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. 2021 Mar 25;149(2):337–346. doi: 10.1002/ijc.33540

TABLE 1.

Model assumptions on the natural disease course of PC and its precursors

Value
Lifetime PC risk 7.5% 1
Treatment mortality 3% 10 , 11
Progressive‐only pathway Indolent Included pathway
Stage Mean duration of progressive stages (years)
Preinvasive stage LGD 3.33 1.11
Preinvasive stage IGD 3.33 1.11
Preinvasive stage HGD 3.33 1.11
Preclinical cancer Stage I 2 0.66
Preclinical cancer Stage II 2 0.66
Preclinical cancer Stage III/IV 1 0.33
Estimated mean total preclinical 14.3 4.8
Stage Mean duration of indolent stages (years)
Preinvasive stage LGD n.a. 7.08 a
Preinvasive stage IGD n.a. 11.78 a
Preinvasive stage HGD n.a. 24.15 a
Preclinical cancer Stage I n.a. Until death from other causes
Stage Probability of being clinically diagnosed, before moving to the next stage 12 b
Cancer Stage I 5.1%
Cancer Stage II 13.1%
Cancer Stage III/IV 100%
Stage 5‐year relative survival 12 b , c
Clinical cancer Stage I 29.1%
Clinical cancer Stage II 11.4%
Clinical cancer Stage III/IV 0%
Stage Screen test sensitivity d
Preinvasive stage LGD 60%
Preinvasive stage IGD 60%
Preinvasive stage HGD 75%
Preclinical cancer Stage I 90%
Preclinical cancer Stage II 93%
Preclinical cancer Stage III/IV 99%
Screen test specificity d
Any pancreatic lesion 90%

Notes: If someone has survived the first 5 years after diagnosis, we assumed lifelong PC survival. Detection (and associated management of preinvasive lesions) was assumed to lead to a 100% cure rate. For resection, we assumed a 3% mortality risk. Stage‐specific survival of screen‐detected invasive cancer was based on observed survival of clinically detected cancer in the Netherlands.

a

Optimized parameter.

b

Weighted averages are used to combine cancer Stage Ia and Ib into Stage I, and IIa and IIb into Stage II.

c

A linear distribution of PC mortality was assumed over 5 years.

d

Combined MRI/EUS.