The potential impact of CAR T-cell treatment delays on society
To date, breakthrough chimeric antigen receptor (CAR) T-cell therapies, such as tisagenlecleucel, indicated for pediatric acute lymphoblastic leukemia (pALL) and diffuse large B-cell lymphoma (DLBCL), and axicabtagene ciloleucel, indicated for DLBCL, although clinically effective, have been limited...
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Veröffentlicht in: | The American journal of managed care 2019-08, Vol.25 (8), p.379-386 |
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creator | Thornton Snider, Julia Brauer, Michelle Kee, Rebecca Batt, Katharine Karaca-Mandic, Pinar Zhang, Jie Goldman, Dana P |
description | To date, breakthrough chimeric antigen receptor (CAR) T-cell therapies, such as tisagenlecleucel, indicated for pediatric acute lymphoblastic leukemia (pALL) and diffuse large B-cell lymphoma (DLBCL), and axicabtagene ciloleucel, indicated for DLBCL, although clinically effective, have been limited by treatment delays. Our study measured the social value of CAR T-cell therapy (CAR T) for relapsed or refractory pALL and DLBCL in the United States and quantified social value lost due to treatment delays.
We used an economic framework for therapy valuation, measuring social value as the sum of consumer surplus and manufacturer profit. Consumer surplus is the difference between the value of health gains from a therapy and its incremental cost, while accounting for indirect costs and benefits to patients.
For 20 incident cohorts of pALL (n = 20 × 400 = 8000) and DLBCL (n = 20 × 5902 = 118,040), we quantified patient value, calculated as the value of additional quality-adjusted life-years gained with CAR T, minus the incremental cost of CAR T compared with standard of care (SOC). We calculated manufacturer profits using a range of production costs given uncertainties in the production process. Patient value and manufacturer profits were summed to obtain total social value. We measured social value lost from treatment delays, assuming that patients received the SOC while awaiting CAR T-cell treatment.
Depending on production costs, as much as $6.5 billion and $34.8 billion in social value was generated for patients with pALL and DLBCL, respectively. However, with 1, 2, or 6 months of treatment delay (assuming $200,000 production costs), the pALL population lost 9.8%, 36.2%, and 67.3% of social value, respectively, whereas the DLBCL population lost 4.2%, 11.5%, and 46.0%, relative to no delay.
The social value of CAR T is significantly limited by treatment delays. Efficient payment mechanisms, adequate capital, and payment policy reform are urgently needed to increase patient access and maximize the value of CAR T. |
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We used an economic framework for therapy valuation, measuring social value as the sum of consumer surplus and manufacturer profit. Consumer surplus is the difference between the value of health gains from a therapy and its incremental cost, while accounting for indirect costs and benefits to patients.
For 20 incident cohorts of pALL (n = 20 × 400 = 8000) and DLBCL (n = 20 × 5902 = 118,040), we quantified patient value, calculated as the value of additional quality-adjusted life-years gained with CAR T, minus the incremental cost of CAR T compared with standard of care (SOC). We calculated manufacturer profits using a range of production costs given uncertainties in the production process. Patient value and manufacturer profits were summed to obtain total social value. We measured social value lost from treatment delays, assuming that patients received the SOC while awaiting CAR T-cell treatment.
Depending on production costs, as much as $6.5 billion and $34.8 billion in social value was generated for patients with pALL and DLBCL, respectively. However, with 1, 2, or 6 months of treatment delay (assuming $200,000 production costs), the pALL population lost 9.8%, 36.2%, and 67.3% of social value, respectively, whereas the DLBCL population lost 4.2%, 11.5%, and 46.0%, relative to no delay.
The social value of CAR T is significantly limited by treatment delays. Efficient payment mechanisms, adequate capital, and payment policy reform are urgently needed to increase patient access and maximize the value of CAR T.</description><identifier>ISSN: 1088-0224</identifier><identifier>EISSN: 1936-2692</identifier><identifier>PMID: 31419095</identifier><language>eng</language><publisher>United States: MultiMedia Healthcare Inc</publisher><subject>Adipocytes ; Antigens ; Health administration ; Leukemia ; Lymphoma ; Medical treatment ; Patients ; Pediatrics ; Production costs</subject><ispartof>The American journal of managed care, 2019-08, Vol.25 (8), p.379-386</ispartof><rights>Copyright Intellisphere, LLC Aug 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31419095$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thornton Snider, Julia</creatorcontrib><creatorcontrib>Brauer, Michelle</creatorcontrib><creatorcontrib>Kee, Rebecca</creatorcontrib><creatorcontrib>Batt, Katharine</creatorcontrib><creatorcontrib>Karaca-Mandic, Pinar</creatorcontrib><creatorcontrib>Zhang, Jie</creatorcontrib><creatorcontrib>Goldman, Dana P</creatorcontrib><title>The potential impact of CAR T-cell treatment delays on society</title><title>The American journal of managed care</title><addtitle>Am J Manag Care</addtitle><description>To date, breakthrough chimeric antigen receptor (CAR) T-cell therapies, such as tisagenlecleucel, indicated for pediatric acute lymphoblastic leukemia (pALL) and diffuse large B-cell lymphoma (DLBCL), and axicabtagene ciloleucel, indicated for DLBCL, although clinically effective, have been limited by treatment delays. Our study measured the social value of CAR T-cell therapy (CAR T) for relapsed or refractory pALL and DLBCL in the United States and quantified social value lost due to treatment delays.
We used an economic framework for therapy valuation, measuring social value as the sum of consumer surplus and manufacturer profit. Consumer surplus is the difference between the value of health gains from a therapy and its incremental cost, while accounting for indirect costs and benefits to patients.
For 20 incident cohorts of pALL (n = 20 × 400 = 8000) and DLBCL (n = 20 × 5902 = 118,040), we quantified patient value, calculated as the value of additional quality-adjusted life-years gained with CAR T, minus the incremental cost of CAR T compared with standard of care (SOC). We calculated manufacturer profits using a range of production costs given uncertainties in the production process. Patient value and manufacturer profits were summed to obtain total social value. We measured social value lost from treatment delays, assuming that patients received the SOC while awaiting CAR T-cell treatment.
Depending on production costs, as much as $6.5 billion and $34.8 billion in social value was generated for patients with pALL and DLBCL, respectively. However, with 1, 2, or 6 months of treatment delay (assuming $200,000 production costs), the pALL population lost 9.8%, 36.2%, and 67.3% of social value, respectively, whereas the DLBCL population lost 4.2%, 11.5%, and 46.0%, relative to no delay.
The social value of CAR T is significantly limited by treatment delays. Efficient payment mechanisms, adequate capital, and payment policy reform are urgently needed to increase patient access and maximize the value of CAR T.</description><subject>Adipocytes</subject><subject>Antigens</subject><subject>Health administration</subject><subject>Leukemia</subject><subject>Lymphoma</subject><subject>Medical treatment</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Production costs</subject><issn>1088-0224</issn><issn>1936-2692</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpd0E1Lw0AQgOFFFFurf0EWvHgJzO4k-3ERSvELCoLUc9ikE0xJsjG7OfTfu2K9eJo5PAwvc8aWwqLKpLLyPO1gTAZS5gt2FcIBAJXJ1SVboMiFBVss2cPuk_joIw2xdR1v-9HVkfuGb9bvfJfV1HU8TuRinwTfU-eOgfuBB1-3FI_X7KJxXaCb01yxj6fH3eYl2749v27W22yUaGNmkGopGtcYQY2oQYJzCOAIQCsjq9xi5axKeQIrxELXrtG51oSiqIxBXLH737vj5L9mCrHs2_AT5wbycyil1IXUYJVK9O4fPfh5GlJdUgYKUFLnSd2e1Fz1tC_Hqe3ddCz_PoPfup9dXA</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Thornton Snider, Julia</creator><creator>Brauer, Michelle</creator><creator>Kee, Rebecca</creator><creator>Batt, Katharine</creator><creator>Karaca-Mandic, Pinar</creator><creator>Zhang, Jie</creator><creator>Goldman, Dana P</creator><general>MultiMedia Healthcare Inc</general><scope>NPM</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20190801</creationdate><title>The potential impact of CAR T-cell treatment delays on society</title><author>Thornton Snider, Julia ; Brauer, Michelle ; Kee, Rebecca ; Batt, Katharine ; Karaca-Mandic, Pinar ; Zhang, Jie ; Goldman, Dana P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p239t-83ec21faf81ef1c020aa300ae007682b493ba9636813b3357caf7477e315b8833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adipocytes</topic><topic>Antigens</topic><topic>Health administration</topic><topic>Leukemia</topic><topic>Lymphoma</topic><topic>Medical treatment</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Production costs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thornton Snider, Julia</creatorcontrib><creatorcontrib>Brauer, Michelle</creatorcontrib><creatorcontrib>Kee, Rebecca</creatorcontrib><creatorcontrib>Batt, Katharine</creatorcontrib><creatorcontrib>Karaca-Mandic, Pinar</creatorcontrib><creatorcontrib>Zhang, Jie</creatorcontrib><creatorcontrib>Goldman, Dana P</creatorcontrib><collection>PubMed</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of managed care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thornton Snider, Julia</au><au>Brauer, Michelle</au><au>Kee, Rebecca</au><au>Batt, Katharine</au><au>Karaca-Mandic, Pinar</au><au>Zhang, Jie</au><au>Goldman, Dana P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The potential impact of CAR T-cell treatment delays on society</atitle><jtitle>The American journal of managed care</jtitle><addtitle>Am J Manag Care</addtitle><date>2019-08-01</date><risdate>2019</risdate><volume>25</volume><issue>8</issue><spage>379</spage><epage>386</epage><pages>379-386</pages><issn>1088-0224</issn><eissn>1936-2692</eissn><abstract>To date, breakthrough chimeric antigen receptor (CAR) T-cell therapies, such as tisagenlecleucel, indicated for pediatric acute lymphoblastic leukemia (pALL) and diffuse large B-cell lymphoma (DLBCL), and axicabtagene ciloleucel, indicated for DLBCL, although clinically effective, have been limited by treatment delays. Our study measured the social value of CAR T-cell therapy (CAR T) for relapsed or refractory pALL and DLBCL in the United States and quantified social value lost due to treatment delays.
We used an economic framework for therapy valuation, measuring social value as the sum of consumer surplus and manufacturer profit. Consumer surplus is the difference between the value of health gains from a therapy and its incremental cost, while accounting for indirect costs and benefits to patients.
For 20 incident cohorts of pALL (n = 20 × 400 = 8000) and DLBCL (n = 20 × 5902 = 118,040), we quantified patient value, calculated as the value of additional quality-adjusted life-years gained with CAR T, minus the incremental cost of CAR T compared with standard of care (SOC). We calculated manufacturer profits using a range of production costs given uncertainties in the production process. Patient value and manufacturer profits were summed to obtain total social value. We measured social value lost from treatment delays, assuming that patients received the SOC while awaiting CAR T-cell treatment.
Depending on production costs, as much as $6.5 billion and $34.8 billion in social value was generated for patients with pALL and DLBCL, respectively. However, with 1, 2, or 6 months of treatment delay (assuming $200,000 production costs), the pALL population lost 9.8%, 36.2%, and 67.3% of social value, respectively, whereas the DLBCL population lost 4.2%, 11.5%, and 46.0%, relative to no delay.
The social value of CAR T is significantly limited by treatment delays. Efficient payment mechanisms, adequate capital, and payment policy reform are urgently needed to increase patient access and maximize the value of CAR T.</abstract><cop>United States</cop><pub>MultiMedia Healthcare Inc</pub><pmid>31419095</pmid><tpages>8</tpages></addata></record> |
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subjects | Adipocytes Antigens Health administration Leukemia Lymphoma Medical treatment Patients Pediatrics Production costs |
title | The potential impact of CAR T-cell treatment delays on society |
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