Prospective Observational Study on Moderate Hypofractionated Radiotherapy for Localized Prostate Cancer in Rwanda: Acute Toxicity in Patients

Felix Sinzabakira*, W D Heemsbergen, Pacifique Mugenzi, A Diane Ndoli, Theoneste Maniragaba, Claire Umubyeyi, Fidel Rubagumya, Emmanuel Mutabazi, Luca Incrocci

*Corresponding author for this work

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Abstract

PURPOSE Moderate hypofractionation (MHF) offers logistical and financial advantages, and has become standard in Western countries but not yet in Africa. This study assessed GI and genitourinary (GU) acute toxicity in Rwandan men undergoing MHF (20 3 3 Gy) treatment. MATERIALS Since 2021, patients with prostate cancer at the Rwanda Cancer Centre have AND METHODS been informed about the study on MHF treatment and could participate by signing an informed consent. The study included patients with confirmed prostate adenocarcinoma (any T, any prostate-specific antigen any Gleason score, N0M0), excluding those with inflammatory bowel disease, previous pelvic irradiation, or previous prostatectomy. Participants received 20 fractions of 3 Gy over 4 weeks using the volumetric modulated arc radiotherapy (RT) technique with a 6 megavoltage linear accelerator. GI and GU acute toxicity was evaluated at week 2, at the end of RT, and 3 months after treatment using the Radiation Therapy Oncology Group (RTOG) acute toxicity grading system. RESULTS Fifty consecutive patients with localized prostate cancer were included. The median patient age was 70 years. Most patients (86%) had high-risk disease and 94% received androgen-deprivation therapy. The cost and treatment time were reduced by 50%. The distribution of maximum acute RTOG toxicity scores were for GI 10% grade 0, 70% grade 1, 20% grade 2, 0% grade 3, and for GU scores were 0%, 40%, 54%, and 6%, respectively. By 3 months, RT symptoms had returned to baseline levels for most patients. CONCLUSION MHF (20 3 3 Gy) was well tolerated in men treated for prostate cancer in Rwanda, showing that MHF is feasible in an African setting. However, further research on acute and late toxicity for more patients is warranted.

Original languageEnglish
Article numbere2400311
JournalJCO Global Oncology
Volume10
DOIs
Publication statusPublished - 20 Dec 2024

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© 2024 by American Society of Clinical Oncology.

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