Obstetrics & Gynecology Email Alerts
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Obstetrics & Gynecology 1992;79:675-682
© 1992 by The American College of Obstetricians and Gynecologists
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by SYRJÄNEN, K.
Right arrow Articles by SAARIKOSKI, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by SYRJÄNEN, K.
Right arrow Articles by SAARIKOSKI, S.

Natural History of Cervical Human Papillomavirus Lesions Does Not Substantiate the Biologic Relevance of the Bethesda System

KARI SYRJÄNEN, MD, PhD, VESA KATAJA, MD, MERJA YLISKOSKI, MD, FUJU CHANG, MD, STINA SYRJÄNEN, DDS, PhD and SEPPO SAARIKOSKI, MD, PhD

From the Departments of Pathology, Radiotherapy and Medical Oncology, and Gynecology and Obstetrics, Kuopio Cancer Research Centre, University of Kuopio; and the A. I. Virtanen Institute, Kuopio, Finland

Abstract

The newly introduced Bethesda System proposes to replace the terms dysplasia, carcinoma in situ (CIS), or cervical intraepithelial neoplasia (CIN) with two terms, low-grade squamous intraepithelial lesion (SID or high-grade SIL. We tested the biologic relevance of the Bethesda System (ie, its ability to establish a close correlation between biologic behavior and the different grades of lesions) in a series of 528 women with genital human papillomavirus (HPV)- associated precancerous lesions prospectively followed for 10 years. The cervical biopsies were reclassified as either low-grade or high-grade SIL, and the data obtained by colposcopy, Papanicolaou smear, and HPV typing, as well as the biological behavior of the lesions, were analyzed in these two groups. Altogether, 77.4% (376 of 486) of the lesions were classified as low-grade SIL lesions; the rest (22.6%) belonged to the high-grade SIL category. In the low-grade SIL category, 46.8% of the women were 24 years old or younger, as compared with 37.3% in the high-grade SIL group. The colposcopic appearance was normal significantly more frequently in the low-grade SIL lesions (22.1%) than in the high-grade category (8.5%) (P < 001). A single Fapanicolaou smear was inadequate to distinguish between low-grade and high-grade SIL, as evidenced by almost identical distributions of Papanicolaou smear class I and II cells in both categories. Noteworthy was the discovery of normal Papanicolaou smears in 8.2% of the high-grade SIL lesions. Four of the HPV types analyzed (6,11,18, 33) were similarly distributed in both categories, whereas HPVs 16 and 31 were significantly more frequent in high-grade as compared with low-grade SIL (P <.001). The spontaneous regression rate was significantly higher in low-grade SIL (63.6%) than in high-grade SIL (38.2%). Progression was significantly higher (39.1%) in the high-grade SIL category (P<.0001). Despite its definitely positive goals, the drawbacks of the Bethesda System still outnumber its advantages. Most important, simplification of the classification into two grades instead of three in the CIN terminology inevitably leads to significant loss of diagnostically and prognostically valuable information. From the patient's point of view, it is essential that clinical terminology does not result in overtreatment, which seems to be a definite risk using only the two categories of the Bethesda System. The present results firmly advocate preservation of the current descriptive terminology, which has proven its effectiveness for many years.




This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
M.-Y. Lee, C.-Y. Chou, M.-J. Tang, and M.-R. Shen
Epithelial-Mesenchymal Transition in Cervical Cancer: Correlation with Tumor Progression, Epidermal Growth Factor Receptor Overexpression, and Snail Up-Regulation
Clin. Cancer Res., August 1, 2008; 14(15): 4743 - 4750.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
J. J. Kim, K. M. Kuntz, N. K. Stout, S. Mahmud, L. L. Villa, E. L. Franco, and S. J. Goldie
Multiparameter Calibration of a Natural History Model of Cervical Cancer
Am. J. Epidemiol., July 15, 2007; 166(2): 137 - 150.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
M.-R. Shen, Y.-M. Hsu, K.-F. Hsu, Y.-F. Chen, M.-J. Tang, and C.-Y. Chou
Insulin-like growth factor 1 is a potent stimulator of cervical cancer cell invasiveness and proliferation that is modulated by {alpha}v{beta}3 integrin signaling
Carcinogenesis, May 1, 2006; 27(5): 962 - 971.
[Abstract] [Full Text] [PDF]


Home page
Eur J Public HealthHome page
U. Siebert, G. Sroczynski, P. Hillemanns, J. Engel, R. Stabenow, C. Stegmaier, K. Voigt, B. Gibis, D. Holzel, and S. J. Goldie
The German Cervical Cancer Screening Model: development and validation of a decision-analytic model for cervical cancer screening in Germany
Eur J Public Health, April 1, 2006; 16(2): 185 - 192.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
J. J. Kim, T. C. Wright, and S. J. Goldie
Cost-effectiveness of Human Papillomavirus DNA Testing in the United Kingdom, The Netherlands, France, and Italy
J Natl Cancer Inst, June 15, 2005; 97(12): 888 - 895.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
S. J. Goldie, M. Kohli, D. Grima, M. C. Weinstein, T. C. Wright, F. X. Bosch, and E. Franco
Projected Clinical Benefits and Cost-effectiveness of a Human Papillomavirus 16/18 Vaccine
J Natl Cancer Inst, April 21, 2004; 96(8): 604 - 615.
[Abstract] [Full Text] [PDF]


Home page
Obstet GynecolHome page
S. J. Goldie, J. J. Kim, and T. C. Wright
Cost-Effectiveness of Human Papillomavirus DNA Testing for Cervical Cancer Screening in Women Aged 30 Years or More
Obstet. Gynecol., April 1, 2004; 103(4): 619 - 631.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
G. F. Sawaya, K. J. McConnell, S. L. Kulasingam, H. W. Lawson, K. Kerlikowske, J. Melnikow, N. C. Lee, G. Gildengorin, E. R. Myers, and A. E. Washington
Risk of Cervical Cancer Associated with Extending the Interval between Cervical-Cancer Screenings
N. Engl. J. Med., October 16, 2003; 349(16): 1501 - 1509.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M.-R. Shen, C.-Y. Chou, K.-F. Hsu, Y.-M. Hsu, W.-T. Chiu, M.-J. Tang, S. L. Alper, and J. C. Ellory
KCl Cotransport Is an Important Modulator of Human Cervical Cancer Growth and Invasion
J. Biol. Chem., October 10, 2003; 278(41): 39941 - 39950.
[Abstract] [Full Text] [PDF]


Home page
CA Cancer J ClinHome page
D. Saslow, C. D. Runowicz, D. Solomon, A.-B. Moscicki, R. A. Smith, H. J. Eyre, and C. Cohen
American Cancer Society Guideline for the Early Detection of Cervical Neoplasia and Cancer
CA Cancer J Clin, November 1, 2002; 52(6): 342 - 362.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
J. J. Kim, T. C. Wright, and S. J. Goldie
Cost-effectiveness of Alternative Triage Strategies for Atypical Squamous Cells of Undetermined Significance
JAMA, May 8, 2002; 287(18): 2382 - 2390.
[Abstract] [Full Text] [PDF]


Home page
Obstet GynecolHome page
A. L. Herbst, K. E. Pickett, M. Follen, and K. L. Noller
The Management of ASCUS Cervical Cytologic Abnormalities and HPV Testing: A Cautionary Note
Obstet. Gynecol., November 1, 2001; 98(5): 849 - 851.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
S. J. Goldie, L. Kuhn, L. Denny, A. Pollack, and T. C. Wright
Policy Analysis of Cervical Cancer Screening Strategies in Low-Resource Settings: Clinical Benefits and Cost-effectiveness
JAMA, June 27, 2001; 285(24): 3107 - 3115.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
A.-B. Moscicki, N. Hills, S. Shiboski, K. Powell, N. Jay, E. Hanson, S. Miller, L. Clayton, S. Farhat, J. Broering, et al.
Risks for Incident Human Papillomavirus Infection and Low-Grade Squamous Intraepithelial Lesion Development in Young Females
JAMA, June 20, 2001; 285(23): 2995 - 3002.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
P. Holowaty, A. B. Miller, T. Rohan, and T. To
Natural History of Dysplasia of the Uterine Cervix
J Natl Cancer Inst, February 3, 1999; 91(3): 252 - 258.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 by the American College of Obstetricians and Gynecologists.