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Brief Summary

GUIDELINE TITLE

American Society of Clinical Oncology 2006 update of the breast cancer follow-up and management guidelines in the adjuvant setting.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates previous versions: American Society of Clinical Oncology. American Society of Clinical Oncology 1998 update of recommended breast cancer surveillance guidelines. J Clin Oncol 1999 Mar;17(3):1080-2.

American Society of Clinical Oncology. Recommended breast cancer surveillance guidelines. J Clin Oncol 1997 May;15(5):2149-56.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Recommended Breast Cancer Surveillance

History, Physical Examination, and Patient Education Regarding Symptoms of Recurrence

2006 recommendation. All women should have a careful history and physical examination every 3 to 6 months for the first 3 years after primary therapy, then every 6 to 12 months for the next 2 years, and then annually. Physicians should counsel patients about the symptoms of recurrence including new lumps, bone pain, chest pain, dyspnea, abdominal pain, or persistent headaches. Helpful Web sites for patient education include www.plwc.org and www.cancer.org.

Women at high risk for familial breast cancer syndromes should be referred for genetic counseling in accordance with clinical guidelines recommended by the U.S. Preventive Services Task Force (USPSTF) (see the National Guideline Clearinghouse [NGC] summary of the USPSTF guideline Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: recommendation statement). Criteria to recommend referral include the following: Ashkenazi Jewish heritage; history of ovarian cancer at any age in the patient or any first- or second-degree relatives; any first-degree relative with a history of breast cancer diagnosed before the age of 50 years; two or more first- or second-degree relatives diagnosed with breast cancer at any age; patient or relative with diagnosis of bilateral breast cancer; and history of breast cancer in a male relative.

Breast Self-Examination

2006 recommendation. All women should be counseled to perform monthly breast self-examination (BSE).

Mammography

2006 recommendation. Women treated with breast-conserving therapy should have their first post-treatment mammogram no earlier than 6 months after definitive radiation therapy. Subsequent mammograms should be obtained every 6 to 12 months for surveillance of abnormalities. Mammography should be performed yearly if stability of mammographic findings is achieved after completion of locoregional therapy.

Coordination of Care

2006 recommendation. The risk of breast cancer recurrence continues through 15 years after primary treatment and beyond. Continuity of care for breast cancer patients is recommended and should be performed by a physician experienced in the surveillance of cancer patients and in breast examination, including the examination of irradiated breasts.

Follow-up by a primary care physician (PCP) seems to lead to the same health outcomes as specialist follow-up with good patient satisfaction. If a patient with early-stage breast cancer (tumor <5 cm and < four positive nodes) desires follow-up exclusively by a PCP, care may be transferred to the PCP approximately 1 year after diagnosis. If care is transferred to a PCP, both the PCP and the patient should be informed of the appropriate follow-up and management strategy. This approach will necessitate referral for oncology assessment if a patient is receiving adjuvant endocrine therapy.

Pelvic Examination

2006 recommendation. Regular gynecologic follow-up is recommended for all women. Patients who receive tamoxifen therapy are at increased risk for developing endometrial cancer and should be advised to report any vaginal bleeding to their physicians. Longer follow-up intervals may be appropriate for women who have had a total hysterectomy and oophorectomy.

Breast Cancer Surveillance Testing: Not Recommended

Complete Blood Count (CBC)

2006 recommendation. CBC testing is not recommended for routine breast cancer surveillance.

Automated Chemistry Studies

2006 recommendation. Automated chemistry studies are not recommended for routine breast cancer surveillance.

Chest X-Rays

2006 recommendation. Chest x-rays are not recommended for routine breast cancer surveillance.

Bone Scan

2006 recommendation. Bone scans are not recommended for routine breast cancer surveillance.

Ultrasound of the Liver

2006 recommendation. Liver ultrasound is not recommended for routine breast cancer surveillance.

Computed Tomography (CT)

2006 recommendation. CT is not recommended for routine breast cancer surveillance.

[18F]Fluorodeoxyglucose–Positron Emission Tomography Scanning

2006 recommendation. [18F]fluorodeoxyglucose-positron emission tomography (FDG-PET) scanning is not recommended for routine breast cancer surveillance.

Breast Magnetic Resonance Imaging

2006 recommendation. Breast magnetic resonance imaging (MRI) is not recommended for routine breast cancer surveillance.

Breast Cancer Tumor Markers CA 15-3 and CA 27.29

2006 recommendation. The use of the CA 15-3 or CA 27.29 is not recommended for routine surveillance of breast cancer patients after primary therapy. The ASCO Breast Cancer Tumor Markers Panel will publish guideline recommendations for selected tumor markers.

Breast Cancer Tumor Marker Carcinoembryonic Antigen

2006 recommendation. Carcinoembryonic antigen testing is not recommended for routine surveillance of breast cancer patients after primary therapy. The ASCO Breast Cancer Tumor Markers Panel will publish guideline recommendations for selected tumor markers.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The evidence supporting each recommendation is presented in the original guideline document under "literature update and discussion" following each recommendation. In general, the literature review supporting these recommendations centered on randomized clinical trials and meta-analyses of data from randomized clinical trials.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

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

DATE RELEASED

1997 May (revised 2006 Nov 1)

GUIDELINE DEVELOPER(S)

American Society of Clinical Oncology - Medical Specialty Society

SOURCE(S) OF FUNDING

American Society of Clinical Oncology (ASCO)

GUIDELINE COMMITTEE

American Society of Clinical Oncology (ASCO) Breast Cancer Tumor Markers Panel

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Panel Members: Nancy E. Davidson, MD (Co-Chair) Johns Hopkins Hospital, Sidney Kimmel Cancer Center; James L. Khatcheressian, MD (Co-Chair) Virginia Commonwealth University/Massey Cancer Center; Martha Bluming, Hematology-Oncology Medical Group of the San Fernando Valley; Laura Esserman, MD, University of California, San Francisco; Eva Grunfeld, MD, DPhil, Dalhousie University; Francine E. Halberg, MD, Marin Cancer Institute, Marin General Hospital; Alexander Hantel, MD, Loyola University, Edward Hospital Cancer Center; Alexander Kennedy, MD, Dartmouth-Hitchcock Manchester; Hyman B. Muss, MD, University of Vermont; Thomas J. Smith, MD, Virginia Commonwealth University/Massey Cancer Center; Victor G. Vogel, MD, MHS, Magee-Womens Hospital of the University of Pittsburgh Medical Center; Antonio C. Wolff, MD, Johns Hopkins Hospital, Sidney Kimmel Cancer Center

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Although all authors completed the disclosure declaration, the following author or immediate family members indicated a financial interest. No conflict exists for drugs or devices used in a study if they are not being evaluated as part of the investigation. For a detailed description of the disclosure categories, or for more information about the American Society of Clinical Oncology's (ASCO's) conflict of interest policy, please refer to the Author Disclosure Declaration and the Disclosures of Potential Conflicts of Interest section in Information for Contributors in the original journal of publication.

Author Employment Leadership Consultant Stock Honoraria Research Funds Testimony Other
Victor G. Vogel     AstraZeneca; Eli Lilly     Eli Lilly; AstraZeneca    

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates previous versions: American Society of Clinical Oncology. American Society of Clinical Oncology 1998 update of recommended breast cancer surveillance guidelines. J Clin Oncol 1999 Mar;17(3):1080-2.

American Society of Clinical Oncology. Recommended breast cancer surveillance guidelines. J Clin Oncol 1997 May;15(5):2149-56.

GUIDELINE AVAILABILITY

Electronic copies: Available from the American Society of Clinical Oncology (ASCO) Web site.

Print copies: Available from American Society of Clinical Oncology, Cancer Policy and Clinical Affairs, 1900 Duke Street, Suite 200, Alexandria, VA 22314; E-mail: guidelines@asco.org.

AVAILABILITY OF COMPANION DOCUMENTS

The following are available:

Guidelines are available for Personal Digital Assistant (PDA) download from the ASCO Web site.

See the related QualityTool tool set on the Health Care Innovations Exchange Web site.

PATIENT RESOURCES

The following is available:

  • ASCO patient guide: follow-up care for breast cancer. 2006 Oct. 4 p.

Available in Portable Document Format (PDF) from the Cancer.Net Web site.

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 September 1, 1998. It was verified by the guideline developer on December 1, 1998. This NGC summary was updated by ECRI on June 11, 1999, and November 22, 2006. The updated information was verified by the guideline developer on December 6, 2006.

COPYRIGHT STATEMENT

This summary is based on the original guideline, which is subject to the American Society of Clinical Oncology's copyright restrictions.

DISCLAIMER

NGC DISCLAIMER

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


 

 

   
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