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. 277 No. 18, May 14, 1997 TABLE OF CONTENTS
  JAMA
  •  Online Features
  Consensus Statement
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in JAMA
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Genetic Testing for Susceptibility to Adult-Onset Cancer

The Process and Content of Informed Consent

Gail Geller, ScD; Jeffrey R. Botkin, MD, MPH; Michael J. Green, MD, MS; Nancy Press, PhD; Barbara B. Biesecker, MS; Benjamin Wilfond, MD; Generosa Grana, MD; Mary B. Daly, MD, PhD; Katherine Schneider, MPH; Mary Jo Ellis Kahn, RN, MSN

JAMA. 1997;277(18):1467-1474.


Abstract

Objective.
—To provide guidance on informed consent to clinicians offering cancer susceptibility testing.

Participants.
—The Task Force on Informed Consent is part of the Cancer Genetics Studies Consortium (CGSC), whose members were recipients of National Institutes of Health grants to assess the implications of cancer susceptibility testing. The 10 task force members represent a range of relevant backgrounds, including various medical specialties, social science, genetic counseling, and consumer advocacy.

Evidence.
—The CGSC held 3 public meetings from 1994 to 1996. At its first meeting, the task force jointly established a list of topics. The cochairs (G.G. and J.R.B) then developed an outline and assigned each topic to an appropriate writer and reviewer. Writers summarized the literature on their topics and drafted recommendations, which were then revised by the reviewers. The cochairs compiled and edited the entire manuscript. All members were involved in writing this report.

Consensus Process.
—The first draft was distributed to task force members, after which a meeting was held to discuss its content and organization. Consensus was reached by voting. A subsequent draft was presented to the entire CGSC at its third meeting, and comments were incorporated.

Conclusions.
—The task force recommends that informed consent for cancer susceptibility testing be an ongoing process of education and counseling in which (1) providers elicit participant, family, and community values and disclose their own, (2) decision making is shared, (3) the style of information disclosure is individualized, and (4) specific content areas are discussed.



Author Affiliations

From Genetics and Public Policy Studies, Department of Pediatrics, Johns Hopkins University, Baltimore, Md (Dr Geller); Utah Center for Human Genome Research, Eccles Institute of Human Genetics, University of Utah, Salt Lake City (Dr Botkin); Department of Humanities, Hershey Medical Center, Hershey, Pa (Dr Green); Department of Psychiatry and Biobehavioral Sciences, School of Medicine, University of California at Los Angeles (Dr Press); Medical Genetics Branch, National Human Genome Research Institute,; Bethesda, Md (Ms Biesecker); Department of Pediatrics, University of Arizona, Tucson (Dr Wilfond); Cancer Center of Southern New Jersey, Camden, NJ (Dr Grana); Fox Chase Cancer Center, Philadelphia, Pa (Dr Daly); Dana Farber Cancer Institute, Boston, Mass (Ms Schneider); and National Breast Cancer Coalition, Richmond, Va (Ms Kahn).


Footnotes

Reprints: Gail Geller, ScD, Johns Hopkins University School of Medicine, 550 N Broadway, Suite 511, Baltimore, MD 21205.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Surrogate Consent for Genomics Research in Intensive Care
Shelton et al.
Am J Crit Care 2009;18:418-426.
ABSTRACT | FULL TEXT  

Obtaining Informed Consent for Genetic Studies: The Multiethnic Study of Atherosclerosis
Green et al.
Am J Epidemiol 2006;164:845-851.
ABSTRACT | FULL TEXT  

The Role of Health Education and Behavior in Public Health Genetics
Kardia and Wang
Health Educ Behav 2005;32:583-588.
ABSTRACT  

Ethics Manual: Fifth Edition
Snyder et al.
ANN INTERN MED 2005;142:560-582.
ABSTRACT | FULL TEXT  

Effect of a Computer-Based Decision Aid on Knowledge, Perceptions, and Intentions About Genetic Testing for Breast Cancer Susceptibility: A Randomized Controlled Trial
Green et al.
JAMA 2004;292:442-452.
ABSTRACT | FULL TEXT  

Minority Recruitment in Hereditary Breast Cancer Research
Hughes et al.
Cancer Epidemiol. Biomarkers Prev. 2004;13:1146-1155.
ABSTRACT | FULL TEXT  

American Thoracic Society/European Respiratory Society Statement: Standards for the Diagnosis and Management of Individuals with Alpha-1 Antitrypsin Deficiency
Am. J. Respir. Crit. Care Med. 2003;168:818-900.
FULL TEXT  

Genetics and the Management of Women at High Risk for Breast Cancer
Mincey
The Oncologist 2003;8:466-473.
ABSTRACT | FULL TEXT  

Genetic Testing and its Implications: Human Genetics Researchers Grapple with Ethical Issues
Rabino
Science Technology Human Values 2003;28:365-402.
ABSTRACT  

"Genetic Exceptionalism" in Medicine: Clarifying the Differences between Genetic and Nongenetic Tests
Green and Botkin
ANN INTERN MED 2003;138:571-575.
ABSTRACT | FULL TEXT  

A community based study on intentions regarding predictive testing for hereditary breast cancer
Welkenhuysen et al.
J. Med. Genet. 2001;38:540-547.
FULL TEXT  

Ethical Issues With Genetic Testing in Pediatrics
Committee on Bioethics
Pediatrics 2001;107:1451-1455.
ABSTRACT | FULL TEXT  

Cost of Genetic Counseling and Testing for BRCA1 and BRCA2 Breast Cancer Susceptibility Mutations
Lawrence et al.
Cancer Epidemiol. Biomarkers Prev. 2001;10:475-481.
ABSTRACT | FULL TEXT  

BRCA1/2 Testing: Complex Themes in Result Interpretation
Peshkin et al.
JCO 2001;19:2555-2565.
ABSTRACT | FULL TEXT  

Solitary Retinal Capillary Hemangioma: Hereditary (von Hippel-Lindau Disease) or Nonhereditary?
Singh et al.
Arch Ophthalmol 2001;119:232-234.
ABSTRACT | FULL TEXT  

Genetic Privacy Laws and Patients' Fear of Discrimination by Health Insurers: The View from Genetic Counselors
Hall and Rich
J Law Med Ethics 2000;28:245-257.
 

Communicating Genetic Risk: Pros, Cons, and Counsel
Penson et al.
The Oncologist 2000;5:152-161.
ABSTRACT | FULL TEXT  

High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects
Goelen et al.
J. Med. Genet. 1999;36:304-308.
ABSTRACT | FULL TEXT  

Attitudes, Knowledge, and Risk Perceptions of Women With Breast and/or Ovarian Cancer Considering Testing for BRCA1 and BRCA2
Bluman et al.
JCO 1999;17:1040-1040.
ABSTRACT | FULL TEXT  

Uncertainties in Genetic Testing for Chronic Disease
Welch and Burke
JAMA 1998;280:1525-1527.
FULL TEXT  

Impact of Laboratory Molecular Diagnosis on Contemporary Diagnostic Criteria for Genetically Transmitted Cardiovascular Diseases: Hypertrophic Cardiomyopathy, Long-QT Syndrome, and Marfan Syndrome : A Statement for Healthcare Professionals From the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association
Maron et al.
Circulation 1998;98:1460-1471.
FULL TEXT  

Genetic Testing for Cancer Risk: How to Reconcile the Conflicts
Kodish et al.
JAMA 1998;279:179-181.
FULL TEXT  

Cancer Genetic Susceptibility Testing: Ethical and Policy Implications for Future Research and Clinical Practice
Wilfond et al.
J Law Med Ethics 1997;25:243-251.
 

Predisposition Genetic Testing for Late-Onset Disorders in Adults: A Position Paper of the National Society of Genetic Counselors
McKinnon et al.
JAMA 1997;278:1217-1220.
ABSTRACT  

Genetic Testing and Informed Consent
Page and Jensen
JAMA 1997;278:821-821.
ABSTRACT  

Informed Consent for Publication
Fontanarosa and Glass
JAMA 1997;278:682-683.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1997 American Medical Association. All Rights Reserved.