reviewPharmaceuticalsOct 20, 2022GOLD OA

[177Lu]Lu-PSMA-617 (PluvictoTM): The First FDA-Approved Radiotherapeutical for Treatment of Prostate Cancer

German Cancer Research Center · Heidelberg University · +2 more institutions

PubMed
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Abstract

In March 2022, [177Lu]Lu-PSMA-617 (PluvictoTM) was approved by the FDA for the treatment of prostate cancer patients. Until now, the approval has been limited to patients with PSMA-positive metastatic castration-resistant prostate cancer who have previously received other therapy options (such as inhibition of the androgen receptor pathway and taxane-based chemotherapy). [177Lu]Lu-PSMA-617, which combines a PSMA-specific peptidomimetic with a therapeutical radionuclide, is used in a radioligand therapy that selectively delivers ionizing radiation to tumor cells, causing their death, while sparing the surrounding healthy tissue. In numerous clinical trials, the efficacy of [177Lu]Lu-PSMA-617 was demonstrated.

Citation impact

275
total citations
FWCI
36.56
Percentile
100%
References
48
Citations per year

Authors

2

Topics & keywords

Keywords
  • Medicine
  • Prostate cancer
  • Taxane
  • Radioligand
  • Oncology
  • Radionuclide therapy
  • Internal medicine
  • Clinical trial
UN Sustainable Development Goals
  • Good health and well-being
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