AI Article Synopsis

  • * Diagnosing DAC is challenging since traditional methods, such as serum PSA tests and multiparametric MRI, might not effectively identify it, and its optimal localized treatment is still unclear due to its rarity.
  • * After treatment, DAC often recurs with metastases even at low PSA levels, and while some systemic therapies for high-risk PAC show promise, they have limited effectiveness for DAC; ongoing genomic studies could help uncover potential new treatments.

Article Abstract

Ductal adenocarcinoma (DAC) is the most common variant histological subtype of prostate carcinoma and has an aggressive clinical course. DAC is usually characterized and treated as high-risk prostatic acinar adenocarcinoma (PAC). However, DAC has a different biology to that of acinar disease, which often poses a challenge for both diagnosis and management. DAC can be difficult to identify using conventional diagnostic modalities such as serum PSA levels and multiparametric MRI, and the optimal management for localized DAC is unknown owing to the rarity of the disease. Following definitive therapy for localized disease with radical prostatectomy or radiotherapy, the majority of DACs recur with visceral metastases at low PSA levels. Various systemic therapies that have been shown to be effective in high-risk PAC have limited use in treating DAC. Although current understanding of the biology of DAC is limited, genomic analyses have provided insights into the pathology behind its aggressive behaviour and potential future therapeutic targets.

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Source
http://dx.doi.org/10.1038/s41585-021-00447-3DOI Listing

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