Literature DB >> 26383917

Enrollment and Stopping Rules for Managing Toxicity Requiring Long Follow-Up in Phase II Oncology Trials.

Guochen Song1, Anastasia Ivanova2.   

Abstract

Monitoring of toxicity is often conducted in Phase II trials in oncology to avoid an excessive number of toxicities if the wrong dose is chosen for Phase II. Existing stopping rules for toxicity use information from patients who have already completed follow-up. We describe a stopping rule that uses all available data to determine whether to stop for toxicity or not when follow-up for toxicity is long. We propose an enrollment rule that prescribes the maximum number of patients that may be enrolled at any given point in the trial.

Entities:  

Keywords:  Delayed outcome; Enrollment rule; Phase II oncology trial; Pocock boundary; Stopping rule.

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Year:  2015        PMID: 26383917      PMCID: PMC4689581          DOI: 10.1080/10543406.2015.1086779

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  3 in total

1.  Continuous toxicity monitoring in phase II trials in oncology.

Authors:  Anastasia Ivanova; Bahjat F Qaqish; Michael J Schell
Journal:  Biometrics       Date:  2005-06       Impact factor: 2.571

2.  Sequential designs for phase I clinical trials with late-onset toxicities.

Authors:  Y K Cheung; R Chappell
Journal:  Biometrics       Date:  2000-12       Impact factor: 2.571

3.  Monitoring late-onset toxicities in phase I trials using predicted risks.

Authors:  B Nebiyou Bekele; Yuan Ji; Yu Shen; Peter F Thall
Journal:  Biostatistics       Date:  2007-12-14       Impact factor: 5.899

  3 in total
  1 in total

1.  Statistical design of Phase II/III clinical trials for testing therapeutic interventions in COVID-19 patients.

Authors:  Shesh N Rai; Chen Qian; Jianmin Pan; Anand Seth; Deo Kumar Srivastava; Aruni Bhatnagar
Journal:  BMC Med Res Methodol       Date:  2020-08-31       Impact factor: 4.615

  1 in total

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