau: Novartis; Piotr Jankowski: Honoraria and grants: Boehringer-Ingelheim,
Novartis, NovoNordisk, Sanofi, Servier, Zentiva; Maciej Niewada: speaking or consultation
fees apart from honorarium for HTA dossiers: Novartis, Novo-Nordisk, Polpharma, Sanofi-Aventis,
Servier, Biogen, Amgen, EverPharma, Polfa Tarchomin, Jansen; Adam Witkowski: speaking
fees and Advisory Boards: Amgen, Novartis, Sanofi; all other authors have no conflict
of interest.