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Case Report: Response to ipilimumab and nivolumab in a patient with adrenocortical carcinoma

BACKGROUND: Adrenocortical carcinoma (ACC) is a rare malignancy with limited treatment options. The evidence for the use of immunotherapy in ACC has been conflicting, with overall response rates ranging from 6 – 33%. CASE PRESENTATION: We describe the case of a 32 year old patient who was initially...

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Detalles Bibliográficos
Autores principales: Charles, Rebecca, Madhu, Divine, Powles, Alexander, Boyde, Adam, Hughes, Owen, Kumar, Nagappan, Moorcraft, Sing Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516602/
https://www.ncbi.nlm.nih.gov/pubmed/37746287
http://dx.doi.org/10.3389/fonc.2023.1242560
Descripción
Sumario:BACKGROUND: Adrenocortical carcinoma (ACC) is a rare malignancy with limited treatment options. The evidence for the use of immunotherapy in ACC has been conflicting, with overall response rates ranging from 6 – 33%. CASE PRESENTATION: We describe the case of a 32 year old patient who was initially thought to have an inoperable clear cell renal cell carcinoma and was treated with immunotherapy with ipilimumab and nivolumab. The patient had an excellent partial response to treatment. Further work-up prior to consideration of surgery demonstrated that the tumour was an ACC, rather than a renal cancer. She had a right adrenalectomy and right hepatectomy, achieving an R0 resection and remains disease-free one year after surgery. CONCLUSION: This case illustrates the challenge of diagnosing ACC, and that doublet immunotherapy with ipilimumab and nivolumab can have significant clinical efficacy in ACC.