Cancer Vaccine
A cancer vaccine is designed to prevent infections caused by cancer-causing
viruses, treat existing cancer, or prevent cancer development in high-risk
individuals. Vaccines that treat existing cancer are termed therapeutic
cancer vaccines.
Certain cancers, like cervical and some liver cancers, result from viral
infections, and vaccines like the HPV and Hepatitis B vaccines can prevent
these cancers. However, these antiviral vaccines are not further discussed
here. Similarly, cancers partly caused by bacterial infections, such as
stomach cancer linked to Helicobacter pylori, are not addressed in this
article.
Researchers are exploring vaccines targeting existing cancers. Some propose
that cancer cells typically emerge and are eliminated by the healthy immune
system, with cancer forming when immune defenses fail.
One approach involves isolating proteins from cancer cells and immunizing
cancer patients against these proteins, aiming to provoke an immune response
that destroys cancer cells. Therapeutic cancer vaccines are under
development for breast, lung, colon, skin, kidney, prostate, and other
cancers.
In a phase III trial involving follicular lymphoma, BiovaxID extended
remission to 44.2 months compared to 30.6 months for the control group, as
reported at the June 2009 meeting of the American Society of Clinical
Oncology.
On April 14, 2009, Dendreon Corporation announced positive results from
their Phase III trial of Provenge, a cancer vaccine for prostate cancer,
showing increased survival rates. Provenge received FDA approval for
advanced prostate cancer treatment on April 29, 2010, sparking interest in
this therapy.
Another therapeutic approach involves generating an immune response within
the patient. BioVex Inc, Woburn, MA, has used this method successfully with
OncoVEX GM-CSF. This modified herpes simplex virus selectively replicates in
tumor tissue and expresses the immune-stimulating protein GM-CSF. Phase 3
trials in melanoma and head and neck cancer have shown promising efficacy
after strong results in Phase 2 trials.
Effective cancer vaccines must overcome several challenges. They target
tumor-specific antigens distinct from self-proteins. Selection of
appropriate adjuvants, molecules that activate immune responses, is crucial.
Currently, only Bacillus Calmette-Guérin (BCG), aluminum-based salts, and a
squalene-oil-water emulsion are approved for clinical use. The vaccine
should also provide long-term memory to prevent tumor recurrence, possibly
by activating both the innate and adaptive immune systems for total tumor
elimination.
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