Literature DB >> 1804808

Phase II trial of ICRF-187 in children with solid tumors and acute leukemia.

T Vats1, B Kamen, J P Krischer.   

Abstract

ICRF-187 is the (+) enantiomer of the racemic mixture razoxane (ICRF-159). This compound is much more water soluble and thus could be formulated for parental use. The maximum tolerated dose in children after phase I trials was determined to be 3500 mg/M2/day x 3 days. A phase II trial of ICRF-187 was done in 21 children with solid tumors and 35 children with acute leukemia. All these patients were less than 21 years of age, had recovered from previous chemotherapy, had normal liver and kidney functions, and had a life expectancy of greater than 4 weeks. ICRF-187 was administered at a dose of 3 g/M2/day for 3 days as a 4 hour infusion each day. In patients with leukemia, no objective response was seen in the bone marrow although a few patients had a decrease in peripheral blast count. There were no measurable responses seen in patients with a solid tumor. ICRF-187 was well tolerated. The major toxicity was hematopoietic depression. Significant but rare toxicities included moderate to severe nausea and vomiting, and elevation of bilirubin and transaminases. Although inactive in the current study, ICRF-187 might be more active in another schedule.

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Year:  1991        PMID: 1804808     DOI: 10.1007/BF00183575

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  5 in total

1.  The bioavailability in man of ICRF-159 a new oral antineoplastic agent.

Authors:  P J Creaven; L M Allen; D A Alford
Journal:  J Pharm Pharmacol       Date:  1975-12       Impact factor: 3.765

2.  Phase I study of ICRF-187 in pediatric cancer patients and comparison of its pharmacokinetics in children and adults.

Authors:  J S Holcenberg; K D Tutsch; R H Earhart; R S Ungerleider; B A Kamen; C B Pratt; T J Gribble; D L Glaubiger
Journal:  Cancer Treat Rep       Date:  1986-06

3.  Phase I study of ICRF-187 using a daily for 3 days schedule.

Authors:  D D Von Hoff; D Howser; B J Lewis; J Holcenberg; R B Weiss; R C Young
Journal:  Cancer Treat Rep       Date:  1981 Mar-Apr

4.  Utilization of an enantiomer as a solution to a pharmaceutical problem: application to solubilization of 1,2-di(4-piperazine-2,6-dione)propane.

Authors:  A J Repta; M J Baltezor; P C Bansal
Journal:  J Pharm Sci       Date:  1976-02       Impact factor: 3.534

5.  Protective effect of the bispiperazinedione ICRF-187 against doxorubicin-induced cardiac toxicity in women with advanced breast cancer.

Authors:  J L Speyer; M D Green; E Kramer; M Rey; J Sanger; C Ward; N Dubin; V Ferrans; P Stecy; A Zeleniuch-Jacquotte
Journal:  N Engl J Med       Date:  1988-09-22       Impact factor: 91.245

  5 in total
  4 in total

1.  Dexrazoxane as a cardioprotectant in children receiving anthracyclines.

Authors:  Dana M Sepe; Jill P Ginsberg; Frank M Balis
Journal:  Oncologist       Date:  2010-11-04

2.  Potent antiviral activity of topoisomerase I and II inhibitors against Kaposi's sarcoma-associated herpesvirus.

Authors:  Lorenzo González-Molleda; Yan Wang; Yan Yuan
Journal:  Antimicrob Agents Chemother       Date:  2011-11-21       Impact factor: 5.191

3.  Administration of Dexrazoxane Improves Cardiac Indices in Children and Young Adults With Acute Myeloid Leukemia (AML) While Maintaining Survival Outcomes.

Authors:  Nathan J Schloemer; Molly Brickler; Raymond Hoffmann; Amy Pan; Pippa Simpson; Vanessa McFadden; Joseph Block; Richard L Tower; Michael J Burke
Journal:  J Pediatr Hematol Oncol       Date:  2017-07       Impact factor: 1.289

Review 4.  The current and future role of dexrazoxane as a cardioprotectant in anthracycline treatment: expert panel review.

Authors:  S M Swain; P Vici
Journal:  J Cancer Res Clin Oncol       Date:  2003-10-17       Impact factor: 4.553

  4 in total

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