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Brief Summary

GUIDELINE TITLE

Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Sections 137-146: cancer and general health screening.

BIBLIOGRAPHIC SOURCE(S)

  • Children's Oncology Group. Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Sections 137-146: cancer and general health screening. Bethesda (MD): Children's Oncology Group; 2006 Mar. 11 p. [45 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

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.

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
137

(Female)
Breast Over age 40
Family history of breast cancer in first degree relative
Early onset of menstruation
Late onset of menopause (age 55 or older)
Older than 30 at birth of first child
Never pregnant
Obesity
Previous breast biopsy with atypical hyperplasia
Hormone replacement therapy
Chest radiation with potential impact to the breast (see Section 68; see list of related summaries at the beginning of the "Major Recommendation" field), including >20 Gy to the following fields:
  • Mantle
  • Mini-Mantle
  • Mediastinal
  • Chest (thorax)
  • Axilla

BRCA1, BRCA2, ATM mutation
PATIENTS AT STANDARD RISK (ACS Recommendation)

Physical

Clinical breast exam

(Every 3 years between ages 20-39, then yearly beginning at age 40)

Screening

Mammogram
(Yearly, beginning at age 40)
Health Links

See "Patient Resources" field

Breast Cancer (for patients at highest risk only)

Counseling

For patients at highest risk, counsel to perform breast self-examination monthly, beginning at puberty. For standard risk patients, provide general guidance regarding routine screening beginning at age 40 per current ACS guidelines.

Considerations for Further Testing and Intervention

Surgery and/or oncology consultation as clinically indicated.
PATIENTS AT HIGHEST RISK

Physical

Breast self exam

(Monthly, beginning at puberty)

Clinical breast exam

(Yearly, beginning at puberty until age 25, then every six months)

Screening

Mammogram

(Yearly, beginning 8 years after radiation or at age 25, whichever occurs last)

Info Link:

There is currently a deficiency in the literature regarding whether or not TBI is a risk factor for the development of breast cancer. Monitoring of patients who received TBI should be determined on an individual basis.

Mammography is currently limited in its ability to evaluate premenopausal breasts. The role of MRI is evolving for screening of other populations at high risk for breast cancer (e.g., premenopausal known or likely carriers of gene mutation of known penetrance).

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
138

(Female)
Cervical Early age at first intercourse
Multiple lifetime sex partners
Smoking
Sexually transmitted diseases
Personal history of cervical dysplasia
Prenatal DES exposure
HPV infection
Immunosuppression
Chronic steroid use
HIV positive
Chronic GVHD
PATIENTS AT STANDARD RISK (ACS Recommendation)

Physical

Pelvic exam

(Every 1 to 2 years)

Screening

Cervical PAP smear

(Yearly for regular PAP test. Every 2 years for liquid-based PAP test. After age 30, if patient has had 3 consecutive normal annual PAP tests, may screen every 2-3 years [with conventional or liquid-based cervical cytology] or every 3 years [with HPV DNA test plus cervical cytology]).

Info Link:

Begin screening (in patients with a cervix) 3 years after first vaginal intercourse, or at age 21, whichever occurs first.
Health Links

See "Patient Resources" field

Reducing the Risk of Second Cancers

Considerations for Further Testing and Intervention

Gynecology and/or oncology consultation as clinically indicated.

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
139 Colorectal High fat/low fiber diet
Age >50 years
Obesity
Radiation with potential impact to the colon/rectum (see Section 78; see list of related summaries at the beginning of the "Major Recommendation" field), including >30 Gy to the following fields:
  • Whole abdomen
  • All upper abdominal fields
  • Pelvic
  • Spine (thoracic, lumbar, sacral)

Personal history of ulcerative colitis, gastrointestinal malignancy, adenomatous polyps, or hepatoblastoma

Familial polyposis

Family history of colorectal cancer or polyps in first degree relative
PATIENTS AT STANDARD RISK (ACS Recommendation)

Screening

Option 1: Fecal occult blood (minimum of 3 cards)

(Yearly, beginning at age 50)

AND/OR

Flexible sigmoidoscopy

(Every 5 years, beginning at age 50)

Note: The combination of yearly fecal occult blood testing and every 5 year flexible sigmoidoscopy is preferable to either test done alone.

Option 2: Double contrast barium enema

(Every 5 years, beginning at age 50)

Option 3: Colonoscopy

(Every 10 years, beginning at age 50)
Health Links

See "Patient Resources" field

Colorectal Cancer

Considerations for Further Testing and Intervention

Gastroenterology, surgery, and/or oncology consultation as clinically indicated.
PATIENTS AT HIGHEST RISK

Screening

Colonoscopy

(Every 5 years [minimum]; more frequently if indicated based on colonoscopy results. Begin monitoring 10 years after radiation or at age 35, whichever occurs last. Monitor more frequently if clinically indicated. Per the ACS, begin screening earlier for the following high-risk groups: HNPCC [at puberty], FAP [at age 21 years], IBD [8 years after diagnosis of IBD]. Information from the first colonoscopy will inform frequency of follow up testing.

Info Link:

Reports of gastrointestinal malignancies in cohorts of long-term survivors suggest that radiation likely increases risk, but the median age of onset is not as well established as that of secondary breast cancer following chest radiation. The expert panel agreed that early onset of screening likely was beneficial, and that a prudent course would be to initiate screening for colorectal cancer for those at highest risk (abdominal, pelvic, and/or spinal radiation >30 Gy) at age 35, or 10 years post radiation, whichever occurs last. Surveillance should be done via colonoscopy as per recommendations for populations at highest risk, with information from the first colonoscopy informing the frequency of follow-up testing.

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
140

(Female)
Endometrial Obesity
Older age
Unopposed estrogen therapy
Tamoxifen
Diabetes
Hypertension
High fat diet
Early menopause
Late menopause
Nulliparity
Infertility
Failure to ovulate
History of/at risk for HNPCC PATIENTS AT HIGHEST RISK (ACS Recommendation)

Screening

Endometrial biopsy

(Yearly, beginning at age 35 for patients at highest risk)

Info Link:

Women at highest risk should be informed that screening recommendation of endometrial biopsy beginning at age 35 is based on expert opinion in the absence of definitive scientific evidence and the potential benefits, risks, and limitations of testing for early endometrial cancer detection should be discussed.
Health Links

See "Patient Resources" field

Reducing the Risk of Second Cancers

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
141 Lung Smoking
Workplace exposures to asbestos, arsenic, radiation
Second hand smoke (in non-smokers)
Chest radiation with potential impact to the lung PATIENTS AT HIGHEST RISK

History

Cough

Wheezing

SOB

DOE

(Yearly, and as clinically indicated)

Physical

Pulmonary Exam

(Yearly, and as clinically indicated)
Health Links

See "Patient Resources" field

Reducing the Risk of Second Cancers

Considerations for Further Testing and Intervention

Imaging and surgery and/or oncology consultation as clinically indicated.

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
142 Oral Tobacco use (smoking cigars, cigarettes, or pipes; dipping, chewing)
Alcohol abuse
Excessive sun exposure (increases risk of cancer of lower lip)
HCT (allogeneic > autologous)
Head/brain radiation
Neck radiation
TBI
Acute/chronic GVHD
PATIENTS AT HIGHEST RISK

Physical

Oral cavity exam

(Yearly)
Health Links

See "Patient Resources" field

Reducing the Risk of Second Cancers
Dental Health

Considerations for Further Testing and Intervention

Head and neck/otolaryngology consultation as indicated.

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
143

(Male)
Prostate Older age, with steadily increasing risk after age 40 years. African-American race
Family history of prostate cancer in first degree relative
ALL PATIENTS

Clinicians should be prepared to discuss prostate cancer testing with patients

Info Link:

The USPSTF found good evidence that PSA screening can detect early-stage prostate cancer but mixed and inconclusive evidence that early detection improves health outcomes. Screening is associated with important harms, including frequent false-positive results and unnecessary anxiety, biopsies, and potential complications of treatment of some cancers that may never have affected a patient's health. The USPSTF concludes that evidence is insufficient to determine whether the benefits outweigh the harms for a screened population. ACS concurs with this conclusion.
Health Links

See "Patient Resources" field

Reducing the Risk of Second Cancers

Considerations for Further Testing and Intervention

Urology and/or oncology consultation as clinically indicated.

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
144 Skin Light skin color
Chronic exposure to sun
Atypical moles or >50 moles
Any history of radiation
Personal history of melanoma or skin cancer
Dysplastic nevi
Family history of melanoma or skin cancer
History of severe sunburn at young age
PATIENTS AT STANDARD RISK

Info Link:

The USPSTF concludes that the evidence is insufficient to recommend for or against routine screening for skin cancer using a total-body skin examination for the early detection of cutaneous melanoma, basal cell cancer, or squamous cell skin cancer. There are no randomized trials or case-control studies that directly examine whether screening by clinicians is associated with improved clinical outcomes such as reduced morbidity or mortality from skin cancer. No studies were found that evaluated whether screening improves the outcomes of these cancers. The ACS recommends skin examination as part of a cancer-related checkup, which should occur on the occasion of the patient's periodic health examination. Self-examination of skin is recommended once a month.
Health Links

See "Patient Resources" field

Reducing the Risk of Second Cancers
Skin Health

Considerations for Further Testing and Intervention

Surgery, dermatology, and/or oncology consultation as clinically indicated.
PATIENTS AT HIGHEST RISK

Physical

Skin self exam

(Monthly)

Dermatologic exam with attention to skin lesions and pigmented nevi in radiation field

(Yearly)

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
145

(Male)
Testicular Young males History of cryptorchidism
History of testicular cancer or carcinoma in-situ in contralateral testis
History of gonadal dysgenesis
Klinefelter's syndrome
Family history of testicular cancer
Info Link:

For standard and high risk populations, the USPSTF recommends against routine screening for testicular cancer in asymptomatic adolescent and adult males. In 2004, the USPSTF found no new evidence that screening with clinical examination or testicular self-examination is effective in reducing mortality from testicular cancer. Even in the absence of screening, the current treatment interventions provide very favorable health outcomes. Given the low prevalence of testicular cancer, limited accuracy of screening tests, and no evidence for the incremental benefits of screening, the USPSTF concluded that the harms of screening exceed any potential benefits. ACS also no longer recommends clinical testicular cancer screening or testicular self-examination.
 

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

Sec # Organ At Risk Population Highest Risk Factors Periodic Evaluation Health Counseling Further Considerations
146 General Health Screening     Screening

Refer to USPSTF recommendations at www.ahrq.gov/clinic/uspstfix.htm

(Yearly)
Considerations for Further Testing and Intervention

Childhood cancer survivors should receive general health maintenance per standard recommendations for age. Recommended preventive services per the USPSTF include screening for hypertension, obesity, depression, tobacco use, and alcohol misuse. In addition, certain subpopulations require screening for lipid disorders, sexually transmitted diseases, and diabetes mellitus. Others require counseling regarding the prevention of cardiovascular disease, osteoporosis, and other disorders. See www.ahrq.gov/clinic/uspstfix.htm for specific recommendations.

Assess immunization status on all patients; reimmunize as indicated. See http://www.cdc.gov/vaccines/recs/schedules/default.htm for current immunization schedules.

For all HCT patients, reimmunization per CDC Guidelines (http://www.cdc.gov/mmwr/preview/mmwrhtml/rr4910a1.htm - see table 4) or EBMT Guidelines (http://www.nature.com/bmt/journal/v23/n7/pdf/1701641a.pdf).

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

Abbreviations

  • ACS, American Cancer Society
  • ATM, ataxia telangiectasia cancer susceptibility gene located on chromosome 11
  • BRCA1, breast cancer early onset gene (cancer susceptibility gene located on chromosome 17)
  • BRCA2, breast cancer 2 early onset gene (cancer susceptibility gene located on chromosome 13)
  • CDC, Centers for Disease Control and Prevention
  • DES, diethylstilbestrol
  • DNA, deoxyribonucleic acid
  • DOE, dyspnea on exertion
  • EBMT, European Group for Blood and Marrow Transplantation
  • FAP, familial adenomatous polyposis
  • GVHD, graft versus host disease
  • Gy, gray
  • HCT, hematopoietic cell transplant
  • HIV, human immunodeficiency virus
  • HNPCC, hereditary nonpolyposis colorectal cancer
  • HPV, human papilloma virus
  • IBD, inflammatory bowel disease
  • MRI, magnetic resonance imaging
  • PAP, Papanicoulau
  • PSA, prostate specific antigen
  • SOB, shortness of breath
  • TBI, total body irradiation
  • USPSTF, United States Preventive Services Task Force

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of evidence supporting the recommendations is not specifically stated.

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 137-146: cancer and general health screening. Bethesda (MD): Children's Oncology Group; 2006 Mar. 11 p. [45 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 137

Sections 138, 140, 141, 142, 143, 144

Section 139

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 Institute on May 11, 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

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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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