Literature DB >> 22740978

Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene.

Koichi Hirose1, Chihiro Kozu, Koshiro Yamashita, Eiji Maruo, Mizuho Kitamura, Junichi Hasegawa, Kei Omoda, Teruo Murakami, Yorinobu Maeda.   

Abstract

In irinotecan (CPT-11)-based chemotherapy, neutropenia and diarrhea are often induced. In the present study, the clinical significance of the concentration ratios of 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronide (SN-38G) and SN-38 in the plasma in predicting CPT-11-induced neutropenia was examined. A total of 17 patients with colorectal cancer and wild-type UDP-glucuronosyltransferase (UGT)1A1 gene were enrolled and treated with CPT-11 as part of the FOLFIRI regimen [CPT-11 and fluorouracil (5-FU)]. Blood was taken exactly 15 min following a 2-h continuous infusion of CPT-11. Plasma concentrations of SN-38, SN-38G and CPT-11 were determined by a modified high-performance liquid chromatography (HPLC) method. The median, maximum and minimum values of plasma SN-38G/SN-38 ratios were 4.25, 7.09 and 1.03, respectively, indicating that UGT activities are variable among patients with the wild-type UGT1A1 gene. The plasma SN-38G/SN-38 ratios decreased with an increase in the trial numbers of chemotherapy (r=0.741, p=0.000669), suggesting that CPT-11 treatment suppresses UGT activity, and the low plasma SN-38G/SN-38 ratios resulted in the induction of greater neutropenia. However, in this analysis, 2 clearly separated regression lines were observed between plasma SN-38G/SN-38 ratios and neutropenia induction. In conclusion, UGT activity involved in SN-38 metabolism is variable among patients with the wild-type UGT1A1 gene, and each CPT-11 treatment suppresses UGT activity. One-point determination of the plasma SN-38G/SN-38 ratio may provide indications for the prediction of CPT-11-induced neutropenia and adjustment of the optimal dose, although further studies are required.

Entities:  

Year:  2011        PMID: 22740978      PMCID: PMC3362497          DOI: 10.3892/ol.2011.533

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  21 in total

Review 1.  Clinical pharmacokinetics of irinotecan.

Authors:  G G Chabot
Journal:  Clin Pharmacokinet       Date:  1997-10       Impact factor: 6.447

2.  High-performance liquid chromatographic method for the simultaneous determination of the camptothecin derivative irinotecan hydrochloride, CPT-11, and its metabolites SN-38 and SN-38 glucuronide in rat plasma with a fully automated on-line solid-phase extraction system, PROSPEKT.

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Journal:  J Chromatogr B Biomed Sci Appl       Date:  1999-03-19

Review 3.  Clinical pharmacokinetics and metabolism of irinotecan (CPT-11).

Authors:  R H Mathijssen; R J van Alphen; J Verweij; W J Loos; K Nooter; G Stoter; A Sparreboom
Journal:  Clin Cancer Res       Date:  2001-08       Impact factor: 12.531

4.  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.

Authors:  Takashi Nozawa; Hironobu Minami; Shigeki Sugiura; Akira Tsuji; Ikumi Tamai
Journal:  Drug Metab Dispos       Date:  2004-12-17       Impact factor: 3.922

5.  Severe toxicities after irinotecan-based chemotherapy in a patient with lung cancer: a homozygote for the SLCO1B1*15 allele.

Authors:  Hiroshi Takane; Masanori Miyata; Naoto Burioka; Jun Kurai; Yasushi Fukuoka; Hisashi Suyama; Yasushi Shigeoka; Kenji Otsubo; Ichiro Ieiri; Eiji Shimizu
Journal:  Ther Drug Monit       Date:  2007-10       Impact factor: 3.681

6.  Organic anion-transporting polypeptide 1B1 mediates transport of Gimatecan and BNP1350 and can be inhibited by several classic ATP-binding cassette (ABC) B1 and/or ABCG2 inhibitors.

Authors:  Roos L Oostendorp; Evita van de Steeg; Cornelia M M van der Kruijssen; Jos H Beijnen; Kathryn E Kenworthy; Alfred H Schinkel; Jan H M Schellens
Journal:  Drug Metab Dispos       Date:  2009-01-12       Impact factor: 3.922

7.  Individualizing dosing of irinotecan.

Authors:  Mark J Ratain; Federico Innocenti
Journal:  Clin Cancer Res       Date:  2010-01-12       Impact factor: 12.531

8.  Population pharmacokinetics and pharmacodynamics of irinotecan (CPT-11) and active metabolite SN-38 during phase I trials.

Authors:  G G Chabot; D Abigerges; G Catimel; S Culine; M de Forni; J M Extra; M Mahjoubi; P Hérait; J P Armand; R Bugat
Journal:  Ann Oncol       Date:  1995-02       Impact factor: 32.976

9.  Prediction of irinotecan and 5-fluorouracil toxicity and response in patients with advanced colorectal cancer.

Authors:  B Glimelius; H Garmo; A Berglund; L A Fredriksson; M Berglund; H Kohnke; P Byström; H Sørbye; M Wadelius
Journal:  Pharmacogenomics J       Date:  2010-02-23       Impact factor: 3.550

10.  A Phase II study of cetuximab (Erbitux) plus FOLFIRI for irinotecan and oxaliplatin-refractory metastatic colorectal cancer.

Authors:  Dong Hoe Koo; Jae Lyun Lee; Tae Won Kim; Heung Moon Chang; Min Hee Ryu; Sung Sook Lee; Min Kyoung Kim; Sun Jin Sym; Jung Shin Lee; Yoon Koo Kang
Journal:  J Korean Med Sci       Date:  2007-09       Impact factor: 2.153

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  15 in total

1.  Correlative analysis of plasma SN-38 levels and DPD activity with outcomes of FOLFIRI regimen for metastatic colorectal cancer with UGT1A1 *28 and *6 wild type and its implication for individualized chemotherapy.

Authors:  Xun Cai; Chuan Tian; Liwei Wang; Rongyuan Zhuang; Xiaowei Zhang; Yuanbiao Guo; Hongmin Lu; Hui Wang; Xiaoyu Li; Junwei Gao; Qi Li; Chungang Wang
Journal:  Cancer Biol Ther       Date:  2017-02-17       Impact factor: 4.742

2.  Development of Pyrosequencing Method for Detection of UGT1A1 Polymorphisms in Thai Colorectal Cancers.

Authors:  Chonlaphat Sukasem; Chalirmporn Atasilp; Pichai Chansriwong; Montri Chamnanphon; Apichaya Puangpetch; Ekapob Sirachainan
Journal:  J Clin Lab Anal       Date:  2014-12-26       Impact factor: 2.352

3.  Non-alcoholic fatty liver disease fibrosis score predicts hematological toxicity of chemotherapy including irinotecan for colorectal cancer.

Authors:  Masashi Yahagi; Masashi Tsuruta; Hirotoshi Hasegawa; Koji Okabayashi; Yuko Kitagawa
Journal:  Mol Clin Oncol       Date:  2017-03-01

4.  Determination of irinotecan, SN-38 and SN-38 glucuronide using HPLC/MS/MS: Application in a clinical pharmacokinetic and personalized medicine in colorectal cancer patients.

Authors:  Chalirmporn Atasilp; Pichai Chansriwong; Ekapob Sirachainan; Thanyanan Reungwetwattana; Apichaya Puangpetch; Santirhat Prommas; Suwannee Sirilerttrakul; Budsaba Rerkarmnuaychoke; Sansanee Wongwaisayawan; Chonlaphat Sukasem
Journal:  J Clin Lab Anal       Date:  2017-04-10       Impact factor: 2.352

5.  Evaluation of UGT1A1 and CYP3A Genotyping and Single-Point Irinotecan and Metabolite Concentrations as Predictors of the Occurrence of Adverse Events in Cancer Treatment.

Authors:  Jeziel Basso; Gilberto Schwartsmann; Mariana Rodrigues Ibaldi; Vitoria Daniela Schaefer; Carla Casagrande Pavei; Roberta Zilles Hahn; Marina Venzon Antunes; Rafael Linden
Journal:  J Gastrointest Cancer       Date:  2022-06-16

6.  Usefulness of one-point plasma SN-38G/SN-38 concentration ratios as a substitute for UGT1A1 genetic information after irinotecan administration.

Authors:  Kouichi Hirose; Koushiro Yamashita; Hirofumi Takada; Noriko Kaneda; Kohei Fukami; Eiji Maruo; Mizuho Kitamura; Junichi Hasegawa; Yorinobu Maeda
Journal:  Int J Clin Oncol       Date:  2013-04-19       Impact factor: 3.402

7.  Relation of Transcriptional Factors to the Expression and Activity of Cytochrome P450 and UDP-Glucuronosyltransferases 1A in Human Liver: Co-Expression Network Analysis.

Authors:  Shilong Zhong; Weichao Han; Chuqi Hou; Junjin Liu; Lili Wu; Menghua Liu; Zhi Liang; Haoming Lin; Lili Zhou; Shuwen Liu; Lan Tang
Journal:  AAPS J       Date:  2016-09-28       Impact factor: 4.009

8.  Severe irinotecan-induced toxicity in a patient with UGT1A1 28 and UGT1A1 6 polymorphisms.

Authors:  Jian-Ming Xu; Yan Wang; Fei-Jiao Ge; Li Lin; Ze-Yuan Liu; Manish R Sharma
Journal:  World J Gastroenterol       Date:  2013-06-28       Impact factor: 5.742

9.  Gene-by-Environment Interaction of Bcrp-/- and Methionine- and Choline-Deficient Diet-Induced Nonalcoholic Steatohepatitis Alters SN-38 Disposition.

Authors:  Erica L Toth; Hui Li; Anika L Dzierlenga; John D Clarke; Anna Vildhede; Michael Goedken; Nathan J Cherrington
Journal:  Drug Metab Dispos       Date:  2018-08-30       Impact factor: 3.922

10.  Analysis of UGT1A1*28 genotype and SN-38 pharmacokinetics for irinotecan-based chemotherapy in patients with advanced colorectal cancer: results from a multicenter, retrospective study in Shanghai.

Authors:  Xun Cai; Weiguo Cao; Honghua Ding; Tianshu Liu; Xinli Zhou; Mei Wang; Ming Zhong; Ziyi Zhao; Qing Xu; Liwei Wang
Journal:  J Cancer Res Clin Oncol       Date:  2013-07-28       Impact factor: 4.553

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