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. Author manuscript; available in PMC: 2012 Sep 1.
Published in final edited form as: Gynecol Oncol. 2011 Jun 12;122(3):473–478. doi: 10.1016/j.ygyno.2011.05.014

Table 2.

Model Estimates - Clinical Assumptions

Clinical Parameter Estimate [refs] Range
Probabilities
  Surgical cytoreduction suboptimal 0.33a 0.00 – 1.00
  Neuropathy | CP 0.07a 0.03 – 0.14
  Neuropathy | CP+P 0.20a 0.10 – 0.40
  Neuropathy | CPB+B 0.07a 0.03 – 0.14
  Bowel Perforation | CPB+B 0.03a 0.015 – 0.10
  Death | Bowel Perforation 0.50a 0.00 – 0.75
Progression Free Survival (months)
  CP
    Optimal 24a reference
    Suboptimal 14a reference
  CP+P
    Optimal 35a 17.5 – 105
    Suboptimal 20a 10 – 60
  CPB+B
    Optimal 35a 17.5 – 105
    Suboptimal 20a 10 – 60
Overall Survival (months)
  CP
    Optimal 48a reference
    Suboptimal 35a reference
  CP+P
    Optimal 70a 35 – 210
    Suboptimal 42a 21 – 126
  CPB+B
    Optimal 70a 35 – 210
    Suboptimal 42a 21 – 126
Quality of Life Utility Index
  Chemotherapy
      CP Cycles 0.77a 0.64 – 0.85
      CPB Cycles 0.77a 0.64 – 0.85
      P Maintenance Cycles 0.80a 0.66 – 0.88
      B Maintenance Cycles 0.82a 0.68 – 0.90
      Months 1–6 Recovery 0.84a 0.70 – 0.93
  PFS 0.85 [34] 0.75 – 1.00
  Cancer recurrence 0.65 [34] 0.50 – 0.85
  Neuropathy 0.94 [35] 0.80 – 1.00
  Bowel perforation 0.85 [36] 0.50 – 0.95
Discount rate 0.03 0.00 – 0.05
a

See text for rationale

Note. CP: Carboplatin and Paclitaxel; CP+P: Carboplatin and Paclitaxel followed by Paclitaxel consolidation; CPB+B: Carboplatin and Paclitaxel and Bevacizumab followed by Bevacizumab consolidation.