Literature DB >> 21246533

Patient willingness to undergo pharmacodynamic and pharmacokinetic tests in early phase oncology trials.

Raoul Tibes1, Barbara F Piper, Jessica A Smith, Raysenia L James, Martin A Benjamin, Jay H Yim, Ramesh K Ramanathan, Daniel D Von Hoff, R Curtis Bay, Mitesh J Borad.   

Abstract

BACKGROUND: Increasingly, early phase clinical trials involve pharmacodynamic (PD) and pharmacokinetic (PK) assays as well as frequent imaging studies. The authors conducted a prospective study examining patients' willingness to undergo such tests and the number of tests the patients would tolerate.
METHODS: A prospective, correlative study was conducted using a self-reported questionnaire to measure patients' willingness on a scale from 1 (not willing) to 10 (very willing) to undergo various procedures (eg, tumor and skin biopsies, blood tests) and imaging studies (eg, magnetic resonance imaging, echocardiogram). In addition, correlations were assessed between the number and type of tests and demographics, previous test experience, inconvenience, and insurance coverage. Sixty-one patients (22 women and 39 men) with advanced malignancies were enrolled. Descriptive, nonparametric, and parametric inferential statistics were used.
RESULTS: Overall willingness to undergo study-required tests was very high. Patients were most willing to undergo urine, blood, ultrasound, x-rays, echocardiogram, and computed tomography studies and were least willing to undergo tumor and skin biopsies and magnetic resonance imaging (all P ≤ .01). Significant inverse relations were observed between the frequency of a particular test and patient's willingness to undergo such tests. Inconvenience and prior negative experiences for more invasive tests (eg, skin biopsies) modestly affected willingness to undergo these tests again. College education, insurance coverage, and the requirement of tests for enrollment were correlated positively with willingness to undergo tests.
CONCLUSIONS: The current findings provide the first prospectively collected data on patients' willingness to undergo PK/PD tests and imaging studies associated with early stage oncology drug trials and can serve as basis for further exploration toward the design of patient-friendly, biomarker-driven clinical studies in oncology.
Copyright © 2011 American Cancer Society.

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Mesh:

Year:  2011        PMID: 21246533     DOI: 10.1002/cncr.25885

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  3 in total

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Authors:  Davinia S Seah; Sarah Scott; Hao Guo; Julie Najita; Ruth Lederman; Elizabeth Frank; Jessica Sohl; Zsofia Stadler; Stuart Silverman; Jeffrey Peppercorn; Eric Winer; Steve Come; Nancy U Lin
Journal:  Oncologist       Date:  2015-08-03

2.  An International MDS/MPN Working Group's perspective and recommendations on molecular pathogenesis, diagnosis and clinical characterization of myelodysplastic/myeloproliferative neoplasms.

Authors:  Tariq I Mughal; Nicholas C P Cross; Eric Padron; Ramon V Tiu; Michael Savona; Luca Malcovati; Raoul Tibes; Rami S Komrokji; Jean-Jacques Kiladjian; Guillermo Garcia-Manero; Attilio Orazi; Ruben Mesa; Jaroslaw P Maciejewski; Pierre Fenaux; Raphael Itzykson; Ghulam Mufti; Eric Solary; Alan F List
Journal:  Haematologica       Date:  2015-09       Impact factor: 9.941

Review 3.  Overcoming implementation challenges of personalized cancer therapy.

Authors:  Funda Meric-Bernstam; Gordon B Mills
Journal:  Nat Rev Clin Oncol       Date:  2012-07-31       Impact factor: 66.675

  3 in total

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