Advances in Vulvar Cancer Biology and Management

R Rania Chehade (Queen's University, Kingston, ON, Canada) K Katarzyna J. Jerzak (Odette Cancer Centre, Sunnybrook Health Sciences Centre, University of Toronto, Toronto) F Farideh Tavanger (Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, ON, Canada) A Anna Plotkin (Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada) L Lilian T. Gien (Division of Gynecological Oncology, Odette Cancer Centre, Sunnybrook Health Sciences Research Centre, Toronto, ON, Canada) E Eric Leung (Sunnybrook Health Sciencies, Toronto, ON, Canada) H Helen Mackay (Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada)

Abstract

PURPOSE Vulvar squamous cell carcinoma (VSCC), a rare gynecologic malignancy, has been rising in incidence. Molecular classification on the basis of human papilloma virus (HPV) and tumor protein 53 (p53) status has identified three clinically distinct subtypes, but we still treat all VSCCs the same. Here, we review molecular classification of VSCC, outline treatment landscape, and highlight potential for targeted therapies in advanced VSCC. DESIGN We conducted a comprehensive review of the literature on treatment of advanced VSCC with particular focus on the implications of molecular stratification on the basis of HPV and p53 status on the treatment landscape of advanced VSCC. RESULTS Incorporation of HPV and p53 status in locoregional treatment decision making has the potential to advise (de)escalation strategies. The role of immunotherapy, alone and in combination, requires further exploration particularly earlier in the course of the disease. In advanced stages, potential for targeted therapies in VSCCs include inhibitors of vascular endothelial growth factor, endothelial growth factor receptor, cell cycle, and DNA damage response, particularly in HPV-negative (HPV–) VSCCs. Targeting the phosphoinositide 3 kinase/mammalian target of rapamycin pathway is attractive in HPV-positive and HPV–/p53 wildtype VSCCs. Trials incorporating antibody-drug conjugates (eg, trophoblast cell-surface antigen 2, human epidermal growth factor receptor 2) should be considered, and basket trials in perineal squamous cell cancers are warranted. Preclinical models are limited and should be expanded to inform trial design. CONCLUSION Like other rare cancers, vulvar cancer lags behind in the identification and optimization of precision medicine strategies. Molecular-based preclinical models and rationally designed clinical trials, incorporating high-quality translational studies, are urgently required. These trials will require international collaboration to ensure feasibility and improvement of outcomes for women diagnosed with this disease.

Article Details

Volume / Issue Vol. 43, Issue 1
Published January 01, 2025
Pages 89-100
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (7)

R

Rania Chehade

Queen's University, Kingston, ON, Canada

K

Katarzyna J. Jerzak

Odette Cancer Centre, Sunnybrook Health Sciences Centre, University of Toronto, Toronto

F

Farideh Tavanger

Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, ON, Canada

A

Anna Plotkin

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada

L

Lilian T. Gien

Division of Gynecological Oncology, Odette Cancer Centre, Sunnybrook Health Sciences Research Centre, Toronto, ON, Canada

E

Eric Leung

Sunnybrook Health Sciencies, Toronto, ON, Canada

H

Helen Mackay

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada