Cost-effectiveness of single, high-dose, liposomal amphotericin regimen for HIV-associated cryptococcal meningitis in five countries in sub-Saharan Africa: an economic analysis of the AMBITION-cm trial.
Journal
The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665
Informations de publication
Date de publication:
12 2022
12 2022
Historique:
received:
30
04
2022
revised:
25
09
2022
accepted:
30
09
2022
pubmed:
19
11
2022
medline:
23
11
2022
entrez:
18
11
2022
Statut:
ppublish
Résumé
HIV-associated cryptococcal meningitis is a leading cause of AIDS-related mortality. The AMBITION-cm trial showed that a regimen based on a single high dose of liposomal amphotericin B deoxycholate (AmBisome group) was non-inferior to the WHO-recommended treatment of seven daily doses of amphotericin B deoxycholate (control group) and was associated with fewer adverse events. We present a five-country cost-effectiveness analysis. The AMBITION-cm trial enrolled patients with HIV-associated cryptococcal meningitis from eight hospitals in Botswana, Malawi, South Africa, Uganda, and Zimbabwe. Taking a health service perspective, we collected country-specific unit costs and individual resource-use data per participant over the 10-week trial period, calculating mean cost per participant by group, mean cost-difference between groups, and incremental cost-effectiveness ratio per life-year saved. Non-parametric bootstrapping and scenarios analyses were performed including hypothetical real-world resource use. The trial registration number is ISRCTN72509687, and the trial has been completed. The AMBITION-cm trial enrolled 844 participants, and 814 were included in the intention-to-treat analysis (327 from Uganda, 225 from Malawi, 107 from South Africa, 84 from Botswana, and 71 from Zimbabwe) with 407 in each group, between Jan 31, 2018, and Feb 17, 2021. Using Malawi as a representative example, mean total costs per participant were US$1369 (95% CI 1314-1424) in the AmBisome group and $1237 (1181-1293) in the control group. The incremental cost-effectiveness ratio was $128 (59-257) per life-year saved. Excluding study protocol-driven cost, using a real-world toxicity monitoring schedule, the cost per life-year saved reduced to $80 (15-275). Changes in the duration of the hospital stay and antifungal medication cost showed the greatest effect in sensitivity analyses. Results were similar across countries, with the cost per life-year saved in the real-world scenario ranging from $71 in Botswana to $121 in Uganda. The AmBisome regimen was cost-effective at a low incremental cost-effectiveness ratio. The regimen might be even less costly and potentially cost-saving in real-world implementation given the lower drug-related toxicity and the potential for shorter hospital stays. European Developing Countries Clinical Trials Partnership, Swedish International Development Cooperation Agency, Wellcome Trust and Medical Research Council, UKAID Joint Global Health Trials, and the National Institute for Health Research. For the Chichewa, Isixhosa, Luganda, Setswana and Shona translations of the abstract see Supplementary Materials section.
Sections du résumé
BACKGROUND
HIV-associated cryptococcal meningitis is a leading cause of AIDS-related mortality. The AMBITION-cm trial showed that a regimen based on a single high dose of liposomal amphotericin B deoxycholate (AmBisome group) was non-inferior to the WHO-recommended treatment of seven daily doses of amphotericin B deoxycholate (control group) and was associated with fewer adverse events. We present a five-country cost-effectiveness analysis.
METHODS
The AMBITION-cm trial enrolled patients with HIV-associated cryptococcal meningitis from eight hospitals in Botswana, Malawi, South Africa, Uganda, and Zimbabwe. Taking a health service perspective, we collected country-specific unit costs and individual resource-use data per participant over the 10-week trial period, calculating mean cost per participant by group, mean cost-difference between groups, and incremental cost-effectiveness ratio per life-year saved. Non-parametric bootstrapping and scenarios analyses were performed including hypothetical real-world resource use. The trial registration number is ISRCTN72509687, and the trial has been completed.
FINDINGS
The AMBITION-cm trial enrolled 844 participants, and 814 were included in the intention-to-treat analysis (327 from Uganda, 225 from Malawi, 107 from South Africa, 84 from Botswana, and 71 from Zimbabwe) with 407 in each group, between Jan 31, 2018, and Feb 17, 2021. Using Malawi as a representative example, mean total costs per participant were US$1369 (95% CI 1314-1424) in the AmBisome group and $1237 (1181-1293) in the control group. The incremental cost-effectiveness ratio was $128 (59-257) per life-year saved. Excluding study protocol-driven cost, using a real-world toxicity monitoring schedule, the cost per life-year saved reduced to $80 (15-275). Changes in the duration of the hospital stay and antifungal medication cost showed the greatest effect in sensitivity analyses. Results were similar across countries, with the cost per life-year saved in the real-world scenario ranging from $71 in Botswana to $121 in Uganda.
INTERPRETATION
The AmBisome regimen was cost-effective at a low incremental cost-effectiveness ratio. The regimen might be even less costly and potentially cost-saving in real-world implementation given the lower drug-related toxicity and the potential for shorter hospital stays.
FUNDING
European Developing Countries Clinical Trials Partnership, Swedish International Development Cooperation Agency, Wellcome Trust and Medical Research Council, UKAID Joint Global Health Trials, and the National Institute for Health Research.
TRANSLATIONS
For the Chichewa, Isixhosa, Luganda, Setswana and Shona translations of the abstract see Supplementary Materials section.
Identifiants
pubmed: 36400090
pii: S2214-109X(22)00450-8
doi: 10.1016/S2214-109X(22)00450-8
pmc: PMC10009915
mid: NIHMS1875082
pii:
doi:
Substances chimiques
liposomal amphotericin B
0
Amphotericin B
7XU7A7DROE
Banques de données
ISRCTN
['ISRCTN72509687']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1845-e1854Subventions
Organisme : Department of Health
ID : RP-2017–08-ST2–012
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_MR/P006922/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P006922/1
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : K23 AI138851
Pays : United States
Organisme : Wellcome Trust
ID : 212638/Z/18/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 214321/Z/18/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 098316
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 211360/Z/18/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 203135/Z/16/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V033417/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P020526/1
Pays : United Kingdom
Investigateurs
Jack Goodall
(J)
Kwana Lechiile
(K)
Norah Mawoko
(N)
Tshepiso Mbangiwa
(T)
James Milburn
(J)
Refilwe Mmipi
(R)
Ponego Ponatshego
(P)
Ikanyang Rulaganyang
(I)
Kaelo Seatla
(K)
Keatlaretse Siamisang
(K)
Nametso Tlhako
(N)
Katlego Tsholo
(K)
Samantha April
(S)
Abulele Bekiswa
(A)
Linda Boloko
(L)
Hloni Bookholane
(H)
Thomas Crede
(T)
Lee-Ann Davids
(LA)
Rene Goliath
(R)
Siphokazi Hlungulu
(S)
Regina Hoffman
(R)
Henriette Kyepa
(H)
Noma Masina
(N)
Deborah Maughan
(D)
Trevor Mnguni
(T)
Sumaiyya Moosa
(S)
Tania Morar
(T)
Mkanyiseli Mpalali
(M)
Jonathan Naude
(J)
Ida Oliphant
(I)
Achita Singh
(A)
Sumaya Sayed
(S)
Leago Sebesho
(L)
Muki Shey
(M)
Loraine Swanepoel
(L)
Madalitso Chasweka
(M)
Wezi Chimang'anga
(W)
Tipatseni Chimphambano
(T)
Ebbie Gondwe
(E)
Henry Mzinganjira
(H)
Aubrey Kadzilimbile
(A)
Steven Kateta
(S)
Evelyn Kossam
(E)
Christopher Kukacha
(C)
Bright Lipenga
(B)
John Ndaferankhande
(J)
Maureen Ndalama
(M)
Reya Shah
(R)
Andreas Singini
(A)
Katherine Stott
(K)
Agness Zambasa
(A)
Towera Banda
(T)
Tarsizio Chikaonda
(T)
Gladys Chitulo
(G)
Lorren Chiwoko
(L)
Nelecy Chome
(N)
Mary Gwin
(M)
Timothy Kachitosi
(T)
Beauty Kamanga
(B)
Mussah Kazembe
(M)
Emily Kumwenda
(E)
Masida Kumwenda
(M)
Chimwemwe Maya
(C)
Wilberforce Mhango
(W)
Chimwemwe Mphande
(C)
Lusungu Msumba
(L)
Tapiwa Munthali
(T)
Doris Ngoma
(D)
Simon Nicholas
(S)
Lusayo Simwinga
(L)
Anthony Stambuli
(A)
Gerald Tegha
(G)
Janet Zambezi
(J)
Cynthia Ahimbisibwe
(C)
Andrew Akampurira
(A)
Anamudde Alice
(A)
Fiona Cresswell
(F)
Jane Gakuru
(J)
Enock Kagimu
(E)
John Kasibante
(J)
Daniel Kiiza
(D)
John Kisembo
(J)
Richard Kwizera
(R)
Florence Kugonza
(F)
Eva Laker
(E)
Tonny Luggya
(T)
Andrew Lule
(A)
Abdu Musubire
(A)
Rhona Muyise
(R)
Carol Olivie Namujju
(CO)
Jane Francis Ndyetukira
(JF)
Laura Nsangi
(L)
Michael Okirworth
(M)
Joshua Rhein
(J)
Morris K Rutakingirwa
(MK)
Alisat Sadiq
(A)
Kenneth Ssebambulidde
(K)
Kiiza Tadeo
(K)
Asmus Tukundane
(A)
Leo Atwine
(L)
Peter Buzaare
(P)
Muganzi Collins
(M)
Ninsima Emily
(N)
Christine Inyakuwa
(C)
Samson Kariisa
(S)
James Mwesigye
(J)
Simpson Nuwamanya
(S)
Ankunda Rodgers
(A)
Joan Rukundo
(J)
Irene Rwomushana
(I)
Mike Ssemusu
(M)
Gavin Stead
(G)
Kathyrn Boyd
(K)
Secrecy Gondo
(S)
Prosper Kufa
(P)
Edward Makaha
(E)
Colombus Moyo
(C)
Takudzwa Mtisi
(T)
Shepherd Mudzinga
(S)
Constantine Mutata
(C)
Taddy Mwarumba
(T)
Tawanda Zinyandu
(T)
Alexandre Alanio
(A)
Francoise Dromer
(F)
Olivier Lortholary
(O)
Aude Sturny-Leclere
(A)
Philippa Griffin
(P)
Sophia Hafeez
(S)
Angela Loyse
(A)
Erik van Widenfelt
(E)
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests TSH was the recipient of an investigator award to his institution from Gilead Sciences; speaker fees from Pfizer and Gilead Sciences; and serves as an adviser for F2G. JNJ and GM both declare speaker fees from Gilead Sciences. All other authors declare no competing interests.
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