You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT JAMA
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 290 No. 4, July 23, 2003 TABLE OF CONTENTS
  JAMA
  •  Online Features
  Original Contribution
 This Article
 •Full text
 •PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (66)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in JAMA
 Topic Collections
 •Journalology/ Peer Review/ Authorship
 •Medical Ethics
 •Randomized Controlled Trial
 •Alert me on articles by topic

Factors Associated With Failure to Publish Large Randomized Trials Presented at an Oncology Meeting

Monika K. Krzyzanowska, MD, MPH; Melania Pintilie, MSc; Ian F. Tannock, MD, PhD

JAMA. 2003;290:495-501.

Context  Large clinical trials are the criterion standard for making treatment decisions, and nonpublication of the results of such trials can lead to bias in the literature and contribute to inappropriate medical decisions.

Objectives  To determine the rate of full publication of large randomized trials presented at annual meetings of the American Society of Clinical Oncology (ASCO), quantify bias against publishing nonsignificant results, and identify factors associated with time to publication.

Design  Survey of 510 abstracts from large (sample size, >=200), phase 3, randomized controlled trials presented at ASCO meetings between 1989 and 1998. Trial results were classified as significant (P<=.05 for the primary outcome measure) or nonsignificant (P>.05 or not reported), and the type of presentation and sponsorship were identified. Subsequent full publication was identified using a search of MEDLINE and EMBASE, completed November 1, 2001; the search was updated in November 2002, using the Cochrane Register of Controlled Trials. Authors were contacted if the searches did not find evidence of publication.

Main Outcome Measures  Publication rate at 5 years; time from presentation to full publication.

Results  Of 510 randomized trials, 26% were not published in full within 5 years after presentation at the meeting. Eighty-one percent of the studies with significant results had been published by this time compared with 68% of the studies with nonsignificant results (P<.001). Studies with oral or plenary presentation were published sooner than those not presented (P = .002), and studies with pharmaceutical sponsorship were published sooner than studies with cooperative group sponsorship or studies for which sponsorship was not specified (P = .02). These factors remained significant in a multivariable model. The most frequent reason cited by authors for not publishing was lack of time, funds, or other resources.

Conclusions  A substantial number of large phase 3 trials presented at an international oncology meeting remain unpublished 5 years after presentation. Bias against publishing nonsignificant results is a problem even for large randomized trials. Nonpublication breaks the contract that investigators make with trial participants, funding agencies, and ethics boards.


Author Affiliations: Center for Outcomes and Policy Research, Department of Adult Oncology, Dana-Farber Cancer Institute, Boston, Mass (Dr Krzyzanowska); Departments of Biostatistics (Ms Pintilie) and Medical Oncology (Dr Tannock), Princess Margaret Hospital and University of Toronto, Toronto, Ontario.


RELATED ARTICLE

Registering Clinical Trials
Kay Dickersin and Drummond Rennie
JAMA. 2003;290(4):516-523.
ABSTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Better reporting of randomized trials in biomedical journal and conference abstracts
Hopewell et al.
Journal of Information Science 2008;34:162-173.
ABSTRACT  

Analysis of Phase II Studies on Targeted Agents and Subsequent Phase III Trials: What Are the Predictors for Success?
Chan et al.
JCO 2008;26:1511-1518.
ABSTRACT | FULL TEXT  

Improving the Quality of Abstract Reporting for Phase I Cancer Trials
Strevel et al.
Clin. Cancer Res. 2008;14:1782-1787.
ABSTRACT | FULL TEXT  

Publication Bias in Orthopaedic Research: An Analysis of Scientific Factors Associated with Publication in The Journal of Bone and Joint Surgery (American Volume)
Okike et al.
JBJS 2008;90:595-601.
ABSTRACT | FULL TEXT  

Reflections on Medical Oncology: 25 Years of Clinical Trials Where Have We Come and Where Are We Going?
Booth and Tannock
JCO 2008;26:6-8.
FULL TEXT  

Disclosure of Conflicts of Interest by Authors of Clinical Trials and Editorials in Oncology
Riechelmann et al.
JCO 2007;25:4642-4647.
ABSTRACT | FULL TEXT  

Statistical Power of Negative Randomized Controlled Trials Presented at American Society for Clinical Oncology Annual Meetings
Bedard et al.
JCO 2007;25:3482-3487.
ABSTRACT | FULL TEXT  

Publication bias in the medical literature: a review by a Canadian Research Ethics Board: [Biais de publication dans la litterature medicale : un compte rendu d'un Comite d'ethique de recherche canadien]
Hall et al.
Canadian J. Anesthesia 2007;54:380-388.
ABSTRACT | FULL TEXT  

Statistical and Clinical Interpretation of Research Results
Allison
J. Am. Podiatr. Med. Assoc. 2007;97:165-170.
ABSTRACT | FULL TEXT  

Comparison of Outcomes of Phase II Studies and Subsequent Randomized Control Studies Using Identical Chemotherapeutic Regimens
Zia et al.
JCO 2005;23:6982-6991.
ABSTRACT | FULL TEXT  

Acute Endophthalmitis Following Cataract Surgery: A Systematic Review of the Literature
Taban et al.
Arch Ophthalmol 2005;123:613-620.
ABSTRACT | FULL TEXT  

Features of a High Quality Phase 3 Trial
Tannock
aacredbook 2005;2005:207-210.
FULL TEXT  

Response by McDonald and Molony
McDonald and Molony
West J Nurs Res 2004;26:858-859.
 

Trends in the Risks and Benefits to Patients With Cancer Participating in Phase 1 Clinical Trials
Roberts et al.
JAMA 2004;292:2130-2140.
ABSTRACT | FULL TEXT  

Risks and Benefits of Phase 1 Clinical Trials Evaluating New Anticancer Agents: A Case for More Innovation
Chen and Tannock
JAMA 2004;292:2150-2151.
FULL TEXT  

Task force 2: Investigator participation in clinical research
Califf et al.
J Am Coll Cardiol 2004;44:1729-1736.
FULL TEXT  

Task Force 2: Investigator Participation in Clinical Research
Califf et al.
Circulation 2004;110:2517-2524.
FULL TEXT  

Quality of cancer care
Vardy and Tannock
Ann Oncol 2004;15:1001-1006.
ABSTRACT | FULL TEXT  

Are Chemotherapy Response Rates Related to Treatment-Induced Survival Prolongations in Patients With Advanced Cancer?
Shanafelt et al.
JCO 2004;22:1966-1974.
ABSTRACT | FULL TEXT  

Quality of Abstracts Describing Randomized Trials in the Proceedings of American Society of Clinical Oncology Meetings: Guidelines for Improved Reporting
Krzyzanowska et al.
JCO 2004;22:1993-1999.
ABSTRACT | FULL TEXT  

Randomized clinical trials: What gets published, and when?
Hirsch
CMAJ 2004;170:481-483.
FULL TEXT  

ABSTRACTS
Obstet Gynecol 2003;102:1085-1087.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2003 American Medical Association. All Rights Reserved.