Literature DB >> 16737672

How to design a phase I trial of an anticancer botanical.

Andrew J Vickers1.   

Abstract

Phase I trials are an important part of traditional drug development in oncology. Such trials address two key issues: safety and dose. Currently, there is a dearth of phase I trials of anticancer botanicals. This may result from the apparently widespread view that a history of human use precludes the need for early-phase study. However, the safe use of a botanical by the population at large does not guarantee safety when the botanical is used in combination with other agents in the complex medical setting of oncology. Several cases of unpredictable adverse events have been recorded following the use of botanicals by cancer patients. We propose a simple, robust design for phase I trials of anticancer botanicals. This design incorporates important characteristics of botanical medicines including low toxicity, prior data on a likely safe dose, a limit on the highest dose it is feasible to administer, and the unknown relationship between dose-toxicity and dose-response curves. Two principal design features are the use of predetermined dose levels and the direct measurement of a response endpoint such as survival or immunity. This response end point can be used to determine the optimal dose if toxicity is acceptable at all dose levels. Increasing the use of phase I methodology would ensure a more systematic development of botanicals as anticancer agents. This would likely increase the chance that at least one such agent would be proven to extend lives.

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Year:  2006        PMID: 16737672      PMCID: PMC1533748     

Source DB:  PubMed          Journal:  J Soc Integr Oncol        ISSN: 1715-894X


  7 in total

1.  Efficacy of traditional Chinese herbal therapy in adult atopic dermatitis.

Authors:  M P Sheehan; M H Rustin; D J Atherton; C Buckley; D W Harris; J Brostoff; L Ostlere; A Dawson; D J Harris
Journal:  Lancet       Date:  1992-07-04       Impact factor: 79.321

Review 2.  Use of antioxidants during chemotherapy and radiotherapy should be avoided.

Authors:  Gabriella M D'Andrea
Journal:  CA Cancer J Clin       Date:  2005 Sep-Oct       Impact factor: 508.702

3.  Design and analysis of phase I clinical trials.

Authors:  B E Storer
Journal:  Biometrics       Date:  1989-09       Impact factor: 2.571

4.  Phase I and pharmacokinetic study of aplidine, a new marine cyclodepsipeptide in patients with advanced malignancies.

Authors:  Sandrine Faivre; Stéphanie Chièze; Catherine Delbaldo; Nora Ady-Vago; Cecilia Guzman; Luis Lopez-Lazaro; Stéphanie Lozahic; José Jimeno; Fernando Pico; Jean Pierre Armand; José Antonio Lopez Martin; Eric Raymond
Journal:  J Clin Oncol       Date:  2005-09-19       Impact factor: 44.544

5.  Design of phase I and II clinical trials in cancer: a statistician's view.

Authors:  N L Geller
Journal:  Cancer Invest       Date:  1984       Impact factor: 2.176

6.  Potential of chemotherapy-herb interactions in adult cancer patients.

Authors:  Jeannine S McCune; Amy J Hatfield; Anne A R Blackburn; Patricia O Leith; Robert B Livingston; Georgiana K Ellis
Journal:  Support Care Cancer       Date:  2004-02-27       Impact factor: 3.603

7.  Effects of St. John's wort on irinotecan metabolism.

Authors:  Ron H J Mathijssen; Jaap Verweij; Peter de Bruijn; Walter J Loos; Alex Sparreboom
Journal:  J Natl Cancer Inst       Date:  2002-08-21       Impact factor: 13.506

  7 in total
  3 in total

Review 1.  Which botanicals or other unconventional anticancer agents should we take to clinical trial?

Authors:  Andrew J Vickers
Journal:  J Soc Integr Oncol       Date:  2007

2.  A phase I/II trial of a polysaccharide extract from Grifola frondosa (Maitake mushroom) in breast cancer patients: immunological effects.

Authors:  Gary Deng; Hong Lin; Andrew Seidman; Monica Fornier; Gabriella D'Andrea; Kathleen Wesa; Simon Yeung; Susanna Cunningham-Rundles; Andrew J Vickers; Barrie Cassileth
Journal:  J Cancer Res Clin Oncol       Date:  2009-03-01       Impact factor: 4.553

3.  A first-in-class, first-in-human, phase I trial of p28, a non-HDM2-mediated peptide inhibitor of p53 ubiquitination in patients with advanced solid tumours.

Authors:  M A Warso; J M Richards; D Mehta; K Christov; C Schaeffer; L Rae Bressler; T Yamada; D Majumdar; S A Kennedy; C W Beattie; T K Das Gupta
Journal:  Br J Cancer       Date:  2013-02-28       Impact factor: 7.640

  3 in total

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