Irinogenetics: what is the right star?

The response of patients to drug therapy is variable and unpredictable. The current focus of pharmacogenetics is to find common genetic variants that are predictors of clinical phenotypes associated with drug therapy. This goal is usually pursued by genotyping patients for a particular polymorphism (a genetic variant occurring in 1% of the population), a set of polymorphisms in the same gene, or different polymorphisms in different genes. The genes of interest in pharmacogenetics are those involved in the mechanism of action and/or disposition of a certain drug. For the classic cytotoxic agents commonly used in oncology, the elucidation of potential genetic predispositions of patients to severe toxicity has been of interest with a goal of improving their therapeutic index. The pharmacogenetics of irinotecan (irinogenetics) indicate that a common polymorphism in the uridine diphosphateglucuronosyltransferase 1A1 (UGT1A1) gene predisposes patients to severe toxicity. This variant is a TA repeat promoter polymorphism reducing the expression of the UGT1A1 gene. In this issue, Han et al analyzed the association between common variants in several UGT1A genes, including UGT1A1, and evaluated the impact of these variants on toxicity and efficacy of irinotecan administered with cisplatin in a population of Korean non– small-cell lung cancer (NSCLC) patients. This article indicates that, in addition to the TA repeat polymorphism, another common variant found only in individuals of East Asian descent might have a predictive role. Moreover, this article suggests that these polymorphisms might have an impact on the antitumor efficacy of irinotecan. To have a better understanding of the findings of Han et al, we need to clarify the structure of the UGT1A gene. In humans, there are nine functional UGT1A enzymes with different patterns of tissue distribution. As partly shown in Figure 1 of the article by Han et al, UGT1A isoforms are generated from a single UGT1A gene by splicing of individual exons 1 with common exons 2 to 5, spanning more than 200 Kb of genomic sequence on chromosome 2. Polymorphisms in the common exons are relatively uncommon but would potentially affect the expression or function of all UGT1A isoforms. However, there are many common polymorphisms that affect the expression or function of single isoforms, either in their exon 1 or in the upstream promoter area. Irinotecan is mainly used in metastatic colorectal cancer patients. Regimens containing irinotecan are often relegated to second-line therapy because of unpredictable toxicity and the availability of equally effective agents (eg, oxaliplatin). Irinotecan causes severe diarrhea and neutropenia in 20% to 35% of patients. The late-onset grade 3 or 4 diarrhea often does not respond to the recommended loperamide therapy and can require hospitalization, irinotecan dose modifications, and/or dose interruptions, potentially compromising efficacy. Fatal events (up to 5.3% prevalence) during single-agent irinotecan treatment have been reported, and concerns have been expressed regarding an excessive rate of early deaths in colorectal cancer patients receiving irinotecan/fluorouracil regimens. Despite this discouraging scenario, recent studies have shown that irinotecan is an active drug with an important role in standard-of-care treatment regimens for colorectal cancer. Overall survival of metastatic colorectal cancer patients can be excellent if patients receive all active drugs, including irinotecan, during their course of treatment. The understanding of irinotecan pharmacology and genetic variability of key genes has made possible the identification of a subset of patients who are genetically predisposed to severe toxicity. In normal and tumor tissues, the hydrolysis of irinotecan leads to the formation of SN-38, a potent topoisomerase inhibitor. SN-38 formation within the tumor may be an important determinant of antitumor activity. The inactivation of SN-38 occurs by glucuronidation to SN-38 glucuronide (SN-38G), mainly through UGT1A1, an isoform expressed in the liver and also in extrahepatic tissues. In addition to UGT1A1, other UGT1A isoforms (including UGT1A6, UGT1A7, UGT1A9, and UGT1A10) are capable of metabolizing SN-38. It is likely that the exposure of patients to SN-38 is the ultimate result of the contribution of several UGT1As, in particular those that are highly expressed in the liver. High interpatient variability in irinotecan clearance and SN-38 area under the curve (AUC) has been observed, but there is no consistency across different studies on whether the AUC of irinotecan, SN-38, SN-38G, or a combination of these three parameters (the biliary index) is the strongest predictor of either severe neutropenia or diarrhea. However, it is certainly clear that changes in function of the UGT1A1 gene in patients will affect the exposure to SN-38, resulting in different susceptibility to toxicity among patients. The most studied polymorphism in irinogenetics is a common TA repeat variant in the UGT1A1 promoter. In the population, five, six, seven, and eight TA repeats can be found. UGT1A1 expression in individuals is inversely correlated with the number of TA repeats. In pharmacogenetics, gene variants are numbered with a “*” (star) preceding a number. The *1 allele of a gene is the allele of the reference sequence (previously referred to as wild-type allele, a term that is becoming obsolete). Hence, the six TA repeat allele is JOURNAL OF CLINICAL ONCOLOGY E D I T O R I A L VOLUME 24 NUMBER 15 MAY 2

[1]  C. Guillemette,et al.  Identification of common polymorphisms in the promoter of the UGT1A9 gene: evidence that UGT1A9 protein and activity levels are strongly genetically controlled in the liver. , 2004, Pharmacogenetics.

[2]  R. Goldberg,et al.  A review of oxaliplatin and its clinical use in colorectal cancer , 2004, Expert opinion on pharmacotherapy.

[3]  Jeffrey Cummings,et al.  Glucuronidation as a mechanism of intrinsic drug resistance in human colon cancer: reversal of resistance by food additives. , 2003, Cancer research.

[4]  M. Schwab,et al.  Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians. , 2003, Biochemical pharmacology.

[5]  M. Baiget,et al.  UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer , 2004, British Journal of Cancer.

[6]  M. Fukuoka,et al.  A phase II trial of combination of CPT-11 and cisplatin for advanced non-small-cell lung cancer. CPT-11 Lung Cancer Study Group. , 1998, British Journal of Cancer.

[7]  David H. Johnson,et al.  Phase II study of irinotecan plus cisplatin in patients with advanced non-small-cell lung cancer. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[8]  J Verweij,et al.  Clinical pharmacokinetics and metabolism of irinotecan (CPT-11). , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.

[9]  D. Sargent,et al.  Recommendation for caution with irinotecan, fluorouracil, and leucovorin for colorectal cancer. , 2001, The New England journal of medicine.

[10]  K. Yamamoto,et al.  Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II. , 1998, Biochimica et biophysica acta.

[11]  J. Crowley,et al.  Survival determinants in extensive-stage non-small-cell lung cancer: the Southwest Oncology Group experience. , 1991, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[12]  Yoshiro Saito,et al.  Human liver UDP-glucuronosyltransferase isoforms involved in the glucuronidation of 7-ethyl-10-hydroxycamptothecin , 2001, Xenobiotica; the fate of foreign compounds in biological systems.

[13]  M. Ratain,et al.  Effects of Ketoconazole on Glucuronidation by UDP-Glucuronosyltransferase Enzymes , 2005, Clinical Cancer Research.

[14]  J. Clegg,et al.  The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications. , 2003, Blood cells, molecules & diseases.

[15]  U. Vanhoefer,et al.  Irinotecan in the treatment of colorectal cancer: clinical overview. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[16]  Kazuo Komamura,et al.  UGT1A1 Haplotypes Associated with Reduced Glucuronidation and Increased Serum Bilirubin in Irinotecan‐administered Japanese Patients with Cancer , 2004, Clinical pharmacology and therapeutics.

[17]  S. Groshen,et al.  Frequency and prognostic importance of pretreatment clinical characteristics in patients with advanced non-small-cell lung cancer treated with combination chemotherapy. , 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[18]  M. Valerio,et al.  Phase III randomized trial of FOLFIRI versus FOLFOX4 in the treatment of advanced colorectal cancer: a multicenter study of the Gruppo Oncologico Dell'Italia Meridionale. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[19]  Yoshiro Saito,et al.  Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38), an active metabolite of irinotecan (CPT-11), by human UGT1A1 variants, G71R, P229Q, and Y486D. , 2003, Drug metabolism and disposition: the biological fate of chemicals.

[20]  Hee-Jin Kim,et al.  Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population. , 2003, Clinical chemistry.

[21]  S. Kudoh,et al.  Randomised phase III trial of irinotecan combined with cisplatin for advanced non-small-cell lung cancer , 2003, British Journal of Cancer.

[22]  M. Ratain,et al.  “Irinogenetics” and UGT1A: from Genotypes to Haplotypes , 2004, Clinical pharmacology and therapeutics.

[23]  R. Rosell,et al.  Weekly regimen of irinotecan/docetaxel in previously treated non-small cell lung cancer patients and correlation with uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) polymorphism , 2003, Investigational New Drugs.

[24]  Christian Jacques,et al.  Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer , 1998, The Lancet.

[25]  M. Ratain,et al.  Haplotypes of variants in the UDP-glucuronosyltransferase1A9 and 1A1 genes , 2005, Pharmacogenetics and genomics.

[26]  R. Schilsky,et al.  A phase I trial of pharmacologic modulation of irinotecan with cyclosporine and phenobarbital , 2004, Clinical pharmacology and therapeutics.

[27]  H. Saka,et al.  Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis. , 2000, Cancer research.

[28]  H. McLeod,et al.  A novel polymorphism in the promoter region of human UGT1A9 gene (UGT1A9*22) and its effects on the transcriptional activity. , 2004, Pharmacogenetics.

[29]  A. Di Rienzo,et al.  Variability at the uridine diphosphate glucuronosyltransferase 1A1 promoter in human populations and primates. , 1999, Pharmacogenetics.

[30]  Y. Fujiwara,et al.  The Role of Glucuronidation in 7‐Ethyl‐10‐hydroxycamptothecin Resistance in vitro , 1997, Japanese journal of cancer research : Gann.

[31]  C. Bokemeyer,et al.  Phase III study of weekly high-dose infusional fluorouracil plus folinic acid with or without irinotecan in patients with metastatic colorectal cancer: European Organisation for Research and Treatment of Cancer Gastrointestinal Group Study 40986. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[32]  M. Manns,et al.  Polymorphic expression of the UDP-glucuronosyltransferase UGT1A gene locus in human gastric epithelium. , 1998, Molecular pharmacology.

[33]  E. Gamelin,et al.  Relevance of Different UGT1A1 Polymorphisms in Irinotecan-Induced Toxicity , 2004, Clinical Cancer Research.

[34]  M. Manns,et al.  Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene. , 2001, Gastroenterology.

[35]  N. Meropol,et al.  UGT1A7 and UGT1A9 polymorphisms predict response and toxicity in colorectal cancer patients treated with capecitabine/irinotecan. , 2005, Clinical cancer research : an official journal of the American Association for Cancer Research.

[36]  Soma Das,et al.  Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[37]  J. Verweij,et al.  Impact of body-size measures on irinotecan clearance: alternative dosing recommendations. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[38]  L. Saltz,et al.  Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. Irinotecan Study Group. , 2000, The New England journal of medicine.

[39]  C. Fuchs,et al.  Phase III comparison of two irinotecan dosing regimens in second-line therapy of metastatic colorectal cancer. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[40]  E. Beutler,et al.  Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[41]  Philip Lazarus,et al.  Glucuronidation: an important mechanism for detoxification of benzo[a]pyrene metabolites in aerodigestive tract tissues. , 2002, Drug metabolism and disposition: the biological fate of chemicals.

[42]  J. Supko,et al.  Current perspectives on the clinical experience, pharmacology, and continued development of the camptothecins. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.

[43]  E. Shin,et al.  Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[44]  C. Guillemette,et al.  Common human UGT1A polymorphisms and the altered metabolism of irinotecan active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38). , 2002, Molecular pharmacology.

[45]  R. Labianca,et al.  Randomised trial of irinotecan versus fluorouracil by continuous infusion after fluorouracil failure in patients with metastatic colorectal cancer , 1998, The Lancet.

[46]  Y. Adachi,et al.  Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase. , 1995, Human molecular genetics.

[47]  D. Ettinger,et al.  Long-term survivors in metastatic non-small-cell lung cancer: an Eastern Cooperative Oncology Group Study. , 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.