TABLE I.
Treatment | Pathway | Currently Used in Practice? | Currently in Prospective Clinical Trials? | Strengths | Weaknesses |
---|---|---|---|---|---|
Cidofovir | Viral DNA replication | Yes | No | Safe for repeat administration | Unclear clinical benefit, no induction of HPV immunity |
Celecoxib | COX-2 inhibitor | No | No | Targets mitogenic signaling | No clinical benefit, no induction of HPV immunity |
I-3-C | Viral DNA replication | Yes | No | Likely safe for long-term use | Unclear clinical benefit, no induction of HPV immunity |
Bevacizumab | Angiogenesis and vessel stability | Yes | No | Can induce rapid regression of lesions | Nephrotoxicity when used systemically, no induction of HPV immunity |
Gardasil | Induces humoral immunity | Yes | No | May increase intersurgery interval | Does not induce T cell immunity |
Immune checkpoint blockade | Induces cellular immunity | Yes | Yes | May unleash existing anti-HPV immunity | Risk of immune-related adverse events |
Therapeutic vaccines | Induces cellular immunity | No | Yes | May induce new anti-HPV immunity | Unknown |
HPV = human papillomavirus; I-3-C = indole-3-carbinol; COX-2 = cyclooxygenase-2; T cell = T-lymphocyte.