Rapid disease progression in patient with mismatch-repair deficiency pituitary ACTH-secreting adenoma treated with checkpoint inhibitor pembrolizumab.


Journal

Anti-cancer drugs
ISSN: 1473-5741
Titre abrégé: Anticancer Drugs
Pays: England
ID NLM: 9100823

Informations de publication

Date de publication:
02 2020
Historique:
pubmed: 9 11 2019
medline: 2 2 2021
entrez: 9 11 2019
Statut: ppublish

Résumé

Secreting pituitary adenomas are tumors for which few treatment options are available, including surgical treatment and management of hormonal imbalance due to altered pituitary secretion. In case of inoperable relapse, radiotherapy or chemotherapeutic treatment can be considered; the effectiveness of these treatments, however, remains limited. In the immunotherapy era, it is necessary to select patients who can benefit from immunotherapeutic treatment. Mismatch repair deficiency is strongly associated with responsiveness to anti-PD-1 in other cancers and can be detected using immunohistochemistry for MLH1, MSH2, MHS6, and PMS2. In this case report, we report a case of rapid disease progression to pembrolizumab in a patient with a MMRd pituitary adrenocorticotropic hormone (ACTH)-secreting adenoma. For the best of our knowledge, we described for the first time, a poor efficacy of pembrolizumab in a patient with ACTH-secreting pituitary adenoma having mismatch repair deficiency probably caused by high levels of cortisol in this patient. Prospective study should be performed to assess the activity of immune checkpoint inhibitor alone or in association with temozolomide in this subsetting of pituitary adenomas.

Identifiants

pubmed: 31702999
doi: 10.1097/CAD.0000000000000856
pii: 00001813-202002000-00014
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
pembrolizumab DPT0O3T46P

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

199-204

Références

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Auteurs

Mario Caccese (M)

Department of Oncology, Medical Oncology 1, Veneto Institute of Oncology IOV-IRCCS.
Clinical and Experimental Oncology and Immunology PhD program, Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua.

Mattia Barbot (M)

Department of Medicine DIMED, Endocrinology Unit - University of Padua.

Filippo Ceccato (F)

Department of Medicine DIMED, Endocrinology Unit - University of Padua.

Marta Padovan (M)

Department of Oncology, Medical Oncology 1, Veneto Institute of Oncology IOV-IRCCS.

Marina Paola Gardiman (MP)

Surgical Pathology Unit, Department of Medicine (DIMED), University Hospital of Padua.

Matteo Fassan (M)

Surgical Pathology Unit, Department of Medicine (DIMED), University Hospital of Padua.

Luca Denaro (L)

Accademic Neurosurgery, Department of Neurosciences, University of Padua, Medical School.

Enzo Emanuelli (E)

Department of Neuroscience, Institute of Otorhinolaryngology, University of Padua, Padua, Italy.

Domenico D'Avella (D)

Accademic Neurosurgery, Department of Neurosciences, University of Padua, Medical School.

Carla Scaroni (C)

Department of Medicine DIMED, Endocrinology Unit - University of Padua.

Vittorina Zagonel (V)

Department of Oncology, Medical Oncology 1, Veneto Institute of Oncology IOV-IRCCS.

Giuseppe Lombardi (G)

Department of Oncology, Medical Oncology 1, Veneto Institute of Oncology IOV-IRCCS.

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