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. Author manuscript; available in PMC: 2015 Sep 14.
Published in final edited form as: Gynecol Oncol. 2010 Aug 14;119(2):237–242. doi: 10.1016/j.ygyno.2010.07.004

Table 1.

Input variables and sources*

Clinical variable Base-case value Range Source
Population variables
Annual hysterectomy rate (%) 0.02 – 1.17 Keshavarz (2002)
Age-specific prevalence of HR HPV infection(%) 4 – 31 0.5 – 2x baseline Apple

Probability of disease progression
HPV infection progressing to CIN 1 (%) 8.1 5.4-15.0 Ho (1998)
Prevalence of LSIL among patients with non 16/18 HR HPV infection (%) 14 0.5 – 2x baseline Herrero (2005)
RR of LSIL among patients with HPV-16 infection§ 1 Assumption
RR of LSIL among patients with HPV-18 infection§ 1 Assumption
HPV infection progressing to CIN 2,3 (%) 0.56 0.54-1.5 Ho (1998), Myers (2000)
Prevalence of CIN 2,3 among patients with non 16/18 HR HPV infection (%) 4 0.5 – 2x baseline Khan (2005)
Progression from CIN 1 to CIN 2,3 (%) 1.7 – 5.7 1.7-8.3 Myers (2000)
Annual rate of progression among patients with non 16/18 HR HPV infection 0.09 0.5 -2x baseline Khan (2005)
RR of CIN 2,3 in patients with HPV-16 infection§ 4.6 Khan (2005)
RR of CIN 2,3 in patients with HPV-18 infection§ 2.5
Progression from CIN 2,3 to cervical cancer (%) 3.8 3.0-6.2 Sanders (2003)
Incidence rate of cervical cancer in the United States (per 100,000 women) 9.4 0.5 – 2x baseline Saraiya (2007)
Prevalence of HPV-16 in patients with cervical cancer (%) 59 55-63 Clifford (2003), Munoz (2003)
Prevalence of HPV-18 in patients with cervical cancer (%) 13 11-15
Prevalence of non 16/18 HR HPV types in patients with cervical cancer (%) 28 22-34

Probability of cervical cancer progression (%) ¥ 43.7-68.3 40-70 Myers (2000), Sanders (2003)

Probability of disease regression
Age-specific probability of regression of HPV infection (%) 3.3 – 37.3 1.7-60.0 Myers (2000), Ho (1998)
Rate of clearance of non 16/18 HR HPV infection 1.29 0.5 – 2x baseline Trottier (unpublished manuscript)
RR of clearance of HPV-16 infection§ 0.85 Trottier
RR of clearance of HPV-18 infection§ 0.96 Trottier
Regression of CIN 1 (%) 2.7 – 14.2 2 – 16 Sanders (2003)
Patients regressing to HPV infection without lesion (%) 10 0 – 20 Sanders (2003), Myers (2000)
Regression rate of LSIL among patients with non 16/18 HR HPV infection 0.98 0.5 – 2x baseline Schlecht (2003)
RR of regression of LSIL in patients with HPV-16§ 0.91
RR of regression of LSIL in patients with HPV-18§ 0.91 Assumption
Regression of CIN 2,3 (%) 3.7 – 5.8 3-7 Sanders (2003), Myers (2000)
Patients regressing to normal (%) 45 40-50
Patients regressing to HPV infection without lesion (%) 5 0-10
Patients regressing to CIN 1 (%) 50 40-60
Regression rate of HSIL among patients with non 16/18 HR HPV infection 0.77 0.5 – 2x baseline Schlecht (2003)
RR of regression of HSIL in patients with HPV-16§ 0.27
RR of regression of HSIL in patients with HPV-18§ 0.27

Annual symptom detection probability for cervical cancer (%) ¥ 15-90 12-93 Sanders (2003)

5-year survival rates (% alive at 5 years) ¥ 85-12 84-10 NCDB commission on cancer (2006)

Disease-specific utilities Sanders (2003)
HPV infection 1 0.8-1
CIN 1 0.97 0.8-1
CIN 2,3 0.97 0.5-1
Invasive cervical cancer ¥ 0.79-0.62 0.25-1

Initial efficacy of treatment (%) Karyn Goodman (personal communication), Assumption
CIN 1 98 95-100
CIN 2 95 90-98
Invasive cervical cancer¥ 90-15 10-100
Probability HPV persists after effective treatment (%) Sanders (2003)
 CIN 1 10 0-25
 CIN 2,3 10 0-25
 Invasive cervical cancer 0 --- Assumption

Screening tests (%) Sensitivity Specificity
Liquid-based cytology (ASCUS or worse)
 CIN 1 or worse 43 85 Ratnam (2000)
 CIN 2,3 or worse 53 96 Cuzick (2006)
HPV positive
 CIN 1 or worse 57 96 Bigras (2005)
 CIN 2,3 or worse 96 91 Cuzick (2006)
*

All variables are annual unless otherwise noted. HR denotes high risk, HPV human papillomavirus, CIN cervical intraepithelial neoplasia, LSIL low-grade squamous intraepithelial lesion, RR relative risk, FIGO International Federation of Gynecology and Obstetrics, HSIL high-grade squamous intraepithelial lesion, NCDB National Cancer Database, and ASCUS atypical squamous cells of undetermined significance.

These data vary based on age. The range of values is shown.

These data also vary by HPV type.

§

Compared to patients with non 16/18 HR HPV infection

Estimated using a Markov model to match the incidence of CIN 2,3 and cervical cancer in the United States

¥

These data vary based on cervical cancer stage (FIGO I, II, III or IV)