3.8 Article

Soluble Programmed Death-Ligand 1 (sPD-L1) is Elevated in Aggressive Prostate Cancer Disease Among African Men

期刊

ONCOLOGY AND THERAPY
卷 10, 期 1, 页码 185-193

出版社

SPRINGER
DOI: 10.1007/s40487-022-00184-6

关键词

Immune checkpoint inhibitors; Immunotherapy; Prostate cancer; sPD-1; sPD-L1

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资金

  1. African Development bank under Uganda Cancer Institute [P-Z1-IB0-024]
  2. Office of the Director, National Institutes of Health (OD)
  3. National Institute of Neurological Disorders and Stroke (NINDS)
  4. National Heart, Lung, And Blood Institute (NHLBI)
  5. Fogarty International Center (FIC)
  6. National Institute on Minority Health and Health Disparities (NIMHD) [D43TW010132]
  7. Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID) [D43TW010132]
  8. National Institute of Dental & Craniofacial Research (NIDCR)

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The study found significant differences in plasma concentrations of PD-L1 and PD-1 between prostate cancer cases and normal healthy controls, with elevated levels of PD-L1 significantly associated with higher Gleason scores among patients with prostate cancer. This suggests that elevated PD-L1 levels could serve as a prognostic marker for assessing patients and selecting suitable candidates for anti-PD-L1 immunotherapy.
Introduction: Programmed death 1 (PD-1)/programmed death-ligand 1 (PD-L1)-targeted immunotherapies have become a new mode of treatment for several tumours; however, there is limited evidence on the expression and prognostic value of PD-1/PD-L1 in prostate cancer, especially in African men. Methods: Plasma concentrations of PD-L1/PD-1 were assessed using enzyme-linked immunosorbent assay in patients with prostate cancer and normal healthy controls at the Uganda Cancer Institute. The associations between plasma PD-L1/PD-1 concentration levels and serum prostate-specific antigen (PSA) levels, Gleason scores, age, and body mass index (BMI) were determined. Results: We found significant differences in the median plasma concentrations of PD-L1 and PD-1 immune checkpoint molecules between prostate cancer cases and normal healthy controls of 0.285 vs 0.035 (p = 0.001) and 0.596 vs 0.355 (p = 0.017), respectively. We found no significant association between age, serum PSA levels, BMI and Gleason scores, and PD-1 among patients with prostate cancer and controls. However, elevated levels of PD-L1 were significantly associated with higher Gleason scores among patients with prostate cancer (p = 0.014). Conclusions: Elevated PD-L1 levels were statistically significantly linked to high Gleason scores. These results may guide clinicians in assessing the prognosis of patients individually and selecting patients who will be suitable candidates for anti-PD-L1 immunotherapy.

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