Tyrosine Kinase Inhibitors and Proton Pump Inhibitors: An Evaluation of Treatment Options

Although the absorption of TKIs may be influenced by many factors, the major determinant in TKI absorption is the pH-dependent solubility [1, 11]. Since TKIs are weakly basic, there is an equilibrium between the ionized and non-ionized form that is dependent on intragastric pH. At normal acidic intragastric pH (pH range 1–2), the equilibrium shifts to the ionized form. Since the ionized form has better solubility, TKI absorption from the gastrointestinal tract is optimal at low intragastric pH; however, when the intragastric pH is elevated (e.g. due to concurrent PPI use), the balance shifts towards the non-ionized form of the drug and solubility and bioavailability may decrease significantly [1, 12].

Besides TKI bioavailability, the pharmacological profile of PPIs is important to consider for the management of DDIs between TKIs and PPIs. PPIs are highly effective acid-inhibitory agents and are registered in a once-daily dose for the majority of their indications. Although this dosing strategy is usually effective in controlling gastroesophageal reflux disease, PPIs do not elevate the intragastric pH over the full 24-h range (see Fig. 1) [13‐16]. There are two important explanations for this 24-h variation in acid suppression: (1) the delayed onset of the pharmacological effect of PPIs; and (2) the duration of pharmacological action [16, 17].

For most PPIs, the acid-inhibitory effects (defined by an intragastric pH >4) will only be reached 3–4 h after intake [16‐19]. This delayed onset of action is caused predominantly by the use of enteric-coated tablets or capsules. Since PPIs are easily protonated, they are unstable at low (intragastric) pH and therefore a coating is indicated. Polymer coatings are stable at low intragastric pH, but break down easily at higher intestinal pH. As a result, the PPI is protected against degradation in the stomach and arrives intact in the duodenum where absorption takes place. Furthermore, the mechanism of action of PPIs through inhibiting the hydrogen/potassium adenosine triphosphatase enzyme (H+/K+ ATPase) in gastric cells may also cause a further delay of action [20]. The resulting delay of acid-inhibitory effects after administration amounts to an average of 3–4 h (Fig. 1).

Although most PPIs are characterized by a short half-life (t _½) of approximately 1–2 h, the pharmacodynamic effects on intragastric pH last much longer because of its irreversible covalent binding to the proton pumps. After 2–3 days of daily use, a steady state in acid inhibition is reached [13, 20]. Meanwhile, new proton pumps are generated in vivo on a continuous basis, and, subsequently, gastric acid will be secreted from these new pumps, compensating the elevated pH [16]. As a consequence, the intragastric pH will start to decrease again and drops to pH values <4 within 12–14 h after PPI administration (Fig. 1) [16]. On the other hand, during nighttime, physiological duodenogastric reflux occurs as a result of the supine position during sleep. As a result, there is an elevation in intragastric pH during nighttime which sharply returns to baseline after getting out of bed (Fig. 1) [16]. Furthermore, a substantial proportion of patients above 80 years of age experience achlorhydria, a state in which the production of hydrochloric acid in the stomach is low or absent and the intragastric pH is substantially elevated [21]. Both nighttime duodenogastric reflux and achlorhydria in older patients may profoundly alter TKI bioavailability. Moreover, TKI bioavailability can be profoundly influenced when taken with food (e.g. lapatinib) [22]. Food may significantly enhance TKI bioavailability by elevating intragastric pH and drug absorption, resulting in high intra- and interpatient variability. For this reason, patients are often advised to take a TKI in a fasting state. Of note, in serious gastroesophageal reflux disease, physicians may prescribe a PPI in a twice-daily dose. In contrast to a once-daily dose, more frequent dosing of PPIs (e.g. twice-daily or continuous dosing) leads to a greater and more constant elevation of intragastric pH over the full 24-h range [10].

As mentioned in Sect. 2.2, the intragastric pH is not elevated over the full 24-h range during PPI therapy. Therefore, the outcomes of DDI studies between a PPI and a TKI are highly dependent on the study design, especially the time of intake for both the TKI and the PPI. Two types of studies can be distinguished: (1) the TKI and PPI are administered concomitantly; and (2) the TKI is administered 2–3 h after the intake of the PPI. There are strengths and limitations for both types of study designs.

When the drugs are taken concomitantly, and if the observed effect is low/nihil, this may indicate that there is indeed no interaction between the two drugs, but it may also well be that a DDI would have been observed if the PPI had been taken at another time [2, 23]. As mentioned previously, when the TKI and PPI are administered concomitantly, there is a time window of low intragastric pH after PPI intake in which the TKI absorption will not be significantly affected, which may potentially lead to a false perception that, regardless of the time of intake of either the PPI and TKI, no DDI occurs. For some TKIs (e.g. axitinib and nilotinib [2]), the question remains whether an alternative time schedule of PPI to TKI intake would lead to an increase or decrease in the TKI absorption, as this is unfortunately rarely studied. Therefore, if no clinically relevant effect is seen in studies while these drugs are taken at the same time, the subsequently drawn conclusion that ‘TKIs and PPIs may be used concomitantly’ should, in our opinion, be replaced by ‘TKIs and PPIs must be used concomitantly’, to guarantee safe use.

When a TKI is administered a few hours after a PPI, the intragastric pH is almost certainly elevated. When no pH-dependent solubility is expected, a study setup where the TKI is administered a few hours after the PPI might be best in order to completely rule out an absorption-based DDI, as was shown for cabozantinib [24].

There is often a hard indication for concomitant use of TKIs and PPIs; however, in clinical practice, clinicians are often advised to avoid the combination [13], often resulting in the patient being deprived of optimal therapy for gastroesophageal reflux disease.

For several TKIs approved by the FDA, the effect on bioavailability has only been studied in vitro, whereas pH-dependent solubility and TKI absorption in vivo is often multifactorial [4]. In this case, only preclinical in vitro data on chemical pH-dependent solubility may not predict the true in vivo effects on bioavailability (e.g. afatinib, regorafenib, sunitinib, trametinib and vemurafenib [2]) of concomitantly used PPIs. If it is stated that there is no significant DDI between a certain TKI and PPI, this should be confirmed in an adequately designed in vivo pharmacokinetic DDI study, or should be based on population pharmacokinetics for DDI assessment using data from large clinical trials.

A lot of discussion has taken place as to whether TKIs and PPIs are really incompatible. There is the interesting suggestion by Ter Heine et al. that when the PPI dose (in this case pantoprazole) is relatively low, erlotinib can be used concomitantly. However, this recommendation is based on a single case study, and solid pharmacokinetic data provided in the FDA assessment report stated otherwise (mentioning a 46 and 61% decrease in erlotinib area under the concentration–time curve [AUC] and maximum concentration [C _max], respectively) [2, 25]. Although many pharmacokinetic DDI studies have already been conducted and have been published in either an EMA/FDA assessment report or scientific literature, clear advice on the management of the DDI between PPIs and TKIs is rarely given. Studies on alternative time schedules of PPI to TKI intake to completely rule out a DDI are also scarcely available, and drawn conclusions on the management (e.g. can be used concomitantly) may not always be 100% solid. Clearly, the investigated effect of a PPI on a certain TKI should always be placed in the context of clinical relevance. For instance, if the effect of a PPI on TKI bioavailability does not influence drug efficacy (e.g. ≤20% decrease), this DDI should be considered as non-significant.

Due to the nocturnal duodenogastric reflux peak, intragastric pH is elevated during sleep [16, 26]. Because of this, the advice to take a TKI without food in the evening concomitantly with a PPI, as was stated in the label of pazopanib, may significantly influence TKI bioavailability [2]. On theoretical grounds (and regardless of PPI use), the bioavailability of TKIs may not be optimal when taken ante noctem and should be avoided accordingly. Furthermore, patients receiving TKI therapy, especially those 80 years of age and older, might experience achlorhydria with a suboptimal absorption as a result [21]. More research is needed to investigate TKI bioavailability during nighttime sleep, and achlorhydria. Although it may significantly enhance TKI bioavailability, patients are often advised to take a TKI without food. As a result, the management of the DDI between the PPI and TKI with regard to food intake (2 h before and 1 h after TKI intake), in clinical practice, also appears to be challenging. When using pantoprazole instead of other PPIs, TKI pharmacokinetics may be altered through inhibition of drug transporters such as Breast Cancer Resistance Protein (BCRP) and P-glycoprotein (P-gp) [27]. Since many TKIs are substrates for BCRP and/or P-gp, physicians should prescribe pantoprazole with caution, or switch to other PPIs, such as omeprazole, during TKI therapy. Moreover, for these TKIs, results obtained from drug interaction studies with omeprazole may not be extrapolated directly to pantoprazole. More research is needed to explore the clinical significance of the DDI between pantoprazole and TKIs.

Several studies have shown that there is large interpatient variability in the onset of action of PPIs. Moreover, there is also large variability in the onset of action between different PPIs and between brand and generic formulas (inter-PPI variability) [16, 17, 28, 29]. Due to these factors, in theory, the delayed onset of action may be significantly shorter. To completely rule out any interpatient and inter-PPI variability, and to give suitable advice for the management of the DDI between TKIs and all PPIs, TKIs should be taken 2 h before the PPI. Furthermore, PPIs can be administered either as an enteric-coated (e.g. Losec^® or Nexium^®) or instant-release formula (e.g. Zegerid^®). Since the abovementioned delayed onset of action and subsequent window of low intragastric pH is used to manage the DDI between TKIs and PPIs, only the enteric-coated formula should be used.

We recently showed that the intake of erlotinib with an acidic beverage (cola) enhanced bioavailability by almost 40% in patients also taking esomeprazole [30]. Through temporarily lowering the intragastric pH by administering the TKI with cola, the DDI between TKIs and PPIs can be bypassed (partly). In particular, when there is a hard indication for twice-daily use of a PPI, in our opinion cola may be a simple and practical solution to manage the DDI between TKIs and PPIs.

When all pharmacological characteristics and data of either TKIs and PPIs are considered, balanced, practical and safe advice on how to manage this drug combination can be given. Since the intragastric pH is not elevated over the whole 24-h range (as shown in Fig. 1), a target period of low intragastric pH can be used to safely administer the TKI.