Feasibility and Safety of Implementing Volumetric Arc Therapy (VMAT) for Pediatric Craniospinal Irradiation in a Low-Middle-Income Region: The Nigerian Experience.


Journal

Advances in radiation oncology
ISSN: 2452-1094
Titre abrégé: Adv Radiat Oncol
Pays: United States
ID NLM: 101677247

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 24 05 2023
accepted: 19 07 2023
medline: 26 2 2024
pubmed: 26 2 2024
entrez: 26 2 2024
Statut: epublish

Résumé

Volumetric modulated arc therapy (VMAT) is a relatively new treatment technique in sub-Saharan Africa. Although craniospinal irradiation (CSI) in the pediatric population has been practiced in Nigeria for many years, the use of VMAT to deliver this treatment is previously undocumented. We reviewed the first set of patients to undergo CSI at a cancer center in Nigeria, detailing the treatment technique, the progress experienced, dose statistics achieved, treatment toxicities, and cancer outcomes to date. This was a prospective case series of 5 children with histologically diagnosed cancers requiring CSI whose parents consented to the study. They were recruited at evaluation and followed through the process of their therapy. Toxicity was monitored at weekly review appointments using the Common Terminology Criteria for Adverse Events version 5.0. Follow-up of the children will continue in the long-term effects clinic. Five patients with a median age of 6 were recruited. Diagnoses were intracranial germ cell tumor (n = 2), medulloblastoma (n = 1), pineoblastoma (n = 1), and ependymoma (n = 1). For all patients, a dose of 36.0 Gy in 1.8 Gy daily fractions was prescribed to the entire neuraxis. A subsequent boost of 18 Gy (n = 4) to 19.8 Gy (n = 1) in 10 daily fractions to the primary tumor bed (n = 2) and posterior fossa (n = 2) was delivered. Four patients had chemotherapy before, during, or after radiation therapy. No patient experienced grade 3 or greater toxicity. Our results indicate great progress has been made in the delivery of CSI in Nigeria, demonstrating tolerable acute side effects using VMAT. This series suggests the feasibility of implementing VMAT technology in low- or middle-income countries. Additional follow-up will be needed to determine whether survival rates and chronic toxicity rates are similar to those reported in the literature.

Identifiants

pubmed: 38405304
doi: 10.1016/j.adro.2023.101325
pii: S2452-1094(23)00153-7
pmc: PMC10885594
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101325

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Adedayo Joseph (A)

NSIA-LUTH Cancer Center, Lagos University Teaching Hospital, Lagos, Nigeria.

Adeseye Akinsete (A)

Department of Pediatrics, College of Medicine, University of Lagos, Lagos, Nigeria.

Samuel Adeneye (S)

NSIA-LUTH Cancer Center, Lagos University Teaching Hospital, Lagos, Nigeria.
Department of Radiation Biology, Radiotherapy and Radiodiagnosis, College of Medicine, University of Lagos, Lagos, Nigeria.

Onyinye Balogun (O)

Department of Radiation Oncology, Weill Cornell Medicine, New York, New York.

Opeyemi Awofeso (O)

Psychosocial Oncology & Palliative Care, Dana Farber Cancer Institute, Boston, Massachusetts.

Aishat Oladipo (A)

NSIA-LUTH Cancer Center, Lagos University Teaching Hospital, Lagos, Nigeria.

Azeezat Ajose (A)

NSIA-LUTH Cancer Center, Lagos University Teaching Hospital, Lagos, Nigeria.

Ibrahim Elhamamsi (I)

NSIA-LUTH Cancer Center, Lagos University Teaching Hospital, Lagos, Nigeria.

Kenneth Merrell (K)

Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.

Wilfred Ngwa (W)

Sidney Kimmel Comprehensive Cancer Center, School of Medicine, Johns Hopkins University, Baltimore, Maryland.

David Puthoff (D)

Office of Research and Sponsored Programs, Marshfield Clinic Research Institute, Marshfield Clinic Health System, Marshfield, Wisconsin.

Abdul R Shour (AR)

Cancer Care and Research Center, Marshfield Clinic Research Institute, Marshfield Clinic Health System, Marshfield, Wisconsin.

Adedayo Onitilo (A)

Cancer Care and Research Center, Marshfield Clinic Research Institute, Marshfield Clinic Health System, Marshfield, Wisconsin.
Department of Oncology, Cancer Care and Research Center, Marshfield Clinic Health System, Marshfield, Wisconsin.

Classifications MeSH