Reducing irinotecan‐associated diarrhea in children
暂无分享,去创建一个
A. Pappo | C. Rodríguez-Galindo | W. Furman | L. Wagner | C. Stewart | K. Crews | K. Albritton | R. McNall-Knapp | C. Rodríguez‐Galindo
[1] M Beth McCarville,et al. Temozolomide and intravenous irinotecan for treatment of advanced Ewing sarcoma , 2007, Pediatric blood & cancer.
[2] B. Geoerger,et al. Phase II trial of irinotecan in children with relapsed or refractory rhabdomyosarcoma: a joint study of the French Society of Pediatric Oncology and the United Kingdom Children's Cancer Study Group. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[3] P. Houghton,et al. Two consecutive phase II window trials of irinotecan alone or in combination with vincristine for the treatment of metastatic rhabdomyosarcoma: the Children's Oncology Group. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[4] J. Verweij,et al. Prophylaxis of irinotecan-induced diarrhea with neomycin and potential role for UGT1A1*28 genotype screening: a double-blind, randomized, placebo-controlled study. , 2006, The oncologist.
[5] J. Panetta,et al. UGT1A1 promoter genotype correlates with pharmacokinetics but not toxicity in patients receiving protracted irinotecan (IRN). , 2006, Journal of Clinical Oncology.
[6] 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.
[7] M. Rocchi,et al. Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism predicts the risk of gastrointestinal toxicity and fatigue induced by irinotecan‐based chemotherapy , 2006, Cancer.
[8] G. Brandi,et al. Intestinal microflora and digestive toxicity of irinotecan in mice. , 2006, Clinical cancer research : an official journal of the American Association for Cancer Research.
[9] P. Houghton,et al. Cefixime allows greater dose escalation of oral irinotecan: a phase I study in pediatric patients with refractory solid tumors. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[10] M. Carli,et al. Phase II study of a protracted irinotecan schedule in children with refractory or recurrent soft tissue sarcoma , 2006, Cancer.
[11] P. Beale,et al. A pilot study on the safety of combining chrysin, a non-absorbable inducer of UGT1A1, and irinotecan (CPT-11) to treat metastatic colorectal cancer , 2006, Cancer Chemotherapy and Pharmacology.
[12] T. Kamataki,et al. Optimal antidiarrhea treatment for antitumor agent irinotecan hydrochloride (CPT-11)-induced delayed diarrhea , 2006, Cancer Chemotherapy and Pharmacology.
[13] J. Kuttesch,et al. A phase I study of irinotecan administered on a weekly schedule in pediatric patients , 2006, Pediatric blood & cancer.
[14] N. Vasudev,et al. Intravenous irinotecan plus oral ciclosporin. , 2005, Clinical oncology (Royal College of Radiologists (Great Britain)).
[15] K. Kobayashi,et al. A phase I/II trial of irinotecan–cisplatin combined with an anti-late-diarrhoeal programme to evaluate the safety and antitumour response of this combination therapy in patients with advanced non-small-cell lung cancer , 2005, British Journal of Cancer.
[16] J. Bowen,et al. Palifermin reduces diarrhea and increases survival following irinotecan treatment in tumor‐bearing DA rats , 2005, International journal of cancer.
[17] H. Messmann,et al. Prospective, Double-Blind, Placebo-Controlled, Multicenter, Randomized Phase III Study with Orally Administered Budesonide for Prevention of Irinotecan (CPT-11)-Induced Diarrhea in Patients with Advanced Colorectal Cancer , 2005, Oncology.
[18] J. Sussman,et al. The Crystal Structure of the Complex of the Anticancer Prodrug 7-Ethyl-10-[4-(1-piperidino)-1-piperidino]-carbonyloxycamptothecin (CPT-11) with Torpedo californica Acetylcholinesterase Provides a Molecular Explanation for Its Cholinergic Action , 2005, Molecular Pharmacology.
[19] M. Ratain,et al. Modulation of irinotecan with cyclosporine: a phase II trial in advanced colorectal cancer , 2005, Cancer Chemotherapy and Pharmacology.
[20] H. Bouzourène,et al. Irinotecan-induced Colitis , 2005, International journal of surgical pathology.
[21] N. Cheung,et al. Five‐day courses of irinotecan as palliative therapy for patients with neuroblastoma , 2005, Cancer.
[22] 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.
[23] A. Friedman,et al. Phase II trial of irinotecan plus celecoxib in adults with recurrent malignant glioma , 2005, Cancer.
[24] A. Oza,et al. Phase II study of activated charcoal to prevent irinotecan-induced diarrhea. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[25] A. Vecchione,et al. New approaches to prevent intestinal toxicity of irinotecan-based regimens. , 2004, Cancer treatment reviews.
[26] D. Richel,et al. A randomised phase II multicentre trial of irinotecan (CPT-11) using four different schedules in patients with metastatic colorectal cancer , 2004, British Journal of Cancer.
[27] S. Rosenoff. Octreotide LAR resolves severe chemotherapy-induced diarrhoea (CID) and allows continuation of full-dose therapy. , 2004, European journal of cancer care.
[28] T. Murakami,et al. Prevention of irinotecan-induced diarrhoea by oral carbonaceous adsorbent (Kremezin) in cancer patients. , 2004, Oncology reports.
[29] E. Thiel,et al. Neomycin as secondary prophylaxis for irinotecan-induced diarrhea. , 2004, Annals of oncology : official journal of the European Society for Medical Oncology.
[30] W. Abdullah. Pediatr Blood Cancer , 2004 .
[31] M. Baiget,et al. UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer , 2004, British Journal of Cancer.
[32] J. Ajani,et al. Recommended guidelines for the treatment of cancer treatment-induced diarrhea. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[33] 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.
[34] R. Buelow,et al. Oral RDP58 Allows CPT-11 Dose Intensification for Enhanced Tumor Response by Decreasing Gastrointestinal Toxicity , 2004, Clinical Cancer Research.
[35] P. Houghton,et al. Phase I Trial of Temozolomide and Protracted Irinotecan in Pediatric Patients with Refractory Solid Tumors , 2004, Clinical Cancer Research.
[36] F. Lévi,et al. Circadian Rhythm of Irinotecan Tolerability in Mice , 2004, Chronobiology international.
[37] D. Frappaz,et al. A phase I study of irinotecan as a 3-week schedule in children with refractory or recurrent solid tumors. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[38] A. Vecchione,et al. Prevention of irinotecan plus 5-fluorouracil/leucovorin-induced diarrhoea by oral administration of neomycin plus bacitracin in first-line treatment of advanced colorectal cancer. , 2003, Annals of oncology : official journal of the European Society for Medical Oncology.
[39] Y. Cheung,et al. The modulation of irinotecan-induced diarrhoea and pharmacokinetics by three different classes of pharmacologic agents. , 2003, Oncology reports.
[40] K. Mori,et al. Preventive effect of Kampo medicine (Hangeshashin-to) against irinotecan-induced diarrhea in advanced non-small-cell lung cancer , 2003, Cancer Chemotherapy and Pharmacology.
[41] G. Hall,et al. Phase I and pharmacokinetic study of intravenous irinotecan plus oral ciclosporin in patients with fuorouracil-refractory metastatic colon cancer. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[42] B. Levine,et al. Cyclooxygenase-2 inhibition with celecoxib enhances antitumor efficacy and reduces diarrhea side effect of CPT-11. , 2002, Cancer research.
[43] Y. Sugiyama,et al. Reduced Gastrointestinal Toxicity Following Inhibition of the Biliary Excretion of Irinotecan and Its Metabolites by Probenecid in Rats , 2002, Pharmaceutical Research.
[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] J. Hecht,et al. Phase II trial of irinotecan in combination with amifostine in patients with advanced colorectal carcinoma , 2002, Cancer.
[46] I. Cameron,et al. Consumption of an omega-3 fatty acids product, INCELL AAFA™, reduced side-effects of CPT-11 (irinotecan) in mice , 2002, British Journal of Cancer.
[47] 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.
[48] W. Gerald,et al. Irinotecan for Pediatric Solid Tumors: The Memorial Sloan-Kettering Experience , 2002, Journal of pediatric hematology/oncology.
[49] G. Koumakis,et al. Control of irinotecan-induced diarrhea by octreotide after loperamide failure , 2001, Supportive Care in Cancer.
[50] J. Verweij,et al. Modulation of irinotecan-induced diarrhea by cotreatment with neomycin in cancer patients. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[51] P. Halushka,et al. Disposition and metabolism of the flavonoid chrysin in normal volunteers. , 2001, British journal of clinical pharmacology.
[52] R. Goldberg,et al. Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. , 2001, The New England journal of medicine.
[53] 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.
[54] H. Saka,et al. Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis. , 2000, Cancer research.
[55] P. Houghton,et al. Clinical use of topoisomerase I inhibitors in anticancer treatment. , 2000, Medical and pediatric oncology.
[56] L. Saltz,et al. Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. Irinotecan Study Group. , 2000, The New England journal of medicine.
[57] C. Morton,et al. Proficient metabolism of irinotecan by a human intestinal carboxylesterase. , 2000, Cancer research.
[58] M. Hauer-Jensen,et al. Effect of thalidomide on gastrointestinal toxic effects of irinotecan , 2000, The Lancet.
[59] M. Ychou,et al. Randomized comparison of prophylactic antidiarrheal treatment versus no prophylactic antidiarrheal treatment in patients receiving CPT-11 (irinotecan) for advanced 5-FU-resistant colorectal cancer: an open-label multicenter phase II study. , 2000, American journal of clinical oncology.
[60] S. Kudoh,et al. pH‐dependent uptake of irinotecan and its active metabolite, SN‐38, by intestinal cells , 1999, International journal of cancer.
[61] T. Loeffler,et al. Substantial activity of budesonide in patients with irinotecan (CPT-11) and 5-fluorouracil induced diarrhea and failure of loperamide treatment. , 1999, Annals of oncology : official journal of the European Society for Medical Oncology.
[62] C. Bucana,et al. Oral administration of the immunomodulator JBT-3002 induces endogenous interleukin 15 in intestinal macrophages for protection against irinotecan-mediated destruction of intestinal epithelium. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.
[63] M. Ciotti,et al. Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38) by the human UDP-glucuronosyltransferases encoded at the UGT1 locus. , 1999, Biochemical and biophysical research communications.
[64] P. Houghton,et al. Direct translation of a protracted irinotecan schedule from a xenograft model to a phase I trial in children. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[65] A. Di Rienzo,et al. Phenotype‐genotype correlation of in vitro SN‐38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism , 1999, Clinical pharmacology and therapeutics.
[66] Y. Sugiyama,et al. Biliary excretion mechanism of CPT-11 and its metabolites in humans: involvement of primary active transporters. , 1998, Cancer research.
[67] P. Houghton,et al. Animal models for studying the action of topoisomerase I targeted drugs. , 1998, Biochimica et biophysica acta.
[68] J. Black,et al. Interleukin 15 offers selective protection from irinotecan-induced intestinal toxicity in a preclinical animal model. , 1998, Cancer research.
[69] J. Hecht. Gastrointestinal toxicity or irinotecan. , 1998, Oncology.
[70] G. Vassal,et al. Pathophysiology and therapy of irinotecan-induced delayed-onset diarrhea in patients with advanced colorectal cancer: a prospective assessment. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[71] M. Ratain,et al. Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes. , 1998, The Journal of clinical investigation.
[72] T Ishizaki,et al. Cell cycle-dependent chronotoxicity of irinotecan hydrochloride in mice. , 1997, The Journal of pharmacology and experimental therapeutics.
[73] T. Kamataki,et al. Relevance of irinotecan hydrochloride-induced diarrhea to the level of prostaglandin E2 and water absorption of large intestine in rats. , 1997, Japanese journal of pharmacology.
[74] A. Ikari,et al. Thromboxane A2, released by the anti‐ tumour drug irinotecan, is a novel stimulator of Cl− secretion in isolated rat colon , 1997, The Journal of physiology.
[75] T. Hodge,et al. Re:Irinotecan (CPT-11) and characteristic mucosal changes in the mouse ileum and cecum. , 1996, Journal of the National Cancer Institute.
[76] S. Kudoh,et al. Irinotecan (CPT-11): pharmacology and clinical applications. , 1996, Critical reviews in oncology/hematology.
[77] M Nomura,et al. Involvement of beta-glucuronidase in intestinal microflora in the intestinal toxicity of the antitumor camptothecin derivative irinotecan hydrochloride (CPT-11) in rats. , 1996, Cancer research.
[78] G. Vassal,et al. Therapeutic activity of CPT-11, a DNA-topoisomerase I inhibitor, against peripheral primitive neuroectodermal tumour and neuroblastoma xenografts. , 1996, British Journal of Cancer.
[79] H. Soda,et al. Irinotecan (CPT-11) and characteristic mucosal changes in the mouse ileum and cecum. , 1995, Journal of the National Cancer Institute.
[80] P. Hérait,et al. Irinotecan (CPT-11) high-dose escalation using intensive high-dose loperamide to control diarrhea. , 1994, Journal of the National Cancer Institute.
[81] P. Houghton,et al. Therapeutic efficacy of the topoisomerase I inhibitor 7-ethyl-10-(4-[1-piperidino]-1-piperidino)-carbonyloxy-camptothecin against human tumor xenografts: lack of cross-resistance in vivo in tumors with acquired resistance to the topoisomerase I inhibitor 9-dimethylaminomethyl-10-hydroxycamptothecin. , 1993, Cancer research.
[82] K. Akahane,et al. Inhibitory Activity of Camptothecin Derivatives Against Acetylcholinesterase in Dogs and Their Binding Activity to Acetylcholine Receptors in Rats , 1993, The Journal of pharmacy and pharmacology.
[83] J. Schwartz,et al. Effects of acetorphan, an enkephalinase inhibitor, on experimental and acute diarrhoea. , 1992, Gut.
[84] T. Mcelwain,et al. The modification of melphalan toxicity in tumor bearing mice by S‐2‐(3‐aminopropylamino)‐ethylphosphorothioic acid (WR2721) , 1982, American journal of clinical oncology.
[85] R. Arceci. Two consecutive phase II window trials of irinotecan alone or in combination with vincristine for the treatment of metastatic rhabdomyosarcoma: the Children's Oncology Group , 2008 .
[86] P. Houghton,et al. Efficacy of topoisomerase I inhibitors, topotecan and irinotecan, administered at low dose levels in protracted schedules to mice bearing xenografts of human tumors , 2004, Cancer Chemotherapy and Pharmacology.
[87] G. Hall,et al. Phase I and pharmacokinetic study of intravenous irinotecan plus oral ciclosporin in patients with fuorouracil-refractory metastatic colon cancer. , 2003, Journal of Clinical Oncology.
[88] R. Schilsky,et al. UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity , 2002, The Pharmacogenomics Journal.
[89] D. Amadori,et al. High-dose loperamide in the treatment of 5-fluorouracil-induced diarrhea in colorectal cancer patients , 2000, Supportive Care in Cancer.
[90] D. Savarese,et al. Glutamine for irinotecan diarrhea. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.