Table 1.

Model clinical parameters

Result or transitionEstimateRangeReferences
PFS for ibrutinib first-line therapy Exponential: λ = 0.005904 — 8  
PFS for R-bendamustine, entire cohort Gompertz: λ = 0.0089865, γ = 0.0257203 — 8  
PFS for R-bendamustine, IGHV mutated only Gompertz: λ = 0.0038591, γ = 0.0315173 — 8  
PFS for R-bendamustine, IGHV unmutated only Gompertz: λ = 0.0107668, γ = 0.0293043 — 8  
PFS for R-venetoclax Gompertz: λ = 0.0044257, γ = 0.0399164 — 11  
PFS for ibrutinib third-line therapy Exponential: λ = 0.015356 — 46  
PFS for R-idelalisib Weibull: λ = 0.0050368, κ = 1.794209 — 15  
PFS for ofatumumab Gompertz: λ = 0.0231548, γ = 0.3048745 — 14  
Time from progression to start of next therapy, mo 10.3 9-12 21  
Probability of treatment discontinuation, ibrutinib first-line, yearly, %   23  
 Year 0-1 6.725 5.38-8.07  
 Year 1-2 5.798 4.64-6.96  
 Year 2-3 5.388 4.31-6.47  
 Year 3+   
Probability of treatment discontinuation, ibrutinib third-line, yearly, %   23  
 Year 0-1 6.728 5.38-8.07  
 Year 1-2 2.714 2.17-3.25  
 Year 2-3 1.999 1.60-2.40  
 Year 3+ 2.599 2.07-3.12  
Time from discontinuation because of toxicity to start of next therapy, ibrutinib, mo 6.5 6-9 24  
Probability of treatment discontinuation, R-bendamustine, 6 cycles, % 13.3 10.6-15.9 22  
Probability of treatment mortality because of R-bendamustine, 6 cycles, % 0.8-2.0 8,22  
Probability of receiving pegfilgrastim during R-bendamustine, cycles 2-6, % 14.3 11.4-17.2 35,36  
Probability of receiving best supportive care after progression from third-line treatment, % 11.6 9.28-13.92 16  
Probability of background death — — 26  
Probability of death from best supportive care state, yearly, % 55 44-66 25  
Probability of receiving IV rituximab rather than SQ, % 80 64-96 Expert opinion 
Discount rate 0.03 0.015-0.06 17,54  
Median starting age of cohort, y 71 65-77 8  
Result or transitionEstimateRangeReferences
PFS for ibrutinib first-line therapy Exponential: λ = 0.005904 — 8  
PFS for R-bendamustine, entire cohort Gompertz: λ = 0.0089865, γ = 0.0257203 — 8  
PFS for R-bendamustine, IGHV mutated only Gompertz: λ = 0.0038591, γ = 0.0315173 — 8  
PFS for R-bendamustine, IGHV unmutated only Gompertz: λ = 0.0107668, γ = 0.0293043 — 8  
PFS for R-venetoclax Gompertz: λ = 0.0044257, γ = 0.0399164 — 11  
PFS for ibrutinib third-line therapy Exponential: λ = 0.015356 — 46  
PFS for R-idelalisib Weibull: λ = 0.0050368, κ = 1.794209 — 15  
PFS for ofatumumab Gompertz: λ = 0.0231548, γ = 0.3048745 — 14  
Time from progression to start of next therapy, mo 10.3 9-12 21  
Probability of treatment discontinuation, ibrutinib first-line, yearly, %   23  
 Year 0-1 6.725 5.38-8.07  
 Year 1-2 5.798 4.64-6.96  
 Year 2-3 5.388 4.31-6.47  
 Year 3+   
Probability of treatment discontinuation, ibrutinib third-line, yearly, %   23  
 Year 0-1 6.728 5.38-8.07  
 Year 1-2 2.714 2.17-3.25  
 Year 2-3 1.999 1.60-2.40  
 Year 3+ 2.599 2.07-3.12  
Time from discontinuation because of toxicity to start of next therapy, ibrutinib, mo 6.5 6-9 24  
Probability of treatment discontinuation, R-bendamustine, 6 cycles, % 13.3 10.6-15.9 22  
Probability of treatment mortality because of R-bendamustine, 6 cycles, % 0.8-2.0 8,22  
Probability of receiving pegfilgrastim during R-bendamustine, cycles 2-6, % 14.3 11.4-17.2 35,36  
Probability of receiving best supportive care after progression from third-line treatment, % 11.6 9.28-13.92 16  
Probability of background death — — 26  
Probability of death from best supportive care state, yearly, % 55 44-66 25  
Probability of receiving IV rituximab rather than SQ, % 80 64-96 Expert opinion 
Discount rate 0.03 0.015-0.06 17,54  
Median starting age of cohort, y 71 65-77 8  

—, not applicable.

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