Survival of children with endemic Burkitt lymphoma in a prospective clinical care project in Uganda.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
09 2019
Historique:
received: 25 07 2018
revised: 10 04 2019
accepted: 26 04 2019
pubmed: 4 6 2019
medline: 23 1 2020
entrez: 4 6 2019
Statut: ppublish

Résumé

"Endemic" Burkitt lymphoma (BL) is a common childhood cancer in Africa. Social and treatment factors may contribute to poor survival. With the aim of improving BL outcomes in Uganda, we undertook a comprehensive project (BL Project) that provided diagnostic support, access to standard chemotherapy, nutritional evaluations, and case management. We evaluated survival of children with BL in the context of the project. Patients followed by the BL Project who consented to research were enrolled in this study. Children with a pathology diagnosis consistent with BL were eligible. Data were collected prospectively. First-line chemotherapy generally consisted of six cycles of cyclophosphamide, vincristine, low-dose methotrexate (COM). We used Kaplan-Meier and Cox regression analyses to evaluate factors associated with overall survival (OS). Between July 2012 and June 2017, 341 patients with suspected BL presented to the BL Project. One hundred eighty patients with a pathology-based diagnosis were included in this study. The median age was seven years (interquartile range, 5-9), 74% lived ≥100 km from the Uganda Cancer Institute, 61% had late-stage disease, 84% had ECOG performance status < 3, 63% reported B-symptoms, and 22% showed neurologic symptoms. Fewer than 10% abandoned therapy. The four-year OS rate was 44% (95% CI, 36%-53%). In a multivariate model, ECOG status was significantly associated with mortality. The BL Project reduced effects of lacking supportive care and oncology resources, and allowed patients from Uganda to receive curative intent therapy with minimal loss to follow-up. Nonetheless, OS remains unacceptably low. Improved therapeutic approaches to endemic BL are urgently needed in Africa.

Identifiants

pubmed: 31157502
doi: 10.1002/pbc.27813
doi:

Substances chimiques

Vincristine 5J49Q6B70F
Cyclophosphamide 8N3DW7272P
Methotrexate YL5FZ2Y5U1

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e27813

Subventions

Organisme : NICHD NIH HHS
ID : F31 HD101149
Pays : United States
Organisme : NIH HHS
ID : U54 CA190146
Pays : United States
Organisme : NIH HHS
ID : P30 CA015704
Pays : United States

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Suzanne M McGoldrick (SM)

Fred Hutchinson Cancer Research Center, Seattle, Washington.

Innocent Mutyaba (I)

Hutchinson Centre Research Institute, Kampala, Uganda.

Scott V Adams (SV)

Fred Hutchinson Cancer Research Center, Seattle, Washington.

Anna Larsen (A)

Fred Hutchinson Cancer Research Center, Seattle, Washington.

Elizabeth M Krantz (EM)

Fred Hutchinson Cancer Research Center, Seattle, Washington.

Constance Namirembe (C)

Hutchinson Centre Research Institute, Kampala, Uganda.

Peter Mooka (P)

Hutchinson Centre Research Institute, Kampala, Uganda.

Susan Nabakooza (S)

Hutchinson Centre Research Institute, Kampala, Uganda.

Mariam Ndagire (M)

Hutchinson Centre Research Institute, Kampala, Uganda.

Kelvin Mubiru (K)

Hutchinson Centre Research Institute, Kampala, Uganda.

Martin Nabwana (M)

Hutchinson Centre Research Institute, Kampala, Uganda.

Rose Nankinga (R)

Hutchinson Centre Research Institute, Kampala, Uganda.

Sarah Gerdts (S)

Fred Hutchinson Cancer Research Center, Seattle, Washington.

Cristin Gordon-Maclean (C)

Seattle Children's Hospital, Seattle, Washington.

Fadhil Geriga (F)

Uganda Cancer Institute, Kampala, Uganda.

Abrahams Omoding (A)

Uganda Cancer Institute, Kampala, Uganda.

Erica Sessle (E)

PATH, Seattle, Washington.

Joyce Kambugu (J)

Uganda Cancer Institute, Kampala, Uganda.

Thomas S Uldrick (TS)

Fred Hutchinson Cancer Research Center, Seattle, Washington.

Jackson Orem (J)

Uganda Cancer Institute, Kampala, Uganda.

Corey Casper (C)

Departments of Medicine and Global Health, Infectious Disease Research Institute and the University of Washington, Seattle, Washington.

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Classifications MeSH