TY - JOUR
T1 - Target prices for mass production of tyrosine kinase inhibitors for global cancer treatment
AU - Hill, Andrew
AU - Gotham, Dzintars
AU - Fortunak, Joseph
AU - Meldrum, Jonathan
AU - Erbacher, Isabelle
AU - Martin, Manuel
AU - Shoman, Haitham
AU - Levi, Jacob
AU - Powderly, William G.
AU - Bower, Mark
PY - 2016
Y1 - 2016
N2 - Objective: To calculate sustainable generic prices for 4 tyrosine kinase inhibitors (TKIs). Background: TKIs have proven survival benefits in the treatment of several cancers, including chronic myeloid leukaemia, breast, liver, renal and lung cancer. However, current high prices are a barrier to treatment. Mass production of low-cost generic antiretrovirals has led to over 13 million people being on HIV/AIDS treatment worldwide. This analysis estimates target prices for generic TKIs, assuming similar methods of mass production. Methods: Four TKIs with patent expiry dates in the next 5 years were selected for analysis: imatinib, erlotinib, lapatinib and sorafenib. Chemistry, dosing, published data on per-kilogram pricing for commercial transactions of active pharmaceutical ingredient (API), and quotes from manufacturers were used to estimate costs of production. Analysis included costs of excipients, formulation, packaging, shipping and a 50% profit margin. Target prices were compared with current prices. Global numbers of patients eligible for treatment with each TKI were estimated. Results: API costs per kg were $347-$746 for imatinib, $2470 for erlotinib, $4671 for lapatinib, and $3000 for sorafenib. Basing on annual dose requirements, costs of formulation/packaging and a 50% profit margin, target generic prices per person-year were $128-$216 for imatinib, $240 for erlotinib, $1450 for sorafenib, and $4020 for lapatinib. Over 1 million people would be newly eligible to start treatment with these TKIs annually. Conclusions: Mass generic production of several TKIs could achieve treatment prices in the range of $128-$4020 per person-year, versus current US prices of $75161-$139 138. Generic TKIs could allow significant savings and scaling-up of treatment globally, for over 1 million eligible patients.
AB - Objective: To calculate sustainable generic prices for 4 tyrosine kinase inhibitors (TKIs). Background: TKIs have proven survival benefits in the treatment of several cancers, including chronic myeloid leukaemia, breast, liver, renal and lung cancer. However, current high prices are a barrier to treatment. Mass production of low-cost generic antiretrovirals has led to over 13 million people being on HIV/AIDS treatment worldwide. This analysis estimates target prices for generic TKIs, assuming similar methods of mass production. Methods: Four TKIs with patent expiry dates in the next 5 years were selected for analysis: imatinib, erlotinib, lapatinib and sorafenib. Chemistry, dosing, published data on per-kilogram pricing for commercial transactions of active pharmaceutical ingredient (API), and quotes from manufacturers were used to estimate costs of production. Analysis included costs of excipients, formulation, packaging, shipping and a 50% profit margin. Target prices were compared with current prices. Global numbers of patients eligible for treatment with each TKI were estimated. Results: API costs per kg were $347-$746 for imatinib, $2470 for erlotinib, $4671 for lapatinib, and $3000 for sorafenib. Basing on annual dose requirements, costs of formulation/packaging and a 50% profit margin, target generic prices per person-year were $128-$216 for imatinib, $240 for erlotinib, $1450 for sorafenib, and $4020 for lapatinib. Over 1 million people would be newly eligible to start treatment with these TKIs annually. Conclusions: Mass generic production of several TKIs could achieve treatment prices in the range of $128-$4020 per person-year, versus current US prices of $75161-$139 138. Generic TKIs could allow significant savings and scaling-up of treatment globally, for over 1 million eligible patients.
UR - http://www.scopus.com/inward/record.url?scp=84960412502&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2015-009586
DO - 10.1136/bmjopen-2015-009586
M3 - Article
C2 - 26817636
AN - SCOPUS:84960412502
SN - 2044-6055
VL - 6
JO - BMJ Open
JF - BMJ Open
IS - 1
M1 - e009586
ER -