Literature DB >> 19237631

Stopping or reporting early for positive results in randomized clinical trials: the National Cancer Institute Cooperative Group experience from 1990 to 2005.

Edward L Korn1, Boris Freidlin, Margaret Mooney.   

Abstract

Randomized clinical trials are designed with stopping boundaries to guide data monitoring committees with their decision making concerning ongoing trials. In particular, when extremely positive results are seen and a boundary is crossed, the data monitoring committee may recommend releasing the results earlier to the public than at the definitive final analysis time specified in the protocol. For trials that are still accruing, this also means stopping accrual. Because the information about treatment efficacy is more limited in an early analysis than in a final analysis, questions have been raised about the appropriateness of incorporating early stopping for positive results in trial designs. In particular, there are concerns that treatment effects seen early may not be real or may be overly optimistic. To examine this issue, we collected information about treatment efficacy on National Cancer Institute Cooperative Group trials that were stopped early for positive results (information both at the time the trial was stopped/released and at times of further follow-up). Twenty-seven such trials were located. For 17 of 18 of these trials with sufficient follow-up information, the treatment effect was similar or only slightly smaller at last follow-up compared with the stopping/release time. We critically evaluate reasons why one might be concerned about early stopping for positive results. We conclude that for trials with well-designed interim monitoring plans, the ability to stop early for positive results is an important component of the trial design, allowing the public to benefit as soon as possible from the study conclusions.

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Mesh:

Year:  2009        PMID: 19237631      PMCID: PMC2668973          DOI: 10.1200/JCO.2008.19.5339

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


  46 in total

1.  Stopping at nothing? Some dilemmas of data monitoring in clinical trials.

Authors:  Steven N Goodman
Journal:  Ann Intern Med       Date:  2007-06-19       Impact factor: 25.391

2.  Ethical issues in stopping randomized trials early because of apparent benefit.

Authors:  Paul S Mueller; Victor M Montori; Dirk Bassler; Barbara A Koenig; Gordon H Guyatt
Journal:  Ann Intern Med       Date:  2007-06-19       Impact factor: 25.391

Review 3.  Early stopping of randomized clinical trials for overt efficacy is problematic.

Authors:  Dirk Bassler; Victor M Montori; Matthias Briel; Paul Glasziou; Gordon Guyatt
Journal:  J Clin Epidemiol       Date:  2008-03       Impact factor: 6.437

Review 4.  Randomized trials in oncology stopped early for benefit.

Authors:  Ryan A Wilcox; Benjamin Djulbegovic; H Lee Moffitt; Gordon H Guyatt; Victor M Montori
Journal:  J Clin Oncol       Date:  2008-01-01       Impact factor: 44.544

5.  A comparison of early intensive methotrexate/mercaptopurine with early intensive alternating combination chemotherapy for high-risk B-precursor acute lymphoblastic leukemia: a Pediatric Oncology Group phase III randomized trial.

Authors:  S J Lauer; J J Shuster; D H Mahoney; N Winick; S Toledano; L Munoz; G Kiefer; J D Pullen; C P Steuber; B M Camitta
Journal:  Leukemia       Date:  2001-07       Impact factor: 11.528

6.  Phase III randomized intergroup trial of subtotal lymphoid irradiation versus doxorubicin, vinblastine, and subtotal lymphoid irradiation for stage IA to IIA Hodgkin's disease.

Authors:  O W Press; M LeBlanc; A S Lichter; T M Grogan; J M Unger; T H Wasserman; E R Gaynor; B A Peterson; T P Miller; R I Fisher
Journal:  J Clin Oncol       Date:  2001-11-15       Impact factor: 44.544

7.  Concurrent chemotherapy and pelvic radiation therapy compared with pelvic radiation therapy alone as adjuvant therapy after radical surgery in high-risk early-stage cancer of the cervix.

Authors:  W A Peters; P Y Liu; R J Barrett; R J Stock; B J Monk; J S Berek; L Souhami; P Grigsby; W Gordon; D S Alberts
Journal:  J Clin Oncol       Date:  2000-04       Impact factor: 44.544

8.  Paclitaxel plus bevacizumab versus paclitaxel alone for metastatic breast cancer.

Authors:  Kathy Miller; Molin Wang; Julie Gralow; Maura Dickler; Melody Cobleigh; Edith A Perez; Tamara Shenkier; David Cella; Nancy E Davidson
Journal:  N Engl J Med       Date:  2007-12-27       Impact factor: 91.245

9.  An update of the phase III trial comparing whole pelvic to prostate only radiotherapy and neoadjuvant to adjuvant total androgen suppression: updated analysis of RTOG 94-13, with emphasis on unexpected hormone/radiation interactions.

Authors:  Colleen A Lawton; Michelle DeSilvio; Mack Roach; Valery Uhl; Robert Kirsch; Michael Seider; Marvin Rotman; Christopher Jones; Sucha Asbell; Richard Valicenti; Stephen Hahn; Charles R Thomas
Journal:  Int J Radiat Oncol Biol Phys       Date:  2007-05-24       Impact factor: 7.038

10.  Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4) for previously treated metastatic colorectal cancer: results from the Eastern Cooperative Oncology Group Study E3200.

Authors:  Bruce J Giantonio; Paul J Catalano; Neal J Meropol; Peter J O'Dwyer; Edith P Mitchell; Steven R Alberts; Michael A Schwartz; Al B Benson
Journal:  J Clin Oncol       Date:  2007-04-20       Impact factor: 44.544

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  12 in total

1.  How to interpret a randomized controlled study stopped early.

Authors:  G Leandro
Journal:  Intensive Care Med       Date:  2013-09       Impact factor: 17.440

2.  Quantifying over-estimation in early stopped clinical trials and the "freezing effect" on subsequent research.

Authors:  Hao Wang; Gary L Rosner; Steven N Goodman
Journal:  Clin Trials       Date:  2016-06-07       Impact factor: 2.486

3.  Adjuvant trastuzumab for breast cancer: uncertainties in clinical and economic evidence following early stopping of the HERA trial.

Authors:  Tallal Younis; Chris Skedgel
Journal:  Pharmacoeconomics       Date:  2011-05       Impact factor: 4.981

4.  Prematurely ended phase III trials in Sweden during the years 2002-2008.

Authors:  Karin Hedenmalm; Annika Johansson; Kristoffer Bäckman; Patrik Ohagen
Journal:  Eur J Clin Pharmacol       Date:  2011-03-12       Impact factor: 2.953

5.  Can we trust in trials stopped early for benefit?

Authors:  Giovanni Casazza; Francesco Casella
Journal:  Intern Emerg Med       Date:  2012-10-31       Impact factor: 3.397

6.  Bioethics in Practice: Considerations for Stopping a Clinical Trial Early.

Authors:  Richard E Deichmann; Marie Krousel-Wood; Joseph Breault
Journal:  Ochsner J       Date:  2016

7.  Rosuvastatin for primary prevention in older persons with elevated C-reactive protein and low to average low-density lipoprotein cholesterol levels: exploratory analysis of a randomized trial.

Authors:  Robert J Glynn; Wolfgang Koenig; Børge G Nordestgaard; James Shepherd; Paul M Ridker
Journal:  Ann Intern Med       Date:  2010-04-20       Impact factor: 25.391

Review 8.  Rosuvastatin, inflammation, C-reactive protein, JUPITER, and primary prevention of cardiovascular disease--a perspective.

Authors:  Richard Kones
Journal:  Drug Des Devel Ther       Date:  2010-12-09       Impact factor: 4.162

9.  Use of a bioabsorbable mesh in midline laparotomy closure to prevent incisional hernia: randomized controlled trial.

Authors:  S Valverde; M A Arbós; M T Quiles; E Espín; J L Sánchez-Garcia; V Rodrigues; J A Pereira; R Villalobos; J M García-Alamino; M Armengol; M López-Cano
Journal:  Hernia       Date:  2021-05-31       Impact factor: 2.920

Review 10.  Endovascular treatment versus medical care alone for ischaemic stroke: systematic review and meta-analysis.

Authors:  Filipe Brogueira Rodrigues; Joana Briosa Neves; Daniel Caldeira; José M Ferro; Joaquim J Ferreira; João Costa
Journal:  BMJ       Date:  2016-04-18
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