Literature DB >> 31335389

Biostatistical and Logistical Considerations in the Development of Basket and Umbrella Clinical Trials.

Laura M Yee1, Lisa M McShane, Boris Freidlin, Margaret M Mooney, Edward L Korn.   

Abstract

Oncology clinical trials are undergoing transformation to evaluate targeted therapies addressing a wider variety of biologically defined cancer subgroups. Multiarm basket and umbrella trials conducted under master protocols have become more prominent mechanisms for the clinical evaluation of promising new biologically driven anticancer therapies that are integral to precision oncology medicine. These new trial designs permit efficient clinical evaluation of multiple therapies in a variety of histologically and biologically defined cancers. These complex trials require extensive planning and attention to many factors, including choice of biomarker assay platform, mechanism for processing clinicopathologic and biomarker data to assign patients to substudies, and statistical design, monitoring, and analysis of substudies. Trial teams have expanded to include expertise in the interface between biology, clinical oncology, bioinformatics, and statistics. Strategies for the design, conduct, and analysis of these complex trials will continue to evolve to meet new challenges and opportunities in precision oncology medicine.

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Year:  2019        PMID: 31335389      PMCID: PMC6658126          DOI: 10.1097/PPO.0000000000000384

Source DB:  PubMed          Journal:  Cancer J        ISSN: 1528-9117            Impact factor:   3.360


  46 in total

1.  Hierarchical Bayesian approaches to phase II trials in diseases with multiple subtypes.

Authors:  Peter F Thall; J Kyle Wathen; B Nebiyou Bekele; Richard E Champlin; Laurence H Baker; Robert S Benjamin
Journal:  Stat Med       Date:  2003-03-15       Impact factor: 2.373

2.  Monitoring for lack of benefit: a critical component of a randomized clinical trial.

Authors:  Boris Freidlin; Edward L Korn
Journal:  J Clin Oncol       Date:  2008-12-08       Impact factor: 44.544

3.  Randomized clinical trials with biomarkers: design issues.

Authors:  Boris Freidlin; Lisa M McShane; Edward L Korn
Journal:  J Natl Cancer Inst       Date:  2010-01-14       Impact factor: 13.506

4.  Multiple Histology Phase II Trials.

Authors:  Michael Leblanc; Cathryn Rankin; John Crowley
Journal:  Clin Cancer Res       Date:  2009-06-23       Impact factor: 12.531

5.  Guidelines for the development and incorporation of biomarker studies in early clinical trials of novel agents.

Authors:  Janet E Dancey; Kevin K Dobbin; Susan Groshen; J Milburn Jessup; Andrew H Hruszkewycz; Maria Koehler; Ralph Parchment; Mark J Ratain; Lalitha K Shankar; Walter M Stadler; Lawrence D True; Amy Gravell; Michael R Grever
Journal:  Clin Cancer Res       Date:  2010-03-09       Impact factor: 12.531

6.  A general inefficacy interim monitoring rule for randomized clinical trials.

Authors:  Boris Freidlin; Edward L Korn; Robert Gray
Journal:  Clin Trials       Date:  2010-04-27       Impact factor: 2.486

Review 7.  Validation of analytic methods for biomarkers used in drug development.

Authors:  Cindy H Chau; Olivier Rixe; Howard McLeod; William D Figg
Journal:  Clin Cancer Res       Date:  2008-10-01       Impact factor: 12.531

8.  A prospective randomized controlled trial of tumour chemosensitivity assay directed chemotherapy versus physician's choice in patients with recurrent platinum-resistant ovarian cancer.

Authors:  Ian A Cree; Christian M Kurbacher; Alan Lamont; Andrew C Hindley; Sharon Love
Journal:  Anticancer Drugs       Date:  2007-10       Impact factor: 2.248

9.  Adaptive two-stage designs for single-arm phase IIA cancer clinical trials.

Authors:  Yong Lin; Weichung J Shih
Journal:  Biometrics       Date:  2004-06       Impact factor: 2.571

10.  Issues in clinical trial design for tumor marker studies.

Authors:  Daniel Sargent; Carmen Allegra
Journal:  Semin Oncol       Date:  2002-06       Impact factor: 4.929

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  3 in total

Review 1.  Novel clinical trial design and analytic methods to tackle challenges in therapeutic development in rare diseases.

Authors:  Yimei Li; Rima Izem
Journal:  Ann Transl Med       Date:  2022-09

2.  Approach for reporting master protocol study designs on ClinicalTrials.gov: qualitative analysis.

Authors:  Rebecca J Williams; Heather D Dobbins; Tony Tse; Sandy D Chon; David Loose; Gisele A Sarosy; Sheila A Prindiville; Frank W Rockhold; Deborah A Zarin
Journal:  BMJ       Date:  2022-06-10

3.  Moving Molecular Profiling to Routine Clinical Practice: A Way Forward?

Authors:  Boris Freidlin; Carmen J Allegra; Edward L Korn
Journal:  J Natl Cancer Inst       Date:  2020-08-01       Impact factor: 13.506

  3 in total

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