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Sipuleucel-T (Provenge)

Sipuleucel-T (Provenge) is a cellular vaccine approved by the FDA in 2010 — the first therapeutic cancer vaccine to reach the market. It is used in metastatic prostate cancer that no longer responds to hormone therapy and causes few or no symptoms. The NCI classifies it as a dendritic cell vaccine: every course is manufactured individually from the patient's own immune cells.

How it works

The patient's white blood cells are collected in a procedure similar to blood donation (leukapheresis). In the laboratory, the antigen-presenting cells among them are cultured with a protein that couples a prostate cancer antigen — prostatic acid phosphatase (PAP), found on most prostate cancer cells — to an immune-stimulating factor (GM-CSF). The activated cells are then returned to the patient by infusion; a full course consists of three such cycles, roughly two weeks apart. Back in the body, the activated cells act as instructors: they present the prostate antigen to T cells and prompt them to seek out and attack cancer cells that carry it. Typical side effects are flu-like — fever, chills, fatigue, muscle and joint aches; the NCI also lists rare but serious events, including severe allergic reactions and stroke.

Used in

Prostate C61

cellular immunotherapy option in selected metastatic castration-resistant cases (approved in the US)

Sources

  1. NCI – Cancer Treatment Vaccines ↗
  2. NCI – Sipuleucel-T (drug information) ↗