Literature DB >> 18650079

A phase I and pharmacokinetic study of the quinoxaline antitumour Agent R(+)XK469 in patients with advanced solid tumours.

Samir D Undevia1, Federico Innocenti, Jacqueline Ramirez, Larry House, Apurva A Desai, Linda A Skoog, Deepti A Singh, Theodore Karrison, Hedy L Kindler, Mark J Ratain.   

Abstract

PURPOSE: To investigate the safety and pharmacokinetics of R(+)XK469, a quinoxaline analogue, in patients with advanced refractory solid tumours. Preclinical studies suggested that efficacy was independent of schedule but that toxicity was decreased by dividing the dose.
METHODS: R(+)XK469 was initially administered as a 30 min intravenous infusion on days 1-5 of a 21-d cycle. Based on the demonstration of a long half-life, the dosing schedule was subsequently amended to infusion on days 1, 3 and 5 of a 21-d cycle. An alternate single-dose schedule of once every 21 d was also explored. Blood samples were collected for pharmacokinetic studies.
RESULTS: Dose-limiting toxicity (DLT) was neutropaenia. There was significant interindividual variability in clearance as evidenced by a coefficient of variation of 46%. A flat-dosing scheme (not based on body surface area) was justified by the absence of correlation between clearance and body surface area. A partial response was observed in a patient with nasopharyngeal carcinoma.
CONCLUSIONS: The recommended phase II doses are 850-1100 mg/d on days 1, 3 and 5 of a 21-d cycle and 2500 mg on day 1 of a 21-d cycle. The observed interpatient pharmacokinetic variability should prompt investigation into the presence of genetic polymorphism in relevant metabolizing enzymes.

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Year:  2008        PMID: 18650079      PMCID: PMC2731567          DOI: 10.1016/j.ejca.2008.05.018

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  18 in total

1.  Pro-apoptotic interactions between XK469 and the peripheral benzodiazepine receptor.

Authors:  D Kessel; J P Horwitz
Journal:  Cancer Lett       Date:  2001-07-26       Impact factor: 8.679

2.  New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada.

Authors:  P Therasse; S G Arbuck; E A Eisenhauer; J Wanders; R S Kaplan; L Rubinstein; J Verweij; M Van Glabbeke; A T van Oosterom; M C Christian; S G Gwyther
Journal:  J Natl Cancer Inst       Date:  2000-02-02       Impact factor: 13.506

Review 3.  Pharmacokinetic variability of anticancer agents.

Authors:  Samir D Undevia; Gonzalo Gomez-Abuin; Mark J Ratain
Journal:  Nat Rev Cancer       Date:  2005-06       Impact factor: 60.716

4.  Preclinical antitumor efficacy of analogs of XK469: sodium-(2-[4-(7-chloro-2-quinoxalinyloxy)phenoxy]propionate.

Authors:  T H Corbett; P LoRusso; L Demchick; C Simpson; S Pugh; K White; J Kushner; L Polin; J Meyer; J Czarnecki; L Heilbrun; J P Horwitz; J L Gross; C H Behrens; B A Harrison; R J McRipley; G Trainor
Journal:  Invest New Drugs       Date:  1998       Impact factor: 3.850

5.  Bioavailability and pharmacokinetics of the investigational anticancer agent XK469 (NSC 698215) in rats following oral and intravenous administration.

Authors:  Ramesh R Boinpally; Sen-Lin Zhou; Patricia M LoRusso; Ralph E Parchment
Journal:  Cancer Chemother Pharmacol       Date:  2004-12-09       Impact factor: 3.333

6.  A phase 1 trial of XK469: toxicity profile of a selective topoisomerase IIbeta inhibitor.

Authors:  Amin M Alousi; Ramesh Boinpally; Richard Wiegand; Ralph Parchment; Shirish Gadgeel; Lance K Heilbrun; Antionette J Wozniak; Pamela DeLuca; Patricia M LoRusso
Journal:  Invest New Drugs       Date:  2006-11-11       Impact factor: 3.850

7.  Metabolic profile of XK469 (2(R)-[4-(7-chloro-2-quinoxalinyl)oxyphenoxy]-propionic acid; NSC698215) in patients and in vitro: low potential for active or toxic metabolites or for drug-drug interactions.

Authors:  Lawrence W Anderson; Jerry M Collins; Raymond W Klecker; Aspandiar G Katki; Ralph E Parchment; Ramesh R Boinpally; Patricia M LoRusso; S Percy Ivy
Journal:  Cancer Chemother Pharmacol       Date:  2005-05-13       Impact factor: 3.333

8.  Cytotoxic mechanism of XK469: resistance of topoisomerase IIbeta knockout cells and inhibition of topoisomerase I.

Authors:  R M Snapka; H Gao; D R Grabowski; D Brill; K K Chan; L Li; G C Li; R Ganapathi
Journal:  Biochem Biophys Res Commun       Date:  2001-02-02       Impact factor: 3.575

9.  A phase I and pharmacokinetic study of XK469R (NSC 698215), a quinoxaline phenoxypropionic acid derivative, in patients with refractory acute leukemia.

Authors:  Wendy Stock; Samir D Undevia; Carol Bivins; Farhad Ravandi; Olatoyosi Odenike; Stefan Faderl; Elizabeth Rich; Gautam Borthakur; Lucy Godley; Srdan Verstovsek; Andrew Artz; William Wierda; Richard A Larson; Yanming Zhang; Jorge Cortes; Mark J Ratain; Francis J Giles
Journal:  Invest New Drugs       Date:  2008-04-19       Impact factor: 3.850

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  8 in total

1.  Perturbing pro-survival proteins using quinoxaline derivatives: a structure-activity relationship study.

Authors:  Rajkumar Rajule; Vashti C Bryant; Hernando Lopez; Xu Luo; Amarnath Natarajan
Journal:  Bioorg Med Chem       Date:  2012-02-16       Impact factor: 3.641

2.  The quinoxaline anti-tumor agent (R+)XK469 inhibits neuroblastoma tumor growth.

Authors:  Nisha C Kakodkar; Radhika Peddinti; Morris Kletzel; Yufeng Tian; Lisa J Guerrero; Samir D Undevia; David Geary; Alexandre Chlenski; Qiwei Yang; Helen R Salwen; Susan L Cohn
Journal:  Pediatr Blood Cancer       Date:  2011-01       Impact factor: 3.167

3.  A pharmacogenetic study of aldehyde oxidase I in patients treated with XK469.

Authors:  Jacqueline Ramírez; Tae Won Kim; Wanqing Liu; Jamie L Myers; Snezana Mirkov; Kouros Owzar; Dorothy Watson; Flora Mulkey; Eric R Gamazon; Wendy Stock; Samir Undevia; Federico Innocenti; Mark J Ratain
Journal:  Pharmacogenet Genomics       Date:  2014-02       Impact factor: 2.089

4.  R(+)XK469 inhibits hydroxylation of S-warfarin by CYP2C9.

Authors:  Wei Peng Yong; Tae Won Kim; Samir D Undevia; Federico Innocenti; Mark J Ratain
Journal:  Eur J Cancer       Date:  2009-05-21       Impact factor: 9.162

5.  An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using recyclable alumina-supported heteropolyoxometalates.

Authors:  Diego M Ruiz; Juan C Autino; Nancy Quaranta; Patricia G Vázquez; Gustavo P Romanelli
Journal:  ScientificWorldJournal       Date:  2012-03-12

6.  I2-Catalyzed Carbonylation of α-Methylene Ketones to Synthesize 1,2-Diaryl Diketones and Antiviral Quinoxalines in One Pot.

Authors:  Lingkai Kong; Jieru Meng; Wenyue Tian; Jiazheng Liu; Xueping Hu; Zhi-Hong Jiang; Wei Zhang; Yanzhong Li; Li-Ping Bai
Journal:  ACS Omega       Date:  2021-12-21

7.  Cucurbit[6]uril-Supported Fe3O4 Magnetic Nanoparticles Catalyzed Green and Sustainable Synthesis of 2-Substituted Benzimidazoles via Acceptorless Dehydrogenative Coupling.

Authors:  Shruti Verma; Shelly Kujur; Richa Sharma; Devendra D Pathak
Journal:  ACS Omega       Date:  2022-03-14

8.  Novel quinoxaline derivatives as dual EGFR and COX-2 inhibitors: synthesis, molecular docking and biological evaluation as potential anticancer and anti-inflammatory agents.

Authors:  Eman A Ahmed; Mamdouh F A Mohamed; Omran A Omran
Journal:  RSC Adv       Date:  2022-09-05       Impact factor: 4.036

  8 in total

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