Idiosyncratic drug-induced liver injury (IDILI) is a rare but potentially severe adverse drug reaction that should be considered in patients who develop laboratory criteria for liver injury secondary to the administration of a potentially hepatotoxic drug. Although currently used liver parameters are sensitive in detecting DILI, they are neither specific nor able to predict the patient's subsequent clinical course. Genetic risk assessment is useful mainly due to its high negative predictive value, with several human leucocyte antigen alleles being associated with DILI. New emerging biomarkers which could be useful in assessing DILI include total keratin18 (K18) and caspase-cleaved keratin18 (ccK18), macrophage colony-stimulating factor receptor 1, high mobility group box 1 and microRNA-122. From the numerous in vitro test systems that are available, monocyte-derived hepatocytes generated from patients with DILI show promise in identifying the DILI-causing agent from among a panel of coprescribed drugs. Several computer-based algorithms are available that rely on cumulative scores of known risk factors such as the administered dose or potential liabilities such as mitochondrial toxicity, inhibition of the bile salt export pump or the formation of reactive metabolites. A novel DILI cluster score is being developed which predicts DILI from multiple complimentary cluster and classification models using absorption–distribution–metabolism–elimination-related as well as physicochemical properties, diverse substructural descriptors and known structural liabilities. The provision of more advanced scientific and regulatory guidance for liver safety assessment will depend on validating the new diagnostic markers in the ongoing DILI registries, biobanks and public–private partnerships.
- HEPATOBILIARY DISEASE
- DRUG INDUCED HEPATOTOXICITY
- BILE ACID
- ADVERSE DRUG REACTIONS
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Importance of DILI diagnosis
Drug-induced liver injury (DILI) accounts for <1% of cases of acute liver injury seen by gastroenterologists, but is the most common cause for acute liver failure in the USA and Europe.1–3 According to surveys in France and Iceland, DILI occurs with an annual incidence of about 14–19 per 100 000 inhabitants.4 ,5 DILI is also a leading cause of attrition of compounds in drug development and one of the two most frequent causes for drug withdrawals, restrictions and project terminations (figure 1).6–11 Of 76 drugs withdrawn from the market between 1969 and 2002, 12 were attributable to liver damage.12 Whereas liver signals that escape detection during drug approval result in postmarketing restrictions (eg, pazopanib, temozolomide and flupirtine in 2013), the risk of false-positive DILI adjudication may lead to unnecessary attrition, thereby contributing to the considerable economic issues associated with DILI.
Patients who consume acetaminophen (APAP) at a single dose exceeding 7.5 g experience acute liver toxicity, notably if plasma concentrations exceed 200 or 100 μg/L 4 or 8 hours after ingestion, respectively. APAP intake at the licensed dose of 4 g/day over a period of 2 weeks results in elevations of alanine aminotransferase (ALT) above 3× the upper limit of normal (ULN) in one-third of patients.13 This form of dose-dependent APAP-induced toxicity is termed intrinsic DILI: it is predictable, reproducible in preclinical models and much insight has been gained into the underlying mechanisms.14 ,15
In contrast to intrinsic DILI, the onset of idiosyncratic DILI (IDILI), which is very rare but nonetheless responsible for about 10–15% of acute liver failures in the USA,16 is almost impossible to predict. IDILI is characterised by a variable latency to onset (weeks to months) and a lack of clear dose dependency.17 Drug–protein adducts, formed by drugs or their metabolites that interact with host proteins, are presented as neoantigens by major histocompatibility complex class II, thereby triggering an immunoallergic reaction. Individuals with underlying hepatic injury such as viral hepatitis or inflammatory conditions may be more susceptible to immunoallergic injury.18 Following the initial insult, additional mechanisms such as inhibition of transporters, mitochondrial injury, endoplasmic reticulum and oxidative stress and proinflammatory cytokines can further amplify the injury mechanisms that lead to acute DILI.19 Identification of host factors that render an individual susceptible is the focus of ongoing pharmacogenetic studies.20 This review article focuses on IDILI and the subsequent use of the term DILI essentially implies IDILI.
A major problem in drug development is the frequency of adverse hepatic reactions induced by the newer molecular targeted agents (MTAs) in oncology. Hepatotoxicity occurs in one-third of patients treated with a protein kinase inhibitor, with fatal outcome reported for pazopanib, sunitinib and regorafenib.21 Ten per cent of patients treated with immune checkpoint inhibitors, notably ipilimumab, develop liver injury with high rates of recurrent liver injury upon rechallenge.21 The epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) gefitinib is associated with a 18.5% frequency of hepatotoxicity and casualties have occurred for all EGFR TKIs.22 The oncology population that is treated with MTAs is more likely to have multiple comorbidities and comedications and is therefore at risk for hepatotoxicity. The Food and Drug Administration (FDA) issues detailed recommendations in drug labels as to liver test monitoring intervals and stopping rules; however, intensive postmarketing surveillance of MTA-associated liver injury is required. The standard recommendations contained in the current FDA Guidance to Industry23 are not applicable to the oncology population and new methods of liver safety assessment are required.24 For the management of IDILI, a key question is whether a patient in whom DILI has been diagnosed will progress to severe liver injury with potentially fatal outcome or recover spontaneously after cessation of the causative agent. A diagnostic algorithm that allows identification of risk factors and prediction of the subsequent clinical course would greatly facilitate the management of acute DILI. The current lack of predictive safety testing before administration of a potentially hepatotoxic compound reinforces the need for rapid identification of a high-risk DILI situation that requires intensified surveillance. Novel biomarkers such as those evaluated in the European Union Innovative Medicines Initiative (IMI) Safer and Faster Evidence-based Translation (SAFE-T) Consortium have gained regulatory support for systematic implementation by sponsors in future trials.25–27
Current diagnosis of IDILI depends on expert opinion that is based on patient data and the typical ‘signatures’ associated with certain drugs.28 Causality scores such as the Roussel-Uclaf Causality Assessment Method (RUCAM, figure 2) are intended to confirm or exclude the suspicion of DILI.29 Limitations of such scoring algorithms are poor inter-rater reliability and arbitrary scoring, for example, for alcohol use.30 This can be mitigated by a consensus process such as the one employed by the US Drug-Induced Liver Injury Network (DILIN), even though consensus opinion carries the risk of overruling a more insightful minority opinion.31 ,32 Liver injury caused by herbal and dietary supplements presents unique challenges to hepatotoxicity assessment and its incidence is increasing.33 ,34 Due to the lack of a reliable diagnostic in vitro test, there is no objective method beyond expert opinion that assesses causality of a given drug in individual cases.
Standard of diagnosis: role of currently performed liver tests in assessing DILI
DILI most often presents as an acute viral hepatitis-like syndrome, without symptoms that specifically point to the drug aetiology unless rash or other cutaneous manifestations35 reinforce the suspicion of drug toxicity. The clinical spectrum of DILI can mimic almost every other liver disorder. Accompanying blood eosinophilia is uncommon in large series of patients with DILI,36 ,37 but is clearly suggestive of drug allergy. Histopathological findings in DILI can resemble many other liver disorders, thereby limiting the value of liver biopsy in DILI diagnosis. However, biopsy can be of use to establish an alternative diagnosis when the underlying liver disease worsens (ie, alcoholic hepatitis, autoimmune hepatitis (AIH))38 (table 1).
A diagnostic workflow for assessing cases of suspected DILI is shown in figure 3. Serum aminotransferases, that is, ALT and aspartate aminotransferase (AST), alkaline phosphatase (ALP) and total bilirubin (TB) levels, although not specific for DILI, remain the hallmark for detecting and classifying liver damage.40 Minor increases in aminotransferases that can result from adaptive and reversible liver responses to the drug (eg, statins) or from pre-existing liver disease (eg, fatty liver) should not be classified as DILI. An international expert group41 proposed the following thresholds for a diagnosis of DILI: (a) ALT value ≥5× ULN, (b) ALP value ≥2× ULN or (c) ALT value ≥3× ULN and TB ≥2× ULN. The latter constellation defines ‘Hy's Law’, which anticipates a 10% risk of mortality/liver transplantation,42 as confirmed in large databases of DILI cases.36 ,43 The FDA guidance for DILI extends the interpretation of Hy's Law by stating that ‘there should not be a prominent cholestatic component’ in the hepatocellular nature of the liver injury,23 suggesting that a cholestatic component as defined by elevated ALP levels is associated with less risk of progression. However, a recent analysis from the Spanish DILI Registry showed that raised ALP >2 ULN did not decrease the risk of acute liver failure in cases fulfilling Hy's Law.44 A marked increase of AST and an AST/ALT ratio >1.5 at DILI recognition also predict a worse prognosis.43 ,44
The presence of autoimmune features such as antinuclear antibodies (ANAs), smooth muscle antibodies (SMAs) and elevated IgG levels as well as histological features of AIH may cause diagnostic confusion in DILI.45 Screening for autoantibodies and serum IgG in hepatocellular injury is mandatory, although the typical laboratory and pathological features of AIH may also be drug induced. Moreover, recurrent DILI induced by a different drug tends to present with an AIH phenotype.46 DILI with autoimmune features should be clearly distinguished from idiopathic AIH and typically resolves after stopping the causative drug. If treated with corticosteroids, a lack of recurrence following corticosteroid cessation supports a diagnosis of drug-induced AIH rather than idiopathic AIH.47 As yet there are no diagnostic tests to differentiate idiopathic from drug-related AIH, although histological findings can help in the differential diagnosis.48 ,49
Rechallenge with the suspected drug, although considered the gold standard for diagnostic confirmation,50 carries ethical and practical issues. First, it confers a risk that is only justified when an alternative drug is not available. Second, the definition of a ‘positive rechallenge’ is controversial regarding the required threshold, if any, of liver enzyme elevation and symptoms, partly due to the lack of data on ‘negative rechallenge’.51 In the RUCAM score, the re-exposure test is positive if ALT is ≥2× baseline upon re-exposure, provided that ALT was below 5× ULN before re-exposure, and negative if one or both criteria are not fulfilled.29 Follow-up in patients with DILI must include routine liver biochemistry until complete normalisation. Rapid normalisation of aminotransferases supports the diagnosis, whereas slow or incomplete resolution suggests alternative causes. In such instances, a liver biopsy can be helpful (figure 3). Persistently elevated TB and ALP 30–60 days after the initial DILI diagnosis can predict a chronic outcome.52
In vitro and in silico tools for the assessment and prediction of DILI
The risk of IDILI has hung like the sword of Damocles over the drug approval process since decades, leading to fatal liver failures and subsequent market withdrawals and creating nervousness on the part of sponsors and regulators alike. These signals may occur in only very few individuals, making it impossible to identify the risk in premarketing registration trials. Thus, the quest for predictive tools that would allow an a priori identification of both host factors as well as compound features conferring a DILI risk has led to the development of numerous cell-based systems, animal models and in silico algorithms. Whereas none of these has lived up to the crystal ball promises that frequently accompany marketing initiatives, the spectrum of predictive tools available today may allow implementation of a panel of select methodologies which, in combination, yield new insight into IDILI.
Cell-based assays include primary human hepatocytes, immortalised hepatocytes, hepatoma cell lines and induced pluripotent stem cell-derived hepatocytes.53–57 These systems have been reviewed in detail and the development of coculture systems with non-parenchymal cells as well as 3D organoids has allowed the in vitro analysis of several mechanisms of DILI, including mitochondrial toxicity, oxidative and endoplasmic reticulum stress and inhibition of transporters such as the bile salt export pump (BSEP).58 ,59 Animal models used to study mechanisms of DILI include the heterozygous superoxide dismutase (Sod2)±mouse, panels of inbred mouse strains and chimeric mice with humanised livers.60–62 These models have proven useful to elucidate mechanisms such as troglitazone-induced mitochondrial toxicity.63 The prediction of IDILI in a susceptible individual has not been made possible by any of these in vitro systems.
A frequent problem in assessing causality in patients with polypharmacy who have experienced DILI is which of the drugs, especially if some of them are known to be potential hepatotoxins, was causative in the given patient. A test system called MetaHeps allows the identification of the DILI-causing drug out of a panel of comedications. This test uses monocyte-derived hepatocyte-like cells (MH cells) from the affected patient (figure 4). MH cells possess donor-specific hepatocyte characteristics when compared with primary human hepatocytes derived from the same donor.64 MH cells from patients with IDILI are more susceptible to toxicity induced by the causative drug than MH cells from patients with non-drug liver injury or healthy donors.65 ,66 MH cells show high sensitivity and specificity for the diagnosis and exclusion of IDILI and outperform the RUCAM score67 in identifying the causative drug in cases of polypharmacy. MH cells may furthermore be useful in assessing the role of drug–drug interactions in the onset of IDILI. The identification of true positives among patients with multiple comedications could help to develop more specific biomarkers that identify patients at risk of progressing to more severe DILI.
In addition to studying the biological effects that drugs have in ex vivo test systems, predictive algorithms are being developed that correlate structural and chemical properties of the parent drug as well as of its metabolites with the clinical risk of DILI. The FDA's Liver Toxicity Knowledge Database (LTKB) contains a benchmark data set of drugs whose potential to cause DILI is categorised into most-DILI-concern drugs (boxed warning or withdrawn from the market due to hepatotoxicity), less-DILI-concern drugs (DILI risk mentioned in the label) and no-DILI-concern drugs (no DILI indication in the label).68 This DILI classification has been refined by incorporating the causality assessment from clinical studies together with drug labelling information to improve its accuracy.69 FDA investigators reported the Rule-of-2 which identified lipophilicity, that is, an octanol–water partitioning coefficient (logP) of ≥3, as well as a daily dose of ≥100 mg as risk factors for DILI.70 By analysing data on 254 orally administered drugs in the LTKB benchmark data set, the FDA group found that drugs that are substrates of cytochrome P450 (CYP) enzymes have a higher likelihood of causing DILI irrespective of the administered dose, whereas mere inhibitors of P450 enzymes were only associated with a risk of DILI at high daily doses.71 By factoring in the formation of reactive metabolites, the predictive value of logP and daily dose could be improved, as shown in an analysis of 159 clinical cases collected from the National Institutes of Health's LiverTox Database.72
Other groups have applied inhibition of BSEP and mitochondrial toxicity as parameters to the most-concern, less-concern and no-concern-DILI drugs in the LTKB and found that dual potency as mitochondrial and BSEP inhibitors was highly associated with more severe human DILI as well as with an exposure–safety correlation represented by the maximum plasma concentration Cmax.73 The role of BSEP inhibition as a mechanism of DILI first became evident from transport studies using isolated membrane vesicles from Sf9 insect cells that overexpress Bsep.74 This technique was employed by various industry groups to systematically correlate the risk of DILI of selected compounds with their inhibitory potential towards BSEP as a function of their exposure.75 ,76 The Critical Path Institute's Predictive Safety Testing Consortium (C-Path PSTC) hosted a webinar in 2016 focused on BSEP inhibition and perturbation of bile acid homeostasis as mechanisms of DILI and a broad industry-wide consensus was reached on the importance of testing lead compounds in BSEP inhibition assays so as to identify potential DILI liabilities at an early stage.77
Based on the knowledge about mechanisms which cause DILI, in silico algorithms are being developed that allow modelling of various parameters to extrapolate the risk of DILI in vivo. The DILIsym model, for example, predicts that the BSEP inhibitor bosentan, but not the BSEP inhibitor telmisartan, causes mild hepatocellular ATP decline and serum ALT elevation in a simulated population.78 The catechol-O-methyltransferase inhibitors tolcapone and entacapone both cause mitochondrial impairment and inhibit BSEP, but liver injury has only been associated with the use of tolcapone. DILIsym identified patient-specific risk factors for tolcapone-induced liver injury and in a simulated population (SimPops) increases in ALT were predicted in 2.2% of the population.79 The Virtual Liver Network is a German research initiative that bridges investigations from the subcellular level to patient and healthy volunteer studies in an integrated workflow to generate validated computer models of human liver physiology.80 These in silico approaches rely on cumulative scores of known risk factors such as the administered dose or on potential liabilities such as mitochondrial toxicity, BSEP inhibition or the formation of reactive metabolites which can be measured in vitro. The major challenge when constructing predictive DILI models is to account for the broad range of chemotypes which have been associated with clinically relevant liver findings as well as the various mechanistic (pathway) considerations which translate into different clinical phenotypes of liver injury. A ‘DILI cluster score’ is being developed at Novartis that correlates a comprehensive set of several hundred compound properties against validated clinical scores as obtained from an extended version of the LTKB Database. Predictions are obtained from multiple complimentary cluster and classification models using calculated and measured compound properties related to absorption–distribution–metabolism–elimination and physicochemical properties, diverse substructural descriptors and known structural liabilities. This also allows for successful prediction of compounds which may not be classified based on typical risk factor profiles or are administered at fairly low doses (eg, methotrexate). The current algorithm is limited to orally administered drugs given over a prolonged period or in a chronic dosing regimen.
There have been recent efforts mainly by public–private partnerships such as the IMI SAFE-T Consortium together with C-Path PSTC and DILIN to develop and qualify new liver safety biomarkers that outperform current standard markers in terms of sensitivity, specificity and predictivity. From the new markers investigated by IMI SAFE-T and PSTC (table 2), a subset has recently received regulatory support from both European Medicines Agency (EMA) and FDA for more systematic use in an exploratory development setting,26 ,27 which will ultimately enable full qualification of the most promising markers. Once qualified in well-controlled trials, regulatory guidance will then also have to account for the new markers and incorporate them into existing guidelines.
Several new biomarkers have been studied in the context of APAP-induced DILI.99 MicroRNA-122 (miR-122) is a hepatocyte-specific miRNA that is elevated in the plasma of patients within hours of an APAP overdose. Together with high mobility group box-1 (HMGB1) and keratin-18, it has been shown to predict the subsequent onset of liver injury at an early time point before ALT is elevated.83 Previous studies in mice already showed that miR-122 and miR-192 are enriched in liver tissue and exhibit dose-dependent and exposure-dependent changes in plasma that parallel serum aminotransferase levels and the histopathology of liver degeneration.81
HMGB1 is a chromatin-binding protein released by necrotic cells. HMGB1 subsequently targets Toll-like receptors and the receptor for advanced glycation end products (RAGE), thus acting as a damage-associated molecular pattern molecule.100 A hyperacetylated form is released from immune cells and acts as a marker of immune activation. Given the role of immune activation in IDILI, HMGB1 has been studied in the context of APAP-induced (intrinsic) DILI and as a marker of IDILI in the IMI SAFE-T Consortium DILI cohort.
Another marker of immune activation is macrophage colony-stimulating factor receptor 1 (MCSFR1). In 10 cases of IDILI caused by the centrally acting non-opioid analgesic flupirtine, the use of which has been restricted by the EMA because of hepatotoxicity, MCSFR1 levels were considerably higher than in 19 cases of APAP-induced DILI, despite ALT levels being markedly higher in APAP-induced DILI. Furthermore, both MCSFR1 and the biomarker osteopontin (table 2) were higher in 31 patients with DILI that fulfilled Hy's Law criteria compared with 70 patients with DILI who did not fulfil Hy's Law criteria (SAFE-T Consortium, unpublished data).
Serum bile acids have traditionally been considered to have little use in the workup of liver disease with the possible exception of intrahepatic cholestasis of pregnancy, given the multitude of analytes and the complexity of bile acid metabolism. Glycodeoxycholic acid (GDCA) has been shown to have prognostic value in predicting the outcome of acute liver failure induced by APAP, with GDCA levels being considerably higher in non-surviving patients with acute liver failure (ALF).101 With the availability of new analytical multiplexing methods based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-mass spectrometry (GC/MS), circulating bile acid (BA) profiles are now being evaluated as biomarkers for hepatotoxicity.102 A targeted LC-MS/MS approach identified cholic acid, glycocholic acid and taurocholic acid (TCA) as potential biomarkers of liver injury in rodent models.103 In the IMI SAFE-T Consortium DILI cohort, several bile acids were markedly elevated in flupirtine-induced DILI, including glycochenodeoxycholic acid, taurochenodeoxycholic acid and TCA. This was not simply the result of cholestasis since ALP was normal. This suggests that selected bile acids could be markers of IDILI.
Serum autoantibodies and pyrrole–protein adducts
Certain drugs causing IDILI are associated with the formation of serum autoantibodies. Examples include anti-CYP 2C9 in tielinic acid-induced hepatitis, anti-epoxide hydrolase in germander-induced liver injury, anti-CYP1A2 in dihydralazine hepatitis, anti-CYP3A in anticonvulsant hepatitis and anti-CYP2E1 in halothane hepatitis.104 ,105 Autoimmune reactions involving CYP2E1 are a feature of DILI induced by halogenated hydrocarbons and isoniazid (INH), but are also detectable in about one-third of patients with alcoholic liver disease and chronic hepatitis C.106 From 19 patients enrolled in the Acute Liver Failure Study Group for INH-induced acute liver failure, eight tested positive for anti-INH antibodies.107 These were not detectable in patients with only mild INH-induced liver injury, suggesting that mild cases of INH DILI resolve with immune tolerance.
In pyrrolizidine-induced liver injury, blood pyrrole–protein adducts (PPAs) predict the onset of sinusoidal obstruction syndrome with a positive predictive value of 96% and a negative predictive value of 100%.108 The blood PPA concentration is related to the severity and clinical outcome of pyrrolizidine alkaloid-associated hepatic sinusoidal obstruction syndrome.
Genetic testing in the assessment of DILI
In keeping with their reputation as ‘hypothesis generating’ research methodology, genome-wide association studies (GWASs) have unearthed a number of novel associations, in particular between human leucocyte antigen (HLA) class I and II alleles and DILI.
In contrast to GWASs focused on other complex traits, those investigating DILI have identified risk alleles with substantially higher risk ratios for susceptibility to DILI. As demonstrated in table 3 (modified from ref. 120), there is substantial overlap among the risk alleles associated with clinically varied phenotypes of toxicities due to structurally dissimilar compounds. For example, DRB1*0701 is a risk allele for flucloxacillin, ximelagatran and lapatinib-related DILI, while DRB1*1501 is associated with DILI secondary to amoxicillin-clavulanate and lumiracoxib. Conversely, DRB1*1501 is associated with reduced risk of flucloxacillin DILI and DRB1*0701 is protective of amoxicillin-clavulanate DILI.121 Such associations extend beyond DILI into a variety of other adverse reactions, including cutaneous hypersensitivity and drug-induced pancreatitis. For example, carriage of HLA-B*5701 allele increases by 80-fold the risk of flucloxacillin-induced DILI and the same allele is also strongly associated with hypersensitivity due to abacavir.111 Another example of common genetic factors underlying different organ toxicities is the link between DRB1*0701 and pancreatitis induced by thiopurine immunosuppressants as well as DILI due to a number of drugs listed above.122 Recently, GWASs led by the international DILI Consortium demonstrated HLA-A*33:01 as a risk factor for a cholestatic or mixed pattern of DILI when these are considered as a single phenotype irrespective of the causative drugs.118
Interaction between drugs and HLA molecules
These investigations highlight the role of the adaptive immune response in DILI pathogenesis.123 The ‘hapten hypothesis’ states that an individual's susceptibility to DILI is determined by the covalent binding of a drug or its metabolites to a cellular or circulating protein and the interaction of the resultant complex with the peptide-binding groove of a specific HLA molecule (figure 5). Alternatively, the ‘pharmacological interaction (pi) concept’ proposes that a drug or drug metabolite can directly bind to the HLA molecule (as in the case of ximelagatran and HLA-DRB1*0701)110 or T cell receptor to trigger T cell activation, leading to immune-mediated liver injury. Recently, it has been proposed that drugs may make van der Waals contacts with the antigen-binding cleft (as in the case of minocycline and HLA-B*3502119) and alter the shape and chemistry of the antigen-binding cleft, thus altering the repertoire of endogenous peptides that subsequently bind to it, which in turn leads to an adaptive immune response.
The majority of HLA alleles associated with DILI have a very high negative predictive value of >0.95. Therefore, genotyping can be used to rule out adverse hepatic reactions due to particular drugs (listed in table 3) so that alternative diagnoses are considered.20 The HLA-B*35:02 genotype is a useful diagnostic test in the setting of suspected minocycline DILI, especially in distinguishing it from idiopathic AIH as both conditions share similar serological markers such as ANAs and SMAs.124 A high negative predictive value of a genetic test can also be used to identify the correct agent underlying DILI when the patient has been exposed to two concomitant medications.
Overall, the strength of association between HLA genotypes and DILI has raised controversy (eg, in relation to lumiracoxib) regarding the use of genetic testing in risk stratification.125 The incidence of DILI is less than 1 in 10 000 for most drugs used in clinical practice126 and thus too low for preprescription genotyping to be cost-effective at present. It is foreseeable, however, that personal genetic information such as the HLA profile may become routinely accessible to assist precision medicine and to minimise adverse drug reactions.
DILI has raised less awareness in routine patient care than it has in the regulatory and industry setting, where DILI is a leading cause of drug attrition and a major safety issue. Acute liver failure induced by a drug in clinical practice requires immediate supportive management of the patient and referral to a liver transplantation unit if the clinical situation deteriorates. Even with a test system in place that could accurately predict a patient's risk to develop liver failure, the likelihood that this would be routinely employed is low given the rarity of the event. This is in marked contrast to the situation in drug development, where pharmaceutical industry and regulators alike are frequently confronted with liver safety issues requiring expert assessment to quantify the risk and to implement an appropriate action scheme. Several examples of drug failures during development over the last 20 years underscore the need to develop new diagnostic tools and predictive systems which help to manage the challenge imposed by DILI. Genetic testing has identified HLA alleles that increase the risk of idiosyncratic reactions and in this sense has strengthened the pathophysiological concept. In a next step, diagnostic tools are required that assess this immunological risk. There is agreement that preclinical species are not useful for assessing the risk of idiosyncratic reactions, although certain intrinsic mechanisms of toxicity may be reproducible. In vitro tools which may predict a risk of DILI prior to first-in-human studies rely on human-derived cell assays to assess mitochondrial toxicity, inhibition of transporters, induction of oxidative stress and other endpoints. These test systems are used as supportive evidence but rarely trigger a decision with respect to the further development of a drug. Novel computer-based algorithms that integrate these in vitro readouts with structural properties are still at an early stage of development, but may offer potential as learning systems that correlate well-characterised compounds with clinical outcome.
This leaves the DILI community with the task of validating new biomarkers and in vitro tools for causality assessment which classify the type of injury and the risk associated with the observed biomarker pattern. How should a transient but rapidly reversible elevation of ALT to >20-fold ULN be interpreted? Biomarkers that inform us whether this rise in ALT was accompanied by immune activation would help us to classify the incident as an idiosyncratic reaction. Are all cases of DILI that fulfil the Hy's Law criteria in the same risk category or can new biomarkers help to define subcategories? Systematic measurement of new predictive biomarkers should be performed in patients in whom liver injury can be attributed to a specific causative drug by use of the RUCAM score. The choice of biomarkers is a major challenge that is being taken up by numerous initiatives such as the IMI Consortia, DILIN, Pro-Euro DILI and dedicated DILI groups within the International Consortium for Innovation and Quality in Pharmaceutical Development (IQ DILI) and the Council for International Organizations of Medical Sciences (CIOMS). Constructive dialogue and close collaboration of these networks with regulatory and academic DILI experts is but one example of the steps required to advance scientific and regulatory guidance for liver safety assessment and management.
Authors thank all partners of the DILI work package in the IMI SAFE-T Consortium that evaluated new biomarkers in DILI.
Contributors GAK-U planned and wrote parts of the manuscript and contributed table 2; RJA wrote parts of the manuscript and contributed table 1 and figure 3; MM and PE wrote parts of the manuscript; AB contributed figures 1, 2 and 4; ALG wrote parts of the manuscript and GPA wrote parts of the manuscript and contributed table 3 and figure 5.
Funding This work was supported by Swiss National Science Foundation grant no. 320030_144193 (to GAK-U).
Competing interests AB and ALG have equity in the company MetaHeps GmbH. PE and MM are employees and GAK-U is a contractor of Novartis Pharma.
Provenance and peer review Not commissioned; externally peer reviewed.
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