Figures
Abstract
Background
Flavopiridol is a cyclin-dependent kinase inhibitor in phase II clinical development for treatment of various forms of cancer. When administered with a pharmacokinetically (PK)-directed dosing schedule, flavopiridol exhibited striking activity in patients with refractory chronic lymphocytic leukemia. This study aimed to evaluate pharmacogenetic factors associated with inter-individual variability in pharmacokinetics and outcomes associated with flavopiridol therapy.
Methodology/Principal Findings
Thirty-five patients who received single-agent flavopiridol via the PK-directed schedule were genotyped for 189 polymorphisms in genes encoding 56 drug metabolizing enzymes and transporters. Genotypes were evaluated in univariate and multivariate analyses as covariates in a population PK model. Transport of flavopiridol and its glucuronide metabolite was evaluated in uptake assays in HEK-293 and MDCK-II cells transiently transfected with SLCO1B1. Polymorphisms in ABCC2, ABCG2, UGT1A1, UGT1A9, and SLCO1B1 were found to significantly correlate with flavopiridol PK in univariate analysis. Transport assay results indicated both flavopiridol and flavopiridol-glucuronide are substrates of the SLCO1B1/OATP1B1 transporter. Covariates incorporated into the final population PK model included bilirubin, SLCO1B1 rs11045819 and ABCC2 rs8187710. Associations were also observed between genotype and response. To validate these findings, a second set of data with 51 patients was evaluated, and overall trends for associations between PK and PGx were found to be consistent.
Conclusions/Significance
Polymorphisms in transport genes were found to be associated with flavopiridol disposition and outcomes. Observed clinical associations with SLCO1B1 were functionally validated indicating for the first time its relevance as a transporter of flavopiridol and its glucuronide metabolite. A second 51-patient dataset indicated similar trends between genotype in the SLCO1B1 and other candidate genes, thus providing support for these findings. Further study in larger patient populations will be necessary to fully characterize and validate the clinical impact of polymorphisms in SLCO1B1 and other transporter and metabolizing enzyme genes on outcomes from flavopiridol therapy.
Citation: Ni W, Ji J, Dai Z, Papp A, Johnson AJ, Ahn S, et al. (2010) Flavopiridol Pharmacogenetics: Clinical and Functional Evidence for the Role of SLCO1B1/OATP1B1 in Flavopiridol Disposition. PLoS ONE 5(11): e13792. https://doi.org/10.1371/journal.pone.0013792
Editor: Ulrich Zanger, Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Germany
Received: May 24, 2010; Accepted: September 27, 2010; Published: November 1, 2010
Copyright: © 2010 Ni et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Leukemia and Lymphoma Society SCOR grant (to JB), the D. Warren Brown Foundation (to JB), NIH/NCI (5 U01 CA76576-07 to MG, 1 R21 CA112947-02 to TL); P01 CA81534-06/PO 10267714; and 5KL2RR025754-02 (PI: Jackson, Trainee: MP). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: A patent has been filed on this method of administering flavopiridol. Inventors on this patent include J.C.B., M.R.G., T.S.L., and J.T.D. It has no financial value now. The remaining authors declare no competing financial interests. The patent does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials.
Introduction
Flavopiridol (Alvocidib, NSC 649890), is a serine/threonine kinase inhibitor that broadly targets cyclin-dependent kinases (CDKs), including the cyclin 9/cyclin T complex (pTEF-b), preventing activation of RNA polymerase II [1]–[2]. Flavopiridol initiates cell cycle arrest [3],[4] and p53-independent apoptosis [5]–[6] through down-regulation of Mcl-1 and X-linked inactivator of apoptosis (XIAP) [7], [8] [9]. These preclinical characteristics provided the rationale for clinical investigation of flavopiridol in chronic lymphocytic leukemia (CLL), as advanced CLL is commonly associated with elevated Mcl-1 and dysfunctional p53, rendering standard treatments such as alkylating agents, fludarabine and rituximab ineffective [10].
Single agent flavopiridol administered with 72-, 24- and 1-hour infusion schedules produced limited activity in hematologic and solid tumor diseases [11], [12], [13], [14]. Phase I and II studies using flavopiridol in combination with other agents utilizing the various schedules obtained mixed results, although partial and complete responses in these trials indicated potential synergy of flavopiridol with chemotherapy [15]. We previously reported overall response rates of 40–50% in patients with refractory CLL when flavopiridol was administered as a single agent using a pharmacokinetically (PK)-directed schedule [16], [17]. A phase II registration trial is underway for unmet need in refractory CLL patients using this PK-directed schedule.
The activity of the PK-directed schedule in CLL, compared to that of the previously evaluated schedules, clearly indicted the importance of flavopiridol PK for clinical activity, and associations were in fact observed between PK and clinical outcomes, including response, cytokine release syndrome (CRS) and tumor lysis syndrome (TLS) [17]. However, a substantial amount of variability in PK, as well as in response and toxicity, was unexplained by demographic, patient and disease characteristics. We therefore sought to determine the role of pharmacogenetic factors in flavopiridol PK and treatment outcomes within this patient population.
Flavopiridol elimination occurs via excretion and metabolism and is known through in vitro studies to be influenced by the multi-drug resistance protein-2 (MRP2, ABCC2) [18], [19] and the breast cancer resistance protein (BCRP, ABCG2) [20], [21], [22], [23], [24], which contribute to biliary excretion of both parent drug and glucuronide metabolites. Glucuronide conjugation to the 5- and 7-hydroxy positions of flavopiridol by uridine diphosphate glucuronosyltransferase isoforms 1A1 and 1A9 (UGT1A1 and UGT1A9, respectively) accounts for the majority of metabolic transformation of flavopiridol [25], [26]. Polymorphic diversity in these and other genes may influence flavopiridol disposition, activity and toxicity in a manner similar to irinotecan disposition [27], [28]. Limited polymorphism effects on flavopiridol interactions have been reported, including a lack of observed effects on clinical PK [29] and in vitro substrate specificity [30]. Although polymorphisms were not directly evaluated by Innocenti and colleagues, their clinical report suggested flavopiridol∶metabolite ratio as a possible predictor of diarrhea with flavopiridol treatment and provided a rationale for evaluation of a genetic link with UGT isoforms [31].
In this report, we present pharmacogenetic (PGx) data for drug metabolizing enzymes and transporters (DMET) in a subset of 35 patients treated in a phase I study of a PK-derived 4.5-hour dosing schedule of single-agent flavopiridol in relapsed CLL. These data comprise a focused analysis of candidate genes known through in vitro studies to interact with flavopiridol, as well as a broader exploratory evaluation of additional DMET genes. The results indicate a novel link between flavopiridol PK and SLCO1B1, as well as functional evidence for OATP1B1 (the organic anion transporting polypeptide 1B1 protein product of SLCO1B1) transport of flavopiridol and its glucuronide metabolite. Preliminary analysis of these associations in a second dataset comprising 51 patients provided additional support for the validity of associations between PK, transporter and UGT1A1 genes and their potential clinical relevance. Importantly, pharmacogenetic factors explain a significant portion of inter-patient variability and improves the accuracy of a developing population PK model for this agent.
Methods
Patients
Ethics Statement.
Samples were obtained from patients who provided informed written consent and were enrolled on clinical protocol NCI-5746 (NCT00058240, ClinicalTrials.gov). The sample collection and analyses reported in this study were outlined in the clinical protocol, as approved by The Ohio State University Institutional Review Board (IRB) and in accordance with the principles expressed in the Declaration of Helsinki. Patient demographics and disease characteristics, as well as clinical outcomes and PK results, were reported previously [17]. DNA was obtainable from peripheral blood mononuclear cells (PBMCs) from 35 of the 52 patients on study. Demographics, baseline labs and disease characteristics for these patients are presented in Table 1.
Pharmacogenetics
Genes known from in vitro studies to specifically affect flavopiridol disposition include UGT1A1, UGT1A9, ABCC2 and ABCG2. These and an additional set of 52 other genes that code for metabolic enzymes and transporters commonly involved in drug disposition were evaluated for the presence of known polymorphisms by direct sequencing and with a high-throughput SNPlex assay (Applied Biosystems) [32]. Genomic DNA was extracted from patient PBMCs and used to sequence promoter TATA box regions of UGT1A1 and UGT1A9 and specifically to identify the presence of the UGT1A1*28 and UGT1A9*22 polymorphisms. Primers for UGT promoter sequencing were as follows: 1A1-forward, 5′ – GGAAGTACTTTGCTGTGTTCACTCAAG; 1A1-reverse, 5′ – AAGGGTCCGTCAGCATGACATCAA; 1A9-forward, 5′ – CTTAACATTGCAGCACAGGGCATGTT; 1A9-reverse, 5′ – CGTACTTGTGCTTTCCATTGAGCATGGG. All sequence data was deposited in GenBank. To validate sequence results of the TATA box regions, single nucleotide polymorphism (SNP) specific primers were used in a fluorescence/gel-migration assay. Polymorphism-specific primers were utilized in the SNPlex assay to identify the presence of 189 other SNPs in drug metabolizing enzymes and transporters. A complete list of the genes and SNPs evaluated was presented previously [32].
Population Pharmacokinetic Modeling and Validation
A population PK (popPK) model for 50 patients on study was previously reported [17]. This model served as the starting point to evaluate SNPs and other covariates for the subset of 35 patients with PGx data using NONMEM VI (Icon, Hanover, MD). With first order conditional estimation, a base structural model was built with proportional and additive residual error considering both between-subject variability (BSV) and between-occasion variability (BOV) on PK parameters, since PK data was available on two occasions from patients who received escalated doses.
Initial screening of the genetic data was completed with the allelic association test in HelixTree software (Golden Helix, Bozeman, MT) which produced unadjusted p-values for correlation with each of the base model-predicted PK parameters. Of the 189 SNPs (191 total including the UGT1A1*28 and UGT1A9*29 promoter polymorphisms from direct sequencing), 16 SNPs in 4 genes known previously to interact with flavopiridol (UGT1A1/9, ABCC2 and ABCG2), were retained for further analysis. From the remaining 175 total SNPs in 52 genes that were known to be involved in drug disposition, we filtered out from consideration SNPs with p-values>0.05 and minor allele frequencies less than 0.15. For direct fitting of selected polymorphisms to PK parameters, SNPs were converted to dichotomous categorical variables whereby the heterozygous category (M/m) for the major (M) and minor (m) alleles was combined with either the major or minor allele category as previously reported [33], [34].
Demographic, baseline laboratory covariates, and the total of 43 SNPs from above screening were then introduced with general additive modeling (GAM) and visual inspection of diagnostic plots using R v.2.9.0 and Xpose 4.0.4. These covariates identified by visual inspection and GAM as potentially meaningful (according to the Akaike information criterion, AIC) were introduced into the population model for further evaluation of the SNP associations. Using GAM, four sets of covariates including SNPs were retained for further evaluation in a full structural model.
For completeness, each individual covariate was fit to the structural model using the power (equation 1) or fractional change (equation 2) models,(1)
(2)where θi is the individual PK parameter estimate, θpop is the population parameter estimate for the typical individual, and ηi is the sum of BSV and BOV parameters approximately log-normally distributed with standard deviations ω about a mean of 0. CONji is the value of the continuous covariate j for individual I, CONj-med is the population median value of covariate j for all individuals, CATji is the value of the categorical covariate j for individual i, and Θj is an estimated parameter. All covariates were evaluated in this way with the full 50-patient dataset, except for the SNPs which were evaluated after removal of individuals for whom no genetic data was available.
To identify a final multivariate model for all of the PK parameters simultaneously, we used selection methods that depend on changes in the objective function value. Using a cutoff of p≤.05, which corresponded to a minimum decrease of the objective function value (OFV) of 3.84 upon inclusion of each individual covariate based on the likelihood-ratio test, multivariate analysis with forward stepwise inclusion, backward stepwise deletion, and forward selection followed by backward elimination were applied to finalize the covariate model. Model selection in multivariate analysis was based on 1) minimum reduction of OFV by 3.84 (P≤0.05) for forward inclusion, 2) reduction of OFV by 6.64 or greater (P≤0.01) for backward deletion, and 3) decrease in residual error and/or BSV of the evaluated PK parameter. Interaction between covariates was examined by scatter plot of covariate values and change of OFV between models with single or combined covariates.
For bias evaluation the final model was fitted to replicate datasets using the bootstrap resampling technique in Wings for NONMEM [35], and PK parameter estimates and random effects for each of the replicate datasets were obtained. Two hundred replicate bootstrap datasets were generated and used for evaluation of parameter estimate precision. Model precision was evaluated by comparing mean parameter values and 95% bootstrap confidence intervals (CI) of the replicates with NONMEM outputs.
Cloning and Expression of SLCO1B1.
The human SLC01B1 gene was isolated from the HEP-G2 cell line using methods similar to those previously published [36]. Briefly, RNA was extracted using Trizol Reagent and each half of the gene was PCR-amplified and cloned into the pcr-blunt II Topo vector (Invitrogen, Carlsbad, CA). The second half of the gene was digested with NotI and SnaBI and combined with the first half in the pcr-blunt II topo vector. The full length clone was then digested with KpnI and NotI and transferred into pcDNA 3.1 (+) (Invitrogen). Base pairs that were different from the reference sequence (NCBI Genbank ID, BC114376) were mutated using QuickChange (Stratagene, La Jolla, CA) via the manufacturer's protocols to match the reference and non-synonymous polymorphic variant sequences. Gene orientation and homology of reference, rs11045819 (T155P), rs2306283 (D130N), and rs4149056 (V174A) SLCO1B1 SNPs were confirmed through direct full length sequencing of clones prior to experimentation. A list of primers used for cloning, sequencing and mutagenesis (for introduction of nonsynonymous SNPs) is presented in Table 2.
Flavopiridol and Flavo-G Uptake Assays.
Flavopiridol was obtained from the National Cancer Institute Cancer Therapy Evaluation Program. Flavopiridol-glucuronide (flavo-G) was extracted from patient urine and purified. Total urine through 24-hours after the start of flavopiridol dosing was collected from patients enrolled in an IRB-approved phase II protocol (NCI-7000). Octanol extraction followed by C-18 solid phase extraction was employed to isolate flavo-G from flavopiridol and other urine components. To quantify recovered flavo-G and verify purity, samples were incubated with β-Glucuronidase as previously described [19] and quantified via LC-MS/MS analysis with methods modified from those previously reported [37]. Purity was estimated at >95% via mass and UV chromatography.
Madin-Darby canine kidney (MDCK-II) and human embryonic kidney (HEK-293) cells, purchased from ATCC (Manassas, VA), were cultured in 5% CO2 at 37°C in Dulbecco's modified Eagle's medium supplemented with L-glutamine, 10% FBS, 100 units/ml penicillin, and 100 µg/ml streptomycin. Plates (24-well) were seeded with 2×105 cells/well and transfected with the reference and polymorphic OATP1B1-containing vectors using FuGENE®6 Transfection Reagent per the manufacturer's protocols (Roche). Transfection efficiency and gene expression were evaluated with GFP vectors and real-time PCR, respectively. Forty-eight hours post-transfection, cells were dosed with 10 µM flavopiridol or flavo-G in OptiMEM® I (Invitrogen, Carlsbad, California) incubation media containing 4% bovine serum albumin for 10 and 30 minutes, respectively, at 37°C. After incubation, cells were washed with 4°C versene, trypsinized, and resuspended in 37°C versene at a total volume of 350 ul. A 150 µL aliquot of the cell suspension was lysed with 30 µl 6% Triton X-100 in PBS, and protein concentration was determined using Pierce® BCA protein assay (Thermo Scientific, Rockford, IL). The remaining 200µL cell suspensions were precipitated with 1mL, 4°C acetonitrile containing 200nM genistein, followed by vortex mixing and centrifugation at 16,000g for 10 min. The supernatant (1mL) was removed and dried in a vacuum concentrator then samples were resuspended in 150µL 95∶5 water∶acetonitrile plus 0.1% acetic acid, vortexed, and centrifuged. Supernatants (100 µL) were analyzed using liquid chromatography and mass spec conditions as described previously [38]. SN-38 (7-ethyl-10-hydroxycamptothecin, Sigma, St Louis, MO) and lenalidomide (obtained by extraction from donated patient capsules as previously reported [39]) were used as positive and negative control, respectively. Analytical methods for LC-MS/MS quantification lenalidomide was used as previously published [38]. For SN-38 LC-MS/MS quantification, a previously published method was modified and partially validated [40]. Calculated uptake velocities were normalized to total protein in each well, and results were compared against empty vector controls using Student's t-test.
Evaluation of Associations Between PGx, PK and Outcomes.
To identify associations with genetics, the means of flavopiridol and flavo-G [17] PK parameters were compared based on SNP genotypes using Student's t-test and analysis of variance (ANOVA). For comparisons of PGx and clinical outcomes, SNP genotypes and response or toxicity grading was evaluated using Fisher's exact test. P-values were not further adjusted for multiple testing.
Results
Pharmacogenetic Analysis
DNA of adequate quality and quantity for analysis was available from 35 of the 52 patients treated on study, and both SNPlex and direct sequencing data were generated for these individuals (see Table 1 for demographics and pre-treatment characteristics of this patient subset). In addition to the 4 genes of interest, 17 genes and 27 SNPs met our criteria for further study (see Table 3). Among these, SLCO1B1 was selected for further evaluation given its known physiological relevance for a broad set of drugs and its potential role of transporting flavopiridol into liver for subsequent metabolism and excretion.
PK Modeling
Base structural model.
A total of 577 plasma concentration-time values from 50 of 52 patients in the clinical study were included for PK data analysis using two-compartmental kinetics with first-order elimination, as described previously [17]. Based on this previous analysis, BSV was initially assumed on each parameter in the model. However, removal of BSV for V1 did not significantly change OFV (increase of 1 unit). After removal of BSV on V1, addition of BOV on single or multiple parameters was tested in the model. Addition of BOV on clearance (CL) resulted in the most significant change in OFV. The final base model thus included BSV on CL, inter-compartmental clearance (Q) and volume of peripheral compartment (V2), and BOV on CL. Base model parameter estimates and random effects are presented in Table 4.
Covariate model.
Demographic and lab covariates from GAM screening were subsequently evaluated in the base model with univariate analysis (see Table 5). With the modified random error in the base model, bilirubin was indicated as the most significant covariate with a direct positive effect on Q. Addition of bilirubin decreased OFV by 8.07 and BSV (on Q) from 63.64% to 55.41% (see Figure 1).
Regression analysis; Q = 11.21 * Bilirubin level+0.7422 (P<0.01).
To evaluate genetic covariates, the dataset was reduced by removing patients for whom no genetic data was available. This reduced the dataset from 50 to 35 subjects and from 577 to 388 records. Univariate analysis on genetic covariates with this dataset identified the 14 most significant covariate-parameter relationships (see Table 6). Using the selection methods discussed above, we retained in all of the final models SLCO1B1 rs11045819 and ABCC2 rs8187710. The relationships between these SNPs and their respective base model-estimated PK parameters are displayed in Figure 2.
Box plots represent the scatter of individual V1 estimates vs. SLCO1B1 rs11045819 (Panel A), CL estimates vs. SLCO1B1 rs4149056 (Panel B), and V2 estimates vs. ABCC2 rs8187710 (Panel C). For rs11045819, data is displayed with V1 estimates using BSV on V1.
Functional Validation of SCL01B1's Role in Flavopiridol and Flavo-G Uptake
Although associations between PK and SNPs in ABCC2 may have been expected due to known in vitro interactions of MRP2 and flavopiridol, no such evidence existed prior to this study for the role of SLCO1B1/OATP1B1 in flavopiridol transport. To determine if the observed associations between flavopiridol PK and SLCO1B1 PGx were functionally relevant for flavopiridol disposition, we measured uptake of flavopiridol and flavo-G in cells transfected with SLCO1B1. Transfection efficiencies were estimated at approximately 60% using GFP-containing control vectors. Mean uptake velocities were 261±12 fmol/mg protein/10 min and 38±10 fmol/mg protein/30 min for flavopiridol and flavo-G, respectively, in MDCK-II cells. Flavopiridol transport rates in HEK-293 cells were approximately 2–3 fold higher than in MDCK-II cells suggesting its transport may be affected by the different membrane and transporter compositions in the two cell lines. Flavo-G transport rates were similar in both cell lines. Figure 3 shows normalized uptake velocities of flavopiridol and flavo-G in both HEK293 and MDCK-II cells transfected with either SLCO1B1 or empty vector. Expression of the transfected SLCO1B1 gene was verified with real-time PCR (data not shown). Functional expression of OATP1B1 was verified by evaluating uptake of a positive control substrate, SN-38 [41]. A second agent, lenalidomide, was used as a negative control substrate. Total intracellular accumulation and Initial transport velocities of SN-38, flavopiridol, and flavo-G were significantly increased in HEK293 and MDCK-II cells transiently transfected with SLCO1B1, compared to empty control vectors, whereas no increased uptake was shown for lenalidomide.
The bar graph indicates means + SD for triplicate determinations of 10 µM flavopiridol, flavo-G, SN-38 and lenalidomide uptake rates in cell lines (HEK-293 or MDCK-II) transfected with empty control vector or vector cloned with the OATP1B1 gene (SCLO1B1). Incubations with flavo-G were for 30 min., and all other drugs were for 10 min. Transport rates are expressed as percentages normalized to empty vector control. * p<.05, ** p<0.001,Student's t-test.
We further evaluated the uptake of flavopiridol in MDCK-II cells transfected with the SLCO1B1 polymorphic variants with amino acid changes relative to the reference sequence (i.e. nonsynonymous SNPs). These included rs11045819 (T155P), rs2306283 (D130N), and rs4149056 (V174A). The results indicated significant decreases in flavopiridol transport rates (t-test p-value<0.05) for the rs11045819 and rs4149056 variants, but the transport rate of the rs2306283 polymorph was similar to that in the reference SLCO1B1 transporter. Figure 4 displays these results.
The bar graph indicates means + SD for triplicate determinations of 10 µM flavopiridol uptake rates in MDCK-II cells transfected with empty control vector or vector cloned with the reference or polymorphic SLCO1B1 genes. All incubations were for 10 min. Variants are indicated with respect to their amino acid change; T155P = rs11045819, D130N = rs2306283, V174A = rs4149056. Transport rates were normalized to empty vector control. Differences in uptake rates were compared to the reference OATP1B1 transporter. * p<.05, ** p<0.01, Student's t-test.
Final PK Model Determination
To arrive at a final model with significant PGx, lab and demographic covariates, the reduced data set was used to reevaluate the demographic and lab covariates retained after univariate analysis with the full dataset (see Table 6). Bilirubin effect on Q was apparent and remained the most significant demographic or lab covariate with the reduced dataset. However, significant effects of blood urea nitrogen on CL and alanine aminotransferase on V2 that were observed in the full dataset disappeared with use of the reduced dataset. The remaining four significant demographic or lab covariates and the two significant SNPs (SLCO1B1 rs11045819 and ABCC2 rs8187710) were then evaluated by forward addition and backward deletion. Only the two SNPs and bilirubin were retained as significant covariates with the reduced dataset. Relative to the base model, the final model displayed an OFV reduction of 34.11. Table 7 lists the final model parameter estimates.
The bootstrap method was used to assess bias in the final covariate model. From the reduced data set, 200 replicate data sets were generated and used for the evaluation of the stability of the final covariate model. Table 8 lists the results of the bootstrap procedure, presented as mean and 95% bootstrap confidence intervals of the parameter estimates and random effects of the final model. Mean estimated parameter values from the bootstrap were within 11% of the parameter estimates of the original data set indicating reliability in the developed model [42].
Evaluation of Flavo-G and Bilirubin vs. PGx
Flavo-G PK parameter estimates reported previously in 27 pts on study [17] were evaluated to identify PGx associations. The trends observed indicated that fewer TA repeats in the UGT1A1 promoter were weakly associated with lower flavo-G Cmax (2.17+/−0.99 vs. 5.08+/−4.12 µM) and AUC (26.43+/−30.26 vs. 66.16+/−64.37 hr* µM) (p = .057 and .077, respectively). Only two transporter SNPs were associated with flavo-G PK. The SLCO1B1 rs2306283 SNP correlated with flavo-G plasma concentrations (the total time in hours flavo-G concentrations were below 1.5 µM, p = .019), and the ABCG2 rs1564481 SNP was associated with flavo-G AUC (p = .050). We also evaluated flavopiridol AUC with respect to PGx, and one trend was observed with the ABCG2 rs2231142 SNP (p = 0.08). Bilirubin levels were not associated with SNPs in UGT1A1, but the SLCO1B1 rs3829310 minor C allele was associated with higher baseline bilirubin (p = .011). These relationships are presented in Figure 5.
Flavo-G PK parameter estimates from 27 patients were evaluated for relationships with PGx. Fewer TA repeats in the UGT1A1 promoter were weakly associated with lower flavo-G Cmax (Panel A) and AUC (Panel B). For SLCO1B1, the rs2306283 SNP correlated with flavo-G plasma concentrations (the total time flavo-G plasma concentrations were below 1.5 µM, p = .019; Panel C, one outlier removed). For ABCG2, the rs1564481 SNP was associated with flavo-G AUC (p = .050; Panel D) and the rs2231142 SNP was associated with flavopiridol AUC (p = 0.08, Panel E). The SLCO1B1 rs3829310 minor C allele was associated with higher baseline total bilirubin (p = .011; Panel F). For plots A and B, the x-axis indicates the number of promoter TA repeats for both gene copies (6.7 = 6 and 7 TA repeats; 7 = 7 TA repeats for each gene copy; 7.8 = 7 and 8 TA repeats; 8 = 8 TA repeats for each gene copy).
Correlations of PGx and Outcomes
To determine if the presence of polymorphisms was significantly associated with outcomes, clinical response and the primary toxicities (TLS, diarrhea and CRS) were evaluated against PGx. Results indicated SNPs in SLCO1B1 and ABCG2, but not in UGT1A1/9 or ABCC2, were associated with response. SNPs significantly associated with improved response included the SCLO1B1 rs11045819 (CC genotype, p = .041) and ABCG2 rs1564481 (T allele, p = .037). The SLCO1B1 rs2306283 SNP alone did not meet the significance criteria (T allele, p = .061), but the combination of this and the SLCO1B1 rs11045819 SNP was significant (p = .007). No SNPs met the significance criteria when compared against TLS, although the most closely associated SNP was SLCO1B1 rs4149056 (C allele, p = .056). Similaraly, the most closely associated SNPs with diarrhea and CRS were SCLO1B1 rs2306283 (T allele, p = .055) and ABCG2 rs1564481 (T allele, p = .074).
Validation of findings with a Phase II Study
To evaluate the validity of the findings from the 35-patient dataset, a second dataset was evaluated for associations between PGx and PK. The validation set comprised data from 66 CLL patients who were treated with the same flavopiridol dosing regimen in a separate phase II study (NCI-7000, NCT00098371). As with the phase I study, enrolled patients provided informed written consent, and plasma and PBMC samples were obtained according to The Ohio State University IRB approved protocol. Clinical results of this study were reported previously [43]. Plasma and DNA samples from this study were analyzed using the methods described above to generate flavopiridol and flavo-G concentration-time data, PK parameter estimates, and PGx data for each patient. Covariates found to be significantly associated in univariate analysis with the phase I dataset, including demographic and baseline laboratory covariates and SNPs in UGT1A1, ABCC2, ABCG2 and SLCO1B1, were compared with the phase II pharmacokinetic data.
Significant associations and trends were observed with the validation dataset. For flavopiridol PK, these included significant associations between the SCLO1B1 rs2306283 SNP and Q (p = 0.02) and between both the ABCG2 rs2622624 and rs3114018 SNPs and CL and V1 (rs2622624, p = 0.008 and 0.04; rs3114018, p = 0.004 and 0.006 for CL and V1, respectively). The SLCO1B1 rs3829310 SNP was weakly associated with flavopiridol CL and AUC (p = 0.08 and 0.08, respectively). The ABCG2 rs2231142 SNP showed a similar trend with AUC (p = .08). For flavo-G, significant associations included Cmax and AUC with the UGT1A1*28 promotor SNP (p = 0.02 and 0.04, respectively). Bilirubin levels were significantly associated with the SLCO1B1 rs3829310 and SLCO1B1 rs2291075 SNPs (p = 0.02 and p = 0.04, respectively). Figure 6 displays a subset of these relationships.
Flavopiridol and flavo-G PK parameter estimates from the phase II study was evaluated for relationships with PGx. Presented are flavopiridol CL associations with ABCG2 rs2622624 (p = 0.008, Panel A) and rs3114018 (p = 0.004, Panel B); UGT1A1*28 (promoter) polymorphisms associated with flavo-G Cmax (p = 0.02, Panel C) and AUC (p = 0.04, Panel D); the ABCG2 rs2231142 SNP was weakly associated with flavopiridol AUC (Panel E, p = .08); For plots C and D, the x-axis indicates the number of promoter TA repeats for both gene copies (6.7 = 6 and 7 TA repeats; 7 = 7 TA repeats for each gene copy; 7.8 = 7 and 8 TA repeats; 8 = 8 TA repeats for each gene copy).
Discussion
Safe and effective use of flavopiridol will require a thorough understanding of the factors influencing the onset of hyper-acute tumor lysis syndrome and inter-individual variability in response. We previously reported that at least some of the variability in outcomes may be explained by PK, yet significant portions of this variability remain unexplained. In this first evaluation of pharmacogenetics using the flavopiridol PK-derived schedule, we identified a novel flavopiridol-transporter interaction and confirmed its functional relevance in vitro. Furthermore, a subset of the polymorphisms evaluated in this study was significantly associated with outcomes. The striking activity of this dosing schedule in CLL and flavopiridol's emerging activity with combination chemotherapy in other diseases demand these pharmacogenetic and other factors be identified and further characterized.
To expand on our previous evaluation of flavopiridol using the PK-directed schedule, we sought to characterize the role of PGx in flavopiridol disposition. We combined focused and exploratory approaches, whereby PK data from a phase I dataset was evaluated against SNPs in candidate genes previously shown to metabolize or transport flavopiridol in in vitro studies, as well as SNPs in genes not known to interact with flavopiridol. The candidate genes evaluated included ABCC2, ABCG2, UGT1A1 and UGT1A9. Indeed, at least one SNP in each of these genes was significantly associated in univariate analysis with flavopiridol and flavo-G PK. In multivariate analysis with the phase I dataset, a single SNP in ABCC2 (rs8187710) remained significant. This is a non-synonymous SNP resulting in a C1515Y alteration and is part of a haplotype with the rs17222723 SNP (also a non-synonymous SNP with a V1188E residue change). This haplotype has been reported to be associated with PBMC accumulation of lopinavir [44], susceptibility to nonalcoholic fatty liver disease [45], and doxorubicin-induced cardiotoxicity [46]. This is a relatively infrequent SNP, and only 5 of 35 and 4 of 51 individuals were genotyped for the polymorphic A allele in the phase I and II datasets, respectively. Significant associations between this SNP and PK parameters were not observed in the phase II dataset.
Although UGT1A1 SNPs were not included in the final popPK model, both flavopiridol and flavo-G were correlated with the UGT1A1*28 promoter polymorphism, and fewer TA repeats (6 and 7) were associated with lower flavo-G concentrations and AUC in both the phase I and II datasets. One of the most broadly studied substrates of UGT1A1 and 1A9 is irinotecan/SN-38, which shares metabolic pathways and has a similar toxicity profile (diarrhea) with flavopiridol. Interestingly, the *3 polymorphism of 1A9 was previously shown to be associated with SN-38 but not flavopiridol disposition [30]. Innocenti and colleagues measured ratios of flavo-G∶flavopiridol and identified an indirect relationship between flavo-G levels and diarrhea [31]. Zhai and colleagues reported PK and UGT1A1 polymorphism data in 49 patients with refractory neoplasms treated with 1-hour IV flavopiridol [29]. However, their results indicated no correlation of the TATA box promoter UGT1A1*28 genotype with flavopiridol PK or diarrhea severity. While we did not identify correlations with diarrhea for flavopiridol and flavo-G PK [17], we observed one association with PGx and diarrhea.
The 35-patient dataset evaluated in this study was small with regard to exploratory PGx, and therefore an additional dataset from 51 patients was used to evaluate the validity of the findings. While the associations identified in each dataset were not identical, similar trends were observed between PK parameters and SNPs in the candidate genes. Furthermore, the clinical associations we observed with SLCO1B1 were functionally validated in vitro. SLCO1B1 is important for the disposition of statin drugs [47] and various anti-cancer agents including irinotecan [48]. It was recently highlighted by the International Transporter Consortium as one of the seven most relevant transporters for drug development due to its broad substrate specificity, potential for drug-drug interactions, and clinically relevant polymorphisms [49]. Importantly, functional transport data indicated this gene may play a role in hepatic uptake of both flavopiridol and flavo-G. All five of the SLCO1B1 SNPs evaluated in the phase I dataset were significant in univariate analysis, and two of these (rs11045819 on V1 and rs4149056 on CL) were the strongest associations observed of any covariates evaluated for flavopiridol PK in multivariate analysis. These are non-synonymous SNPs affecting the amino acid sequence in OATP1B1. Previous studies indicated these variants were associated with reduced uptake activity of the OATP1B1 substrates estrone-3-sulfate, estradiol-17β-d-glucuronide, atorvastatin, cerivastatin, pravastatin, the SN-38 metabolite of irinotecan and rifampicin in [50]–[51]. These reports are consistent with our in vitro data which indicated these SNPs significantly reduced flavopiridol transport, while the other nonsynonymous SNP evaluated (rs2306283) had no measureable effect. Interestingly, this was the only SLCO1B1 SNP significantly associated with flavo-G PK. A recently reported study in MDCK-II cells with this SNP indicated increased transport of bromosulfophthalein and decreased transport of cholyltaurine [51]. Collectively, the data may suggest that the altered protein sequence affects OATP1B1 transport of flavopiridol and flavo-G differently. Further in vitro evaluations of these and other SNPs will be required to characterize their functional impact with respect to flavopiridol and flavo-G disposition. Additionally, the data presented suggests flavopridol may be a weak substrate of SLCO1B1 in comparison with SN-38 under the evaluated experimental conditions. However, characterization of the kinetics of flavopiridol and flavo-G transport via SLCO1B1 will be necessary for understanding the full impact this gene has on overall flavopiridol disposition.
The observed associations between PGx and outcomes in this study are encouraging as potential indicators for patient response. While no SNP met the significance criteria for association with TLS, the polymorphism most closely associated with this toxicity was SLCO1B1 rs4149056 (ANOVA p = .056). The strength of the associations between PK, outcomes and multiple SNPs in SLCO1B1 and the confirmation of functional OATP1B1 transport of both flavopiridol and flavo-G support the potential for this gene to be clinically relevant in patients receiving flavopiridol treatment. Overall, analysis of the phase II dataset revealed significant associations with the candidate genes that were supportive of the findings from the phase I dataset. In particular, trends in flavopiridol AUC with respect to the ABCG2 rs2231142 SNP and flavo-G Cmax and AUC with respect to the UGT1A1*28 polymorphism were strikingly similar between the two datasets (see Figures 5 and 6). Again, further validation of these associations will be essential in larger datasets.
This work modifies and develops further our previously reported population model for the PK-directed schedule of flavopiridol. We demonstrate the most significant covariates in the phase I dataset to be polymorphisms in two transporter genes, SCLO1B1 and ABCC2, and the phase II validation set revealed significant associations with polymorphisms in ABCG2. While larger data sets are necessary to fully characterize the clinical impact of polymorphisms in SLCO1B1 and other genes on flavopiridol PK, our findings are supportive of a clinically significant role for PGx in flavopiridol disposition. The composite data to date suggests inter-individual variability in outcomes from flavopiridol therapy will be due to a combination of pharmacokinetics, pharmacogenetics and potentially other factors related to tumor cell sensitivity to flavopiridol's cytotoxic effects. Inter-individual variability is of particular concern for chemotherapeutic drugs with relatively narrow therapeutic windows. The developing model for flavopiridol PK may ultimately help to explain this variability by incorporating pharmacogenetic and other significant factors. With sufficient data and validation, this model may ultimately serve as a tool for predicting PK and associated outcomes in individuals prior to therapy. If sufficiently robust, such a tool would be clinically useful in identifying individuals likely to respond and/or experience severe TLS or other toxicities upon receiving flavopiridol. As a phase II registration study of flavopiridol in relapsed CLL nears completion and additional combination studies in hematologic and solid tumor diseases begin accruing patients, further exploration and characterization of the factors influencing inter-individual variability in outcomes from therapy will be necessary to insure the broad and safe clinical use of this drug.
Author Contributions
Conceived and designed the experiments: ZD ACP AJJ KLF TSL JTD JCB WS MAP. Performed the experiments: WN ZD ACP SA KLF MAP. Analyzed the data: WN JJ ZD ACP XL DJ MAP. Contributed reagents/materials/analysis tools: JTD JCB WS MRG MAP. Wrote the paper: WN JJ TSL XL DJ JCB WS MRG MAP.
References
- 1. Senderowicz AM, Sausville EA (2000) Preclinical and clinical development of cyclin-dependent kinase modulators. J Natl Cancer Inst 92: 376–387.
- 2. Carlson B, Lahusen T, Singh S, Loaiza-Perez A, Worland PJ, et al. (1999) Down-regulation of cyclin D1 by transcriptional repression in MCF-7 human breast carcinoma cells induced by flavopiridol. Cancer Res 59: 4634–4641.
- 3. Carlson BA, Dubay MM, Sausville EA, Brizuela L, Worland PJ (1996) Flavopiridol induces G1 arrest with inhibition of cyclin-dependent kinase (CDK) 2 and CDK4 in human breast carcinoma cells. Cancer Res 56: 2973–2978.
- 4. Worland PJ, Kaur G, Stetler-Stevenson M, Sebers S, Sartor O, et al. (1993) Alteration of the phosphorylation state of p34cdc2 kinase by the flavone L86-8275 in breast carcinoma cells. Correlation with decreased H1 kinase activity. Biochem Pharmacol 46: 1831–1840.
- 5. Decker RH, Dai Y, Grant S (2001) The cyclin-dependent kinase inhibitor flavopiridol induces apoptosis in human leukemia cells (U937) through the mitochondrial rather than the receptor-mediated pathway. Cell Death Differ 8: 715–724.
- 6. Parker BW, Kaur G, Nieves-Neira W, Taimi M, Kohlhagen G, et al. (1998) Early induction of apoptosis in hematopoietic cell lines after exposure to flavopiridol. Blood 91: 458–465.
- 7. Gojo I, Zhang B, Fenton RG (2002) The cyclin-dependent kinase inhibitor flavopiridol induces apoptosis in multiple myeloma cells through transcriptional repression and down-regulation of Mcl-1. Clin Cancer Res 8: 3527–3538.
- 8. Wittmann S, Bali P, Donapaty S, Nimmanapalli R, Guo F, et al. (2003) Flavopiridol down-regulates antiapoptotic proteins and sensitizes human breast cancer cells to epothilone B-induced apoptosis. Cancer Res 63: 93–99.
- 9. Byrd JC, Shinn C, Waselenko JK, Fuchs EJ, Lehman TA, et al. (1998) Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53. Blood 92: 3804–3816.
- 10. Wattel E, Preudhomme C, Hecquet B, Vanrumbeke M, Quesnel B, et al. (1994) p53 mutations are associated with resistance to chemotherapy and short survival in hematologic malignancies. Blood 84: 3148–3157.
- 11. Senderowicz AM, Headlee D, Stinson SF, Lush RM, Kalil N, et al. (1998) Phase I trial of continuous infusion flavopiridol, a novel cyclin-dependent kinase inhibitor, in patients with refractory neoplasms. J Clin Oncol 16: 2986–2999.
- 12. Lin TS, Howard OM, Neuberg DS, Kim HH, Shipp MA (2002) Seventy-two hour continuous infusion flavopiridol in relapsed and refractory mantle cell lymphoma. Leuk Lymphoma 43: 793–797.
- 13. Rudek MA, Bauer KS Jr, Lush RM 3rd, Stinson SF, Senderowicz AM, et al. (2003) Clinical pharmacology of flavopiridol following a 72-hour continuous infusion. Ann Pharmacother 37: 1369–1374.
- 14. Thomas JP, Tutsch KD, Cleary JF, Bailey HH, Arzoomanian R, et al. (2002) Phase I clinical and pharmacokinetic trial of the cyclin-dependent kinase inhibitor flavopiridol. Cancer Chemother Pharmacol 50: 465–472.
- 15. Schwartz GK, O'Reilly E, Ilson D, Saltz L, Sharma S, et al. (2002) Phase I study of the cyclin-dependent kinase inhibitor flavopiridol in combination with paclitaxel in patients with advanced solid tumors. J Clin Oncol 20: 2157–2170.
- 16. Lin TS, Ruppert AS, Johnson AJ, Fischer B, Heerema NA, et al. (2009) Phase II study of flavopiridol in relapsed chronic lymphocytic leukemia demonstrating high response rates in genetically high-risk disease. J Clin Oncol 27: 6012–6018.
- 17. Phelps MA, Lin TS, Johnson AJ, Hurh E, Rozewski DM, et al. (2009) Clinical response and pharmacokinetics from a phase 1 study of an active dosing schedule of flavopiridol in relapsed chronic lymphocytic leukemia. Blood 113: 2637–2645.
- 18. Jager W, Gehring E, Hagenauer B, Aust S, Senderowicz A, et al. (2003) The role of hepatic Mrp2 in the interaction of flavopiridol and bilirubin: impact on therapy. Int J Clin Pharmacol Ther 41: 610–611.
- 19. Jager W, Gehring E, Hagenauer B, Aust S, Senderowicz A, et al. (2003) Biliary excretion of flavopiridol and its glucuronides in the isolated perfused rat liver: role of multidrug resistance protein 2 (Mrp2). Life Sci 73: 2841–2854.
- 20. Nakanishi T, Karp JE, Tan M, Doyle LA, Peters T, et al. (2003) Quantitative analysis of breast cancer resistance protein and cellular resistance to flavopiridol in acute leukemia patients. Clin Cancer Res 9: 3320–3328.
- 21. Robey RW, Medina-Perez WY, Nishiyama K, Lahusen T, Miyake K, et al. (2001) Overexpression of the ATP-binding cassette half-transporter, ABCG2 (Mxr/BCrp/ABCP1), in flavopiridol-resistant human breast cancer cells. Clin Cancer Res 7: 145–152.
- 22. Doyle LA, Ross DD (2003) Multidrug resistance mediated by the breast cancer resistance protein BCRP (ABCG2). Oncogene 22: 7340–7358.
- 23. Nakanishi T, Doyle LA, Hassel B, Wei Y, Bauer KS, et al. (2003) Functional characterization of human breast cancer resistance protein (BCRP, ABCG2) expressed in the oocytes of Xenopus laevis. Mol Pharmacol 64: 1452–1462.
- 24. Sugimoto Y, Tsukahara S, Ishikawa E, Mitsuhashi J (2005) Breast cancer resistance protein: molecular target for anticancer drug resistance and pharmacokinetics/pharmacodynamics. Cancer Sci 96: 457–465.
- 25. Ramirez J, Iyer L, Journault K, Belanger P, Innocenti F, et al. (2002) In vitro characterization of hepatic flavopiridol metabolism using human liver microsomes and recombinant UGT enzymes. Pharm Res 19: 588–594.
- 26. Hagenauer B, Salamon A, Thalhammer T, Kunert O, Haslinger E, et al. (2001) In vitro glucuronidation of the cyclin-dependent kinase inhibitor flavopiridol by rat and human liver microsomes: involvement of UDP-glucuronosyltransferases 1A1 and 1A9. Drug Metab Dispos 29: 407–414.
- 27. Mani S (2001) UGT1A1 polymorphism predicts irinotecan toxicity: evolving proof. AAPS PharmSci 3: 2.
- 28. Nagar S, Blanchard RL (2006) Pharmacogenetics of uridine diphosphoglucuronosyltransferase (UGT) 1A family members and its role in patient response to irinotecan. Drug Metab Rev 38: 393–409.
- 29. Zhai S, Sausville EA, Senderowicz AM, Ando Y, Headlee D, et al. (2003) Clinical pharmacology and pharmacogenetics of flavopiridol 1-h i.v. infusion in patients with refractory neoplasms. Anticancer Drugs 14: 125–135.
- 30. Villeneuve L, Girard H, Fortier LC, Gagne JF, Guillemette C (2003) Novel functional polymorphisms in the UGT1A7 and UGT1A9 glucuronidating enzymes in Caucasian and African-American subjects and their impact on the metabolism of 7-ethyl-10-hydroxycamptothecin and flavopiridol anticancer drugs. J Pharmacol Exp Ther 307: 117–128.
- 31. Innocenti F, Stadler WM, Iyer L, Ramirez J, Vokes EE, et al. (2000) Flavopiridol metabolism in cancer patients is associated with the occurrence of diarrhea. Clin Cancer Res 6: 3400–3405.
- 32. Dai Z, Papp AC, Wang D, Hampel H, Sadee W (2008) Genotyping panel for assessing response to cancer chemotherapy. BMC Med Genomics 1: 24.
- 33. Innocenti F, Kroetz DL, Schuetz E, Dolan ME, Ramirez J, et al. (2009) Comprehensive pharmacogenetic analysis of irinotecan neutropenia and pharmacokinetics. J Clin Oncol 27: 2604–2614.
- 34. Rosner GL, Panetta JC, Innocenti F, Ratain MJ (2008) Pharmacogenetic pathway analysis of irinotecan. Clin Pharmacol Ther 84: 393–402.
- 35. Parke J, Holford NH, Charles BG (1999) A procedure for generating bootstrap samples for the validation of nonlinear mixed-effects population models. Comput Methods Programs Biomed 59: 19–29.
- 36. Hirano M, Maeda K, Shitara Y, Sugiyama Y (2004) Contribution of OATP2 (OATP1B1) and OATP8 (OATP1B3) to the hepatic uptake of pitavastatin in humans. J Pharmacol Exp Ther 311: 139–146.
- 37. Phelps MA, Rozewski DM, Johnston JS, Farley KL, Albanese KA, et al. (2008) Development and validation of a sensitive liquid chromatography/mass spectrometry method for quantitation of flavopiridol in plasma enables accurate estimation of pharmacokinetic parameters with a clinically active dosing schedule. J Chromatogr B Analyt Technol Biomed Life Sci 868: 110–115.
- 38. Liu Q, Farley KL, Johnson AJ, Muthusamy N, Hofmeister CC, et al. (2008) Development and Validation of a Highly Sensitive Liquid Chromatography/Mass Spectrometry Method for Simultaneous Quantification of Lenalidomide and Flavopiridol in Human Plasma. Ther Drug Monit.
- 39. Chen N, Lau H, Kong L, Kumar G, Zeldis JB, et al. (2007) Pharmacokinetics of lenalidomide in subjects with various degrees of renal impairment and in subjects on hemodialysis. J Clin Pharmacol 47: 1466–1475.
- 40. Khan S, Ahmad A, Guo W, Wang YF, Abu-Qare A, et al. (2005) A simple and sensitive LC/MS/MS assay for 7-ethyl-10-hydroxycamptothecin (SN-38) in mouse plasma and tissues: application to pharmacokinetic study of liposome entrapped SN-38 (LE-SN38). J Pharm Biomed Anal 37: 135–142.
- 41. Nozawa T, Minami H, Sugiura S, Tsuji A, Tamai I (2005) Role of organic anion transporter OATP1B1 (OATP-C) in hepatic uptake of irinotecan and its active metabolite, 7-ethyl-10-hydroxycamptothecin: in vitro evidence and effect of single nucleotide polymorphisms. Drug Metab Dispos 33: 434–439.
- 42. Ette EI (1997) Stability and performance of a population pharmacokinetic model. J Clin Pharmacol 37: 486–495.
- 43. Lin TS, Ruppert AS, Johnson AJ, Fischer B, Heerema NA, et al. (2009) Phase II Study of Flavopiridol in Relapsed Chronic Lymphocytic Leukemia Demonstrating High Response Rates in Genetically High-Risk Disease. Journal of Clinical Oncology 27: 6012–6018.
- 44. Elens L, Yombi JC, Lison D, Wallemacq P, Vandercam B, et al. (2009) Association between ABCC2 polymorphism and lopinavir accumulation in peripheral blood mononuclear cells of HIV-infected patients. Pharmacogenomics 10: 1589–1597.
- 45. Sookoian S, Castano G, Gianotti TF, Gemma C, Pirola CJ (2009) Polymorphisms of MRP2 (ABCC2) are associated with susceptibility to nonalcoholic fatty liver disease. J Nutr Biochem 20: 765–770.
- 46. Wojnowski L, Kulle B, Schirmer M, Schluter G, Schmidt A, et al. (2005) NAD(P)H oxidase and multidrug resistance protein genetic polymorphisms are associated with doxorubicin-induced cardiotoxicity. Circulation 112: 3754–3762.
- 47. Niemi M (2009) Transporter pharmacogenetics and statin toxicity. Clin Pharmacol Ther 87: 130–133.
- 48. Takane H, Kawamoto K, Sasaki T, Moriki K, Kitano H, et al. (2009) Life-threatening toxicities in a patient with UGT1A1*6/*28 and SLCO1B1*15/*15 genotypes after irinotecan-based chemotherapy. Cancer Chemother Pharmacol 63: 1165–1169.
- 49. Giacomini KM, Huang SM, Tweedie DJ, Benet LZ, Brouwer KL, et al. Membrane transporters in drug development. Nat Rev Drug Discov 9: 215–236.
- 50. Pasanen MK, Neuvonen PJ, Niemi M (2008) Global analysis of genetic variation in SLCO1B1. Pharmacogenomics 9: 19–33.
- 51. Romaine SP, Bailey KM, Hall AS, Balmforth AJ (2010) The influence of SLCO1B1 (OATP1B1) gene polymorphisms on response to statin therapy. Pharmacogenomics J 10: 1–11.