Literature DB >> 26503199

Clinical Utility of Metrics Based on Tumor Measurements in Phase II Trials to Predict Overall Survival Outcomes in Phase III Trials by Using Resampling Methods.

Ming-Wen An1, Yu Han2, Jeffrey P Meyers2, Jan Bogaerts2, Daniel J Sargent2, Sumithra J Mandrekar2.   

Abstract

PURPOSE: Phase II clinical trials inform go/no-go decisions for proceeding to phase III trials, and appropriate end points in phase II trials are critical for facilitating this decision. Phase II solid tumor trials have traditionally used end points such as tumor response defined by Response Evaluation Criteria for Solid Tumors (RECIST). We previously reported that absolute and relative changes in tumor measurements demonstrated potential, but not convincing, improvement over RECIST to predict overall survival (OS). We have evaluated the metrics by using additional measures of clinical utility and data from phase III trials.
METHODS: Resampling methods were used to assess the clinical utility of metrics to predict phase III outcomes from simulated phase II trials. In all, 2,000 phase II trials were simulated from four actual phase III trials (two positive for OS and two negative for OS). Cox models for three metrics landmarked at 12 weeks and adjusted for baseline tumor burden were fit for each phase II trial: absolute changes, relative changes, and RECIST. Clinical utility was assessed by positive predictive value and negative predictive value, that is, the probability of a positive or negative phase II trial predicting an effective or ineffective phase III conclusion, by prediction error, and by concordance index (c-index).
RESULTS: Absolute and relative change metrics had higher positive predictive value and negative predictive value than RECIST in five of six treatment comparisons and lower prediction error curves in all six. However, differences were negligible. No statistically significant difference in c-index across metrics was found.
CONCLUSION: The absolute and relative change metrics are not meaningfully better than RECIST in predicting OS.
© 2015 by American Society of Clinical Oncology.

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Year:  2015        PMID: 26503199      PMCID: PMC4669590          DOI: 10.1200/JCO.2015.60.8778

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  18 in total

1.  Choosing phase II endpoints and designs: evaluating the possibilities.

Authors:  Michael LeBlanc; Catherine Tangen
Journal:  Clin Cancer Res       Date:  2012-03-08       Impact factor: 12.531

2.  The initial change in tumor size predicts response and survival in patients with metastatic colorectal cancer treated with combination chemotherapy.

Authors:  C Suzuki; L Blomqvist; A Sundin; H Jacobsson; P Byström; Å Berglund; P Nygren; B Glimelius
Journal:  Ann Oncol       Date:  2011-08-10       Impact factor: 32.976

3.  Resampling phase III data to assess phase II trial designs and endpoints.

Authors:  Manish R Sharma; Theodore G Karrison; Yuyan Jin; Robert R Bies; Michael L Maitland; Walter M Stadler; Mark J Ratain
Journal:  Clin Cancer Res       Date:  2012-01-27       Impact factor: 12.531

4.  Evaluation of tumor-size response metrics to predict overall survival in Western and Chinese patients with first-line metastatic colorectal cancer.

Authors:  Laurent Claret; Manish Gupta; Kelong Han; Amita Joshi; Nenad Sarapa; Jing He; Bob Powell; René Bruno
Journal:  J Clin Oncol       Date:  2013-05-06       Impact factor: 44.544

5.  More randomization in phase II trials: necessary but not sufficient.

Authors:  Lawrence Rubinstein; Michael Leblanc; Malcolm A Smith
Journal:  J Natl Cancer Inst       Date:  2011-06-27       Impact factor: 13.506

6.  Resampling the N9741 trial to compare tumor dynamic versus conventional end points in randomized phase II trials.

Authors:  Manish R Sharma; Elizabeth Gray; Richard M Goldberg; Daniel J Sargent; Theodore G Karrison
Journal:  J Clin Oncol       Date:  2014-10-27       Impact factor: 44.544

7.  Comparison of error rates in single-arm versus randomized phase II cancer clinical trials.

Authors:  Hui Tang; Nathan R Foster; Axel Grothey; Stephen M Ansell; Richard M Goldberg; Daniel J Sargent
Journal:  J Clin Oncol       Date:  2010-03-08       Impact factor: 44.544

Review 8.  Assumptions of expected benefits in randomized phase III trials evaluating systemic treatments for cancer.

Authors:  Hui K Gan; Benoit You; Gregory R Pond; Eric X Chen
Journal:  J Natl Cancer Inst       Date:  2012-04-06       Impact factor: 13.506

9.  Evaluation of alternate categorical tumor metrics and cut points for response categorization using the RECIST 1.1 data warehouse.

Authors:  Sumithra J Mandrekar; Ming-Wen An; Jeffrey Meyers; Axel Grothey; Jan Bogaerts; Daniel J Sargent
Journal:  J Clin Oncol       Date:  2014-02-10       Impact factor: 44.544

10.  Designing exploratory cancer trials using change in tumour size as primary endpoint.

Authors:  Thomas Jaki; Valérie André; Ting-Li Su; John Whitehead
Journal:  Stat Med       Date:  2012-12-19       Impact factor: 2.373

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Journal:  J Immunother Cancer       Date:  2019-02-08       Impact factor: 13.751

4.  Modeling tumor measurement data to predict overall survival (OS) in cancer clinical trials.

Authors:  Fang-Shu Ou; Jun Tang; Ming-Wen An; Sumithra J Mandrekar
Journal:  Contemp Clin Trials Commun       Date:  2021-08-09

5.  Utilization of target lesion heterogeneity for treatment efficacy assessment in late stage lung cancer.

Authors:  Dung-Tsa Chen; Wenyaw Chan; Zachary J Thompson; Ram Thapa; Amer A Beg; Andreas N Saltos; Alberto A Chiappori; Jhanelle E Gray; Eric B Haura; Trevor A Rose; Ben Creelan
Journal:  PLoS One       Date:  2021-07-01       Impact factor: 3.240

  5 in total

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