Literature DB >> 17428104

Satraplatin in hormone-refractory prostate cancer and other tumour types: pharmacological properties and clinical evaluation.

Mark J McKeage1.   

Abstract

Satraplatin is the first orally administered platinum drug to be evaluated in the clinic. Oral satraplatin plus prednisone improved progression free survival significantly relative to prednisone alone in patients with hormone-refractory prostate cancer in a randomised study. Furthermore, single-agent satraplatin has demonstrated activity in ovarian cancer and small cell lung cancer similar to that observed with single-agent cisplatin or carboplatin. In >600 treated patients, satraplatin was generally well tolerated and the most common adverse event was non-cumulative myelosuppression.

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Year:  2007        PMID: 17428104     DOI: 10.2165/00003495-200767060-00003

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  30 in total

1.  Phase II study of oral platinum drug JM216 as first-line treatment in patients with small-cell lung cancer.

Authors:  E Fokkema; H J Groen; J Bauer; D R Uges; C Weil; I E Smith
Journal:  J Clin Oncol       Date:  1999-12       Impact factor: 44.544

2.  Satraplatin activation by haemoglobin, cytochrome C and liver microsomes in vitro.

Authors:  Jocelyn L Carr; Malcolm D Tingle; Mark J McKeage
Journal:  Cancer Chemother Pharmacol       Date:  2005-09-20       Impact factor: 3.333

Review 3.  Cellular processing of platinum anticancer drugs.

Authors:  Dong Wang; Stephen J Lippard
Journal:  Nat Rev Drug Discov       Date:  2005-04       Impact factor: 84.694

4.  A phase II trial of JM-216 in cervical cancer: an NCIC CTG study.

Authors:  Marc Trudeau; Gavin Stuart; Hal Hirte; Pierre Drouin; Marie Plante; Paul Bessette; Helene Dulude; David Lebwohl; Bryn Fisher; Lesley Seymour
Journal:  Gynecol Oncol       Date:  2002-02       Impact factor: 5.482

5.  Phase II study of oral bis (aceto) ammine dichloro (cyclohexamine) platinum (IV) (JM-216, BMS-182751) given daily x 5 in hormone refractory prostate cancer (HRPC).

Authors:  Tahir Latif; Laura Wood; Cindy Connell; David C Smith; David Vaughn; David Lebwohl; David Peereboom
Journal:  Invest New Drugs       Date:  2005-01       Impact factor: 3.850

6.  Schedule dependency of orally administered bis-acetato-ammine-dichloro-cyclohexylamine-platinum(IV) (JM216) in vivo.

Authors:  M J McKeage; L R Kelland; F E Boxall; M R Valenti; M Jones; P M Goddard; J Gwynne; K R Harrap
Journal:  Cancer Res       Date:  1994-08-01       Impact factor: 12.701

7.  Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer.

Authors:  Daniel P Petrylak; Catherine M Tangen; Maha H A Hussain; Primo N Lara; Jeffrey A Jones; Mary Ellen Taplin; Patrick A Burch; Donna Berry; Carol Moinpour; Manish Kohli; Mitchell C Benson; Eric J Small; Derek Raghavan; E David Crawford
Journal:  N Engl J Med       Date:  2004-10-07       Impact factor: 91.245

8.  Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer.

Authors:  Ian F Tannock; Ronald de Wit; William R Berry; Jozsef Horti; Anna Pluzanska; Kim N Chi; Stephane Oudard; Christine Théodore; Nicholas D James; Ingela Turesson; Mark A Rosenthal; Mario A Eisenberger
Journal:  N Engl J Med       Date:  2004-10-07       Impact factor: 91.245

9.  Preclinical antitumor evaluation of bis-acetato-ammine-dichloro-cyclohexylamine platinum(IV): an orally active platinum drug.

Authors:  L R Kelland; G Abel; M J McKeage; M Jones; P M Goddard; M Valenti; B A Murrer; K R Harrap
Journal:  Cancer Res       Date:  1993-06-01       Impact factor: 12.701

10.  Rapid biotransformation of satraplatin by human red blood cells in vitro.

Authors:  Jocelyn L Carr; Malcolm D Tingle; Mark J McKeage
Journal:  Cancer Chemother Pharmacol       Date:  2002-05-22       Impact factor: 3.333

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  2 in total

1.  The plasma and cerebrospinal fluid pharmacokinetics of the platinum analog satraplatin after intravenous administration in non-human primates.

Authors:  Leigh Marcus; Robert Murphy; Elizabeth Fox; Cynthia McCully; Raphael Cruz; Katherine E Warren; Thorsten Meyer; Edward McNiff; Frank M Balis; Brigitte C Widemann
Journal:  Cancer Chemother Pharmacol       Date:  2011-06-26       Impact factor: 3.333

2.  RHAMM (CD168) is overexpressed at the protein level and may constitute an immunogenic antigen in advanced prostate cancer disease.

Authors:  Kilian M Gust; Matthias D Hofer; Sven R Perner; Robert Kim; Arul M Chinnaiyan; Sooryanarayana Varambally; Peter Moller; Ludwig Rinnab; Mark A Rubin; Jochen Greiner; Michael Schmitt; Rainer Kuefer; Mark Ringhoffer
Journal:  Neoplasia       Date:  2009-09       Impact factor: 5.715

  2 in total

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