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Brief Summary

GUIDELINE TITLE

Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Sections 1-2: any cancer experience.

BIBLIOGRAPHIC SOURCE(S)

  • Children's Oncology Group. Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Sections 1-2: any cancer experience. Bethesda (MD): Children's Oncology Group; 2006 Mar. 4 p. [50 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Children's Oncology Group. Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Version 1.2. 2004 Mar.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Grades of recommendations (1, 2A, 2B, 3) are defined at the end of the "Major Recommendations" field.

Note from the Children's Oncology Group and the National Guideline Clearinghouse (NGC): The Children's Oncology Group Long-Term Follow-Up Guidelines for Survivors of Childhood, Adolescent, and Young Adult Cancers (COG LTFU) are organized according to therapeutic exposures; this guideline has been divided into individual summaries. In addition to the current summary, the following are available:

In order to accurately derive individualized screening recommendations for a specific childhood cancer survivor using this guideline, see "Using the COG LTFU Guidelines to Develop Individualized Screening Recommendations" in the original guideline document. (Note: For ease of use, a Patient-Specific Guideline Identification Tool has been developed to streamline the process and is included in Appendix I of the original guideline document.)

Guideline Organization

The Children's Oncology Group Long-Term Follow-Up Guidelines for Survivors of Childhood, Adolescent, and Young Adult Cancers are organized according to therapeutic exposures, arranged by column as follows:

System

Body system (e.g., auditory, musculoskeletal) most relevant to each guideline section.

Score

Score assigned by expert panel representing the strength of data from the literature linking a specific late effect with a therapeutic exposure coupled with an assessment of the appropriateness of the screening recommendation based on collective clinical experience.

Section Number

Unique identifier for each guideline section corresponding with listing in Index.

Therapeutic Agent

Therapeutic intervention for malignancy, including chemotherapy, radiation, surgery, blood/serum products, hematopoietic cell transplant, and other therapeutic modalities.

Risk Factors

Host factors (e.g., age, sex, race, genetic predisposition), treatment factors (e.g., cumulative dose of therapeutic agent, mode of administration, combinations of agents), medical conditions (e.g., pre-morbid or co-morbid conditions), and health behaviors (e.g., diet, smoking, alcohol use) that may increase risk of developing the complication.

Highest Risk Factors

Conditions (host factors, treatment factors, medical conditions and/or health behaviors) associated with the highest risk for developing the complication.

Periodic Evaluations

Recommended screening evaluations, including health history, physical examination, laboratory evaluation, imaging, and psychosocial assessment. Recommendation for minimum frequency of periodic evaluations is based on risk factors and magnitude of risk, as supported by the medical literature and/or the combined clinical experience of the reviewers and panel of experts.

Health Counseling/
Further Considerations

Health Links: Health education materials developed specifically to accompany these guidelines. Title(s) of Health Link(s) relevant to each guideline section are referenced in this column. Health Link documents are included in Appendix II of the original guideline document.
Counseling: Suggested patient counseling regarding measures to prevent/reduce risk or promote early detection of the potential treatment complication.
Resources: See the original guideline document for lists of books and web sites that may provide the clinician with additional relevant information.
Considerations for Further Testing and Intervention: Recommendations for further diagnostic evaluations beyond minimum screening for individuals with positive screening tests, recommendations for consultation and/or referral, and recommendations for management of exacerbating or predisposing conditions.

References

References are listed immediately following each guideline section in the original guideline document. Included are medical citations that provide evidence for the association of the therapeutic intervention with the specific treatment complication and/or evaluation of predisposing risk factors. In addition, some general review articles have been included in the Reference section of the original guideline document for clinician convenience.

Note: See the end of the "Major Recommendations" field for explanations of abbreviations included in the summary.

System = Psychosocial
Score = 2A

Sec # Therapeutic Agent(s) Potential Late Effects Risk Factors Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
1 Any Cancer Experience

Info Link: The Children's Oncology Group Follow-Up Guidelines apply to patients who have been off therapy for a minimum of 2 years.
Psychosocial Disorders
Social withdrawal
Educational problems
Host Factors
Female sex
Family history of depression, anxiety or mental illness

Social Factors
Lower household income
Lower educational achievement

Treatment Factors
HCT
Host Factors
CNS tumor
CNS-directed therapy
Premorbid learning or emotional difficulties

Social Factors
Failure to graduate from high school
History
Psychosocial assessment, with attention to:
  • Educational and/or vocational progress
  • Depression
  • Anxiety
  • Post-traumatic stress
  • Social withdrawal
(Yearly)
Health Links
See "Patient Resources" field

Introduction to Long-Term Follow-Up
Emotional Issues
Educational Issues
Chronic Pain after Childhood Cancer

Resources
See the original guideline document for a list of books and web sites that may provide the clinician with additional relevant information.

Considerations for Further Testing and Intervention
Consider psychological consultation in patients with emotional difficulties related to cancer experience, including physical deformities or chronic disabilities. Consider appropriate psychotropic medications. Consider evaluation of parent for post-traumatic stress syndrome. Consider social work consultation. Refer as indicated to school liaison in community or cancer center (psychologist, social worker, school counselor) to facilitate acquisition of educational resources. Screen for physical sources of fatigue, such as anemia, sleep disturbances, nutritional deficiencies, cardiomyopathy, pulmonary fibrosis, hypothyroidism, or other endocrinopathy.
Mental Health Disorders
Depression
Anxiety
Post-traumatic stress
Host Factors
Female sex
Family history of depression, anxiety, or mental illness

Social Factors
Lower household income
Lower educational achievement

Treatment Factors
HCT
Host Factors
CNS tumor
CNS-directed therapy
Premorbid learning or emotional difficulties

Social Factors
Failure to graduate from high school
Risky Behaviors
Behaviors known to increase the likelihood of subsequent illness or injury
Social Factors
Lower household income
Host Factors
Older age at diagnosis

Social Factors
Lower educational achievement
Psychosocial Disability due to Pain Treatment Factors
Amputation
Radiation to bone/joint
Limb-sparing surgery
Vincristine exposure

Medical Conditions
Osteonecrosis
Host Factors
CNS tumor
Hodgkin lymphoma
Fatigue Host Factors
Female sex
Depression
Obesity

Social Factors
Unemployment
Treatment Factors
Pulmonary radiation

Note: See a list of Abbreviations at the end of the "Major Recommendations" field.

System = Psychosocial
Score = 2A

Sec # Therapeutic Agent(s) Potential Late Effects Risk Factors Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
2 Any Cancer Experience Limitations in healthcare and insurance access Social Factors
Lower household income
Lower educational achievement
  History

Psychosocial assessment, with attention to healthcare insurance and access
(Yearly)
Health Links

See "Patient Resources" field
Finding Healthcare

Considerations for Further Testing and Intervention
Social work consultation

Note: See a list of Abbreviations at the end of the "Major Recommendations" field.

Abbreviations

CNS, central nervous system; HCT, hematopoietic cell transplant

Definitions:

Explanation of Scoring for the Long-Term Follow-Up Guidelines

Each item was scored based on the level of evidence currently available to support it. Scores were assigned according to a modified version of the National Comprehensive Cancer Network "Categories of Consensus," as follows:

1  There is uniform consensus of the panel that (1) there is high-level evidence linking the late effect with the therapeutic exposure, and (2) the screening recommendation is appropriate based on the collective clinical experience of panel members.

2A  There is uniform consensus of the panel that (1) there is lower-level evidence linking the late effect with the therapeutic exposure, and (2) the screening recommendation is appropriate based on the collective clinical experience of panel members.

2B  There is non-uniform consensus of the panel that (1) there is lower-level evidence linking the late effect with the therapeutic exposure, and (2) the screening recommendation is appropriate based on the collective clinical experience of panel members.

3  There is major disagreement that the recommendation is appropriate.

Rating Scheme for the Strength of the Evidence

"High-level evidence" (recommendation category 1) was defined as evidence derived from high quality case control or cohort studies.

"Lower-level evidence" (recommendation categories 2A and 2B) was defined as evidence derived from non-analytic studies, case reports, case series, and clinical experience.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations")

Although several well-conducted studies on large populations of childhood cancer survivors have demonstrated associations between specific exposures and late effects, the size of the survivor population and the rate of occurrence of late effects does not allow for clinical studies that would assess the impact of screening recommendations on the morbidity and mortality associated with the late effect. Therefore, scoring of each exposure reflects the expert panel's assessment of the level of literature support linking the therapeutic exposure with the late effect coupled with an assessment of the appropriateness of the recommended screening modality in identifying the potential late effect based on the panel's collective clinical experience.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Children's Oncology Group. Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Sections 1-2: any cancer experience. Bethesda (MD): Children's Oncology Group; 2006 Mar. 4 p. [50 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2003 Sep (revised 2006 Mar)

GUIDELINE DEVELOPER(S)

Children's Oncology Group - Medical Specialty Society

SOURCE(S) OF FUNDING

This work was supported by the Children's Oncology Group grant U10 CA098543 from the National Cancer Institute.

GUIDELINE COMMITTEE

Children's Oncology Group Nursing Discipline and Late Effects Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Melissa M. Hudson, MD
Vice-Chair – COG Late Effects Committee
Member, Department of Hematology-Oncology
Director, After Completion of Therapy Clinic
St. Jude Children's Research Hospital
Memphis, Tennessee

Wendy Landier, RN, MSN, CPNP, CPON®
Chair – COG Nursing Clinical Practice Subcommittee
Clinical Director - Survivorship Clinic
City of Hope Comprehensive Cancer Center
Duarte, California

Smita Bhatia, MD, MPH
Chair – COG Late Effects Committee
Professor and Chair, Division of Population Sciences
City of Hope Comprehensive Cancer Center
Duarte, California

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

All Children's Oncology Group (COG) members have complied with the COG conflict of interest policy, which requires disclosure of any potential financial or other conflicting interests.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Children's Oncology Group. Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Version 1.2. 2004 Mar.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

In an effort led by the Nursing Clinical Practice Subcommittee, complementary patient education materials (Health Links) were developed and are available in Appendix II of the original guideline document. The following Health Links are relevant to this summary:

Section 1

Section 2

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This NGC summary was completed by ECRI on May 4, 2007. The information was verified by the guideline developer on June 11, 2007.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

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Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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