Advances in cancer therapies have improved oncologic outcomes but can
potentially expose patients to risk of cardiovascular toxicity. While left
ventricular (LV) dysfunction is a well-known cardiotoxicity of cancer therapy.
Pulmonary hypertension (PH) and right ventricular (RV) dysfunction are seen with
several cancer therapies, including alkylating agents, tyrosine kinase inhibitors
(TKIs), and immunotherapy, and are associated with significant morbidity and
mortality. Awareness and recognition of cancer therapy-associated PH and RV
dysfunction is critical to identify underlying etiologies and institute the
appropriate therapy. However, gaps exist in the current literature on the
epidemiology of PH and RV dysfunction in cancer, underlying pathophysiology and
optimal management strategies.