Evidence map›Paper›PMID 39543506›Full record

ArticleBMC cancer2024

Clinical characteristics and survival of patients with de novo metastatic prostate cancer treated with androgen deprivation therapy and taxane-based chemotherapy in Uganda: a retrospective study.

Alex Bakenga, Barbra Natukunda, Fred Okuku, Kelvin Roland Mubiru, Edward Kakungulu, Eddy Kyagulanyi, Derrick Bary Abila, Jackson Orem

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Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Alex BakengaDepartment of Medical Oncology and Hematology, Uganda Cancer Institute, Kampala, Uganda. alex.bakenga@uci.or.ug.
Barbra NatukundaDepartment of Medical Oncology and Hematology, Uganda Cancer Institute, Kampala, Uganda.
Fred OkukuDepartment of Medical Oncology and Hematology, Uganda Cancer Institute, Kampala, Uganda.
Kelvin Roland MubiruDepartment of Statistics, Hutchinson Cancer Research Center, Kampala, Uganda.
Edward KakunguluDepartment of Surgical Oncology, Uganda Cancer Institute, Kampala, Uganda.
Eddy KyagulanyiCollege of Health Sciences, Makerere University, Kampala, Uganda.
Derrick Bary AbilaUganda Child Cancer Foundation, Kampala, Uganda.
Jackson OremDepartment of Medical Oncology and Hematology, Uganda Cancer Institute, Kampala, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer is the second most common cancer among men worldwide. Mortality is highest among patients in resource-limited settings (RLS), in part due to late-stage disease. Among patients with metastatic prostate cancer (mPCa), studies have shown significant improvement in overall survival with the use of androgen deprivation therapy (ADT) and taxane-based chemotherapy. However, outcome data among patients treated with chemo-endocrine therapy are scarce in many resource-limited settings. The aim of this study was to determine the clinical characteristics and 5-year overall survival (OS) of patients with de novo mPCa treated at the Uganda Cancer Institute (UCI).

methodsA retrospective chart review study was conducted between 2015 and 2019, and the data of patients with histologically confirmed prostate cancer and radiological evidence of metastasis were reviewed. Sample size was estimated for Cox Proportion Hazard regression. Data on clinical and laboratory characteristics, overall survival, and predictors of survival were extracted. P < 0.05 was considered to indicate statistical significance.

resultsA total of 300 patients were enrolled over the 5-year study period. The median age was 68 (IQR 61.5-74) years. At presentation, lower urinary tract symptoms were reported in nearly all patients (96.7%, n = 290), median total prostate specific antigen (PSA) was 414.75 ng/ml and 40% (n = 120) of patients had grade 5 histological scores. In addition to receiving ADT, majority of patients (70.3%, n = 211) received at least 6 cycles of chemotherapy. Overall survival at one year was 92.4% (95% CI: 88.6-94.9%), but it declined to 45.2% (95% CI: 36.8-53.2%) at 5 years. A high Gleason score, the presence of visceral metastasis and receiving less than 6 cycles of chemotherapy were predictors of poor outcomes.

conclusionPatients with de novo mPCa in Uganda present with high histologic grades and high baseline Prostate Specific Antigen (PSA) levels but have improved 5-year overall survival with a combination of chemotherapy and ADT as a first-line treatment. We recommend interventions to reduce late presentation and prospective studies to evaluate treatment efficacy in this population.

Indexed as

Androgen AntagonistsProstatic NeoplasmsTaxoidsAgedAntineoplastic Combined Chemotherapy ProtocolsBridged-Ring CompoundsHumansMaleMiddle AgedNeoplasm MetastasisProstate-Specific AntigenRetrospective StudiesSurvival RateUgandaAndrogen AntagonistsBridged-Ring CompoundsProstate-Specific AntigentaxaneTaxoidsAndrogen deprivation therapyChemotherapyMetastasisProstate cancer

Identifiers

PMID39543506
PMCPMC11566626

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