Efficacy of PARP inhibitor therapy after targeted BRAF/MEK failure in advanced melanoma
Modern advancements in targeted therapy and immunotherapy have significantly improved survival outcomes for advanced melanoma; however, there remains a need for novel approaches to overcome disease progression and treatment resistance. In recent years, PARPi therapy has shown great promise both as a single regimen and in combination with other therapeutics in melanoma. Here, we describe three unique cases of advanced BRAF V600 mutated melanoma that progressed on targeted BRAF/MEK agents that subsequently exhibited partial to near-complete responses to combinatory PARPi and BRAF/MEK inhibitors. This highlights both a potential synergy underlying this combinatory approach and its efficacy as a treatment option for patients with advanced melanoma refractory to targeted and/or immunotherapies. Prospective clinical trials are needed to explore this synergic effect in larger melanoma cohorts to investigate this combination for treating refractory advanced melanoma.
Authors
- Omar H. Butt (ORCID: https://orcid.org/0000-0003-2252-3673)
- Jordan Phillipps (ORCID: https://orcid.org/0000-0002-9156-3567)
- Tolulope Adeyelu (ORCID: https://orcid.org/0000-0003-0615-0731)
- Andrew Elliott (ORCID: https://orcid.org/0000-0001-8494-8031)
- Ari M. Vanderwalde (ORCID: https://orcid.org/0000-0002-6842-2563)
- Farah Abdulla (ORCID: https://orcid.org/0000-0002-3455-7566)
- George Ansstas (ORCID: https://orcid.org/0000-0002-7178-8777)
- Renée Morecroft (ORCID: https://orcid.org/0009-0003-9333-1123)
- George Nassief (ORCID: https://orcid.org/0009-0000-4271-7868)
- Soohyung Park (ORCID: https://orcid.org/0000-0001-8463-2002)
- Alice Zhou
Institutions
- Washington University in St. Louis (US)
- University of California San Diego (US)
- Caris Life Sciences (United States) (US)
- Saint Louis University (US)
Publication Details
- Journal
- npj Precision Oncology
- Published
- 2024-09-05
- DOI
- https://doi.org/10.1038/s41698-024-00684-w
- Citations
- 14
- Primary Topic
- Melanoma and MAPK Pathways
- Type
- article
- Field-Weighted Citation Impact
- 3.27
Funders
- Natera