cervix cancer power point with slides
TRANSCRIPT
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Cervix Cancer
Prevention and Early Detection
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Obtaining CME CreditThis activity is accredited for up to 1 hour
of AMA PRA Category 1 credit. To
obtain CME credit for this module,complete the evaluation and return with$10 to TMA/POEP, 401 West 15th
Street, Austin, TX 78701-1680.
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Objectives After completion of this module, the physician
will be able to:
1. Identify women at risk for cervix cancer.2. Describe the probable etiologic factors that
contribute to the development of cervix cancer.
3. Explain why cervix cancer is suitable forscreening.
4. Describe the screening procedure for cervixcancer.
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Objectives (continued) After completion of this module, the physician
will be able to:
5. Describe the reporting system(s) used for Papsmear.
6. Describe the recommendations for evaluationand follow-up of women with abnormal Pap
test results.7. Encourage women to be screened for cervix
cancer.
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Cervix Cancer: A Global Problem It is the second most common cancer
site in women worldwide.
It is the most common cancer site andcause of cancer death in women inmany developing countries.
Women with cervical cancer die at ayounger age than those with any othernon-childhood cancer.
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Incidence Rates of Cervix
Cancer in the United States14.2
11.9
10.1
8.7 8.4 8.88.4
7.8
0
24
6
8
1012
14
16
1973 1980 1985 1991
Rates per 100,000
Age-adjusted to1970 U.S. std. Pop.
21-year trend (females only)
Source: SEER Cancer Statistics Review, 1973-1994.
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Mortality Rates for Cervix
Cancer in Texas
Counties with mortality rate above5 per 100,000
Counties with Mortality rate above 2per 100,000 but less than 5 per 100,000
Counties with mortality rate lowerthan 2 per 100,000
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Relationships Between Age, Ethnicity,
and Incidence of Cervix Cancer
0
51015202530
354045
1 5 - 1 9
2 5 - 2 9
3 5 - 3 9
4 5 - 4 9
5 5 - 5 9
6 5 - 6 9
7 5 - 7 9
8 5 +
Age at diagnosis
Black
White
Source: Herrero, Rolando. Journal of the National Cancer Institute Monographs , No. 21:3, 1996.
Age-specific rate1988-1992
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Cervical Cancer Among Blacks
and Whites
0
2
4
6
8
10
12
14
1 9 7 3 7 5 7 7 7 9 8 1 8 3 8 5 8 7 8 9 9 1
Year of death
M o r t a l i t y r
a t e
Black
White
Source: Herrero, Rolando. Journal of the National Cancer Institute Monographs , No. 21:3, 1996
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Incidence of Invasive and
Pre-invasive Cervix Cancer
0
10
20
30
40
50
60
70
1975 1980 1985 1990 1995
Invasive
Carcinoma in situ
Rates are per 100,000
and age-adjusted to the1970 U.S. standard
Source: SEER Registry
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Risk Factors for Cervix Cancer No prior smear screening
History of cervical dysplasia or genital warts
Young age at first coitus
Multiple sex partners
High-risk male partner (e.g., multiple female
partners) Sexually transmitted diseases
Cigarette smoking
Increasing age
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The Normal Cervix
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The Human Papillomavirus
(HPV) and Cervix CancerHPV 16 and 18
E6 protein E7 protein
+ +
p53 retinoblastomatumor suppressor tumor suppressor
gene product gene product
increased cellular proliferation
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Promoters of Cervix Cancer Smoking
Diet
Immunosuppression
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Screening for Cervix CancerCervix cancer is a disease suitable for screening
because it meets the following criteria:
It’s a common disease.
It has serious consequences.
It has a detectable, asymptomatic phase.
Early detection and treatment decreasemorbidity and mortality.
The screening test is acceptable to patients,safe, and affordable.
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Benefits of the Papanicolaou Smear Sensitivity: 50-70%
Specificity: 30-50%
Inexpensive
Minimal risk and discomfort to the patient
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The Papanicolaou Smear:
False Negative ResultsWhy do false negative results occur?
Inadequate smear technique/sample Improper laboratory preparation/evaluation
Failure of health care provider to properlyinterpret and manage an abnormal result
Failure of the patient to comply withrecommendations for evaluation and treatment
Invasive cancer at the time of initial evaluation
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Cervix Cancer Screening:
Recommendations for Frequency Annually after the patient is sexually active or
age 18 until negative x3; then at the
discretion of the physician and patient basedupon a consideration of risk factors.
The American College of Obstetricians and Gynecologist
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Cervix Cancer Screening:
Current Controversies How often should Pap tests be
performed?
Should a woman who has had ahysterectomy continue to have periodicPap tests?
When should the Pap test be repeatedif endocervical cells are not present?
Should Pap tests be performed inpatients older than age 60?
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Pathology of Cervical Dysplasia
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The 1988 Bethesda SystemReporting Cervical Cytologic Diagnosis
Statement about the adequacy of the specimen
General categorization of the diagnosis
Descriptive diagnosis
JAMA 267:1892, 1989.
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The 1988 Bethesda System
(continued)Descriptive Diagnosis
Infection
Reactive and reparative changes
Epithelial cell abnormalities
Nonepithelial malignant neoplasm (specify)
Hormonal evaluation (vaginal smear only)
Other
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The 1988 Bethesda System
(continued)Epithelial Cell Abnormalities: Squamous Cells
Atypical squamous cells of undeterminedsignificance (recommended follow-upspecified)
Squamous intraepithelial lesion (SIL) Low grade SIL: HPV changes and/or CIN I
High grade SIL: CIN II, CIN III, or CIS
Squamous cell carcinoma
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The 1988 Bethesda System
(continued)Epithelial Cell Abnormalities: Glandualr Cells
Presence of endometrial cells
Out of phase in a menstruating woman In a postmenopausal woman
No menstrual history available
Atypical glandular cell of undetermined
significance (recommended follow-upspecified) Endometrial
Endocervical
Not otherwise specified
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The 1988 Bethesda System
(continued)Epithelial Cell Abnormalities: Glandular
Cells (continued)
Adenocarcinoma (probable site of origin specified)
Other epithelial malignant neoplasm: specify
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Follow-up of Abnormal
Papanicolaou SmearsColposcopy: Magnified Inspection of
the Cervix
Identifies the area of abnormality for biopsy
Defines the extent of the cervical lesion
Delineates the areas of greatest abnormality
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Evaluation of the Abnormal
Papanicolaou SmearCOLPOSCOPY
Satisfactory Unsatisfactory
(entire lesion seen) (lesion extends intoendocervical canal)
Biopsy lesion Biopsy any visible lesionEndocervical curettage
Histological Confirmation
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Evaluation of the Abnormal
Papanicolaou SmearTREATMENT OF CERVICAL DYSPLASIA
Lesion confined Lesion extends intoto ectocervix endocervical canal
Cervical biopsies revealmicroinvasion
Ablation of Excision of T-zone
excision of T-zone
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Treatment of Cervix DysplasiaTreatment Modality
Destructive Methods Cryotherapy
Laser ablation
Excision Cervical conization
LEEP
Cure Rate (5-year)Overall
85-95%
85-95%
>90%
>90%
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Evaluation of the Patient with
Cervix CanerHistologic confirmation of cervix cancer
by biopsy, followed by:
HIV test
Staging examination
Metastatic survey
Treatment planning
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Evaluation of the Patient with
Cervix Cancer Staging examination
Complete physical and pelvic examination
Palpation of the lymph node-bearing areas
Cystoscopy/proctoscopy for advanced cancers
Metastatic survey Radiograph of the chest
IVP and barium enema or computerizedtomography of pelvis and abdomen
Treatment planning Surgery for selected Stage I lesions
Radiation therapy for all others
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Post Treatment SurveillanceExams: Palpation of the node-bearing areas, Pelvic, Pap
Year Frequency0-2 every 3-4 months
2-4 every 6 months
5+ annually
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Five Year Survival of Cervix
Cancer by Stage of Disease100%
85%
66%
39%
11%0%
20%
40%
60%
80%
100%
Stage 0 Stage I Stage II Stage III Stage IV
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Role of the Primary Care Physician
in Preventing Cervix Cancer Identify patients who should be
screened
Educate patients regarding theimportance and timing of Pap smears
Conduct Pap smears properly
Follow up abnormal Pap smear results
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Barriers to Screening Embarrassment, unpleasantness
Lack of knowledge of recommended
screening interval
Financial barriers
Lack of knowledge concerning theimportance of screening
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SummaryCervix cancer is highly preventable
Pap smear screening
Treatment of precursor lesions (dysplasia)
Follow-up of abnormal Pap smear results is critical
Colposcopically-directed biopsies
Histologic evaluation and correlation with the Papsmear
Definitive therapy
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Reading List1. American College of Obstetricians and Gynecologists.Recommendations on Frequency of Pap Test Screening. ACOG Committee Opinion 152. Washington, DC: ACOG, 1995.
2. Anderson GH, et al. Organisation and results of the cervical
cytology screening programme in British Columbia, 1955-85,British Medical Journal (Clin Res Ed) 296(6627):975-8, 1988.
3. Broder S. The Bethesda System for reporting cervical/vaginalcytologic diagnoses: report of the 1991 Bethesda workshop.Journal of the American Medical Association 267:1892, 1992.
4. Burack RC, et al. How reminders given to patients andphysicians affected pap smear use in a health maintenanceorganization: results of a randomized controlled trail. Cancer 82(12):2391-400, 1998.
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Reading List (continued)5. Creasman WT, et al. Early invasive carcinoma of the cervix (3
to 5 mm invasion): risk factors and prognosis. A GynecologicOncology Group study. Am J Obstet Gynecol 178(1 Pt 1):62-5, 1998.
6. Devesa SS, et al. Recent trends in cervix uteri cancer. CancerNov. 15; 64(10):2184-90, 1989.
7. Eaker ED, et al. Cervical cancer screening among women withand without hysterectomies. Obstet Gynecol 91(4):551-5,1998.
8. Frame PS, et al. Determinants of cancer screening frequency;the example of screening for cervical cancer. J AM Board Fam Pract 11(2):87-95, 1998.
9. Hopman EH, et al. Positive predictive rate of colposcopicexamination of the cervix uteri: an overview of literature.Obstet Gynecol Surv 53(2):97-106, 1998.
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Reading List (continued)10. Lobell M, et al. Barriers to cancer screening in Mexican-
American women. Mayo Clin Proc 73(4):301-8, 1998.
11. Ollayos CW. Update on the Papanicolaou smear: new issues
for the 1990s. Mil Med 162(8):521-3, 1997.12. Paskett ED, et al. Clinic-based interventions to promote
breast and cervical cancer screening. Prev Med 27(1):120-8,1998.
13. Peters RK, et al. Risk Factors for invasive cervical cancer
among Latinas and non-Latinas in Los Angeles County.Journal of the National Cancer Institute 77(5):1063-77, 1986.
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Other POEP CME Modules Breast Cancer (and in interactive CD-ROM)
Cancer in Special Populations
Colorectal Cancer Head and Neck Caner
Lung Cancer
Nutrition and Cancer Risk Reduction
Prostate Cancer
Skin Cancer
Surveillance of Cancer Patients
To order these modules in spiral bound or 35mm slide format, contactPOEP at [email protected] or call 800-880-1300, ext. 1672.
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EvaluationTo obtain CME credit for this module,
complete the online evaluation and
return with $10 to TMA/POEP, 401 West15th Street, Austin, TX 78701-1680.
Return to POEP online CME