Cost-effectiveness analysis of different combination therapies for the treatment of chronic lymphocytic leukaemia in India.

Chemotherapy Cost effectiveness Economic evaluation Leukaemia

Journal

The Lancet regional health. Southeast Asia
ISSN: 2772-3682
Titre abrégé: Lancet Reg Health Southeast Asia
Pays: England
ID NLM: 9918419282806676

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 17 06 2022
revised: 24 11 2022
accepted: 10 04 2023
medline: 29 6 2023
pubmed: 29 6 2023
entrez: 29 6 2023
Statut: epublish

Résumé

Over the years, there has been introduction of newer drugs, like bendamustine and ibrutinib, for the management of chronic lymphocytic leukaemia (CLL). Though these drugs lead to better survival, they are also associated with higher cost. The existing evidence on cost effectiveness of these drugs is from high-income countries, which has limited generalisability for low-income and middle-income counties. Therefore, the present study was undertaken to assess the cost-effectiveness of three therapeutic regimens, chlorambucil plus prednisolone (CP), bendamustine plus rituximab (BR) and ibrutinib for CLL treatment in India. A Markov model was developed for estimating lifetime costs and consequences in a hypothetical cohort of 1000 CLL patients following treatment with different therapeutic regimens. The analysis was performed based on a limited societal perspective, 3% discount rate and lifetime horizon. The clinical effectiveness of each regime in the form of progression-free survival and occurrence of adverse events were assessed from various randomised controlled trials. A structured comprehensive review of literature was undertaken for the identification of relevant trials. The data on utility values and out of pocket expenditure was obtained from primary data collected from 242 CLL patients across six large cancer hospitals in India. As compared to the most affordable regimen comprising of CP as first-line followed by BR as second-line therapy, none of the other therapeutic regimens were cost-effective at one time per capita gross-domestic product of India. However, if the current price of either combination of BR and ibrutinib or even ibrutinib alone could be reduced by more than 80%, regimen comprising of BR as first-line therapy followed by second-line ibrutinib would become cost-effective. At the current market prices, regimen comprising of CP as first-line followed by BR as second-line therapy is the most cost-effective strategy for CLL treatment in India. Department of Health Research, Government of India.

Sections du résumé

Background UNASSIGNED
Over the years, there has been introduction of newer drugs, like bendamustine and ibrutinib, for the management of chronic lymphocytic leukaemia (CLL). Though these drugs lead to better survival, they are also associated with higher cost. The existing evidence on cost effectiveness of these drugs is from high-income countries, which has limited generalisability for low-income and middle-income counties. Therefore, the present study was undertaken to assess the cost-effectiveness of three therapeutic regimens, chlorambucil plus prednisolone (CP), bendamustine plus rituximab (BR) and ibrutinib for CLL treatment in India.
Methods UNASSIGNED
A Markov model was developed for estimating lifetime costs and consequences in a hypothetical cohort of 1000 CLL patients following treatment with different therapeutic regimens. The analysis was performed based on a limited societal perspective, 3% discount rate and lifetime horizon. The clinical effectiveness of each regime in the form of progression-free survival and occurrence of adverse events were assessed from various randomised controlled trials. A structured comprehensive review of literature was undertaken for the identification of relevant trials. The data on utility values and out of pocket expenditure was obtained from primary data collected from 242 CLL patients across six large cancer hospitals in India.
Findings UNASSIGNED
As compared to the most affordable regimen comprising of CP as first-line followed by BR as second-line therapy, none of the other therapeutic regimens were cost-effective at one time per capita gross-domestic product of India. However, if the current price of either combination of BR and ibrutinib or even ibrutinib alone could be reduced by more than 80%, regimen comprising of BR as first-line therapy followed by second-line ibrutinib would become cost-effective.
Interpretation UNASSIGNED
At the current market prices, regimen comprising of CP as first-line followed by BR as second-line therapy is the most cost-effective strategy for CLL treatment in India.
Funding UNASSIGNED
Department of Health Research, Government of India.

Identifiants

pubmed: 37383548
doi: 10.1016/j.lansea.2023.100201
pii: S2772-3682(23)00061-6
pmc: PMC10305972
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100201

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

Shankar Prinja has formerly served as the Executive Director at the National Health Authority, India. The authors declare no other conflict of interest.

Références

J Clin Oncol. 2017 Jan 10;35(2):166-174
pubmed: 27870563
Value Health. 2016 Jun;19(4):374-82
pubmed: 27325329
Leuk Lymphoma. 2012 Oct;53(10):1961-5
pubmed: 22475243
J Clin Oncol. 2009 Sep 10;27(26):4378-84
pubmed: 19652068
Clinicoecon Outcomes Res. 2014 Apr 01;6:141-9
pubmed: 24729719
Blood. 2020 Oct 22;136(17):1946-1955
pubmed: 32518952
BMJ Glob Health. 2021 Apr;6(4):
pubmed: 33903175
Cancer Med. 2018 Apr;7(4):1043-1055
pubmed: 29533000
CA Cancer J Clin. 2018 Mar;68(2):153-165
pubmed: 29338071
J Oncol Pract. 2015 May;11(3):252-8
pubmed: 25804983
Value Health. 2011 Jul-Aug;14(5 Suppl 1):S60-4
pubmed: 21839901
Pharmacoeconomics. 2006;24(10):1021-33
pubmed: 17002484
Clin Ther. 2016 Apr;38(4):889-904.e14
pubmed: 26970696
Lancet. 2015 May 9;385(9980):1873-83
pubmed: 25882396
N Engl J Med. 2018 Dec 27;379(26):2517-2528
pubmed: 30501481
Value Health. 2019 Nov;22(11):1329-1344
pubmed: 31708071
J Natl Compr Canc Netw. 2010 Mar;8(3):288-334
pubmed: 20202462
N Engl J Med. 2015 Dec 17;373(25):2425-37
pubmed: 26639149
Blood Adv. 2018 Nov 30;2(Suppl 1):33-34
pubmed: 30504196
Biomed Eng Online. 2022 Jan 11;21(1):4
pubmed: 35016695
Leukemia. 2020 Mar;34(3):787-798
pubmed: 31628428
Blood. 2018 Jun 21;131(25):2745-2760
pubmed: 29540348
BMC Med Res Methodol. 2021 Jun 1;21(1):111
pubmed: 34074267
Blood Adv. 2018 Aug 14;2(15):1946-1956
pubmed: 30097461
Clin Lymphoma Myeloma Leuk. 2018 Feb;18(2):e131-e142
pubmed: 29398648
BMJ Open. 2021 Jul 29;11(7):e048513
pubmed: 34326050
J Clin Oncol. 2020 Sep 1;38(25):2849-2861
pubmed: 32459600
Value Health. 2012 Jul-Aug;15(5):759-70
pubmed: 22867787
JCO Glob Oncol. 2020 Jun;6:866-872
pubmed: 32579486
Blood. 2009 Oct 15;114(16):3382-91
pubmed: 19605849
JCO Glob Oncol. 2020 Feb;6:205-216
pubmed: 32045547

Auteurs

Prerika Nehra (P)

Department of Community Medicine and School of Public Health, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Akashdeep Singh Chauhan (AS)

Department of Community Medicine and School of Public Health, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Pankaj Malhotra (P)

Department of Clinical Haematology and Medical Oncology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Lalit Kumar (L)

Department of Medical Oncology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.

Ashish Singh (A)

Department of Medical Oncology, Christian Medical College, Vellore, Tamil Nadu, India.

Nidhi Gupta (N)

Department of Radiation Oncology, Government Medical College and Hospital, Chandigarh, India.

Nikita Mehra (N)

Department of Medical Oncology, Adyar Cancer Institute, Chennai, Tamil Nadu, India.

Anisha Mathew (A)

Department of Medical Oncology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.

Amal Chandra Kataki (AC)

Department of Gynaecologic Oncology, Dr. B. Booroah Cancer Institute, Guwahati, Assam, India.

Sudeep Gupta (S)

Department of Medical Oncology, Tata Memorial Centre, Mumbai, Maharashtra, India.

Shankar Prinja (S)

Department of Community Medicine and School of Public Health, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Classifications MeSH