The cost effectiveness of treating Burkitt lymphoma in Uganda.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 06 2019
Historique:
received: 11 06 2018
revised: 12 10 2018
accepted: 17 10 2018
pubmed: 7 3 2019
medline: 23 2 2020
entrez: 7 3 2019
Statut: ppublish

Résumé

Perceptions of high cost and resource intensity remain political barriers to the prioritization of childhood cancer treatment programs in many low- and middle-income countries (LMICs). Little knowledge exists of the actual cost and cost-effectiveness of such programs. To improve outcomes for children with Burkitt lymphoma (BL), the most common childhood cancer in Africa, the Uganda Cancer Institute implemented a comprehensive BL treatment program in 2012. We undertook an economic evaluation of the program to ascertain the cost-effectiveness of BL therapy in a specific LIC setting. We compared the treatment of BL to usual care in a cohort of 122 patients treated between 2012 and 2014. Costs included variable, fixed, and family costs. Our primary measure of effectiveness was overall survival (OS). Patient outcomes were determined through prospective capture and retrospective chart abstraction. The cost per disability-adjusted life-year (DALY) averted was calculated using the World Health Organization's Choosing Interventions That Are Cost-Effective (WHO-CHOICE) methodology. The 2-year OS with treatment was 55% (95% CI, 45% to 64%). The cost per DALY averted in the treatment group was US$97 (Int$301). Cumulative estimate of national DALYs averted through treatment was 8607 years, and the total national annual cost of treatment was US$834,879 (Int$2,590,845). The cost of BL treatment fell well within WHO-CHOICE cost-effectiveness thresholds. The ratio of cost per DALY averted to per capita gross domestic product was 0.14, reflecting a very cost-effective intervention. This study demonstrates that treating BL with locally tailored protocols is very cost-effective by international standards. Studies of this kind will furnish crucial evidence to help policymakers prioritize the allocation of LMIC health system resources among noncommunicable diseases, including childhood cancer.

Sections du résumé

BACKGROUND
Perceptions of high cost and resource intensity remain political barriers to the prioritization of childhood cancer treatment programs in many low- and middle-income countries (LMICs). Little knowledge exists of the actual cost and cost-effectiveness of such programs. To improve outcomes for children with Burkitt lymphoma (BL), the most common childhood cancer in Africa, the Uganda Cancer Institute implemented a comprehensive BL treatment program in 2012. We undertook an economic evaluation of the program to ascertain the cost-effectiveness of BL therapy in a specific LIC setting.
METHODS
We compared the treatment of BL to usual care in a cohort of 122 patients treated between 2012 and 2014. Costs included variable, fixed, and family costs. Our primary measure of effectiveness was overall survival (OS). Patient outcomes were determined through prospective capture and retrospective chart abstraction. The cost per disability-adjusted life-year (DALY) averted was calculated using the World Health Organization's Choosing Interventions That Are Cost-Effective (WHO-CHOICE) methodology.
RESULTS
The 2-year OS with treatment was 55% (95% CI, 45% to 64%). The cost per DALY averted in the treatment group was US$97 (Int$301). Cumulative estimate of national DALYs averted through treatment was 8607 years, and the total national annual cost of treatment was US$834,879 (Int$2,590,845). The cost of BL treatment fell well within WHO-CHOICE cost-effectiveness thresholds. The ratio of cost per DALY averted to per capita gross domestic product was 0.14, reflecting a very cost-effective intervention.
CONCLUSION
This study demonstrates that treating BL with locally tailored protocols is very cost-effective by international standards. Studies of this kind will furnish crucial evidence to help policymakers prioritize the allocation of LMIC health system resources among noncommunicable diseases, including childhood cancer.

Identifiants

pubmed: 30840316
doi: 10.1002/cncr.32006
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1918-1928

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 American Cancer Society.

Auteurs

Avram E Denburg (AE)

The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Nazeefah Laher (N)

The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Wellesley Institute, Toronto, Ontario, Canada.

Innocent Mutyaba (I)

Uganda Cancer Institute, Makerere University, Kampala, Uganda.
Fred Hutchinson Cancer Research Center, Seattle Children's Hospital, Seattle, Washington.

Suzanne McGoldrick (S)

Fred Hutchinson Cancer Research Center, Seattle Children's Hospital, Seattle, Washington.

Joyce Kambugu (J)

Uganda Cancer Institute, Makerere University, Kampala, Uganda.

Erica Sessle (E)

PATH, Seattle, Washington.

Jackson Orem (J)

Uganda Cancer Institute, Makerere University, Kampala, Uganda.
Fred Hutchinson Cancer Research Center, Seattle Children's Hospital, Seattle, Washington.

Corey Casper (C)

Fred Hutchinson Cancer Research Center, Seattle Children's Hospital, Seattle, Washington.
Infectious Disease Research Institute, University of Washington School of Medicine, Seattle, Washington.

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